Item | Value |
---|---|
geneid | 3356 |
ensemblid | ENSG00000102468.11 |
hgncid | 5293 |
symbol | HTR2A |
name | 5-hydroxytryptamine receptor 2A |
refseq_nuc | NM_000621.5 |
refseq_prot | NP_000612.1 |
ensembl_nuc | ENST00000542664.4 |
ensembl_prot | ENSP00000437737.1 |
mane_status | MANE Select |
chr | chr13 |
start | 46831546 |
end | 46897053 |
strand | - |
ver | v1.2 |
region | chr13:46831546-46897053 |
region5000 | chr13:46826546-46902053 |
regionname0 | HTR2A_chr13_46831546_46897053 |
regionname5000 | HTR2A_chr13_46826546_46902053 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 471 | 311 | 73 | 57 | 139 | 11 | 29 | 110 | HTR2A_chr13_46826546_46902053 | HTR2A | MDILC others(466): Show |
chr13 | 46826546 | 46902053 |
a0002 | 0/0 | 471 | 18 | 7 | 3 | 1 | 2 | 5 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | MDILC others(466): Show |
chr13 | 46826546 | 46902053 |
a0003 | 0/0 | 471 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | MDILC others(466): Show |
chr13 | 46826546 | 46902053 |
a0004 | 0/0 | 471 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | MDILC others(466): Show |
chr13 | 46826546 | 46902053 |
a0005 | 0/0 | 471 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | MDILC others(466): Show |
chr13 | 46826546 | 46902053 |
a0006 | 0/0 | 471 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | MDILC others(466): Show |
chr13 | 46826546 | 46902053 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1413 | 183 | 35 | 41 | 79 | 6 | 20 | HTR2A_chr13_46826546_46902053 | HTR2A | ATGGA others(1408): Show |
chr13 | 46826546 | 46902053 | ||
a0001c0002 | 0/0 | 1413 | 119 | 32 | 14 | 60 | 5 | 8 | HTR2A_chr13_46826546_46902053 | HTR2A | ATGGA others(1408): Show |
chr13 | 46826546 | 46902053 | ||
a0001c0005 | 0/0 | 1413 | 6 | 6 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | ATGGA others(1408): Show |
chr13 | 46826546 | 46902053 | ||
a0001c0010 | 0/0 | 1413 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | ATGGA others(1408): Show |
chr13 | 46826546 | 46902053 | ||
a0001c0012 | 0/0 | 1413 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | ATGGA others(1408): Show |
chr13 | 46826546 | 46902053 | ||
a0001c0013 | 0/0 | 1413 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | ATGGA others(1408): Show |
chr13 | 46826546 | 46902053 | ||
a0002c0003 | 0/0 | 1413 | 10 | 7 | 2 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | ATGGA others(1408): Show |
chr13 | 46826546 | 46902053 | ||
a0002c0004 | 0/0 | 1413 | 8 | 0 | 1 | 1 | 2 | 4 | HTR2A_chr13_46826546_46902053 | HTR2A | ATGGA others(1408): Show |
chr13 | 46826546 | 46902053 | ||
a0003c0006 | 0/0 | 1413 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | ATGGA others(1408): Show |
chr13 | 46826546 | 46902053 | ||
a0003c0007 | 0/0 | 1413 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | ATGGA others(1408): Show |
chr13 | 46826546 | 46902053 | ||
a0004c0009 | 0/0 | 1413 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | ATGGA others(1408): Show |
chr13 | 46826546 | 46902053 | ||
a0005c0008 | 0/0 | 1413 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | ATGGA others(1408): Show |
chr13 | 46826546 | 46902053 | ||
a0006c0011 | 0/0 | 1413 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | ATGGA others(1408): Show |
chr13 | 46826546 | 46902053 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5415 | 109 | 4 | 28 | 58 | 5 | 13 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0002 | 0/0 | 5416 | 23 | 0 | 2 | 18 | 0 | 3 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0004 | 1/0 | 5415 | 10 | 3 | 5 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0005 | 0/0 | 5416 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0006 | 0/0 | 5416 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0008 | 0/0 | 5415 | 3 | 2 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0009 | 0/0 | 5416 | 3 | 0 | 2 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0010 | 0/0 | 5416 | 3 | 2 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0011 | 0/0 | 5415 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0012 | 0/0 | 5416 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0014 | 0/0 | 5415 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0016 | 0/0 | 5415 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0017 | 0/0 | 5416 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0019 | 0/0 | 5416 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0020 | 0/0 | 5416 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0021 | 0/0 | 5415 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0023 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0024 | 0/0 | 5415 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0025 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0035 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0037 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0041 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0042 | 0/0 | 5415 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0043 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0044 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0045 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0046 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0047 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0049 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0050 | 0/0 | 5416 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0001t0051 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0002t0001 | 0/0 | 5415 | 77 | 14 | 13 | 40 | 5 | 5 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0002t0002 | 0/0 | 5416 | 20 | 4 | 0 | 15 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0002t0005 | 0/0 | 5416 | 6 | 6 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0002t0006 | 0/0 | 5416 | 4 | 3 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0002t0012 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0002t0022 | 0/0 | 5415 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0002t0027 | 0/0 | 5416 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0002t0028 | 0/0 | 5417 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5412): Show |
chr13 | 46826546 | 46902053 |
a0001c0002t0029 | 0/0 | 5416 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0002t0030 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0002t0032 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0002t0033 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0002t0036 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0002t0038 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0002t0039 | 0/0 | 5415 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0002t0040 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0005t0007 | 0/0 | 5416 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0005t0015 | 0/0 | 5416 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0005t0026 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0005t0048 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0010t0034 | 0/0 | 5415 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0001c0012t0031 | 0/0 | 5416 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0001c0013t0001 | 0/0 | 5415 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0002c0003t0003 | 0/0 | 5417 | 7 | 5 | 1 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5412): Show |
chr13 | 46826546 | 46902053 |
a0002c0003t0013 | 0/0 | 5416 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0002c0003t0018 | 0/0 | 5417 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5412): Show |
chr13 | 46826546 | 46902053 |
a0002c0004t0003 | 0/0 | 5417 | 7 | 0 | 0 | 1 | 2 | 4 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5412): Show |
chr13 | 46826546 | 46902053 |
a0002c0004t0013 | 0/0 | 5416 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0003c0006t0001 | 0/0 | 5415 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0003c0007t0007 | 0/0 | 5416 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0004c0009t0017 | 0/0 | 5416 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
a0005c0008t0001 | 0/0 | 5415 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5410): Show |
chr13 | 46826546 | 46902053 |
a0006c0011t0002 | 0/0 | 5416 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | AGAGA others(5411): Show |
chr13 | 46826546 | 46902053 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0031 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0004g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0004g0313 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0008g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0008g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0009g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0009g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0010g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0010g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0011g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0012g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0014g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0014g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0016g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0016g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0017g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0019g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0019g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0020g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0020g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0021g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0021g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0023g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0024g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0025g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0035g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0037g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0041g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0042g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0043g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0044g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0045g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0046g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0047g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0049g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0050g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0001t0051g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0006g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0012g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0022g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0027g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0028g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0029g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0030g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0032g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0033g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0036g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0038g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0039g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0002t0040g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0005t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0005t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0005t0015g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0005t0026g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0005t0048g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0010t0034g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0012t0031g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0001c0013t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0002c0003t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0002c0003t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0002c0003t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0002c0003t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0002c0003t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0002c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0002c0003t0013g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0002c0003t0018g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0002c0003t0018g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0002c0004t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0002c0004t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0002c0004t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0002c0004t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0002c0004t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0002c0004t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0002c0004t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0002c0004t0013g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0003c0006t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0003c0006t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0003c0007t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0003c0007t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0004c0009t0017g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0005c0008t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
a0006c0011t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0230 | EUR | GBR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00099 | hp2 | a0004 | c0009 | t0017 | g0290 | EUR | GBR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00140 | hp1 | a0001 | c0001 | t0004 | g0295 | EUR | GBR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00140 | hp2 | a0002 | c0004 | t0003 | g0229 | EUR | GBR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | FIN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00280 | hp2 | a0002 | c0004 | t0003 | g0171 | EUR | FIN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0243 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0247 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | CHS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00639 | hp2 | a0001 | c0001 | t0042 | g0282 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00738 | hp2 | a0002 | c0003 | t0003 | g0152 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01070 | hp1 | a0001 | c0012 | t0031 | g0185 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01074 | hp1 | a0001 | c0001 | t0006 | g0161 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01081 | hp2 | a0002 | c0003 | t0013 | g0144 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0176 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01109 | hp1 | a0001 | c0002 | t0006 | g0183 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01109 | hp2 | a0001 | c0001 | t0010 | g0115 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0293 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01175 | hp1 | a0002 | c0004 | t0013 | g0203 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0222 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0258 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0302 | AMR | PUR | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0221 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01256 | hp1 | a0001 | c0001 | t0009 | g0013 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0198 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01258 | hp2 | a0001 | c0001 | t0009 | g0013 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0191 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01358 | hp2 | a0001 | c0001 | t0004 | g0292 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0170 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01496 | hp2 | a0001 | c0013 | t0001 | g0268 | AMR | CLM | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0195 | EUR | IBS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | IBS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0187 | EUR | IBS | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0272 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01884 | hp2 | a0001 | c0002 | t0012 | g0264 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01891 | hp1 | a0001 | c0002 | t0005 | g0261 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01891 | hp2 | a0001 | c0001 | t0014 | g0142 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0209 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01975 | hp2 | a0001 | c0001 | t0050 | g0312 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0294 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0296 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02015 | hp1 | a0001 | c0002 | t0029 | g0213 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02055 | hp1 | a0001 | c0002 | t0005 | g0260 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02056 | hp1 | a0002 | c0004 | t0003 | g0201 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0274 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CDX | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | CDX | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | CDX | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | CDX | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0307 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0081 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02280 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02280 | hp2 | a0001 | c0002 | t0033 | g0273 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02451 | hp1 | a0001 | c0001 | t0047 | g0308 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02451 | hp2 | a0001 | c0002 | t0005 | g0263 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02572 | hp1 | a0001 | c0002 | t0006 | g0277 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02572 | hp2 | a0001 | c0001 | t0044 | g0285 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02602 | hp1 | a0002 | c0004 | t0003 | g0206 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02602 | hp2 | a0005 | c0008 | t0001 | g0030 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02615 | hp1 | a0001 | c0001 | t0021 | g0305 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0256 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02630 | hp1 | a0001 | c0001 | t0021 | g0304 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02630 | hp2 | a0001 | c0001 | t0014 | g0136 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02647 | hp1 | a0001 | c0001 | t0019 | g0311 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0184 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02683 | hp1 | a0002 | c0004 | t0003 | g0200 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02683 | hp2 | a0002 | c0004 | t0003 | g0192 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0227 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02698 | hp2 | a0001 | c0010 | t0034 | g0123 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02717 | hp1 | a0003 | c0007 | t0007 | g0147 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02717 | hp2 | a0001 | c0001 | t0010 | g0129 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02723 | hp1 | a0003 | c0007 | t0007 | g0148 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02723 | hp2 | a0001 | c0001 | t0046 | g0288 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02809 | hp1 | a0001 | c0001 | t0019 | g0300 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0177 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0275 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02886 | hp2 | a0003 | c0006 | t0001 | g0146 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02895 | hp1 | a0001 | c0001 | t0011 | g0004 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02896 | hp1 | a0001 | c0002 | t0005 | g0276 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02897 | hp1 | a0001 | c0001 | t0011 | g0004 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02922 | hp1 | a0001 | c0001 | t0016 | g0284 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0301 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02965 | hp1 | a0001 | c0002 | t0005 | g0259 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0251 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02970 | hp2 | a0001 | c0001 | t0025 | g0025 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02976 | hp1 | a0003 | c0006 | t0001 | g0145 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02976 | hp2 | a0001 | c0001 | t0023 | g0022 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03041 | hp1 | a0001 | c0001 | t0049 | g0291 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03041 | hp2 | a0001 | c0002 | t0006 | g0262 | AFR | GWD | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03098 | hp1 | a0001 | c0001 | t0020 | g0314 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03098 | hp2 | a0001 | c0005 | t0007 | g0133 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03130 | hp2 | a0002 | c0003 | t0003 | g0131 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03139 | hp1 | a0001 | c0001 | t0020 | g0310 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03139 | hp2 | a0001 | c0005 | t0015 | g0020 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03225 | hp1 | a0001 | c0002 | t0006 | g0265 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03225 | hp2 | a0001 | c0002 | t0038 | g0173 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03239 | hp2 | a0001 | c0002 | t0039 | g0279 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03453 | hp1 | a0001 | c0001 | t0043 | g0283 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0255 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0271 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03486 | hp2 | a0001 | c0001 | t0010 | g0080 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03490 | hp1 | a0001 | c0001 | t0008 | g0023 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03492 | hp1 | a0001 | c0001 | t0024 | g0024 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03516 | hp1 | a0001 | c0005 | t0015 | g0020 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0151 | AFR | ESN | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03579 | hp1 | a0001 | c0005 | t0026 | g0026 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03579 | hp2 | a0002 | c0003 | t0018 | g0309 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0194 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03688 | hp2 | a0001 | c0001 | t0009 | g0157 | SAS | STU | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03704 | hp1 | a0001 | c0002 | t0022 | g0021 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0205 | SAS | PJL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03831 | hp1 | a0002 | c0004 | t0003 | g0220 | SAS | BEB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | BEB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03834 | hp2 | a0001 | c0001 | t0017 | g0297 | SAS | BEB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | BEB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG04115 | hp1 | a0002 | c0003 | t0003 | g0154 | SAS | STU | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG04115 | hp2 | a0006 | c0011 | t0002 | g0232 | SAS | STU | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0214 | SAS | BEB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0202 | SAS | BEB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0218 | SAS | STU | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | STU | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | STU | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18522 | hp1 | a0001 | c0001 | t0041 | g0281 | AFR | YRI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0298 | AFR | YRI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | CHB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18906 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | YRI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0254 | AFR | YRI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18952 | hp1 | a0001 | c0002 | t0040 | g0280 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0266 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18957 | hp2 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18967 | hp1 | a0001 | c0001 | t0037 | g0091 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18974 | hp1 | a0001 | c0002 | t0002 | g0270 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18978 | hp2 | a0001 | c0002 | t0028 | g0168 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19004 | hp2 | a0001 | c0002 | t0027 | g0244 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19010 | hp1 | a0001 | c0002 | t0036 | g0225 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19030 | hp1 | a0002 | c0003 | t0003 | g0007 | AFR | LWK | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19030 | hp2 | a0001 | c0001 | t0016 | g0286 | AFR | LWK | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19043 | hp1 | a0002 | c0003 | t0003 | g0007 | AFR | LWK | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19043 | hp2 | a0002 | c0003 | t0003 | g0141 | AFR | LWK | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19076 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19078 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19078 | hp2 | a0001 | c0001 | t0012 | g0110 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19084 | hp1 | a0001 | c0001 | t0035 | g0079 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19084 | hp2 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19240 | hp1 | a0001 | c0005 | t0048 | g0303 | AFR | YRI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | YRI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0224 | AFR | ASW | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA20129 | hp2 | a0001 | c0005 | t0007 | g0134 | AFR | ASW | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | TSI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | TSI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0204 | EUR | TSI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0231 | EUR | TSI | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02109 | hp1 | a0002 | c0003 | t0018 | g0306 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0278 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02486 | hp1 | a0001 | c0002 | t0005 | g0028 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | ACB | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03471 | hp1 | a0002 | c0003 | t0003 | g0035 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG03471 | hp2 | a0001 | c0001 | t0045 | g0287 | AFR | MSL | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | USA | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
HG06807 | hp2 | a0001 | c0002 | t0032 | g0172 | AFR | USA | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA21309 | hp1 | a0001 | c0001 | t0051 | g0299 | AFR | LWK | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
NA21309 | hp2 | a0001 | c0002 | t0030 | g0178 | AFR | LWK | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0031 | REF | REF | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0313 | REF | REF | HTR2A_chr13_46826546_46902053 | HTR2A | chr13 | 46826546 | 46902053 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:46834895 | G | A | 1 | a0006 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.1358C>T | p.Ser453Phe | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2066/5415 | 1358/1416 | 453/471 | chr13 | 46834895 | |||
chr13:46834899 | G | A | 1 | a0002 | 18 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(15): Show |
missense_variant | MODERATE | c.1354C>T | p.His452Tyr | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2062/5415 | 1354/1416 | 452/471 | chr13 | 46834899 | |||
chr13:46892414 | T | C | 1 | a0003 | 4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
missense_variant | MODERATE | c.589A>G | p.Ile197Val | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/4 | 1297/5415 | 589/1416 | 197/471 | chr13 | 46892414 | |||
chr13:46895833 | G | T | 1 | a0004 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.74C>A | p.Thr25Asn | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | 782/5415 | 74/1416 | 25/471 | chr13 | 46895833 | |||
chr13:46895872 | C | T | 1 | a0005 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.35G>A | p.Ser12Asn | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | 743/5415 | 35/1416 | 12/471 | chr13 | 46895872 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:46835014 | T | A | 3 | a0001c0005 a0001c0012 a0003c0007 |
9 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
synonymous_variant | LOW | c.1239A>T | p.Thr413Thr | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1947/5415 | 1239/1416 | 413/471 | chr13 | 46835014 | |||
chr13:46835359 | C | T | 1 | a0001c0010 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.894G>A | p.Ser298Ser | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1602/5415 | 894/1416 | 298/471 | chr13 | 46835359 | |||
chr13:46892487 | G | A | 1 | a0001c0013 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.516C>T | p.Asp172Asp | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/4 | 1224/5415 | 516/1416 | 172/471 | chr13 | 46892487 | |||
chr13:46895805 | G | A | 6 | a0001c0002 a0001c0012 a0001c0013 others(3): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
synonymous_variant | LOW | c.102C>T | p.Ser34Ser | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | 810/5415 | 102/1416 | 34/471 | chr13 | 46895805 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:46831587 | C | G | 1 | a0001c0002t0032 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3250G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 3250 | chr13 | 46831587 | ||||||
chr13:46831601 | G | A | 2 | a0001c0001t0017 a0004c0009t0017 |
2 | HG00099.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3236C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 3236 | chr13 | 46831601 | ||||||
chr13:46831605 | C | T | 1 | a0001c0002t0032 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3232G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 3232 | chr13 | 46831605 | ||||||
chr13:46831699 | T | A | 3 | a0001c0001t0006 a0001c0001t0050 a0001c0002t0006 |
6 | HG01074.hp1 HG01109.hp1 HG01975.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3138A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 3138 | chr13 | 46831699 | ||||||
chr13:46831840 | T | C | 1 | a0001c0010t0034 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2997A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2997 | chr13 | 46831840 | ||||||
chr13:46832277 | A | C | 1 | a0001c0012t0031 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2560T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2560 | chr13 | 46832277 | ||||||
chr13:46832277 | A | G | 5 | a0001c0005t0007 a0001c0005t0015 a0001c0005t0026 others(2): Show |
8 | HG02717.hp1 HG02723.hp1 HG03098.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2560T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2560 | chr13 | 46832277 | ||||||
chr13:46832493 | A | T | 9 | a0001c0001t0045 a0001c0001t0047 a0001c0002t0030 others(6): Show |
22 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2344T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2344 | chr13 | 46832493 | ||||||
chr13:46832596 | T | C | 9 | a0001c0001t0045 a0001c0001t0047 a0001c0002t0030 others(6): Show |
22 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2241A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2241 | chr13 | 46832596 | ||||||
chr13:46832644 | T | C | 4 | a0001c0001t0045 a0001c0001t0047 a0001c0002t0030 others(1): Show |
4 | HG02451.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2193A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2193 | chr13 | 46832644 | ||||||
chr13:46832701 | T | C | 1 | a0001c0001t0035 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2136A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2136 | chr13 | 46832701 | ||||||
chr13:46832710 | C | T | 25 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0017 others(22): Show |
84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2127G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2127 | chr13 | 46832710 | ||||||
chr13:46832821 | C | T | 9 | a0001c0001t0045 a0001c0001t0047 a0001c0002t0030 others(6): Show |
22 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2016G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 2016 | chr13 | 46832821 | ||||||
chr13:46832900 | T | C | 4 | a0001c0001t0045 a0001c0001t0047 a0001c0002t0030 others(1): Show |
4 | HG02451.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1937A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1937 | chr13 | 46832900 | ||||||
chr13:46833066 | G | A | 4 | a0001c0001t0045 a0001c0001t0047 a0001c0002t0030 others(1): Show |
4 | HG02451.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1771C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1771 | chr13 | 46833066 | ||||||
chr13:46833295 | T | G | 10 | a0001c0001t0020 a0001c0001t0045 a0001c0001t0047 others(7): Show |
24 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1542A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1542 | chr13 | 46833295 | ||||||
chr13:46833327 | G | T | 6 | a0001c0005t0007 a0001c0005t0015 a0001c0005t0026 others(3): Show |
9 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1510C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1510 | chr13 | 46833327 | ||||||
chr13:46833329 | C | G | 2 | a0001c0001t0011 a0001c0001t0014 |
4 | HG01891.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1508G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1508 | chr13 | 46833329 | ||||||
chr13:46833357 | T | C | 2 | a0001c0001t0001 a0001c0010t0034 |
3 | HG02055.hp2 HG02698.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1480A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1480 | chr13 | 46833357 | ||||||
chr13:46833368 | C | CT | 8 | a0001c0001t0010 a0001c0001t0023 a0001c0001t0046 others(5): Show |
23 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1468dupA | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1468 | chr13 | 46833368 | ||||||
chr13:46833597 | C | A | 1 | a0001c0002t0036 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1240G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1240 | chr13 | 46833597 | ||||||
chr13:46833623 | C | T | 1 | a0001c0002t0033 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1214G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1214 | chr13 | 46833623 | ||||||
chr13:46833648 | G | A | 1 | a0001c0002t0032 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1189C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1189 | chr13 | 46833648 | ||||||
chr13:46833799 | T | C | 1 | a0001c0001t0037 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1038A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1038 | chr13 | 46833799 | ||||||
chr13:46833806 | C | T | 1 | a0001c0001t0009 | 3 | HG01256.hp1 HG01258.hp2 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1031G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1031 | chr13 | 46833806 | ||||||
chr13:46833807 | G | A | 1 | a0001c0002t0032 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1030C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 1030 | chr13 | 46833807 | ||||||
chr13:46834042 | A | G | 4 | a0001c0001t0045 a0001c0001t0047 a0001c0002t0030 others(1): Show |
4 | HG02451.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*795T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 795 | chr13 | 46834042 | ||||||
chr13:46834091 | G | A | 4 | a0001c0001t0045 a0001c0001t0047 a0001c0002t0030 others(1): Show |
4 | HG02451.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*746C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 746 | chr13 | 46834091 | ||||||
chr13:46834114 | C | G | 1 | a0001c0002t0027 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*723G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 723 | chr13 | 46834114 | ||||||
chr13:46834215 | T | C | 4 | a0001c0001t0045 a0001c0001t0047 a0001c0002t0030 others(1): Show |
4 | HG02451.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*622A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 622 | chr13 | 46834215 | ||||||
chr13:46834406 | C | T | 4 | a0001c0001t0045 a0001c0001t0047 a0001c0002t0030 others(1): Show |
4 | HG02451.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*431G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 431 | chr13 | 46834406 | ||||||
chr13:46834435 | T | G | 21 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(18): Show |
76 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*402A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 402 | chr13 | 46834435 | ||||||
chr13:46834716 | C | G | 11 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0017 others(8): Show |
54 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*121G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 121 | chr13 | 46834716 | ||||||
chr13:46834767 | A | AT | 36 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(33): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*69dupA | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 4/4 | 69 | chr13 | 46834767 | ||||||
chr13:46895924 | T | C | 1 | a0001c0002t0039 | 1 | HG03239.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-18A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | chr13 | 46895924 | |||||||
chr13:46895936 | T | A | 1 | a0001c0002t0040 | 1 | NA18952.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | 30 | chr13 | 46895936 | ||||||
chr13:46896131 | T | C | 1 | a0001c0001t0043 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-225A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | 225 | chr13 | 46896131 | ||||||
chr13:46896157 | C | G | 5 | a0001c0001t0016 a0001c0001t0044 a0001c0001t0045 others(2): Show |
7 | HG02572.hp2 HG02723.hp2 HG02922.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-251G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | 251 | chr13 | 46896157 | ||||||
chr13:46896158 | C | A | 3 | a0001c0001t0041 a0001c0001t0042 a0001c0001t0043 |
3 | HG00639.hp2 HG03453.hp1 NA18522.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-252G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | chr13 | 46896158 | |||||||
chr13:46896217 | C | T | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(40): Show |
296 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
5_prime_UTR_variant | MODIFIER | c.-311G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/4 | 311 | chr13 | 46896217 | ||||||
chr13:46896689 | C | T | 48 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(45): Show |
303 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
5_prime_UTR_variant | MODIFIER | c.-344G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/4 | 783 | chr13 | 46896689 | ||||||
chr13:46896789 | A | G | 2 | a0001c0001t0011 a0001c0005t0026 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-444T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/4 | 883 | chr13 | 46896789 | ||||||
chr13:46896888 | C | G | 1 | a0001c0001t0025 | 1 | HG02970.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-543G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/4 | chr13 | 46896888 | |||||||
chr13:46896912 | C | G | 1 | a0001c0001t0024 | 1 | HG03492.hp1 | 5_prime_UTR_variant | MODIFIER | c.-567G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/4 | 1006 | chr13 | 46896912 | ||||||
chr13:46896949 | C | T | 2 | a0001c0001t0008 a0001c0001t0023 |
4 | HG02280.hp1 HG02976.hp2 HG03490.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-604G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/4 | 1043 | chr13 | 46896949 | ||||||
chr13:46897032 | C | T | 1 | a0001c0002t0022 | 1 | HG03704.hp1 | 5_prime_UTR_variant | MODIFIER | c.-687G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/4 | 1126 | chr13 | 46897032 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:46835968 | T | A | 132 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0036 others(129): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.614-329A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46835968 | |||||||
chr13:46836190 | TA | T | 56 | a0001c0001t0002g0008 a0001c0001t0002g0037 a0001c0001t0002g0052 others(53): Show |
59 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.614-552delT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46836190 | |||||||
chr13:46836480 | A | G | 1 | a0001c0002t0033g0273 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.614-841T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46836480 | |||||||
chr13:46836563 | A | T | 1 | a0001c0002t0033g0273 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.614-924T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46836563 | |||||||
chr13:46836703 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.614-1064G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46836703 | |||||||
chr13:46836831 | T | C | 8 | a0001c0005t0007g0133 a0001c0005t0007g0134 a0001c0005t0015g0020 others(5): Show |
9 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.614-1192A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46836831 | |||||||
chr13:46836907 | A | C | 1 | a0001c0001t0016g0286 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.614-1268T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46836907 | |||||||
chr13:46837022 | C | G | 1 | a0001c0005t0026g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.614-1383G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837022 | |||||||
chr13:46837035 | G | T | 6 | a0001c0001t0010g0080 a0001c0001t0010g0115 a0001c0001t0010g0129 others(3): Show |
6 | HG01109.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-1396C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837035 | |||||||
chr13:46837072 | G | T | 6 | a0001c0001t0010g0080 a0001c0001t0010g0115 a0001c0001t0010g0129 others(3): Show |
6 | HG01109.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-1433C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837072 | |||||||
chr13:46837078 | G | A | 1 | a0001c0002t0005g0276 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.614-1439C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837078 | |||||||
chr13:46837432 | G | A | 4 | a0001c0001t0004g0301 a0001c0001t0008g0003 a0001c0002t0001g0256 others(1): Show |
5 | HG02280.hp1 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.614-1793C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837432 | |||||||
chr13:46837470 | A | G | 1 | a0001c0002t0001g0233 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.614-1831T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837470 | |||||||
chr13:46837526 | C | T | 81 | a0001c0001t0002g0008 a0001c0001t0002g0037 a0001c0001t0002g0052 others(78): Show |
86 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.614-1887G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837526 | |||||||
chr13:46837556 | G | A | 6 | a0001c0001t0010g0080 a0001c0001t0010g0115 a0001c0001t0010g0129 others(3): Show |
6 | HG01109.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-1917C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837556 | |||||||
chr13:46837850 | A | G | 248 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(245): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.614-2211T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837850 | |||||||
chr13:46837940 | T | C | 51 | a0001c0001t0002g0008 a0001c0001t0002g0037 a0001c0001t0002g0052 others(48): Show |
54 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.614-2301A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46837940 | |||||||
chr13:46838111 | G | C | 6 | a0001c0001t0010g0080 a0001c0001t0010g0115 a0001c0001t0010g0129 others(3): Show |
6 | HG01109.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-2472C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838111 | |||||||
chr13:46838317 | G | A | 1 | a0001c0002t0001g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.614-2678C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838317 | |||||||
chr13:46838606 | G | A | 87 | a0001c0001t0002g0008 a0001c0001t0002g0037 a0001c0001t0002g0052 others(84): Show |
92 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.614-2967C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838606 | |||||||
chr13:46838734 | C | A | 1 | a0001c0002t0001g0218 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.614-3095G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838734 | |||||||
chr13:46838977 | T | C | 7 | a0001c0005t0007g0133 a0001c0005t0007g0134 a0001c0005t0015g0020 others(4): Show |
8 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.614-3338A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838977 | |||||||
chr13:46838977 | T | TAAACACA others(3): Show |
1 | a0001c0001t0001g0101 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.614-3339_614-3338i others(12): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838977 | |||||||
chr13:46838977 | T | TAC | 6 | a0001c0001t0005g0081 a0001c0001t0019g0311 a0001c0001t0045g0287 others(3): Show |
6 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.614-3340_614-3339d others(4): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838977 | |||||||
chr13:46838977 | T | TACAC | 23 | a0001c0001t0004g0298 a0001c0001t0004g0301 a0001c0001t0005g0151 others(20): Show |
24 | HG01074.hp1 HG01109.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.614-3342_614-3339d others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838977 | |||||||
chr13:46838977 | T | TACACAC | 4 | a0001c0001t0021g0304 a0001c0002t0006g0265 a0001c0002t0038g0173 others(1): Show |
4 | HG02630.hp1 HG03225.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-3344_614-3339d others(8): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838977 | |||||||
chr13:46838977 | TAC | T | 116 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(113): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.614-3340_614-3339d others(4): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838977 | |||||||
chr13:46838977 | TACAC | T | 5 | a0001c0001t0002g0052 a0001c0001t0010g0080 a0001c0001t0010g0129 others(2): Show |
5 | HG02300.hp1 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.614-3342_614-3339d others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46838977 | |||||||
chr13:46839008 | A | C | 18 | a0001c0001t0010g0080 a0001c0001t0010g0129 a0001c0001t0023g0022 others(15): Show |
19 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.614-3369T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46839008 | |||||||
chr13:46839011 | C | T | 1 | a0001c0002t0040g0280 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.614-3372G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46839011 | |||||||
chr13:46839236 | T | C | 3 | a0001c0001t0001g0069 a0001c0002t0001g0193 a0001c0002t0029g0213 |
3 | HG02015.hp1 NA18961.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.614-3597A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46839236 | |||||||
chr13:46839423 | G | A | 1 | a0001c0001t0002g0064 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.614-3784C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46839423 | |||||||
chr13:46839751 | C | A | 1 | a0001c0001t0044g0285 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.614-4112G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46839751 | |||||||
chr13:46839823 | A | G | 1 | a0001c0002t0001g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.614-4184T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46839823 | |||||||
chr13:46839830 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.614-4191A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46839830 | |||||||
chr13:46840819 | T | C | 3 | a0001c0001t0045g0287 a0001c0001t0047g0308 a0001c0002t0030g0178 |
3 | HG02451.hp1 HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.614-5180A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46840819 | |||||||
chr13:46840827 | G | A | 1 | a0004c0009t0017g0290 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.614-5188C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46840827 | |||||||
chr13:46840866 | A | C | 153 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0036 others(150): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.614-5227T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46840866 | |||||||
chr13:46840985 | G | A | 8 | a0001c0005t0007g0133 a0001c0005t0007g0134 a0001c0005t0015g0020 others(5): Show |
9 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.614-5346C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46840985 | |||||||
chr13:46841027 | C | T | 8 | a0001c0005t0007g0133 a0001c0005t0007g0134 a0001c0005t0015g0020 others(5): Show |
9 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.614-5388G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46841027 | |||||||
chr13:46841141 | A | C | 32 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0036 others(29): Show |
35 | HG00099.hp1 HG00438.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.614-5502T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46841141 | |||||||
chr13:46841248 | C | T | 50 | a0001c0001t0002g0008 a0001c0001t0002g0037 a0001c0001t0002g0052 others(47): Show |
53 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.614-5609G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46841248 | |||||||
chr13:46841371 | T | C | 1 | a0001c0001t0001g0005 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.614-5732A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46841371 | |||||||
chr13:46841492 | A | G | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.614-5853T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46841492 | |||||||
chr13:46841566 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0004g0296 a0001c0002t0001g0191 |
3 | HG00735.hp2 HG01261.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.614-5927G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46841566 | |||||||
chr13:46841852 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.614-6213T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46841852 | |||||||
chr13:46841907 | C | G | 51 | a0001c0001t0002g0008 a0001c0001t0002g0037 a0001c0001t0002g0052 others(48): Show |
54 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.614-6268G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46841907 | |||||||
chr13:46842048 | C | T | 1 | a0001c0001t0005g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.614-6409G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842048 | |||||||
chr13:46842059 | T | A | 1 | a0001c0001t0047g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.614-6420A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842059 | |||||||
chr13:46842132 | T | G | 2 | a0001c0001t0001g0153 a0001c0001t0004g0292 |
2 | HG01358.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.614-6493A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842132 | |||||||
chr13:46842213 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.614-6574G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842213 | |||||||
chr13:46842251 | C | T | 84 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(81): Show |
87 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.614-6612G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842251 | |||||||
chr13:46842325 | T | C | 1 | a0001c0001t0035g0079 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.614-6686A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842325 | |||||||
chr13:46842495 | G | A | 1 | a0001c0001t0004g0302 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.614-6856C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842495 | |||||||
chr13:46842541 | C | T | 9 | a0001c0001t0010g0115 a0001c0005t0007g0133 a0001c0005t0007g0134 others(6): Show |
10 | HG01070.hp1 HG01109.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.614-6902G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842541 | |||||||
chr13:46842549 | T | C | 1 | a0001c0002t0032g0172 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.614-6910A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842549 | |||||||
chr13:46842577 | A | G | 34 | a0001c0001t0002g0037 a0001c0001t0002g0052 a0001c0001t0002g0054 others(31): Show |
35 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.614-6938T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842577 | |||||||
chr13:46842752 | G | A | 1 | a0001c0001t0016g0286 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.614-7113C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842752 | |||||||
chr13:46842903 | C | T | 2 | a0002c0003t0013g0144 a0002c0004t0013g0203 |
2 | HG01081.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.614-7264G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46842903 | |||||||
chr13:46843014 | T | C | 1 | a0001c0002t0022g0021 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.614-7375A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46843014 | |||||||
chr13:46843147 | G | T | 1 | a0003c0007t0007g0147 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.614-7508C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46843147 | |||||||
chr13:46843742 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.614-8103A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46843742 | |||||||
chr13:46843809 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0072 |
3 | NA19060.hp2 NA19067.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.614-8170C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46843809 | |||||||
chr13:46844001 | C | T | 2 | a0002c0004t0003g0171 a0002c0004t0003g0229 |
2 | HG00140.hp2 HG00280.hp2 |
intron_variant | MODIFIER | c.614-8362G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844001 | |||||||
chr13:46844051 | CCTT | C | 3 | a0001c0001t0010g0115 a0001c0001t0011g0004 a0001c0001t0014g0136 |
4 | HG01109.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-8415_614-8413d others(5): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844051 | |||||||
chr13:46844144 | T | C | 13 | a0001c0001t0010g0080 a0001c0001t0010g0129 a0001c0001t0023g0022 others(10): Show |
14 | HG01070.hp1 HG02717.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.614-8505A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844144 | |||||||
chr13:46844248 | G | A | 18 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0043 others(15): Show |
18 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.614-8609C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844248 | |||||||
chr13:46844311 | A | G | 1 | a0001c0002t0001g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.614-8672T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844311 | |||||||
chr13:46844408 | T | C | 24 | a0001c0001t0005g0081 a0001c0001t0005g0151 a0001c0001t0006g0161 others(21): Show |
24 | HG01074.hp1 HG01109.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.614-8769A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844408 | |||||||
chr13:46844509 | C | T | 1 | a0001c0002t0032g0172 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.614-8870G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844509 | |||||||
chr13:46844593 | C | A | 1 | a0001c0002t0001g0247 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.614-8954G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844593 | |||||||
chr13:46844694 | G | T | 1 | a0001c0001t0001g0126 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.614-9055C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844694 | |||||||
chr13:46844834 | G | C | 9 | a0001c0002t0001g0271 a0001c0005t0007g0133 a0001c0005t0007g0134 others(6): Show |
10 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.614-9195C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46844834 | |||||||
chr13:46845011 | CT | C | 85 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(82): Show |
88 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.614-9373delA | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845011 | |||||||
chr13:46845069 | A | G | 83 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(80): Show |
86 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.614-9430T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845069 | |||||||
chr13:46845147 | A | G | 9 | a0001c0002t0001g0271 a0001c0005t0007g0133 a0001c0005t0007g0134 others(6): Show |
10 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.614-9508T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845147 | |||||||
chr13:46845442 | A | G | 104 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(101): Show |
107 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.614-9803T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845442 | |||||||
chr13:46845577 | G | A | 1 | a0001c0001t0051g0299 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.614-9938C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845577 | |||||||
chr13:46845643 | C | CA | 80 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0082 others(77): Show |
87 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.614-10005dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845643 | |||||||
chr13:46845643 | C | CAA | 9 | a0001c0001t0001g0036 a0001c0001t0009g0157 a0001c0001t0016g0286 others(6): Show |
9 | HG00738.hp2 HG02165.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.614-10006_614-1000 others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845643 | |||||||
chr13:46845643 | CA | C | 87 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(84): Show |
91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.614-10005delT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845643 | |||||||
chr13:46845643 | CAA | C | 7 | a0001c0001t0001g0066 a0001c0001t0001g0078 a0001c0001t0001g0096 others(4): Show |
7 | HG00621.hp1 NA18939.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.614-10006_614-1000 others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845643 | |||||||
chr13:46845685 | G | T | 73 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0036 others(70): Show |
80 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.614-10046C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46845685 | |||||||
chr13:46846111 | A | G | 1 | a0001c0002t0001g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.614-10472T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846111 | |||||||
chr13:46846177 | T | C | 192 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(189): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.614-10538A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846177 | |||||||
chr13:46846277 | A | C | 81 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(78): Show |
84 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.614-10638T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846277 | |||||||
chr13:46846289 | C | G | 3 | a0001c0001t0001g0058 a0001c0001t0004g0296 a0001c0002t0001g0191 |
3 | HG00735.hp2 HG01261.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.614-10650G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846289 | |||||||
chr13:46846293 | A | G | 21 | a0001c0001t0001g0042 a0001c0001t0005g0081 a0001c0001t0005g0151 others(18): Show |
21 | HG00280.hp1 HG01074.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.614-10654T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846293 | |||||||
chr13:46846329 | T | C | 1 | a0001c0002t0002g0167 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.614-10690A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846329 | |||||||
chr13:46846650 | G | C | 1 | a0001c0001t0051g0299 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.614-11011C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846650 | |||||||
chr13:46846718 | G | A | 1 | a0001c0002t0001g0233 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.614-11079C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846718 | |||||||
chr13:46846848 | G | A | 80 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(77): Show |
83 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.614-11209C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46846848 | |||||||
chr13:46847088 | G | A | 84 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(81): Show |
88 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.614-11449C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46847088 | |||||||
chr13:46847131 | C | T | 165 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(162): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.614-11492G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46847131 | |||||||
chr13:46847159 | A | T | 10 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0004g0307 others(7): Show |
10 | HG00738.hp2 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.614-11520T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46847159 | |||||||
chr13:46847701 | C | T | 78 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(75): Show |
81 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.614-12062G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46847701 | |||||||
chr13:46847822 | G | A | 1 | a0001c0002t0001g0211 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.614-12183C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46847822 | |||||||
chr13:46848180 | A | G | 1 | a0001c0001t0047g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.614-12541T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46848180 | |||||||
chr13:46848321 | A | G | 1 | a0002c0003t0003g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.614-12682T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46848321 | |||||||
chr13:46848330 | A | G | 21 | a0001c0001t0005g0081 a0001c0001t0005g0151 a0001c0001t0006g0161 others(18): Show |
21 | HG01074.hp1 HG01109.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.614-12691T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46848330 | |||||||
chr13:46848499 | A | C | 8 | a0001c0005t0007g0133 a0001c0005t0007g0134 a0001c0005t0015g0020 others(5): Show |
9 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.614-12860T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46848499 | |||||||
chr13:46848862 | A | G | 1 | a0002c0003t0003g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.614-13223T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46848862 | |||||||
chr13:46848907 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0032 a0001c0001t0001g0050 others(1): Show |
5 | HG01255.hp2 HG01256.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.614-13268A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46848907 | |||||||
chr13:46848951 | T | C | 92 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0036 others(89): Show |
98 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.614-13312A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46848951 | |||||||
chr13:46848987 | T | C | 2 | a0001c0002t0001g0272 a0001c0002t0033g0273 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.614-13348A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46848987 | |||||||
chr13:46849100 | C | T | 1 | a0001c0002t0001g0195 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.614-13461G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849100 | |||||||
chr13:46849156 | C | T | 202 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(199): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.614-13517G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849156 | |||||||
chr13:46849198 | T | C | 2 | a0001c0001t0016g0284 a0001c0002t0001g0019 |
3 | HG02896.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.614-13559A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849198 | |||||||
chr13:46849256 | C | T | 1 | a0001c0001t0002g0100 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.614-13617G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849256 | |||||||
chr13:46849430 | A | T | 86 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0036 others(83): Show |
93 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.614-13791T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849430 | |||||||
chr13:46849457 | C | T | 86 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0036 others(83): Show |
93 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.614-13818G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849457 | |||||||
chr13:46849721 | A | G | 1 | a0001c0001t0004g0298 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.614-14082T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849721 | |||||||
chr13:46849744 | C | T | 5 | a0001c0005t0007g0133 a0001c0005t0015g0020 a0001c0005t0048g0303 others(2): Show |
6 | HG01070.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-14105G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849744 | |||||||
chr13:46849983 | A | G | 32 | a0001c0001t0001g0053 a0001c0001t0001g0077 a0001c0001t0001g0084 others(29): Show |
33 | HG00423.hp2 HG01074.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.614-14344T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849983 | |||||||
chr13:46849989 | G | A | 25 | a0001c0001t0004g0298 a0001c0001t0005g0081 a0001c0001t0014g0136 others(22): Show |
26 | HG01070.hp1 HG01891.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.614-14350C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46849989 | |||||||
chr13:46850158 | G | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(153): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.614-14519C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850158 | |||||||
chr13:46850208 | C | A | 1 | a0001c0002t0001g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.614-14569G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850208 | |||||||
chr13:46850243 | T | C | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.614-14604A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850243 | |||||||
chr13:46850250 | A | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(200): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.614-14611T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850250 | |||||||
chr13:46850630 | A | G | 1 | a0001c0002t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.614-14991T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850630 | |||||||
chr13:46850635 | C | T | 1 | a0001c0001t0047g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.614-14996G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850635 | |||||||
chr13:46850636 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.614-14997C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850636 | |||||||
chr13:46850674 | T | C | 7 | a0001c0001t0025g0025 a0001c0005t0007g0133 a0001c0005t0015g0020 others(4): Show |
8 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.614-15035A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850674 | |||||||
chr13:46850677 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(197): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.614-15038G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850677 | |||||||
chr13:46850714 | G | T | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.614-15075C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850714 | |||||||
chr13:46850761 | G | A | 7 | a0001c0001t0025g0025 a0001c0005t0007g0133 a0001c0005t0015g0020 others(4): Show |
8 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.614-15122C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850761 | |||||||
chr13:46850809 | C | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(152): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.614-15170G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850809 | |||||||
chr13:46850859 | T | A | 1 | a0001c0001t0001g0085 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.614-15220A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850859 | |||||||
chr13:46850912 | A | T | 1 | a0001c0001t0051g0299 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.614-15273T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850912 | |||||||
chr13:46850940 | C | G | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.614-15301G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46850940 | |||||||
chr13:46851110 | A | G | 22 | a0001c0001t0001g0153 a0001c0001t0004g0298 a0001c0001t0005g0081 others(19): Show |
22 | HG00738.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.614-15471T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46851110 | |||||||
chr13:46851115 | T | C | 1 | a0001c0002t0033g0273 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.614-15476A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46851115 | |||||||
chr13:46851715 | C | T | 1 | a0001c0002t0002g0202 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.614-16076G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46851715 | |||||||
chr13:46851806 | A | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0049 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.614-16167T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46851806 | |||||||
chr13:46851812 | C | T | 1 | a0001c0005t0007g0133 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.614-16173G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46851812 | |||||||
chr13:46851908 | A | G | 3 | a0001c0001t0010g0115 a0001c0001t0011g0004 a0001c0005t0026g0026 |
4 | HG01109.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-16269T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46851908 | |||||||
chr13:46851912 | A | T | 1 | a0001c0002t0001g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.614-16273T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46851912 | |||||||
chr13:46852018 | T | TGATTCAA others(9): Show |
7 | a0001c0001t0025g0025 a0001c0005t0007g0133 a0001c0005t0015g0020 others(4): Show |
8 | HG01070.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.614-16395_614-1638 others(20): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852018 | |||||||
chr13:46852130 | A | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
133 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.614-16491T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852130 | |||||||
chr13:46852176 | C | G | 1 | a0001c0002t0033g0273 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.614-16537G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852176 | |||||||
chr13:46852331 | T | G | 1 | a0001c0001t0047g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.614-16692A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852331 | |||||||
chr13:46852373 | G | T | 2 | a0001c0002t0001g0181 a0001c0002t0040g0280 |
2 | NA18952.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.614-16734C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852373 | |||||||
chr13:46852417 | G | A | 1 | a0001c0002t0001g0194 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.614-16778C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852417 | |||||||
chr13:46852527 | C | T | 3 | a0001c0001t0001g0085 a0001c0001t0001g0092 a0001c0001t0001g0094 |
3 | HG00438.hp1 NA18941.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.614-16888G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852527 | |||||||
chr13:46852587 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(149): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.614-16948T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852587 | |||||||
chr13:46852846 | A | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0049 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.614-17207T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852846 | |||||||
chr13:46852864 | T | C | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(301): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.614-17225A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852864 | |||||||
chr13:46852891 | A | C | 1 | a0001c0001t0001g0084 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.614-17252T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852891 | |||||||
chr13:46852910 | T | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(116): Show |
129 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.614-17271A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852910 | |||||||
chr13:46852968 | G | GT | 120 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(117): Show |
130 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.614-17330_614-1732 others(5): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852968 | |||||||
chr13:46852968 | GC | G | 3 | a0001c0001t0001g0127 a0001c0002t0001g0228 a0001c0002t0001g0236 |
3 | HG02165.hp2 NA18943.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.614-17330delG | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852968 | |||||||
chr13:46852969 | C | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(298): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.614-17330G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852969 | |||||||
chr13:46852998 | ATTC | A | 12 | a0001c0001t0001g0130 a0001c0001t0005g0151 a0001c0001t0016g0286 others(9): Show |
12 | HG00639.hp2 HG01109.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.614-17362_614-1736 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46852998 | |||||||
chr13:46853175 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.614-17536C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853175 | |||||||
chr13:46853209 | T | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(116): Show |
129 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.614-17570A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853209 | |||||||
chr13:46853377 | T | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(116): Show |
129 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.614-17738A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853377 | |||||||
chr13:46853491 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(116): Show |
129 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.614-17852T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853491 | |||||||
chr13:46853501 | T | C | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.614-17862A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853501 | |||||||
chr13:46853541 | T | C | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(301): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.614-17902A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853541 | |||||||
chr13:46853547 | G | C | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.614-17908C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853547 | |||||||
chr13:46853634 | C | G | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.614-17995G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853634 | |||||||
chr13:46853656 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(116): Show |
129 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.614-18017T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853656 | |||||||
chr13:46853785 | A | C | 22 | a0001c0001t0001g0153 a0001c0001t0004g0298 a0001c0001t0005g0081 others(19): Show |
22 | HG00738.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.614-18146T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853785 | |||||||
chr13:46853799 | C | A | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.614-18160G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46853799 | |||||||
chr13:46854046 | T | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(116): Show |
129 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.614-18407A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854046 | |||||||
chr13:46854061 | G | A | 1 | a0001c0001t0016g0286 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.614-18422C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854061 | |||||||
chr13:46854065 | C | T | 117 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(114): Show |
127 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.614-18426G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854065 | |||||||
chr13:46854113 | A | G | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(300): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.614-18474T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854113 | |||||||
chr13:46854252 | C | T | 1 | a0001c0002t0001g0271 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.614-18613G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854252 | |||||||
chr13:46854336 | A | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(181): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.614-18697T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854336 | |||||||
chr13:46854476 | T | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(116): Show |
129 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.614-18837A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854476 | |||||||
chr13:46854616 | G | T | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.614-18977C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854616 | |||||||
chr13:46854728 | A | G | 1 | a0001c0002t0033g0273 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.614-19089T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854728 | |||||||
chr13:46854936 | C | A | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.614-19297G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854936 | |||||||
chr13:46854948 | T | C | 3 | a0001c0001t0001g0149 a0001c0001t0004g0293 a0001c0002t0001g0223 |
3 | HG00639.hp1 HG01074.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.614-19309A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46854948 | |||||||
chr13:46855019 | T | C | 4 | a0001c0001t0020g0310 a0001c0001t0020g0314 a0001c0002t0002g0029 others(1): Show |
4 | HG02970.hp1 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-19380A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855019 | |||||||
chr13:46855092 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.614-19453T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855092 | |||||||
chr13:46855093 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(104): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.614-19454T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855093 | |||||||
chr13:46855162 | C | T | 3 | a0001c0001t0001g0042 a0001c0002t0001g0187 a0002c0003t0013g0144 |
3 | HG00280.hp1 HG01081.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.614-19523G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855162 | |||||||
chr13:46855163 | G | A | 1 | a0002c0003t0018g0309 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.614-19524C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855163 | |||||||
chr13:46855293 | G | A | 3 | a0001c0001t0014g0136 a0001c0002t0001g0271 a0001c0002t0033g0273 |
3 | HG02280.hp2 HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.614-19654C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855293 | |||||||
chr13:46855311 | T | C | 43 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0038 others(40): Show |
47 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.614-19672A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855311 | |||||||
chr13:46855348 | A | G | 1 | a0001c0002t0001g0019 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.614-19709T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855348 | |||||||
chr13:46855410 | T | C | 5 | a0001c0001t0020g0314 a0001c0002t0001g0177 a0001c0002t0001g0278 others(2): Show |
5 | HG02109.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.614-19771A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855410 | |||||||
chr13:46855436 | T | C | 1 | a0001c0010t0034g0123 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.614-19797A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855436 | |||||||
chr13:46855516 | G | C | 1 | a0001c0002t0002g0270 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.614-19877C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855516 | |||||||
chr13:46855542 | A | C | 3 | a0001c0001t0001g0061 a0001c0001t0004g0292 a0001c0002t0001g0204 |
3 | HG00741.hp2 HG01358.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.614-19903T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855542 | |||||||
chr13:46855634 | TA | T | 7 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0061 others(4): Show |
7 | HG00741.hp2 HG01192.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.614-19996delT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855634 | |||||||
chr13:46855635 | A | T | 1 | a0001c0001t0014g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.614-19996T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855635 | |||||||
chr13:46855657 | G | A | 1 | a0001c0005t0026g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.614-20018C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855657 | |||||||
chr13:46855732 | C | A | 1 | a0001c0002t0001g0221 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.614-20093G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855732 | |||||||
chr13:46855742 | A | G | 1 | a0001c0001t0002g0068 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.614-20103T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855742 | |||||||
chr13:46855837 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.614-20198C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46855837 | |||||||
chr13:46856128 | C | G | 67 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0056 others(64): Show |
72 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.614-20489G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856128 | |||||||
chr13:46856128 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.614-20489G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856128 | |||||||
chr13:46856141 | C | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0039 others(80): Show |
88 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.614-20502G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856141 | |||||||
chr13:46856177 | T | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0001t0001g0049 |
3 | HG01346.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.614-20538A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856177 | |||||||
chr13:46856180 | A | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(246): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.614-20541T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856180 | |||||||
chr13:46856231 | G | A | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(302): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.614-20592C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856231 | |||||||
chr13:46856344 | A | G | 146 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
155 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.614-20705T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856344 | |||||||
chr13:46856383 | T | C | 1 | a0001c0001t0001g0011 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.614-20744A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856383 | |||||||
chr13:46856394 | A | G | 6 | a0001c0001t0004g0302 a0001c0001t0020g0310 a0001c0001t0043g0283 others(3): Show |
6 | HG01243.hp2 HG02615.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.614-20755T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856394 | |||||||
chr13:46856467 | T | C | 18 | a0001c0001t0004g0292 a0001c0001t0004g0293 a0001c0001t0004g0296 others(15): Show |
19 | HG00099.hp2 HG01169.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.614-20828A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856467 | |||||||
chr13:46856471 | G | A | 4 | a0001c0002t0001g0255 a0001c0002t0001g0256 a0001c0002t0002g0184 others(1): Show |
4 | HG01109.hp1 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-20832C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856471 | |||||||
chr13:46856594 | T | TA | 18 | a0001c0001t0001g0135 a0001c0001t0004g0301 a0001c0001t0006g0161 others(15): Show |
19 | HG01074.hp1 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.614-20956dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856594 | |||||||
chr13:46856594 | TA | T | 7 | a0001c0001t0001g0116 a0001c0001t0005g0081 a0001c0001t0010g0080 others(4): Show |
7 | HG02155.hp1 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.614-20956delT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856594 | |||||||
chr13:46856625 | T | C | 1 | a0001c0002t0039g0279 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.614-20986A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856625 | |||||||
chr13:46856653 | G | A | 10 | a0001c0001t0004g0302 a0001c0001t0004g0307 a0001c0001t0019g0300 others(7): Show |
11 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.614-21014C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856653 | |||||||
chr13:46856666 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.614-21027A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856666 | |||||||
chr13:46856755 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.614-21116G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856755 | |||||||
chr13:46856849 | C | G | 1 | a0001c0001t0008g0023 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.614-21210G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856849 | |||||||
chr13:46856973 | G | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0039 others(29): Show |
37 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.614-21334C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856973 | |||||||
chr13:46856986 | C | T | 5 | a0001c0002t0001g0181 a0001c0002t0001g0234 a0001c0002t0002g0018 others(2): Show |
6 | NA18965.hp2 NA18969.hp2 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-21347G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46856986 | |||||||
chr13:46857100 | G | C | 4 | a0001c0002t0001g0255 a0001c0002t0001g0256 a0001c0002t0002g0184 others(1): Show |
4 | HG01109.hp1 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-21461C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857100 | |||||||
chr13:46857179 | A | G | 18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0034 others(15): Show |
21 | HG01070.hp1 HG01099.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.614-21540T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857179 | |||||||
chr13:46857228 | G | A | 107 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0067 others(104): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.614-21589C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857228 | |||||||
chr13:46857248 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.614-21609C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857248 | |||||||
chr13:46857297 | T | TA | 30 | a0001c0001t0001g0076 a0001c0001t0001g0106 a0001c0001t0002g0125 others(27): Show |
31 | HG00099.hp2 HG00140.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.614-21659dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857297 | |||||||
chr13:46857297 | T | TAA | 37 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0039 others(34): Show |
42 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.614-21660_614-2165 others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857297 | |||||||
chr13:46857297 | TA | T | 8 | a0001c0001t0001g0086 a0001c0002t0001g0207 a0001c0002t0001g0240 others(5): Show |
8 | HG02129.hp1 HG02717.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.614-21659delT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857297 | |||||||
chr13:46857336 | G | A | 38 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0039 others(35): Show |
43 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.614-21697C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857336 | |||||||
chr13:46857374 | T | C | 31 | a0001c0001t0001g0056 a0001c0001t0004g0292 a0001c0001t0004g0293 others(28): Show |
32 | HG00099.hp2 HG00140.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.614-21735A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857374 | |||||||
chr13:46857441 | A | G | 8 | a0001c0001t0005g0081 a0001c0001t0010g0080 a0001c0001t0016g0284 others(5): Show |
8 | HG02257.hp2 HG02572.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.614-21802T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857441 | |||||||
chr13:46857558 | T | C | 5 | a0001c0001t0014g0142 a0001c0002t0001g0272 a0001c0002t0005g0276 others(2): Show |
5 | HG01884.hp1 HG01891.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.614-21919A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857558 | |||||||
chr13:46857565 | T | C | 1 | a0001c0001t0042g0282 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.614-21926A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857565 | |||||||
chr13:46857815 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0039 others(36): Show |
44 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.614-22176C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857815 | |||||||
chr13:46857909 | C | G | 2 | a0001c0001t0001g0289 a0001c0001t0002g0117 |
2 | HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.614-22270G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46857909 | |||||||
chr13:46858019 | T | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(182): Show |
196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.614-22380A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858019 | |||||||
chr13:46858240 | T | C | 1 | a0001c0012t0031g0185 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.614-22601A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858240 | |||||||
chr13:46858261 | A | C | 2 | a0001c0001t0011g0004 a0001c0005t0026g0026 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.614-22622T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858261 | |||||||
chr13:46858291 | T | A | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(307): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.614-22652A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858291 | |||||||
chr13:46858357 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.614-22718A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858357 | |||||||
chr13:46858475 | T | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
194 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.614-22836A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858475 | |||||||
chr13:46858661 | G | T | 1 | a0001c0002t0001g0179 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.614-23022C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858661 | |||||||
chr13:46858793 | T | G | 21 | a0001c0001t0004g0292 a0001c0001t0004g0293 a0001c0001t0004g0294 others(18): Show |
22 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.614-23154A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858793 | |||||||
chr13:46858827 | T | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
5 | HG02040.hp2 NA18952.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.614-23188A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858827 | |||||||
chr13:46858946 | T | C | 2 | a0001c0002t0002g0266 a0001c0002t0039g0279 |
2 | HG03239.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.614-23307A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46858946 | |||||||
chr13:46859078 | A | G | 1 | a0001c0002t0002g0180 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.614-23439T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859078 | |||||||
chr13:46859175 | A | G | 2 | a0001c0001t0001g0036 a0002c0003t0003g0035 |
2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.614-23536T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859175 | |||||||
chr13:46859212 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.614-23573A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859212 | |||||||
chr13:46859220 | C | G | 117 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(114): Show |
126 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.614-23581G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859220 | |||||||
chr13:46859362 | G | A | 279 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(276): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.614-23723C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859362 | |||||||
chr13:46859379 | A | G | 1 | a0001c0001t0045g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.614-23740T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859379 | |||||||
chr13:46859690 | A | G | 4 | a0001c0002t0001g0182 a0001c0002t0001g0187 a0001c0002t0001g0188 others(1): Show |
4 | HG00735.hp1 HG01358.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-24051T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859690 | |||||||
chr13:46859699 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0002g0121 |
2 | HG00438.hp2 HG00597.hp1 |
intron_variant | MODIFIER | c.614-24060G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859699 | |||||||
chr13:46859709 | C | G | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(62): Show |
73 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.614-24070G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859709 | |||||||
chr13:46859753 | C | T | 2 | a0001c0001t0016g0284 a0001c0001t0045g0287 |
2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.614-24114G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859753 | |||||||
chr13:46859799 | T | C | 1 | a0001c0001t0006g0161 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.614-24160A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859799 | |||||||
chr13:46859803 | C | T | 8 | a0001c0001t0001g0067 a0001c0001t0001g0153 a0001c0001t0001g0155 others(5): Show |
8 | HG00738.hp2 HG01175.hp2 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.614-24164G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859803 | |||||||
chr13:46859818 | G | A | 3 | a0001c0001t0008g0003 a0001c0001t0008g0023 a0001c0001t0023g0022 |
4 | HG02280.hp1 HG02976.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-24179C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46859818 | |||||||
chr13:46860114 | T | C | 2 | a0001c0001t0043g0283 a0001c0002t0006g0265 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.614-24475A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46860114 | |||||||
chr13:46860192 | G | A | 35 | a0001c0001t0001g0012 a0001c0001t0001g0053 a0001c0001t0001g0086 others(32): Show |
36 | HG00438.hp2 HG00597.hp1 HG01981.hp1 others(33): Show |
intron_variant | MODIFIER | c.614-24553C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46860192 | |||||||
chr13:46860336 | A | G | 1 | a0001c0002t0002g0246 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.614-24697T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46860336 | |||||||
chr13:46860487 | T | A | 2 | a0001c0001t0011g0004 a0001c0005t0026g0026 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.614-24848A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46860487 | |||||||
chr13:46860598 | C | T | 15 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0137 others(12): Show |
19 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.614-24959G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46860598 | |||||||
chr13:46860723 | A | G | 1 | a0001c0001t0019g0300 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.614-25084T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46860723 | |||||||
chr13:46860971 | C | G | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0033 others(23): Show |
29 | HG00280.hp1 HG01070.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.614-25332G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46860971 | |||||||
chr13:46861148 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(282): Show |
306 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.614-25509C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861148 | |||||||
chr13:46861200 | A | G | 3 | a0001c0001t0008g0003 a0001c0001t0008g0023 a0001c0001t0023g0022 |
4 | HG02280.hp1 HG02976.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-25561T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861200 | |||||||
chr13:46861208 | A | C | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.614-25569T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861208 | |||||||
chr13:46861251 | A | C | 3 | a0001c0002t0002g0029 a0001c0002t0005g0028 a0001c0002t0032g0172 |
3 | HG02486.hp1 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.614-25612T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861251 | |||||||
chr13:46861325 | C | G | 2 | a0001c0012t0031g0185 a0002c0003t0003g0007 |
3 | HG01070.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.614-25686G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861325 | |||||||
chr13:46861448 | G | T | 2 | a0001c0001t0004g0298 a0001c0001t0051g0299 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.614-25809C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861448 | |||||||
chr13:46861469 | G | A | 2 | a0001c0001t0010g0115 a0001c0001t0010g0129 |
2 | HG01109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.614-25830C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861469 | |||||||
chr13:46861475 | A | C | 1 | a0001c0001t0001g0130 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.614-25836T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861475 | |||||||
chr13:46861476 | A | C | 1 | a0001c0002t0005g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.614-25837T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861476 | |||||||
chr13:46861657 | G | A | 4 | a0001c0001t0001g0065 a0001c0001t0002g0008 a0001c0001t0002g0063 others(1): Show |
5 | NA18612.hp2 NA18982.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.614-26018C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861657 | |||||||
chr13:46861729 | G | C | 3 | a0001c0001t0008g0003 a0001c0001t0008g0023 a0001c0001t0023g0022 |
4 | HG02280.hp1 HG02976.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-26090C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861729 | |||||||
chr13:46861978 | A | C | 1 | a0001c0001t0006g0161 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.614-26339T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46861978 | |||||||
chr13:46862031 | G | A | 1 | a0001c0002t0001g0227 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.614-26392C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862031 | |||||||
chr13:46862191 | C | A | 3 | a0001c0001t0001g0114 a0001c0001t0002g0102 a0001c0001t0002g0125 |
3 | NA18954.hp1 NA18965.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.614-26552G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862191 | |||||||
chr13:46862214 | T | C | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.614-26575A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862214 | |||||||
chr13:46862228 | G | A | 1 | a0001c0001t0006g0161 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.614-26589C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862228 | |||||||
chr13:46862385 | G | T | 1 | a0001c0001t0006g0161 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.614-26746C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862385 | |||||||
chr13:46862558 | G | A | 1 | a0001c0002t0001g0228 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.614-26919C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862558 | |||||||
chr13:46862582 | A | C | 1 | a0001c0001t0001g0066 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.614-26943T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862582 | |||||||
chr13:46862618 | G | A | 2 | a0001c0001t0010g0115 a0001c0001t0010g0129 |
2 | HG01109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.614-26979C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862618 | |||||||
chr13:46862672 | T | A | 2 | a0001c0001t0011g0004 a0001c0005t0026g0026 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.614-27033A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862672 | |||||||
chr13:46862672 | T | C | 1 | a0001c0001t0046g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.614-27033A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862672 | |||||||
chr13:46862794 | A | G | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0137 others(8): Show |
14 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.614-27155T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862794 | |||||||
chr13:46862961 | T | C | 2 | a0001c0002t0001g0230 a0002c0004t0003g0229 |
2 | HG00099.hp1 HG00140.hp2 |
intron_variant | MODIFIER | c.614-27322A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862961 | |||||||
chr13:46862968 | G | C | 51 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0135 others(48): Show |
57 | HG00099.hp2 HG00140.hp1 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.614-27329C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862968 | |||||||
chr13:46862976 | C | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0057 others(4): Show |
9 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.614-27337G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46862976 | |||||||
chr13:46863045 | T | C | 12 | a0001c0002t0001g0019 a0001c0002t0001g0254 a0001c0002t0001g0255 others(9): Show |
13 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.614-27406A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863045 | |||||||
chr13:46863081 | G | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(258): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.614-27442C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863081 | |||||||
chr13:46863247 | G | C | 48 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0137 others(45): Show |
54 | HG00099.hp2 HG00140.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.614-27608C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863247 | |||||||
chr13:46863290 | G | T | 1 | a0001c0001t0006g0161 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.614-27651C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863290 | |||||||
chr13:46863298 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.614-27659C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863298 | |||||||
chr13:46863410 | C | T | 14 | a0001c0002t0001g0019 a0001c0002t0001g0254 a0001c0002t0001g0255 others(11): Show |
15 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.614-27771G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863410 | |||||||
chr13:46863483 | C | A | 1 | a0001c0001t0041g0281 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.614-27844G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863483 | |||||||
chr13:46863517 | A | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(290): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.614-27878T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863517 | |||||||
chr13:46863630 | GA | G | 29 | a0001c0001t0004g0292 a0001c0001t0004g0293 a0001c0001t0004g0294 others(26): Show |
30 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.614-27992delT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863630 | |||||||
chr13:46863645 | A | AAAAG | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(243): Show |
262 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.614-28007_614-2800 others(8): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863645 | |||||||
chr13:46863650 | G | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(251): Show |
270 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.614-28011C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863650 | |||||||
chr13:46863657 | A | AAAAAG | 8 | a0001c0001t0001g0036 a0001c0001t0001g0158 a0001c0001t0002g0109 others(5): Show |
8 | HG01175.hp2 HG02135.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.614-28019_614-2801 others(9): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863657 | |||||||
chr13:46863657 | A | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(251): Show |
270 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.614-28018T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863657 | |||||||
chr13:46863968 | A | T | 1 | a0001c0001t0001g0032 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.614-28329T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863968 | |||||||
chr13:46863982 | G | T | 2 | a0001c0002t0001g0255 a0001c0002t0001g0256 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.614-28343C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46863982 | |||||||
chr13:46864000 | G | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(258): Show |
276 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.614-28361C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864000 | |||||||
chr13:46864011 | A | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(259): Show |
278 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.614-28372T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864011 | |||||||
chr13:46864065 | T | C | 2 | a0001c0001t0044g0285 a0001c0005t0015g0020 |
3 | HG02572.hp2 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.613+28325A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864065 | |||||||
chr13:46864081 | G | A | 27 | a0001c0001t0004g0292 a0001c0001t0004g0293 a0001c0001t0004g0294 others(24): Show |
27 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.613+28309C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864081 | |||||||
chr13:46864280 | G | A | 3 | a0001c0001t0001g0135 a0001c0005t0007g0133 a0001c0005t0007g0134 |
3 | HG03098.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+28110C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864280 | |||||||
chr13:46864369 | A | G | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(260): Show |
279 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.613+28021T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864369 | |||||||
chr13:46864414 | T | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(260): Show |
279 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.613+27976A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864414 | |||||||
chr13:46864439 | T | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(260): Show |
279 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.613+27951A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864439 | |||||||
chr13:46864447 | T | C | 2 | a0001c0001t0005g0081 a0001c0001t0010g0080 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.613+27943A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864447 | |||||||
chr13:46864533 | G | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0137 others(9): Show |
15 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.613+27857C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864533 | |||||||
chr13:46864559 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.613+27831G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864559 | |||||||
chr13:46864587 | A | G | 1 | a0001c0002t0001g0194 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.613+27803T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864587 | |||||||
chr13:46864603 | C | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(260): Show |
279 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.613+27787G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864603 | |||||||
chr13:46864621 | C | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0137 others(5): Show |
10 | HG01081.hp2 HG01099.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+27769G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864621 | |||||||
chr13:46864670 | C | T | 1 | a0001c0001t0047g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.613+27720G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864670 | |||||||
chr13:46864733 | G | A | 1 | a0001c0005t0026g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.613+27657C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864733 | |||||||
chr13:46864772 | AGTT | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0083 a0001c0001t0001g0092 others(130): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.613+27615_613+2761 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864772 | |||||||
chr13:46864839 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): Show |
102 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.613+27551G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864839 | |||||||
chr13:46864931 | T | C | 3 | a0001c0001t0001g0135 a0001c0005t0007g0133 a0001c0005t0007g0134 |
3 | HG03098.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+27459A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864931 | |||||||
chr13:46864944 | GT | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(292): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.613+27445delA | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864944 | |||||||
chr13:46864957 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(254): Show |
273 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.613+27433A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46864957 | |||||||
chr13:46865081 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.613+27309T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865081 | |||||||
chr13:46865084 | G | A | 2 | a0001c0002t0001g0162 a0001c0002t0001g0242 |
2 | NA18941.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.613+27306C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865084 | |||||||
chr13:46865105 | C | T | 1 | a0001c0002t0002g0169 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.613+27285G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865105 | |||||||
chr13:46865236 | A | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0083 a0001c0001t0001g0092 others(102): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.613+27154T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865236 | |||||||
chr13:46865441 | G | GAAGT | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(292): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.613+26948_613+2694 others(8): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865441 | |||||||
chr13:46865533 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.613+26857A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865533 | |||||||
chr13:46865595 | G | T | 23 | a0001c0001t0004g0292 a0001c0001t0004g0293 a0001c0001t0004g0294 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.613+26795C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865595 | |||||||
chr13:46865641 | A | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0053 others(63): Show |
69 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.613+26749T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865641 | |||||||
chr13:46865658 | T | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(257): Show |
277 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.613+26732A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865658 | |||||||
chr13:46865664 | G | T | 1 | a0001c0002t0001g0253 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.613+26726C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865664 | |||||||
chr13:46865685 | T | C | 1 | a0001c0001t0020g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+26705A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865685 | |||||||
chr13:46865741 | C | A | 5 | a0001c0001t0016g0284 a0001c0001t0016g0286 a0001c0001t0044g0285 others(2): Show |
6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+26649G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865741 | |||||||
chr13:46865819 | G | A | 2 | a0001c0001t0002g0143 a0001c0001t0020g0314 |
2 | HG03098.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.613+26571C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865819 | |||||||
chr13:46865820 | C | A | 1 | a0001c0002t0001g0233 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.613+26570G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865820 | |||||||
chr13:46865820 | C | T | 1 | a0001c0001t0020g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+26570G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865820 | |||||||
chr13:46865841 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0053 others(63): Show |
69 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.613+26549G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865841 | |||||||
chr13:46865935 | C | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
100 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.613+26455G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865935 | |||||||
chr13:46865990 | G | A | 1 | a0001c0001t0005g0151 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.613+26400C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46865990 | |||||||
chr13:46866140 | T | C | 1 | a0001c0002t0028g0168 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.613+26250A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866140 | |||||||
chr13:46866284 | C | G | 10 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+26106G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866284 | |||||||
chr13:46866323 | G | C | 26 | a0001c0001t0001g0012 a0001c0001t0001g0084 a0001c0001t0001g0085 others(23): Show |
27 | HG00423.hp2 HG02015.hp2 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.613+26067C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866323 | |||||||
chr13:46866372 | C | T | 1 | a0001c0001t0041g0281 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.613+26018G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866372 | |||||||
chr13:46866425 | C | T | 228 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(225): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.613+25965G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866425 | |||||||
chr13:46866622 | C | G | 1 | a0001c0001t0020g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+25768G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866622 | |||||||
chr13:46866665 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0053 others(64): Show |
70 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.613+25725A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866665 | |||||||
chr13:46866666 | G | A | 4 | a0003c0006t0001g0145 a0003c0006t0001g0146 a0003c0007t0007g0147 others(1): Show |
4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+25724C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866666 | |||||||
chr13:46866693 | T | G | 4 | a0001c0001t0041g0281 a0001c0001t0043g0283 a0001c0002t0006g0265 others(1): Show |
4 | HG03225.hp1 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.613+25697A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866693 | |||||||
chr13:46866735 | G | T | 1 | a0001c0001t0006g0161 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.613+25655C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866735 | |||||||
chr13:46866769 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.613+25621C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866769 | |||||||
chr13:46866844 | T | C | 1 | a0002c0004t0003g0171 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.613+25546A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866844 | |||||||
chr13:46866853 | A | G | 1 | a0002c0004t0003g0192 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.613+25537T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866853 | |||||||
chr13:46866900 | G | A | 1 | a0001c0002t0006g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.613+25490C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866900 | |||||||
chr13:46866924 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.613+25466T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46866924 | |||||||
chr13:46867122 | C | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0132 a0001c0002t0001g0234 others(6): Show |
11 | HG02165.hp2 NA18939.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.613+25268G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867122 | |||||||
chr13:46867288 | A | G | 7 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0057 others(4): Show |
9 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.613+25102T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867288 | |||||||
chr13:46867326 | T | C | 2 | a0001c0001t0011g0004 a0001c0005t0026g0026 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+25064A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867326 | |||||||
chr13:46867375 | A | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(228): Show |
244 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.613+25015T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867375 | |||||||
chr13:46867399 | G | A | 1 | a0001c0001t0049g0291 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.613+24991C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867399 | |||||||
chr13:46867474 | G | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(227): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.613+24916C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867474 | |||||||
chr13:46867481 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(227): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.613+24909C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867481 | |||||||
chr13:46867546 | C | T | 10 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+24844G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867546 | |||||||
chr13:46867572 | T | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(292): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.613+24818A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867572 | |||||||
chr13:46867912 | AT | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0053 others(54): Show |
60 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.613+24477delA | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46867912 | |||||||
chr13:46868029 | G | GTTAATTC | 67 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0053 others(64): Show |
70 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.613+24360_613+2436 others(11): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46868029 | |||||||
chr13:46868160 | C | T | 1 | a0001c0001t0016g0286 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.613+24230G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46868160 | |||||||
chr13:46868193 | A | G | 2 | a0001c0005t0007g0133 a0001c0005t0007g0134 |
2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+24197T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46868193 | |||||||
chr13:46868378 | G | A | 2 | a0001c0001t0043g0283 a0001c0002t0006g0265 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.613+24012C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46868378 | |||||||
chr13:46868577 | A | T | 1 | a0001c0001t0020g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+23813T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46868577 | |||||||
chr13:46868590 | C | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0083 a0001c0001t0001g0092 others(115): Show |
123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.613+23800G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46868590 | |||||||
chr13:46868633 | T | A | 2 | a0001c0001t0008g0003 a0001c0001t0023g0022 |
3 | HG02280.hp1 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.613+23757A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46868633 | |||||||
chr13:46869366 | C | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.613+23024G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46869366 | |||||||
chr13:46869393 | C | T | 11 | a0001c0001t0004g0292 a0001c0001t0004g0293 a0001c0001t0004g0294 others(8): Show |
11 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.613+22997G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46869393 | |||||||
chr13:46869475 | G | A | 1 | a0003c0006t0001g0146 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.613+22915C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46869475 | |||||||
chr13:46869668 | T | C | 23 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0087 others(20): Show |
24 | HG00423.hp2 HG02015.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.613+22722A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46869668 | |||||||
chr13:46869733 | G | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(308): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.613+22657C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46869733 | |||||||
chr13:46869754 | A | G | 27 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0032 others(24): Show |
30 | HG00280.hp1 HG01070.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.613+22636T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46869754 | |||||||
chr13:46869918 | T | C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0032 others(31): Show |
39 | HG00280.hp1 HG01070.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.613+22472A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46869918 | |||||||
chr13:46870129 | T | C | 2 | a0001c0001t0001g0038 a0001c0001t0002g0037 |
2 | NA19055.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.613+22261A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46870129 | |||||||
chr13:46870405 | C | T | 1 | a0001c0001t0020g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+21985G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46870405 | |||||||
chr13:46870414 | A | G | 3 | a0001c0001t0001g0130 a0001c0001t0005g0081 a0001c0001t0010g0080 |
3 | HG01192.hp2 HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.613+21976T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46870414 | |||||||
chr13:46870875 | A | G | 5 | a0001c0001t0016g0284 a0001c0001t0016g0286 a0001c0001t0044g0285 others(2): Show |
6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+21515T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46870875 | |||||||
chr13:46871051 | C | T | 25 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(22): Show |
29 | HG00558.hp2 HG01255.hp2 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.613+21339G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871051 | |||||||
chr13:46871092 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.613+21298C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871092 | |||||||
chr13:46871094 | G | A | 2 | a0001c0001t0011g0004 a0001c0005t0026g0026 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+21296C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871094 | |||||||
chr13:46871449 | T | G | 1 | a0001c0005t0026g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.613+20941A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871449 | |||||||
chr13:46871514 | A | G | 1 | a0001c0001t0004g0298 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.613+20876T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871514 | |||||||
chr13:46871568 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0032 others(66): Show |
72 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.613+20822C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871568 | |||||||
chr13:46871602 | C | A | 3 | a0001c0001t0041g0281 a0001c0001t0043g0283 a0001c0002t0006g0265 |
3 | HG03225.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.613+20788G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871602 | |||||||
chr13:46871620 | A | T | 28 | a0001c0001t0004g0292 a0001c0001t0004g0293 a0001c0001t0004g0294 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.613+20770T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871620 | |||||||
chr13:46871703 | G | GTT | 69 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0032 others(66): Show |
72 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.613+20685_613+2068 others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871703 | |||||||
chr13:46871742 | C | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
100 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.613+20648G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871742 | |||||||
chr13:46871758 | G | A | 2 | a0001c0001t0011g0004 a0001c0005t0026g0026 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+20632C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871758 | |||||||
chr13:46871759 | G | C | 1 | a0001c0001t0006g0161 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.613+20631C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871759 | |||||||
chr13:46871789 | T | C | 3 | a0001c0001t0041g0281 a0001c0001t0043g0283 a0001c0002t0006g0265 |
3 | HG03225.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.613+20601A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871789 | |||||||
chr13:46871832 | A | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0032 others(66): Show |
72 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.613+20558T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871832 | |||||||
chr13:46871859 | A | G | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0033 others(30): Show |
38 | HG00280.hp1 HG01070.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.613+20531T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871859 | |||||||
chr13:46871867 | A | G | 2 | a0001c0002t0001g0174 a0001c0002t0001g0186 |
2 | HG02135.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.613+20523T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46871867 | |||||||
chr13:46872071 | A | G | 26 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(23): Show |
30 | HG00558.hp2 HG01255.hp2 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.613+20319T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872071 | |||||||
chr13:46872269 | A | G | 5 | a0001c0001t0016g0284 a0001c0001t0016g0286 a0001c0001t0044g0285 others(2): Show |
6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+20121T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872269 | |||||||
chr13:46872330 | AT | A | 25 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0033 others(22): Show |
28 | HG00280.hp1 HG01070.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.613+20059delA | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872330 | |||||||
chr13:46872349 | T | G | 1 | a0001c0002t0038g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.613+20041A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872349 | |||||||
chr13:46872363 | C | T | 28 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0033 others(25): Show |
32 | HG00280.hp1 HG01070.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.613+20027G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872363 | |||||||
chr13:46872477 | CTTTA | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(159): Show |
171 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.613+19909_613+1991 others(8): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872477 | |||||||
chr13:46872530 | C | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.613+19860G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872530 | |||||||
chr13:46872662 | C | T | 1 | a0001c0001t0043g0283 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.613+19728G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872662 | |||||||
chr13:46872687 | C | T | 1 | a0001c0001t0004g0292 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.613+19703G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872687 | |||||||
chr13:46872712 | C | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.613+19678G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872712 | |||||||
chr13:46872781 | C | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0033 others(22): Show |
28 | HG00280.hp1 HG01070.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.613+19609G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872781 | |||||||
chr13:46872828 | C | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0058 |
4 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+19562G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872828 | |||||||
chr13:46872898 | T | A | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.613+19492A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872898 | |||||||
chr13:46872952 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.613+19438C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46872952 | |||||||
chr13:46873101 | G | A | 171 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(168): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.613+19289C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873101 | |||||||
chr13:46873152 | CT | C | 52 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0032 others(49): Show |
55 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.613+19237delA | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873152 | |||||||
chr13:46873247 | AG | A | 56 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0033 others(53): Show |
61 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.613+19142delC | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873247 | |||||||
chr13:46873405 | C | CATT | 231 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(228): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.613+18982_613+1898 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873405 | |||||||
chr13:46873427 | T | TTTA | 18 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0036 others(15): Show |
18 | HG00558.hp2 HG00639.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.613+18960_613+1896 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | |||||||
chr13:46873427 | T | TTTATTA | 60 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(57): Show |
65 | HG00280.hp1 HG00423.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.613+18957_613+1896 others(10): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | |||||||
chr13:46873427 | T | TTTATTAT others(2): Show |
6 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0124 others(3): Show |
6 | HG00438.hp2 HG00597.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.613+18954_613+1896 others(13): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | |||||||
chr13:46873427 | T | TTTATTAT others(5): Show |
4 | a0001c0001t0001g0130 a0001c0001t0016g0286 a0001c0001t0043g0283 others(1): Show |
4 | HG01081.hp2 HG01192.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.613+18951_613+1896 others(16): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | |||||||
chr13:46873427 | TTTA | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0056 others(47): Show |
56 | HG00099.hp2 HG00140.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.613+18960_613+1896 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | |||||||
chr13:46873427 | TTTATTA | T | 9 | a0001c0001t0016g0284 a0001c0001t0044g0285 a0001c0001t0045g0287 others(6): Show |
11 | HG01070.hp1 HG02572.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.613+18957_613+1896 others(10): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | |||||||
chr13:46873427 | TTTATTAT others(2): Show |
T | 5 | a0001c0001t0001g0061 a0001c0002t0001g0177 a0001c0002t0001g0278 others(2): Show |
5 | HG00741.hp2 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.613+18954_613+1896 others(13): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | |||||||
chr13:46873427 | TTTATTAT others(5): Show |
T | 107 | a0001c0001t0001g0002 a0001c0001t0001g0083 a0001c0001t0001g0084 others(104): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.613+18951_613+1896 others(16): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | |||||||
chr13:46873427 | TTTATTAT others(11): Show |
T | 1 | a0001c0002t0001g0250 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.613+18945_613+1896 others(22): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873427 | |||||||
chr13:46873505 | G | A | 3 | a0001c0001t0001g0135 a0001c0005t0007g0133 a0001c0005t0007g0134 |
3 | HG03098.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+18885C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873505 | |||||||
chr13:46873517 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.613+18873A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873517 | |||||||
chr13:46873575 | T | C | 49 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0033 others(46): Show |
52 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.613+18815A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873575 | |||||||
chr13:46873598 | C | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(169): Show |
182 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.613+18792G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873598 | |||||||
chr13:46873653 | G | T | 2 | a0001c0001t0002g0100 a0001c0001t0002g0109 |
2 | HG02135.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.613+18737C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873653 | |||||||
chr13:46873925 | C | A | 5 | a0001c0001t0016g0284 a0001c0001t0016g0286 a0001c0001t0044g0285 others(2): Show |
6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+18465G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873925 | |||||||
chr13:46873925 | C | T | 149 | a0001c0001t0001g0002 a0001c0001t0001g0083 a0001c0001t0001g0084 others(146): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.613+18465G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46873925 | |||||||
chr13:46874196 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.613+18194C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46874196 | |||||||
chr13:46874235 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.613+18155T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46874235 | |||||||
chr13:46874337 | A | G | 1 | a0001c0001t0009g0013 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.613+18053T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46874337 | |||||||
chr13:46874512 | G | A | 3 | a0001c0002t0001g0245 a0001c0002t0002g0243 a0001c0002t0027g0244 |
3 | HG00423.hp1 HG00621.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.613+17878C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46874512 | |||||||
chr13:46874526 | T | G | 171 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(168): Show |
180 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.613+17864A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46874526 | |||||||
chr13:46874767 | G | C | 2 | a0001c0002t0001g0278 a0001c0002t0006g0277 |
2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.613+17623C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46874767 | |||||||
chr13:46875011 | G | C | 1 | a0001c0001t0001g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.613+17379C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875011 | |||||||
chr13:46875029 | T | C | 168 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(165): Show |
177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.613+17361A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875029 | |||||||
chr13:46875063 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.613+17327G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875063 | |||||||
chr13:46875172 | T | C | 2 | a0001c0001t0011g0004 a0001c0005t0026g0026 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+17218A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875172 | |||||||
chr13:46875191 | T | C | 5 | a0001c0001t0016g0284 a0001c0001t0016g0286 a0001c0001t0044g0285 others(2): Show |
6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+17199A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875191 | |||||||
chr13:46875306 | T | C | 3 | a0001c0001t0001g0135 a0001c0005t0007g0133 a0001c0005t0007g0134 |
3 | HG03098.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+17084A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875306 | |||||||
chr13:46875394 | T | G | 2 | a0001c0001t0001g0111 a0001c0010t0034g0123 |
2 | HG02698.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.613+16996A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875394 | |||||||
chr13:46875400 | A | C | 1 | a0001c0001t0020g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+16990T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875400 | |||||||
chr13:46875430 | G | T | 31 | a0001c0001t0004g0292 a0001c0001t0004g0293 a0001c0001t0004g0294 others(28): Show |
33 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.613+16960C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875430 | |||||||
chr13:46875566 | T | G | 1 | a0001c0001t0009g0157 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.613+16824A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875566 | |||||||
chr13:46875622 | A | G | 3 | a0001c0001t0001g0135 a0001c0005t0007g0133 a0001c0005t0007g0134 |
3 | HG03098.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+16768T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875622 | |||||||
chr13:46875703 | C | G | 10 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+16687G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875703 | |||||||
chr13:46875726 | G | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0083 a0001c0001t0001g0084 others(133): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.613+16664C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875726 | |||||||
chr13:46875905 | T | G | 1 | a0001c0002t0001g0179 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.613+16485A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875905 | |||||||
chr13:46875989 | G | T | 1 | a0002c0003t0003g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.613+16401C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46875989 | |||||||
chr13:46876081 | C | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0053 others(51): Show |
57 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.613+16309G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876081 | |||||||
chr13:46876143 | C | G | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0137 others(8): Show |
14 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.613+16247G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876143 | |||||||
chr13:46876300 | T | A | 229 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(226): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.613+16090A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876300 | |||||||
chr13:46876385 | C | CATAT | 4 | a0001c0001t0001g0124 a0001c0001t0002g0109 a0001c0001t0008g0003 others(1): Show |
5 | HG00438.hp2 HG02135.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.613+16001_613+1600 others(8): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876385 | |||||||
chr13:46876385 | C | CATATAT | 24 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0058 others(21): Show |
25 | HG00423.hp2 HG00597.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.613+15999_613+1600 others(10): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876385 | |||||||
chr13:46876385 | C | CATATATA others(1): Show |
3 | a0001c0001t0001g0053 a0001c0001t0001g0289 a0001c0001t0002g0054 |
3 | HG01981.hp1 HG01993.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.613+15997_613+1600 others(12): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876385 | |||||||
chr13:46876385 | C | CATATATA others(3): Show |
3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0099 |
3 | NA18747.hp2 NA19005.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.613+15995_613+1600 others(14): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876385 | |||||||
chr13:46876385 | CAT | C | 10 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+16003_613+1600 others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876385 | |||||||
chr13:46876385 | CATAT | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0092 a0001c0001t0001g0094 others(94): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.613+16001_613+1600 others(8): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876385 | |||||||
chr13:46876385 | CATATAT | C | 5 | a0001c0001t0043g0283 a0001c0002t0001g0247 a0001c0002t0002g0246 others(2): Show |
5 | HG00597.hp2 HG02896.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.613+15999_613+1600 others(10): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876385 | |||||||
chr13:46876394 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.613+15996T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876394 | |||||||
chr13:46876396 | A | G | 9 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(6): Show |
9 | HG00639.hp1 HG00738.hp2 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.613+15994T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876396 | |||||||
chr13:46876399 | TATA | T | 12 | a0001c0001t0001g0083 a0001c0002t0001g0162 a0001c0002t0001g0181 others(9): Show |
13 | HG00735.hp1 HG01109.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.613+15988_613+1599 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876399 | |||||||
chr13:46876399 | TATATA | T | 16 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0160 others(13): Show |
16 | HG00621.hp2 HG01099.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.613+15986_613+1599 others(9): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876399 | |||||||
chr13:46876401 | TATA | T | 3 | a0001c0002t0001g0187 a0001c0002t0001g0188 a0001c0002t0001g0252 |
3 | HG01358.hp1 HG01517.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.613+15986_613+1598 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876401 | |||||||
chr13:46876404 | A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0088 a0001c0001t0002g0089 |
2 | NA18946.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.613+15985_613+1598 others(15): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876404 | |||||||
chr13:46876404 | A | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0083 a0001c0001t0001g0132 others(85): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.613+15986T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876404 | |||||||
chr13:46876404 | ATTT | A | 6 | a0001c0001t0006g0161 a0001c0002t0038g0173 a0003c0006t0001g0145 others(3): Show |
6 | HG01074.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.613+15983_613+1598 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876404 | |||||||
chr13:46876404 | ATTTT | A | 9 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0011g0004 others(6): Show |
12 | HG01070.hp1 HG02895.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.613+15982_613+1598 others(8): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876404 | |||||||
chr13:46876404 | ATTTTT | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0033 others(16): Show |
21 | HG00280.hp1 HG01167.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.613+15981_613+1598 others(9): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876404 | |||||||
chr13:46876404 | ATTTTTT | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0046 a0001c0001t0004g0302 others(6): Show |
11 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.613+15980_613+1598 others(10): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876404 | |||||||
chr13:46876404 | ATTTTTTT | A | 19 | a0001c0001t0004g0292 a0001c0001t0004g0293 a0001c0001t0004g0294 others(16): Show |
19 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.613+15979_613+1598 others(11): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876404 | |||||||
chr13:46876405 | T | TA | 17 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(14): Show |
20 | HG00558.hp2 HG01255.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.613+15984_613+1598 others(5): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876405 | |||||||
chr13:46876405 | T | TATA | 9 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0077 others(6): Show |
10 | HG00639.hp2 HG01109.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+15984_613+1598 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876405 | |||||||
chr13:46876405 | T | TATATA | 8 | a0001c0001t0001g0061 a0001c0001t0001g0098 a0001c0001t0001g0112 others(5): Show |
8 | HG00741.hp2 HG03490.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.613+15984_613+1598 others(9): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876405 | |||||||
chr13:46876405 | T | TATATATA | 6 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0060 others(3): Show |
8 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.613+15984_613+1598 others(11): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876405 | |||||||
chr13:46876405 | T | TATATATA others(4): Show |
1 | a0001c0001t0010g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.613+15984_613+1598 others(15): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876405 | |||||||
chr13:46876406 | T | A | 36 | a0001c0001t0001g0012 a0001c0001t0001g0053 a0001c0001t0001g0057 others(33): Show |
38 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.613+15984A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876406 | |||||||
chr13:46876407 | T | A | 38 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(35): Show |
42 | HG00558.hp2 HG00639.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.613+15983A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876407 | |||||||
chr13:46876408 | T | A | 18 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0076 others(15): Show |
18 | HG00438.hp2 HG00597.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.613+15982A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876408 | |||||||
chr13:46876409 | T | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0002g0125 others(6): Show |
9 | HG02257.hp2 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.613+15981A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876409 | |||||||
chr13:46876410 | T | A | 8 | a0001c0001t0001g0051 a0001c0001t0001g0126 a0001c0001t0001g0289 others(5): Show |
10 | HG01081.hp1 HG02300.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+15980A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876410 | |||||||
chr13:46876411 | T | A | 9 | a0001c0001t0005g0081 a0001c0001t0016g0284 a0001c0001t0016g0286 others(6): Show |
9 | HG02257.hp2 HG02572.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.613+15979A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876411 | |||||||
chr13:46876412 | T | A | 3 | a0001c0001t0014g0136 a0001c0001t0045g0287 a0001c0005t0015g0020 |
4 | HG02630.hp2 HG03139.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+15978A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876412 | |||||||
chr13:46876413 | T | A | 3 | a0001c0001t0016g0284 a0001c0001t0020g0310 a0001c0001t0044g0285 |
3 | HG02572.hp2 HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.613+15977A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876413 | |||||||
chr13:46876414 | T | A | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.613+15976A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876414 | |||||||
chr13:46876434 | G | C | 1 | a0001c0001t0020g0310 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.613+15956C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876434 | |||||||
chr13:46876449 | G | C | 1 | a0001c0001t0020g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+15941C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876449 | |||||||
chr13:46876471 | G | A | 1 | a0001c0002t0001g0250 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.613+15919C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876471 | |||||||
chr13:46876474 | A | G | 1 | a0001c0002t0038g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.613+15916T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876474 | |||||||
chr13:46876502 | C | T | 2 | a0001c0001t0041g0281 a0001c0001t0043g0283 |
2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.613+15888G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876502 | |||||||
chr13:46876503 | G | A | 10 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+15887C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876503 | |||||||
chr13:46876534 | T | G | 1 | a0001c0001t0024g0024 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.613+15856A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876534 | |||||||
chr13:46876552 | A | G | 3 | a0001c0001t0001g0135 a0001c0005t0007g0133 a0001c0005t0007g0134 |
3 | HG03098.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+15838T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876552 | |||||||
chr13:46876575 | AATTTTCT others(6812): Show |
A | 1 | a0001c0001t0024g0024 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.613+8996_613+15814 others(3): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876575 | |||||||
chr13:46876619 | T | C | 9 | a0001c0001t0001g0135 a0001c0001t0011g0004 a0001c0005t0007g0133 others(6): Show |
10 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+15771A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876619 | |||||||
chr13:46876651 | T | C | 10 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+15739A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876651 | |||||||
chr13:46876774 | A | C | 1 | a0001c0001t0002g0109 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.613+15616T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876774 | |||||||
chr13:46876799 | C | T | 1 | a0001c0002t0001g0208 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.613+15591G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46876799 | |||||||
chr13:46877066 | G | C | 1 | a0001c0001t0005g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.613+15324C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877066 | |||||||
chr13:46877123 | T | C | 1 | a0001c0002t0038g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.613+15267A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877123 | |||||||
chr13:46877151 | T | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(226): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.613+15239A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877151 | |||||||
chr13:46877185 | A | G | 167 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(164): Show |
175 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.613+15205T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877185 | |||||||
chr13:46877229 | C | T | 3 | a0001c0002t0001g0197 a0001c0002t0002g0189 a0006c0011t0002g0232 |
3 | HG04115.hp2 NA18947.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.613+15161G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877229 | |||||||
chr13:46877509 | C | T | 5 | a0001c0001t0016g0284 a0001c0001t0016g0286 a0001c0001t0044g0285 others(2): Show |
6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+14881G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877509 | |||||||
chr13:46877644 | C | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0137 others(8): Show |
14 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.613+14746G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877644 | |||||||
chr13:46877713 | G | A | 1 | a0001c0001t0006g0161 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.613+14677C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877713 | |||||||
chr13:46877810 | T | G | 3 | a0001c0001t0008g0003 a0001c0001t0008g0023 a0001c0001t0023g0022 |
4 | HG02280.hp1 HG02976.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.613+14580A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877810 | |||||||
chr13:46877869 | G | A | 4 | a0003c0006t0001g0145 a0003c0006t0001g0146 a0003c0007t0007g0147 others(1): Show |
4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+14521C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877869 | |||||||
chr13:46877903 | A | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0053 others(53): Show |
59 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.613+14487T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877903 | |||||||
chr13:46877998 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0053 others(53): Show |
59 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.613+14392C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46877998 | |||||||
chr13:46878022 | A | C | 1 | a0001c0002t0001g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.613+14368T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878022 | |||||||
chr13:46878034 | T | C | 1 | a0004c0009t0017g0290 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.613+14356A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878034 | |||||||
chr13:46878204 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.613+14186T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878204 | |||||||
chr13:46878207 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.613+14183A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878207 | |||||||
chr13:46878309 | G | C | 2 | a0001c0001t0002g0100 a0001c0001t0002g0109 |
2 | HG02135.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.613+14081C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878309 | |||||||
chr13:46878414 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0053 others(49): Show |
55 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.613+13976C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878414 | |||||||
chr13:46878461 | G | A | 1 | a0001c0001t0020g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+13929C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878461 | |||||||
chr13:46878592 | G | C | 1 | a0002c0003t0003g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.613+13798C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878592 | |||||||
chr13:46878659 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.613+13731C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878659 | |||||||
chr13:46878752 | C | G | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.613+13638G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878752 | |||||||
chr13:46878770 | A | G | 1 | a0001c0001t0020g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+13620T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878770 | |||||||
chr13:46878836 | T | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.613+13554A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878836 | |||||||
chr13:46878878 | T | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0057 others(4): Show |
9 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.613+13512A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46878878 | |||||||
chr13:46879051 | G | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(277): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.613+13339C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879051 | |||||||
chr13:46879062 | A | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0083 a0001c0001t0001g0084 others(134): Show |
142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.613+13328T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879062 | |||||||
chr13:46879177 | T | C | 4 | a0003c0006t0001g0145 a0003c0006t0001g0146 a0003c0007t0007g0147 others(1): Show |
4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+13213A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879177 | |||||||
chr13:46879258 | C | A | 1 | a0001c0001t0006g0161 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.613+13132G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879258 | |||||||
chr13:46879308 | T | C | 3 | a0001c0002t0001g0237 a0001c0002t0001g0239 a0001c0002t0001g0240 |
3 | NA18948.hp2 NA18991.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.613+13082A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879308 | |||||||
chr13:46879435 | C | T | 4 | a0001c0002t0001g0177 a0001c0002t0001g0278 a0001c0002t0006g0277 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+12955G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879435 | |||||||
chr13:46879500 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0053 others(49): Show |
55 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.613+12890T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879500 | |||||||
chr13:46879538 | G | A | 2 | a0002c0004t0003g0200 a0002c0004t0003g0201 |
2 | HG02056.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.613+12852C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879538 | |||||||
chr13:46879585 | T | C | 1 | a0001c0002t0001g0170 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.613+12805A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879585 | |||||||
chr13:46879595 | G | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.613+12795C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879595 | |||||||
chr13:46879666 | A | G | 26 | a0001c0001t0004g0292 a0001c0001t0004g0293 a0001c0001t0004g0294 others(23): Show |
27 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.613+12724T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879666 | |||||||
chr13:46879804 | A | G | 1 | a0001c0002t0002g0018 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.613+12586T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879804 | |||||||
chr13:46879826 | G | GAAAGCCC | 3 | a0001c0001t0001g0135 a0001c0005t0007g0133 a0001c0005t0007g0134 |
3 | HG03098.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+12557_613+1256 others(11): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46879826 | |||||||
chr13:46880010 | C | CA | 225 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.613+12379dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880010 | |||||||
chr13:46880117 | T | G | 1 | a0001c0002t0001g0222 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.613+12273A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880117 | |||||||
chr13:46880305 | G | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0032 others(23): Show |
29 | HG00280.hp1 HG01070.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.613+12085C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880305 | |||||||
chr13:46880362 | C | T | 5 | a0001c0002t0001g0204 a0002c0004t0003g0200 a0002c0004t0003g0201 others(2): Show |
5 | HG01175.hp1 HG02056.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.613+12028G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880362 | |||||||
chr13:46880446 | T | A | 1 | a0001c0002t0001g0197 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.613+11944A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880446 | |||||||
chr13:46880449 | C | G | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.613+11941G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880449 | |||||||
chr13:46880465 | T | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.613+11925A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880465 | |||||||
chr13:46880551 | A | T | 4 | a0003c0006t0001g0145 a0003c0006t0001g0146 a0003c0007t0007g0147 others(1): Show |
4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+11839T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880551 | |||||||
chr13:46880570 | G | A | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.613+11820C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880570 | |||||||
chr13:46880708 | G | A | 10 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+11682C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880708 | |||||||
chr13:46880849 | G | GA | 51 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0032 others(48): Show |
55 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.613+11540dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880849 | |||||||
chr13:46880890 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.613+11500G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46880890 | |||||||
chr13:46881012 | A | G | 1 | a0002c0003t0003g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.613+11378T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881012 | |||||||
chr13:46881081 | C | T | 2 | a0001c0001t0002g0008 a0001c0002t0001g0236 |
2 | HG02165.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.613+11309G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881081 | |||||||
chr13:46881144 | G | A | 10 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+11246C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881144 | |||||||
chr13:46881230 | C | T | 180 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): Show |
189 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.613+11160G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881230 | |||||||
chr13:46881240 | C | T | 1 | a0001c0002t0001g0181 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.613+11150G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881240 | |||||||
chr13:46881265 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.613+11125C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881265 | |||||||
chr13:46881301 | C | T | 3 | a0001c0001t0001g0135 a0001c0005t0007g0133 a0001c0005t0007g0134 |
3 | HG03098.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.613+11089G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881301 | |||||||
chr13:46881323 | G | A | 2 | a0001c0001t0010g0115 a0001c0001t0010g0129 |
2 | HG01109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.613+11067C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881323 | |||||||
chr13:46881349 | T | C | 2 | a0001c0001t0011g0004 a0001c0005t0026g0026 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+11041A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881349 | |||||||
chr13:46881478 | G | T | 10 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+10912C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881478 | |||||||
chr13:46881488 | A | C | 5 | a0001c0002t0001g0016 a0001c0002t0001g0217 a0001c0002t0001g0228 others(2): Show |
6 | HG00558.hp1 NA18943.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.613+10902T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881488 | |||||||
chr13:46881508 | G | A | 4 | a0001c0001t0016g0284 a0001c0001t0044g0285 a0001c0001t0045g0287 others(1): Show |
5 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+10882C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881508 | |||||||
chr13:46881590 | G | A | 169 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(166): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.613+10800C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881590 | |||||||
chr13:46881622 | T | C | 1 | a0001c0001t0016g0286 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.613+10768A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881622 | |||||||
chr13:46881625 | T | C | 2 | a0003c0006t0001g0145 a0003c0006t0001g0146 |
2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.613+10765A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881625 | |||||||
chr13:46881728 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.613+10662T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881728 | |||||||
chr13:46881751 | A | G | 2 | a0001c0001t0047g0308 a0002c0003t0018g0309 |
2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.613+10639T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881751 | |||||||
chr13:46881790 | T | C | 1 | a0001c0002t0002g0180 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.613+10600A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881790 | |||||||
chr13:46881916 | G | A | 214 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(211): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.613+10474C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881916 | |||||||
chr13:46881957 | C | A | 1 | a0001c0001t0001g0001 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.613+10433G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881957 | |||||||
chr13:46881958 | C | A | 1 | a0002c0003t0018g0306 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.613+10432G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46881958 | |||||||
chr13:46882039 | A | G | 1 | a0001c0002t0001g0214 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.613+10351T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882039 | |||||||
chr13:46882055 | T | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.613+10335A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882055 | |||||||
chr13:46882057 | C | T | 221 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(218): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.613+10333G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882057 | |||||||
chr13:46882229 | T | TA | 18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0044 others(15): Show |
21 | HG01081.hp2 HG01099.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.613+10160dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882229 | |||||||
chr13:46882229 | T | TAA | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(238): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.613+10159_613+1016 others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882229 | |||||||
chr13:46882229 | T | TAAA | 7 | a0001c0001t0001g0036 a0001c0001t0016g0284 a0001c0001t0044g0285 others(4): Show |
8 | HG02572.hp2 HG02895.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.613+10158_613+1016 others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882229 | |||||||
chr13:46882290 | T | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.613+10100A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882290 | |||||||
chr13:46882304 | T | A | 2 | a0001c0002t0001g0257 a0001c0002t0005g0261 |
2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.613+10086A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882304 | |||||||
chr13:46882340 | A | G | 10 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+10050T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882340 | |||||||
chr13:46882413 | A | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0053 others(54): Show |
60 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.613+9977T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882413 | |||||||
chr13:46882450 | G | A | 1 | a0001c0002t0001g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.613+9940C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882450 | |||||||
chr13:46882549 | C | T | 4 | a0003c0006t0001g0145 a0003c0006t0001g0146 a0003c0007t0007g0147 others(1): Show |
4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+9841G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882549 | |||||||
chr13:46882637 | A | C | 2 | a0001c0001t0001g0122 a0001c0001t0002g0120 |
2 | NA19009.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.613+9753T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882637 | |||||||
chr13:46882722 | G | A | 1 | a0001c0002t0001g0253 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.613+9668C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882722 | |||||||
chr13:46882805 | T | A | 2 | a0001c0001t0011g0004 a0001c0005t0026g0026 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+9585A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882805 | |||||||
chr13:46882837 | T | C | 1 | a0001c0001t0004g0293 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.613+9553A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882837 | |||||||
chr13:46882839 | T | A | 10 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+9551A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882839 | |||||||
chr13:46882864 | A | G | 14 | a0001c0002t0001g0254 a0001c0002t0001g0255 a0001c0002t0001g0256 others(11): Show |
14 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.613+9526T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882864 | |||||||
chr13:46882893 | A | C | 1 | a0001c0001t0020g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+9497T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46882893 | |||||||
chr13:46883081 | G | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(308): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.613+9309C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883081 | |||||||
chr13:46883106 | A | T | 3 | a0001c0001t0041g0281 a0001c0001t0042g0282 a0001c0001t0043g0283 |
3 | HG00639.hp2 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.613+9284T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883106 | |||||||
chr13:46883159 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.613+9231T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883159 | |||||||
chr13:46883223 | C | T | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(276): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.613+9167G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883223 | |||||||
chr13:46883264 | A | AAGGTTAG others(16): Show |
69 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0053 others(66): Show |
72 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.613+9125_613+9126i others(25): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883264 | |||||||
chr13:46883455 | CTGAAATG others(5688): Show |
C | 1 | a0001c0001t0024g0024 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.613+3240_613+8934d others(2): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883455 | |||||||
chr13:46883491 | T | C | 1 | a0001c0001t0016g0286 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.613+8899A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883491 | |||||||
chr13:46883506 | C | T | 4 | a0003c0006t0001g0145 a0003c0006t0001g0146 a0003c0007t0007g0147 others(1): Show |
4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+8884G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883506 | |||||||
chr13:46883520 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.613+8870C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883520 | |||||||
chr13:46883558 | T | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0057 others(3): Show |
8 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.613+8832A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883558 | |||||||
chr13:46883724 | A | G | 4 | a0003c0006t0001g0145 a0003c0006t0001g0146 a0003c0007t0007g0147 others(1): Show |
4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+8666T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883724 | |||||||
chr13:46883784 | C | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0053 others(66): Show |
72 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.613+8606G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883784 | |||||||
chr13:46883793 | G | A | 1 | a0001c0001t0020g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+8597C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883793 | |||||||
chr13:46883913 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.613+8477G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883913 | |||||||
chr13:46883917 | C | A | 2 | a0002c0004t0003g0200 a0002c0004t0003g0201 |
2 | HG02056.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.613+8473G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883917 | |||||||
chr13:46883917 | C | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(280): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.613+8473G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883917 | |||||||
chr13:46883959 | G | C | 3 | a0001c0002t0001g0271 a0001c0002t0001g0274 a0001c0002t0033g0273 |
3 | HG02145.hp1 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.613+8431C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46883959 | |||||||
chr13:46884026 | G | A | 2 | a0001c0001t0011g0004 a0001c0005t0026g0026 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+8364C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884026 | |||||||
chr13:46884123 | A | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(307): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.613+8267T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884123 | |||||||
chr13:46884168 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.613+8222G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884168 | |||||||
chr13:46884182 | C | T | 1 | a0002c0003t0003g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.613+8208G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884182 | |||||||
chr13:46884257 | G | A | 1 | a0001c0002t0001g0187 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.613+8133C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884257 | |||||||
chr13:46884281 | A | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0137 others(9): Show |
15 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.613+8109T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884281 | |||||||
chr13:46884446 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.613+7944G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884446 | |||||||
chr13:46884457 | C | G | 216 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(213): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.613+7933G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884457 | |||||||
chr13:46884535 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(96): Show |
107 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.613+7855T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884535 | |||||||
chr13:46884580 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.613+7810G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884580 | |||||||
chr13:46884596 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.613+7794C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884596 | |||||||
chr13:46884603 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0002g0054 |
2 | HG01981.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.613+7787C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884603 | |||||||
chr13:46884675 | A | G | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0137 others(8): Show |
14 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.613+7715T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884675 | |||||||
chr13:46884705 | C | T | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(307): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.613+7685G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884705 | |||||||
chr13:46884739 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(88): Show |
98 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.613+7651G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884739 | |||||||
chr13:46884798 | TTGTG | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(85): Show |
95 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.613+7588_613+7591d others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884798 | |||||||
chr13:46884820 | A | T | 3 | a0001c0002t0001g0230 a0002c0004t0003g0220 a0002c0004t0003g0229 |
3 | HG00099.hp1 HG00140.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.613+7570T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884820 | |||||||
chr13:46884827 | C | CAT | 107 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(104): Show |
115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.613+7561_613+7562d others(4): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884827 | |||||||
chr13:46884827 | C | CATAT | 5 | a0001c0001t0016g0284 a0001c0001t0045g0287 a0001c0002t0002g0029 others(2): Show |
6 | HG02486.hp1 HG02922.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.613+7559_613+7562d others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46884827 | |||||||
chr13:46885069 | G | A | 3 | a0001c0001t0008g0003 a0001c0001t0008g0023 a0001c0001t0023g0022 |
4 | HG02280.hp1 HG02976.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.613+7321C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885069 | |||||||
chr13:46885071 | G | A | 4 | a0001c0001t0016g0284 a0001c0001t0044g0285 a0001c0001t0045g0287 others(1): Show |
5 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+7319C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885071 | |||||||
chr13:46885324 | T | C | 1 | a0001c0002t0001g0239 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.613+7066A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885324 | |||||||
chr13:46885385 | T | C | 6 | a0001c0001t0004g0298 a0001c0001t0051g0299 a0003c0006t0001g0145 others(3): Show |
6 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+7005A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885385 | |||||||
chr13:46885448 | T | A | 1 | a0001c0001t0002g0008 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.613+6942A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885448 | |||||||
chr13:46885451 | T | C | 1 | a0001c0001t0020g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+6939A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885451 | |||||||
chr13:46885572 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.613+6818G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885572 | |||||||
chr13:46885713 | G | C | 1 | a0001c0002t0040g0280 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.613+6677C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885713 | |||||||
chr13:46885937 | C | T | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.613+6453G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46885937 | |||||||
chr13:46886009 | A | G | 4 | a0003c0006t0001g0145 a0003c0006t0001g0146 a0003c0007t0007g0147 others(1): Show |
4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+6381T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886009 | |||||||
chr13:46886048 | G | A | 1 | a0001c0001t0041g0281 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.613+6342C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886048 | |||||||
chr13:46886054 | A | G | 23 | a0001c0001t0004g0292 a0001c0001t0004g0293 a0001c0001t0004g0294 others(20): Show |
24 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.613+6336T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886054 | |||||||
chr13:46886070 | T | C | 2 | a0001c0001t0011g0004 a0001c0005t0026g0026 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+6320A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886070 | |||||||
chr13:46886277 | G | T | 1 | a0001c0002t0001g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.613+6113C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886277 | |||||||
chr13:46886307 | G | T | 10 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+6083C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886307 | |||||||
chr13:46886330 | T | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(307): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.613+6060A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886330 | |||||||
chr13:46886345 | T | TAAATG | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(301): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.613+6044_613+6045i others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886345 | |||||||
chr13:46886378 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.613+6012T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886378 | |||||||
chr13:46886479 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(85): Show |
95 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.613+5911T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886479 | |||||||
chr13:46886490 | CAT | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(85): Show |
95 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.613+5898_613+5899d others(4): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886490 | |||||||
chr13:46886605 | C | T | 10 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+5785G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886605 | |||||||
chr13:46886609 | A | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(275): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.613+5781T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886609 | |||||||
chr13:46886696 | G | A | 1 | a0001c0005t0015g0020 | 2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.613+5694C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886696 | |||||||
chr13:46886755 | G | A | 2 | a0001c0001t0014g0142 a0002c0003t0003g0141 |
2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.613+5635C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886755 | |||||||
chr13:46886885 | G | A | 3 | a0001c0002t0001g0272 a0001c0002t0002g0275 a0001c0002t0005g0276 |
3 | HG01884.hp1 HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.613+5505C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886885 | |||||||
chr13:46886967 | A | T | 1 | a0001c0002t0001g0226 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.613+5423T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46886967 | |||||||
chr13:46887085 | A | G | 1 | a0001c0002t0001g0253 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.613+5305T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887085 | |||||||
chr13:46887145 | C | T | 2 | a0001c0002t0001g0217 a0001c0002t0001g0228 |
2 | NA18943.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.613+5245G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887145 | |||||||
chr13:46887191 | G | A | 4 | a0003c0006t0001g0145 a0003c0006t0001g0146 a0003c0007t0007g0147 others(1): Show |
4 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+5199C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887191 | |||||||
chr13:46887295 | C | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0137 others(9): Show |
15 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.613+5095G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887295 | |||||||
chr13:46887295 | C | T | 1 | a0001c0001t0020g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+5095G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887295 | |||||||
chr13:46887410 | G | A | 2 | a0001c0001t0005g0081 a0001c0001t0010g0080 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.613+4980C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887410 | |||||||
chr13:46887422 | C | CA | 8 | a0001c0001t0001g0135 a0001c0001t0025g0025 a0001c0002t0001g0017 others(5): Show |
8 | HG01167.hp1 HG02015.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.613+4967dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887422 | |||||||
chr13:46887422 | C | CAA | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(221): Show |
239 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.613+4966_613+4967d others(4): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887422 | |||||||
chr13:46887422 | C | CAAA | 16 | a0001c0001t0001g0103 a0001c0001t0010g0115 a0001c0001t0010g0129 others(13): Show |
16 | HG01109.hp2 HG02630.hp2 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.613+4965_613+4967d others(5): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887422 | |||||||
chr13:46887422 | C | CAAAA | 31 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0032 others(28): Show |
33 | HG00099.hp2 HG00280.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.613+4964_613+4967d others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887422 | |||||||
chr13:46887422 | C | CAAAAA | 20 | a0001c0001t0004g0292 a0001c0001t0004g0294 a0001c0001t0004g0295 others(17): Show |
21 | HG00140.hp1 HG01243.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.613+4963_613+4967d others(7): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887422 | |||||||
chr13:46887480 | G | A | 10 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+4910C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887480 | |||||||
chr13:46887503 | G | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0137 others(9): Show |
15 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.613+4887C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887503 | |||||||
chr13:46887599 | A | G | 10 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.613+4791T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887599 | |||||||
chr13:46887615 | T | A | 54 | a0001c0001t0001g0012 a0001c0001t0001g0053 a0001c0001t0001g0083 others(51): Show |
55 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.613+4775A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887615 | |||||||
chr13:46887792 | A | G | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(307): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.613+4598T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46887792 | |||||||
chr13:46888086 | C | CA | 240 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(237): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.613+4303dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888086 | |||||||
chr13:46888086 | C | CAA | 41 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(38): Show |
47 | HG00558.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.613+4302_613+4303d others(4): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888086 | |||||||
chr13:46888086 | C | CAAAA | 9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0137 others(6): Show |
12 | HG01099.hp2 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.613+4300_613+4303d others(6): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888086 | |||||||
chr13:46888189 | C | T | 2 | a0001c0001t0011g0004 a0001c0005t0026g0026 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+4201G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888189 | |||||||
chr13:46888355 | G | A | 1 | a0001c0001t0020g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+4035C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888355 | |||||||
chr13:46888356 | C | A | 1 | a0001c0001t0020g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.613+4034G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888356 | |||||||
chr13:46888470 | G | GA | 172 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0014 others(169): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.613+3919dupT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888470 | |||||||
chr13:46888470 | GA | G | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0032 others(23): Show |
29 | HG00280.hp1 HG01081.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.613+3919delT | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888470 | |||||||
chr13:46888600 | T | G | 2 | a0001c0001t0001g0069 a0001c0001t0002g0068 |
2 | NA18946.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.613+3790A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888600 | |||||||
chr13:46888601 | T | C | 2 | a0001c0001t0001g0069 a0001c0001t0002g0068 |
2 | NA18946.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.613+3789A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888601 | |||||||
chr13:46888665 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(85): Show |
95 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.613+3725T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888665 | |||||||
chr13:46888802 | G | A | 5 | a0001c0001t0016g0284 a0001c0001t0016g0286 a0001c0001t0044g0285 others(2): Show |
6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+3588C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46888802 | |||||||
chr13:46889038 | G | A | 2 | a0001c0001t0047g0308 a0002c0003t0018g0309 |
2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.613+3352C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889038 | |||||||
chr13:46889057 | C | T | 1 | a0003c0007t0007g0147 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.613+3333G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889057 | |||||||
chr13:46889063 | A | G | 12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0137 others(9): Show |
15 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.613+3327T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889063 | |||||||
chr13:46889320 | T | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0137 others(9): Show |
15 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.613+3070A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889320 | |||||||
chr13:46889345 | A | C | 1 | a0001c0001t0001g0083 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.613+3045T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889345 | |||||||
chr13:46889364 | C | T | 12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0137 others(9): Show |
15 | HG01081.hp2 HG01099.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.613+3026G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889364 | |||||||
chr13:46889488 | A | G | 12 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(9): Show |
13 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.613+2902T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889488 | |||||||
chr13:46889511 | G | T | 1 | a0001c0002t0032g0172 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.613+2879C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889511 | |||||||
chr13:46889684 | A | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(277): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.613+2706T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889684 | |||||||
chr13:46889855 | C | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0032 others(22): Show |
28 | HG00280.hp1 HG01081.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.613+2535G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889855 | |||||||
chr13:46889877 | C | T | 1 | a0001c0001t0014g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.613+2513G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889877 | |||||||
chr13:46889984 | T | C | 1 | a0001c0001t0035g0079 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.613+2406A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46889984 | |||||||
chr13:46890036 | T | A | 2 | a0003c0006t0001g0145 a0003c0006t0001g0146 |
2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.613+2354A>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890036 | |||||||
chr13:46890133 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0132 a0001c0001t0006g0161 others(136): Show |
146 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.613+2257G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890133 | |||||||
chr13:46890179 | A | G | 12 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(9): Show |
13 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.613+2211T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890179 | |||||||
chr13:46890203 | C | T | 3 | a0001c0002t0001g0017 a0001c0002t0001g0170 a0002c0004t0003g0171 |
4 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.613+2187G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890203 | |||||||
chr13:46890204 | G | A | 1 | a0001c0002t0002g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.613+2186C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890204 | |||||||
chr13:46890283 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.613+2107G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890283 | |||||||
chr13:46890330 | C | T | 1 | a0002c0003t0003g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.613+2060G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890330 | |||||||
chr13:46890593 | G | C | 2 | a0001c0002t0001g0252 a0001c0002t0001g0253 |
2 | HG02083.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.613+1797C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890593 | |||||||
chr13:46890722 | A | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0132 a0001c0002t0001g0016 others(111): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.613+1668T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890722 | |||||||
chr13:46890757 | A | G | 2 | a0001c0001t0005g0081 a0001c0001t0010g0080 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.613+1633T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890757 | |||||||
chr13:46890804 | C | A | 4 | a0001c0001t0041g0281 a0001c0001t0042g0282 a0001c0001t0043g0283 others(1): Show |
4 | HG00639.hp2 HG02723.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.613+1586G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890804 | |||||||
chr13:46890902 | G | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(29): Show |
38 | HG00558.hp2 HG00735.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.613+1488C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890902 | |||||||
chr13:46890939 | G | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0132 a0001c0001t0006g0161 others(130): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.613+1451C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46890939 | |||||||
chr13:46891009 | C | T | 1 | a0001c0002t0002g0169 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.613+1381G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891009 | |||||||
chr13:46891124 | G | A | 1 | a0001c0002t0002g0266 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.613+1266C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891124 | |||||||
chr13:46891139 | T | C | 1 | a0001c0001t0016g0286 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.613+1251A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891139 | |||||||
chr13:46891303 | A | C | 2 | a0001c0001t0011g0004 a0001c0005t0026g0026 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.613+1087T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891303 | |||||||
chr13:46891379 | A | G | 7 | a0001c0002t0001g0163 a0001c0002t0001g0164 a0001c0002t0001g0165 others(4): Show |
7 | NA18962.hp1 NA18971.hp2 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.613+1011T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891379 | |||||||
chr13:46891554 | G | A | 1 | a0001c0002t0001g0267 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.613+836C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891554 | |||||||
chr13:46891604 | C | A | 1 | a0002c0003t0003g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.613+786G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891604 | |||||||
chr13:46891648 | A | G | 5 | a0001c0001t0016g0284 a0001c0001t0016g0286 a0001c0001t0044g0285 others(2): Show |
6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+742T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891648 | |||||||
chr13:46891796 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | NA18986.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.613+594C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891796 | |||||||
chr13:46891893 | G | A | 1 | a0002c0003t0003g0007 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.613+497C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891893 | |||||||
chr13:46891948 | C | A | 1 | a0001c0001t0010g0129 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.613+442G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46891948 | |||||||
chr13:46892095 | C | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(236): Show |
254 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.613+295G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46892095 | |||||||
chr13:46892249 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.613+141A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | 46892249 | |||||||
chr13:46892646 | T | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.413-56A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46892646 | |||||||
chr13:46892815 | T | G | 55 | a0001c0001t0001g0012 a0001c0001t0001g0053 a0001c0001t0001g0083 others(52): Show |
56 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.413-225A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46892815 | |||||||
chr13:46892902 | G | T | 2 | a0001c0001t0001g0053 a0001c0001t0002g0054 |
2 | HG01981.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.413-312C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46892902 | |||||||
chr13:46892935 | T | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(87): Show |
97 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.413-345A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46892935 | |||||||
chr13:46892969 | A | C | 11 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(8): Show |
11 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.413-379T>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46892969 | |||||||
chr13:46892981 | C | A | 2 | a0003c0007t0007g0147 a0003c0007t0007g0148 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.413-391G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46892981 | |||||||
chr13:46893060 | A | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0032 others(21): Show |
27 | HG00280.hp1 HG01081.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.413-470T>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893060 | |||||||
chr13:46893228 | A | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(308): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.413-638T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893228 | |||||||
chr13:46893232 | G | C | 1 | a0001c0002t0002g0270 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.413-642C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893232 | |||||||
chr13:46893305 | C | G | 1 | a0001c0001t0045g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.413-715G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893305 | |||||||
chr13:46893326 | C | A | 6 | a0001c0002t0001g0271 a0001c0002t0001g0272 a0001c0002t0001g0274 others(3): Show |
6 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.413-736G>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893326 | |||||||
chr13:46893351 | T | G | 1 | a0001c0001t0045g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.413-761A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893351 | |||||||
chr13:46893469 | C | G | 1 | a0001c0002t0001g0016 | 2 | NA18971.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.413-879G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893469 | |||||||
chr13:46893491 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
123 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.413-901C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893491 | |||||||
chr13:46893638 | T | C | 7 | a0001c0001t0011g0004 a0001c0001t0016g0284 a0001c0001t0016g0286 others(4): Show |
9 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.413-1048A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893638 | |||||||
chr13:46893743 | C | T | 24 | a0001c0001t0004g0292 a0001c0001t0004g0293 a0001c0001t0004g0294 others(21): Show |
25 | HG00099.hp2 HG00140.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.413-1153G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893743 | |||||||
chr13:46893836 | C | G | 5 | a0001c0001t0016g0284 a0001c0001t0016g0286 a0001c0001t0044g0285 others(2): Show |
6 | HG02572.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.413-1246G>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46893836 | |||||||
chr13:46894117 | G | C | 11 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(8): Show |
11 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+1378C>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46894117 | |||||||
chr13:46894174 | T | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(165): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.412+1321A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46894174 | |||||||
chr13:46894277 | G | A | 11 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(8): Show |
11 | HG00639.hp1 HG00738.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+1218C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46894277 | |||||||
chr13:46894414 | T | G | 2 | a0001c0002t0001g0278 a0001c0002t0006g0277 |
2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.412+1081A>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46894414 | |||||||
chr13:46894420 | A | G | 1 | a0001c0002t0001g0162 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.412+1075T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46894420 | |||||||
chr13:46894445 | T | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(163): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.412+1050A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46894445 | |||||||
chr13:46894702 | G | A | 1 | a0001c0001t0019g0311 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.412+793C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46894702 | |||||||
chr13:46894726 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.412+769A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46894726 | |||||||
chr13:46895177 | G | A | 1 | a0001c0001t0006g0161 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.412+318C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46895177 | |||||||
chr13:46895200 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(274): Show |
296 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.412+295A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46895200 | |||||||
chr13:46895301 | G | A | 1 | a0001c0001t0020g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.412+194C>T | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 2/3 | chr13 | 46895301 | |||||||
chr13:46896306 | C | T | 2 | a0001c0002t0002g0029 a0001c0002t0005g0028 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-328-72G>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/3 | chr13 | 46896306 | |||||||
chr13:46896346 | G | T | 1 | a0001c0001t0001g0027 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-328-112C>A | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/3 | chr13 | 46896346 | |||||||
chr13:46896465 | A | G | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(304): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.-329+209T>C | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/3 | chr13 | 46896465 | |||||||
chr13:46896655 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-329+19A>G | HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 1/3 | chr13 | 46896655 |