Item | Value |
---|---|
geneid | 4293 |
ensemblid | ENSG00000006432.16 |
hgncid | 6861 |
symbol | MAP3K9 |
name | mitogen-activated protein kinase kinase kinase 9 |
refseq_nuc | NM_001284230.2 |
refseq_prot | NP_001271159.1 |
ensembl_nuc | ENST00000554752.7 |
ensembl_prot | ENSP00000451612.2 |
mane_status | MANE Select |
chr | chr14 |
start | 70722526 |
end | 70809513 |
strand | - |
ver | v1.2 |
region | chr14:70722526-70809513 |
region5000 | chr14:70717526-70814513 |
regionname0 | MAP3K9_chr14_70722526_70809513 |
regionname5000 | MAP3K9_chr14_70717526_70814513 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1104 | 361 | 78 | 64 | 173 | 13 | 31 | 133 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | MEPSR others(1099): Show |
chr14 | 70717526 | 70814513 |
a0002 | 0/0 | 1104 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | MEPSR others(1099): Show |
chr14 | 70717526 | 70814513 |
a0003 | 0/0 | 1104 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | MEPSR others(1099): Show |
chr14 | 70717526 | 70814513 |
a0004 | 0/0 | 1104 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | MEPSR others(1099): Show |
chr14 | 70717526 | 70814513 |
a0005 | 0/0 | 1104 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | MEPSR others(1099): Show |
chr14 | 70717526 | 70814513 |
a0006 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | MEPSR others(1099): Show |
chr14 | 70717526 | 70814513 |
a0007 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | MEPSR others(1099): Show |
chr14 | 70717526 | 70814513 |
a0008 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | MEPSR others(1099): Show |
chr14 | 70717526 | 70814513 |
a0009 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | MEPSR others(1099): Show |
chr14 | 70717526 | 70814513 |
a0010 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | MEPSR others(1099): Show |
chr14 | 70717526 | 70814513 |
a0011 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | MEPSR others(1099): Show |
chr14 | 70717526 | 70814513 |
a0012 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | MEPSR others(1099): Show |
chr14 | 70717526 | 70814513 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3312 | 262 | 49 | 46 | 134 | 8 | 23 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0001c0002 | 0/0 | 3312 | 70 | 11 | 15 | 37 | 1 | 6 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0001c0003 | 0/0 | 3312 | 10 | 4 | 3 | 0 | 1 | 2 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0001c0004 | 0/0 | 3312 | 5 | 5 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0001c0005 | 0/0 | 3312 | 4 | 4 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0001c0006 | 0/0 | 3312 | 4 | 4 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0001c0009 | 0/0 | 3312 | 2 | 0 | 0 | 0 | 2 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0001c0011 | 0/0 | 3312 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0001c0013 | 0/0 | 3312 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0001c0018 | 0/0 | 3312 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0001c0021 | 0/0 | 3312 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0002c0007 | 0/0 | 3312 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0003c0008 | 0/0 | 3312 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0004c0016 | 0/0 | 3312 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0005c0020 | 0/0 | 3312 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0006c0022 | 0/0 | 3312 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0007c0017 | 0/0 | 3312 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0008c0014 | 0/0 | 3312 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0009c0010 | 0/0 | 3312 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0010c0019 | 0/0 | 3312 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0011c0015 | 0/0 | 3312 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 | ||
a0012c0012 | 0/0 | 3312 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | ATGGA others(3307): Show |
chr14 | 70717526 | 70814513 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/1 | 11516 | 29 | 1 | 7 | 11 | 2 | 7 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0003 | 0/0 | 11510 | 30 | 4 | 0 | 25 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11505): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0004 | 1/0 | 11511 | 27 | 1 | 3 | 19 | 0 | 3 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0005 | 0/0 | 11516 | 22 | 0 | 2 | 20 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0006 | 0/0 | 11511 | 18 | 0 | 7 | 8 | 2 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0007 | 0/0 | 11497 | 10 | 7 | 1 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11492): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0009 | 0/0 | 11518 | 10 | 0 | 7 | 0 | 1 | 2 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11513): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0010 | 0/0 | 11511 | 9 | 0 | 0 | 9 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0011 | 0/0 | 11516 | 6 | 0 | 3 | 0 | 1 | 2 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0012 | 0/0 | 11496 | 5 | 5 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11491): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0013 | 0/0 | 11517 | 5 | 0 | 3 | 1 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11512): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0014 | 0/0 | 11510 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11505): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0015 | 0/0 | 11516 | 4 | 2 | 0 | 1 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0016 | 0/0 | 11516 | 3 | 2 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0019 | 0/0 | 11511 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0021 | 0/0 | 11510 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11505): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0024 | 0/0 | 11512 | 3 | 0 | 1 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11507): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0025 | 0/0 | 11512 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11507): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0026 | 0/0 | 11517 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11512): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0027 | 0/0 | 11498 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11493): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0029 | 0/0 | 11510 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11505): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0030 | 0/0 | 11517 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11512): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0033 | 0/0 | 11516 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0034 | 0/0 | 11516 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0035 | 0/0 | 11517 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11512): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0036 | 0/0 | 11515 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11510): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0038 | 0/0 | 11511 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0039 | 0/0 | 11511 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0040 | 0/0 | 11517 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11512): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0043 | 0/0 | 11512 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11507): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0044 | 0/0 | 11511 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0045 | 0/0 | 11511 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0046 | 0/0 | 11510 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11505): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0047 | 0/0 | 11509 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11504): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0051 | 0/0 | 11519 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11514): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0052 | 0/0 | 11517 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11512): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0053 | 0/0 | 11514 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11509): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0054 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0056 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0057 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0064 | 0/0 | 11511 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0065 | 0/0 | 11511 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0068 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0071 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0072 | 0/0 | 11518 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11513): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0073 | 0/0 | 11514 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11509): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0074 | 0/0 | 11514 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11509): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0075 | 0/0 | 11514 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11509): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0076 | 0/0 | 11513 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11508): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0077 | 0/0 | 11512 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11507): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0078 | 0/0 | 11518 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11513): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0079 | 0/0 | 11516 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0080 | 0/0 | 11512 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11507): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0082 | 0/0 | 11517 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11512): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0083 | 0/0 | 11511 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0084 | 0/0 | 11512 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11507): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0085 | 0/0 | 11518 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11513): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0086 | 0/0 | 11517 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11512): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0087 | 0/0 | 11520 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11515): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0088 | 0/0 | 11519 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11514): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0089 | 0/0 | 11519 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11514): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0090 | 0/0 | 11517 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11512): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0091 | 0/0 | 11516 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0093 | 0/0 | 11513 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11508): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0095 | 0/0 | 11512 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11507): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0097 | 0/0 | 11516 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0098 | 0/0 | 11511 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0099 | 0/0 | 11518 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11513): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0100 | 0/0 | 11517 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11512): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0101 | 0/0 | 11517 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11512): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0102 | 0/0 | 11518 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11513): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0103 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0104 | 0/0 | 11518 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11513): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0105 | 0/0 | 11517 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11512): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0108 | 0/0 | 11511 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0109 | 0/0 | 11496 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11491): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0110 | 0/0 | 11496 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11491): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0111 | 0/0 | 11497 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11492): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0112 | 0/0 | 11511 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0001c0001t0113 | 0/0 | 11514 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11509): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0001 | 0/0 | 11499 | 34 | 2 | 13 | 15 | 1 | 3 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11494): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0008 | 0/0 | 11500 | 8 | 0 | 1 | 6 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11495): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0017 | 0/0 | 11499 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11494): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0020 | 0/0 | 11499 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11494): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0022 | 0/0 | 11499 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11494): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0023 | 0/0 | 11498 | 3 | 1 | 1 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11493): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0028 | 0/0 | 11498 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11493): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0031 | 0/0 | 11499 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11494): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0037 | 0/0 | 11500 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11495): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0041 | 0/0 | 11500 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11495): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0042 | 0/0 | 11500 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11495): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0049 | 0/0 | 11499 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11494): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0058 | 0/0 | 11500 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11495): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0059 | 0/0 | 11499 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11494): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0060 | 0/0 | 11499 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11494): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0061 | 0/0 | 11500 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11495): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0062 | 0/0 | 11501 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11496): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0067 | 0/0 | 11499 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11494): Show |
chr14 | 70717526 | 70814513 |
a0001c0002t0069 | 0/0 | 11500 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11495): Show |
chr14 | 70717526 | 70814513 |
a0001c0003t0001 | 0/0 | 11499 | 5 | 1 | 3 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11494): Show |
chr14 | 70717526 | 70814513 |
a0001c0003t0008 | 0/0 | 11500 | 2 | 1 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11495): Show |
chr14 | 70717526 | 70814513 |
a0001c0003t0048 | 0/0 | 11499 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11494): Show |
chr14 | 70717526 | 70814513 |
a0001c0003t0055 | 0/0 | 11501 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11496): Show |
chr14 | 70717526 | 70814513 |
a0001c0003t0107 | 0/0 | 11511 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0001c0004t0007 | 0/0 | 11497 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11492): Show |
chr14 | 70717526 | 70814513 |
a0001c0004t0027 | 0/0 | 11498 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11493): Show |
chr14 | 70717526 | 70814513 |
a0001c0004t0066 | 0/0 | 11497 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11492): Show |
chr14 | 70717526 | 70814513 |
a0001c0005t0005 | 0/0 | 11516 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0005t0035 | 0/0 | 11517 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11512): Show |
chr14 | 70717526 | 70814513 |
a0001c0005t0096 | 0/0 | 11511 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0001c0006t0018 | 0/0 | 11513 | 4 | 4 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11508): Show |
chr14 | 70717526 | 70814513 |
a0001c0009t0032 | 0/0 | 11514 | 2 | 0 | 0 | 0 | 2 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11509): Show |
chr14 | 70717526 | 70814513 |
a0001c0011t0050 | 0/0 | 11516 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0013t0005 | 0/0 | 11516 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0001c0018t0081 | 0/0 | 11512 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11507): Show |
chr14 | 70717526 | 70814513 |
a0001c0021t0070 | 0/0 | 11512 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11507): Show |
chr14 | 70717526 | 70814513 |
a0002c0007t0063 | 0/0 | 11511 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0002c0007t0094 | 0/0 | 11512 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11507): Show |
chr14 | 70717526 | 70814513 |
a0003c0008t0002 | 0/0 | 11516 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0004c0016t0002 | 0/0 | 11516 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0005c0020t0106 | 0/0 | 11511 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0006c0022t0092 | 0/0 | 11512 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11507): Show |
chr14 | 70717526 | 70814513 |
a0007c0017t0025 | 0/0 | 11512 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11507): Show |
chr14 | 70717526 | 70814513 |
a0008c0014t0016 | 0/0 | 11516 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0009c0010t0002 | 0/0 | 11516 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11511): Show |
chr14 | 70717526 | 70814513 |
a0010c0019t0025 | 0/0 | 11512 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11507): Show |
chr14 | 70717526 | 70814513 |
a0011c0015t0004 | 0/0 | 11511 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11506): Show |
chr14 | 70717526 | 70814513 |
a0012c0012t0001 | 0/0 | 11499 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | GCGGA others(11494): Show |
chr14 | 70717526 | 70814513 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0224 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0342 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0007g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0007g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0007g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0007g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0007g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0007g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0007g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0009g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0009g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0009g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0009g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0009g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0009g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0009g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0009g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0009g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0009g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0010g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0010g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0010g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0010g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0010g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0010g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0010g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0010g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0010g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0011g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0011g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0011g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0011g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0012g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0012g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0012g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0012g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0012g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0013g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0013g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0013g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0013g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0013g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0014g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0014g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0014g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0014g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0015g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0015g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0015g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0015g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0016g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0016g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0016g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0019g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0019g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0019g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0019g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0021g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0021g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0021g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0024g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0024g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0024g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0025g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0026g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0026g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0026g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0027g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0029g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0029g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0030g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0030g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0033g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0033g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0034g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0034g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0035g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0036g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0036g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0038g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0039g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0040g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0043g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0044g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0045g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0046g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0047g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0051g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0052g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0053g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0054g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0056g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0057g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0064g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0065g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0068g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0071g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0072g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0073g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0074g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0075g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0076g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0077g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0078g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0079g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0080g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0082g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0083g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0084g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0085g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0086g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0087g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0088g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0089g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0090g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0091g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0093g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0095g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0097g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0098g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0099g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0100g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0101g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0102g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0103g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0104g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0105g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0108g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0109g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0110g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0111g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0112g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0001t0113g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0008g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0008g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0008g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0008g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0008g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0008g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0008g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0008g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0017g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0017g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0017g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0020g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0020g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0022g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0022g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0022g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0023g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0023g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0023g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0028g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0031g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0031g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0037g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0041g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0042g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0049g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0058g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0059g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0060g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0061g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0062g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0067g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0002t0069g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0003t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0003t0008g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0003t0048g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0003t0055g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0003t0107g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0004t0007g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0004t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0004t0027g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0004t0027g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0004t0066g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0005t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0005t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0005t0035g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0005t0096g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0006t0018g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0006t0018g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0006t0018g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0006t0018g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0009t0032g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0009t0032g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0011t0050g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0013t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0018t0081g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0001c0021t0070g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0002c0007t0063g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0002c0007t0094g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0003c0008t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0003c0008t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0004c0016t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0005c0020t0106g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0006c0022t0092g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0007c0017t0025g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0008c0014t0016g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0009c0010t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0010c0019t0025g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0011c0015t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
a0012c0012t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0095 | EUR | GBR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00099 | hp2 | a0001 | c0009 | t0032 | g0123 | EUR | GBR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00140 | hp1 | a0001 | c0001 | t0102 | g0285 | EUR | GBR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0213 | EUR | GBR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00280 | hp1 | a0001 | c0001 | t0006 | g0147 | EUR | FIN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00280 | hp2 | a0001 | c0001 | t0011 | g0292 | EUR | FIN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00323 | hp1 | a0001 | c0003 | t0001 | g0087 | EUR | FIN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00323 | hp2 | a0001 | c0001 | t0009 | g0303 | EUR | FIN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00408 | hp1 | a0001 | c0001 | t0021 | g0121 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00438 | hp1 | a0001 | c0002 | t0008 | g0173 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00438 | hp2 | a0001 | c0001 | t0034 | g0229 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00597 | hp1 | a0001 | c0001 | t0038 | g0015 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00609 | hp1 | a0001 | c0018 | t0081 | g0227 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00609 | hp2 | a0001 | c0001 | t0005 | g0309 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00621 | hp1 | a0001 | c0002 | t0008 | g0171 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0335 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00639 | hp2 | a0001 | c0001 | t0009 | g0289 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00642 | hp2 | a0001 | c0001 | t0105 | g0290 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00673 | hp1 | a0001 | c0001 | t0005 | g0263 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0349 | EAS | CHS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00733 | hp1 | a0001 | c0001 | t0007 | g0284 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00735 | hp1 | a0001 | c0001 | t0099 | g0274 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00735 | hp2 | a0001 | c0001 | t0013 | g0203 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00741 | hp1 | a0001 | c0001 | t0009 | g0291 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG00741 | hp2 | a0001 | c0003 | t0001 | g0078 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0345 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01070 | hp1 | a0001 | c0002 | t0023 | g0106 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01070 | hp2 | a0001 | c0001 | t0005 | g0268 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0344 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01071 | hp2 | a0001 | c0001 | t0005 | g0297 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01074 | hp1 | a0001 | c0001 | t0104 | g0260 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01074 | hp2 | a0001 | c0001 | t0011 | g0010 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01081 | hp1 | a0004 | c0016 | t0002 | g0204 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01081 | hp2 | a0001 | c0001 | t0040 | g0019 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01099 | hp1 | a0001 | c0001 | t0011 | g0010 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0115 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01106 | hp2 | a0001 | c0001 | t0110 | g0324 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01109 | hp1 | a0005 | c0020 | t0106 | g0333 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01109 | hp2 | a0002 | c0007 | t0063 | g0149 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01167 | hp1 | a0001 | c0003 | t0001 | g0070 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0071 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0107 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01192 | hp1 | a0001 | c0001 | t0075 | g0186 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0346 | AMR | PUR | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0109 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0112 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01256 | hp1 | a0001 | c0001 | t0006 | g0162 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01257 | hp2 | a0001 | c0001 | t0009 | g0262 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01346 | hp1 | a0001 | c0001 | t0078 | g0191 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01346 | hp2 | a0001 | c0001 | t0097 | g0283 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01358 | hp1 | a0001 | c0001 | t0009 | g0272 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0108 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01361 | hp1 | a0001 | c0001 | t0013 | g0220 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01433 | hp1 | a0001 | c0001 | t0051 | g0172 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01433 | hp2 | a0001 | c0001 | t0016 | g0130 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01496 | hp1 | a0001 | c0001 | t0013 | g0192 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01496 | hp2 | a0002 | c0007 | t0094 | g0256 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0146 | EUR | IBS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0225 | EUR | IBS | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01884 | hp1 | a0001 | c0004 | t0007 | g0275 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01884 | hp2 | a0001 | c0006 | t0018 | g0164 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01891 | hp1 | a0001 | c0001 | t0012 | g0032 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01891 | hp2 | a0001 | c0001 | t0054 | g0086 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01943 | hp1 | a0001 | c0002 | t0008 | g0119 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01943 | hp2 | a0001 | c0001 | t0009 | g0280 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01952 | hp1 | a0001 | c0001 | t0088 | g0248 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01952 | hp2 | a0001 | c0001 | t0024 | g0142 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01981 | hp1 | a0001 | c0001 | t0006 | g0150 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0073 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01993 | hp2 | a0001 | c0001 | t0006 | g0155 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02004 | hp1 | a0001 | c0001 | t0006 | g0152 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02004 | hp2 | a0001 | c0001 | t0091 | g0251 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02015 | hp2 | a0001 | c0002 | t0017 | g0005 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02040 | hp1 | a0001 | c0002 | t0031 | g0079 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0340 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02055 | hp1 | a0001 | c0001 | t0085 | g0249 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02055 | hp2 | a0006 | c0022 | t0092 | g0258 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02056 | hp1 | a0001 | c0001 | t0026 | g0244 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02071 | hp1 | a0001 | c0001 | t0005 | g0298 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02074 | hp1 | a0001 | c0001 | t0086 | g0253 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0304 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02083 | hp1 | a0001 | c0001 | t0034 | g0230 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02083 | hp2 | a0001 | c0002 | t0031 | g0177 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02132 | hp1 | a0001 | c0002 | t0017 | g0092 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02132 | hp2 | a0001 | c0001 | t0005 | g0301 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02135 | hp2 | a0001 | c0001 | t0095 | g0252 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02145 | hp1 | a0001 | c0001 | t0016 | g0136 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02145 | hp2 | a0001 | c0001 | t0076 | g0182 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | CDX | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02155 | hp2 | a0001 | c0002 | t0067 | g0102 | EAS | CDX | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02257 | hp1 | a0001 | c0001 | t0080 | g0226 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0084 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02258 | hp1 | a0001 | c0001 | t0012 | g0021 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02258 | hp2 | a0001 | c0001 | t0015 | g0126 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02273 | hp2 | a0001 | c0001 | t0006 | g0159 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02280 | hp1 | a0001 | c0001 | t0113 | g0318 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02293 | hp1 | a0001 | c0001 | t0009 | g0287 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02293 | hp2 | a0001 | c0001 | t0006 | g0158 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02300 | hp1 | a0001 | c0001 | t0006 | g0151 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02300 | hp2 | a0001 | c0001 | t0009 | g0354 | AMR | PEL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02451 | hp1 | a0001 | c0001 | t0074 | g0188 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02451 | hp2 | a0001 | c0001 | t0016 | g0132 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02523 | hp1 | a0001 | c0001 | t0006 | g0144 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02523 | hp2 | a0001 | c0001 | t0005 | g0314 | EAS | KHV | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02572 | hp1 | a0001 | c0005 | t0005 | g0322 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02572 | hp2 | a0007 | c0017 | t0025 | g0179 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02602 | hp2 | a0001 | c0002 | t0062 | g0114 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02615 | hp1 | a0001 | c0001 | t0025 | g0026 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02615 | hp2 | a0001 | c0002 | t0049 | g0069 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02622 | hp1 | a0001 | c0001 | t0072 | g0189 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02622 | hp2 | a0001 | c0002 | t0028 | g0006 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02630 | hp2 | a0001 | c0001 | t0033 | g0129 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02647 | hp1 | a0008 | c0014 | t0016 | g0134 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02647 | hp2 | a0001 | c0001 | t0027 | g0243 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0101 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02698 | hp1 | a0009 | c0010 | t0002 | g0208 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02698 | hp2 | a0001 | c0001 | t0009 | g0288 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02717 | hp1 | a0001 | c0001 | t0111 | g0355 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02717 | hp2 | a0001 | c0006 | t0018 | g0138 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02723 | hp1 | a0001 | c0002 | t0022 | g0024 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02723 | hp2 | a0001 | c0001 | t0012 | g0033 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02738 | hp1 | a0001 | c0001 | t0013 | g0223 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02738 | hp2 | a0001 | c0002 | t0008 | g0113 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02809 | hp1 | a0001 | c0006 | t0018 | g0139 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02809 | hp2 | a0001 | c0001 | t0012 | g0031 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02895 | hp1 | a0001 | c0001 | t0007 | g0282 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02895 | hp2 | a0001 | c0003 | t0107 | g0326 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0265 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02897 | hp2 | a0001 | c0001 | t0033 | g0128 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02922 | hp1 | a0001 | c0001 | t0007 | g0325 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02922 | hp2 | a0001 | c0001 | t0057 | g0133 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0278 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02965 | hp2 | a0001 | c0002 | t0023 | g0074 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02970 | hp2 | a0001 | c0002 | t0058 | g0025 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0329 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03041 | hp1 | a0001 | c0001 | t0109 | g0279 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03041 | hp2 | a0001 | c0004 | t0066 | g0034 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03098 | hp1 | a0001 | c0003 | t0055 | g0068 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03098 | hp2 | a0001 | c0001 | t0030 | g0135 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03130 | hp1 | a0001 | c0001 | t0068 | g0127 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03130 | hp2 | a0001 | c0005 | t0035 | g0321 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03139 | hp1 | a0001 | c0002 | t0059 | g0022 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0273 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03195 | hp1 | a0001 | c0005 | t0005 | g0323 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03195 | hp2 | a0001 | c0004 | t0027 | g0246 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03209 | hp1 | a0001 | c0001 | t0029 | g0166 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03209 | hp2 | a0001 | c0001 | t0101 | g0261 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03453 | hp1 | a0001 | c0005 | t0096 | g0319 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03453 | hp2 | a0001 | c0001 | t0012 | g0035 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03486 | hp1 | a0001 | c0001 | t0103 | g0259 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03486 | hp2 | a0010 | c0019 | t0025 | g0180 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03490 | hp1 | a0001 | c0001 | t0011 | g0011 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03490 | hp2 | a0001 | c0001 | t0064 | g0148 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03492 | hp1 | a0001 | c0001 | t0011 | g0011 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03516 | hp1 | a0001 | c0002 | t0022 | g0023 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03516 | hp2 | a0001 | c0002 | t0022 | g0085 | AFR | ESN | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03540 | hp1 | a0001 | c0001 | t0053 | g0124 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03540 | hp2 | a0001 | c0003 | t0008 | g0169 | AFR | GWD | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03579 | hp1 | a0001 | c0001 | t0029 | g0167 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03579 | hp2 | a0001 | c0001 | t0015 | g0125 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03654 | hp1 | a0001 | c0003 | t0008 | g0178 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03654 | hp2 | a0001 | c0001 | t0015 | g0185 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03669 | hp1 | a0001 | c0003 | t0048 | g0088 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0341 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0072 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03710 | hp2 | a0001 | c0001 | t0089 | g0247 | SAS | PJL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03831 | hp1 | a0001 | c0001 | t0093 | g0257 | SAS | BEB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03831 | hp2 | a0001 | c0001 | t0079 | g0209 | SAS | BEB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03834 | hp1 | a0001 | c0001 | t0098 | g0339 | SAS | BEB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03834 | hp2 | a0001 | c0001 | t0009 | g0264 | SAS | BEB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG04115 | hp1 | a0001 | c0001 | t0108 | g0331 | SAS | STU | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0197 | SAS | STU | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG04184 | hp1 | a0001 | c0001 | t0006 | g0165 | SAS | BEB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0350 | SAS | BEB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | STU | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG04199 | hp2 | a0001 | c0002 | t0042 | g0018 | SAS | STU | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0110 | SAS | STU | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0193 | SAS | STU | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | YRI | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18522 | hp2 | a0001 | c0002 | t0028 | g0006 | AFR | YRI | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18612 | hp1 | a0001 | c0001 | t0005 | g0305 | EAS | CHB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | CHB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18747 | hp1 | a0001 | c0001 | t0100 | g0266 | EAS | CHB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18747 | hp2 | a0001 | c0001 | t0006 | g0154 | EAS | CHB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18906 | hp1 | a0001 | c0004 | t0027 | g0242 | AFR | YRI | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18906 | hp2 | a0001 | c0001 | t0077 | g0181 | AFR | YRI | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18939 | hp1 | a0001 | c0001 | t0021 | g0052 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18939 | hp2 | a0001 | c0001 | t0004 | g0327 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18941 | hp1 | a0001 | c0001 | t0019 | g0359 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18943 | hp1 | a0001 | c0002 | t0060 | g0096 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18945 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18946 | hp2 | a0001 | c0001 | t0005 | g0306 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18948 | hp1 | a0001 | c0001 | t0047 | g0063 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18948 | hp2 | a0001 | c0001 | t0005 | g0316 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18949 | hp1 | a0001 | c0001 | t0045 | g0047 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18949 | hp2 | a0001 | c0001 | t0084 | g0234 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18950 | hp1 | a0001 | c0001 | t0014 | g0045 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18950 | hp2 | a0001 | c0001 | t0052 | g0091 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18954 | hp1 | a0001 | c0002 | t0023 | g0075 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18954 | hp2 | a0001 | c0001 | t0005 | g0277 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18956 | hp1 | a0001 | c0001 | t0039 | g0016 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18957 | hp2 | a0001 | c0001 | t0005 | g0299 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18960 | hp2 | a0001 | c0001 | t0019 | g0358 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18962 | hp1 | a0001 | c0001 | t0005 | g0312 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18962 | hp2 | a0001 | c0001 | t0006 | g0156 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18963 | hp2 | a0001 | c0001 | t0004 | g0338 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18964 | hp1 | a0001 | c0001 | t0010 | g0239 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18964 | hp2 | a0003 | c0008 | t0002 | g0215 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18967 | hp1 | a0001 | c0002 | t0020 | g0014 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18967 | hp2 | a0001 | c0001 | t0026 | g0254 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18968 | hp2 | a0001 | c0001 | t0010 | g0238 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18970 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18971 | hp1 | a0001 | c0001 | t0005 | g0311 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18971 | hp2 | a0001 | c0001 | t0004 | g0337 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18972 | hp1 | a0001 | c0002 | t0037 | g0013 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18972 | hp2 | a0001 | c0001 | t0005 | g0295 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18973 | hp1 | a0001 | c0001 | t0005 | g0300 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0332 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18975 | hp2 | a0001 | c0001 | t0090 | g0250 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18978 | hp1 | a0001 | c0001 | t0010 | g0240 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18978 | hp2 | a0001 | c0001 | t0014 | g0043 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18979 | hp1 | a0001 | c0013 | t0005 | g0281 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18980 | hp1 | a0001 | c0001 | t0021 | g0120 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18980 | hp2 | a0001 | c0002 | t0017 | g0005 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18982 | hp2 | a0001 | c0002 | t0069 | g0093 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18983 | hp1 | a0001 | c0001 | t0007 | g0269 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18983 | hp2 | a0001 | c0001 | t0006 | g0153 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18984 | hp2 | a0001 | c0001 | t0065 | g0145 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18986 | hp2 | a0001 | c0001 | t0004 | g0343 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18989 | hp2 | a0001 | c0001 | t0007 | g0308 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18990 | hp1 | a0001 | c0001 | t0013 | g0199 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18990 | hp2 | a0001 | c0001 | t0010 | g0236 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18991 | hp1 | a0001 | c0001 | t0004 | g0334 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18991 | hp2 | a0001 | c0001 | t0082 | g0228 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18992 | hp2 | a0003 | c0008 | t0002 | g0217 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18994 | hp1 | a0001 | c0001 | t0035 | g0293 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0348 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18995 | hp1 | a0001 | c0001 | t0015 | g0184 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18995 | hp2 | a0001 | c0001 | t0014 | g0036 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18998 | hp2 | a0001 | c0001 | t0019 | g0356 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18999 | hp1 | a0001 | c0001 | t0014 | g0044 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0336 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19000 | hp1 | a0001 | c0001 | t0087 | g0255 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19000 | hp2 | a0001 | c0002 | t0061 | g0080 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19001 | hp1 | a0001 | c0001 | t0006 | g0143 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19001 | hp2 | a0001 | c0001 | t0005 | g0315 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19003 | hp1 | a0001 | c0002 | t0017 | g0090 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19003 | hp2 | a0001 | c0001 | t0036 | g0267 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19004 | hp1 | a0001 | c0002 | t0020 | g0003 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19004 | hp2 | a0001 | c0001 | t0010 | g0232 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19007 | hp1 | a0001 | c0001 | t0004 | g0330 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0352 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0313 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19010 | hp1 | a0011 | c0015 | t0004 | g0270 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19011 | hp2 | a0001 | c0001 | t0010 | g0235 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19012 | hp1 | a0001 | c0001 | t0019 | g0357 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19012 | hp2 | a0001 | c0001 | t0026 | g0245 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19030 | hp1 | a0001 | c0021 | t0070 | g0141 | AFR | LWK | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19030 | hp2 | a0001 | c0004 | t0007 | g0276 | AFR | LWK | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0294 | AFR | LWK | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19043 | hp2 | a0001 | c0006 | t0018 | g0140 | AFR | LWK | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19056 | hp1 | a0001 | c0001 | t0005 | g0296 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19056 | hp2 | a0001 | c0002 | t0041 | g0017 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19057 | hp2 | a0001 | c0001 | t0036 | g0310 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19058 | hp2 | a0001 | c0002 | t0008 | g0117 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19060 | hp1 | a0001 | c0001 | t0044 | g0046 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19062 | hp1 | a0001 | c0001 | t0046 | g0057 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19062 | hp2 | a0001 | c0001 | t0006 | g0160 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19076 | hp1 | a0001 | c0001 | t0083 | g0241 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19076 | hp2 | a0001 | c0001 | t0024 | g0168 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19078 | hp1 | a0001 | c0001 | t0043 | g0020 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0353 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19082 | hp1 | a0001 | c0001 | t0010 | g0233 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19084 | hp2 | a0001 | c0001 | t0010 | g0237 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19085 | hp2 | a0001 | c0001 | t0004 | g0351 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19086 | hp1 | a0001 | c0002 | t0008 | g0170 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19086 | hp2 | a0001 | c0001 | t0024 | g0161 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19087 | hp1 | a0001 | c0002 | t0008 | g0077 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19087 | hp2 | a0001 | c0001 | t0010 | g0231 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19088 | hp2 | a0001 | c0001 | t0006 | g0157 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19090 | hp1 | a0001 | c0001 | t0006 | g0163 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19090 | hp2 | a0001 | c0002 | t0008 | g0081 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19091 | hp1 | a0001 | c0001 | t0005 | g0302 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA19091 | hp2 | a0001 | c0002 | t0020 | g0003 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | ASW | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA20129 | hp2 | a0001 | c0001 | t0073 | g0187 | AFR | ASW | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA20752 | hp1 | a0001 | c0011 | t0050 | g0183 | EUR | TSI | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0027 | EUR | TSI | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA20805 | hp1 | a0012 | c0012 | t0001 | g0111 | EUR | TSI | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA20805 | hp2 | a0001 | c0009 | t0032 | g0122 | EUR | TSI | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01123 | hp1 | a0001 | c0001 | t0011 | g0307 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0105 | AMR | CLM | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02486 | hp1 | a0001 | c0001 | t0071 | g0190 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG02486 | hp2 | a0001 | c0001 | t0030 | g0137 | AFR | ACB | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
HG03471 | hp2 | a0001 | c0001 | t0007 | g0317 | AFR | MSL | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | USA | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA20300 | hp2 | a0001 | c0001 | t0112 | g0320 | AFR | USA | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA21309 | hp1 | a0001 | c0001 | t0056 | g0131 | AFR | LWK | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0347 | AFR | LWK | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0224 | REF | REF | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0342 | REF | REF | MAP3K9_chr14_70717526_70814513 | MAP3K9 | chr14 | 70717526 | 70814513 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:70730667 | C | A | 1 | a0010 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.3028G>T | p.Val1010Leu | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3370/11511 | 3028/3315 | 1010/1104 | chr14 | 70730667 | |||
chr14:70732700 | C | T | 1 | a0007 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.2669G>A | p.Arg890Gln | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 3011/11511 | 2669/3315 | 890/1104 | chr14 | 70732700 | |||
chr14:70732718 | C | T | 1 | a0004 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.2651G>A | p.Arg884Gln | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 2993/11511 | 2651/3315 | 884/1104 | chr14 | 70732718 | |||
chr14:70732740 | G | A | 1 | a0002 | 2 | HG01109.hp2 HG01496.hp2 |
missense_variant | MODERATE | c.2629C>T | p.His877Tyr | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 2971/11511 | 2629/3315 | 877/1104 | chr14 | 70732740 | |||
chr14:70733094 | C | T | 1 | a0011 | 1 | NA19010.hp1 | missense_variant | MODERATE | c.2275G>A | p.Val759Ile | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 2617/11511 | 2275/3315 | 759/1104 | chr14 | 70733094 | |||
chr14:70733198 | A | C | 1 | a0008 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.2171T>G | p.Val724Gly | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 2513/11511 | 2171/3315 | 724/1104 | chr14 | 70733198 | |||
chr14:70733255 | C | T | 1 | a0012 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.2114G>A | p.Arg705His | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 2456/11511 | 2114/3315 | 705/1104 | chr14 | 70733255 | |||
chr14:70733304 | G | A | 1 | a0003 | 2 | NA18964.hp2 NA18992.hp2 |
missense_variant | MODERATE | c.2065C>T | p.Arg689Cys | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 2407/11511 | 2065/3315 | 689/1104 | chr14 | 70733304 | |||
chr14:70734475 | T | C | 1 | a0005 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1937A>G | p.Tyr646Cys | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/12 | 2279/11511 | 1937/3315 | 646/1104 | chr14 | 70734475 | |||
chr14:70761150 | G | T | 1 | a0009 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.853C>A | p.Leu285Met | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/12 | 1195/11511 | 853/3315 | 285/1104 | chr14 | 70761150 | |||
chr14:70809047 | G | C | 1 | a0006 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.125C>G | p.Ala42Gly | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/12 | 467/11511 | 125/3315 | 42/1104 | chr14 | 70809047 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:70730455 | G | A | 1 | a0001c0005 | 4 | HG02572.hp1 HG03130.hp2 HG03195.hp1 others(1): Show |
synonymous_variant | LOW | c.3240C>T | p.Thr1080Thr | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3582/11511 | 3240/3315 | 1080/1104 | chr14 | 70730455 | |||
chr14:70730494 | G | A | 1 | a0001c0021 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.3201C>T | p.Leu1067Leu | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3543/11511 | 3201/3315 | 1067/1104 | chr14 | 70730494 | |||
chr14:70730533 | C | T | 1 | a0001c0018 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.3162G>A | p.Pro1054Pro | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3504/11511 | 3162/3315 | 1054/1104 | chr14 | 70730533 | |||
chr14:70732735 | G | A | 4 | a0001c0002 a0001c0003 a0006c0022 others(1): Show |
82 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
synonymous_variant | LOW | c.2634C>T | p.Asn878Asn | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 2976/11511 | 2634/3315 | 878/1104 | chr14 | 70732735 | |||
chr14:70733185 | C | A | 1 | a0001c0004 | 5 | HG01884.hp1 HG03041.hp2 HG03195.hp2 others(2): Show |
synonymous_variant | LOW | c.2184G>T | p.Thr728Thr | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/12 | 2526/11511 | 2184/3315 | 728/1104 | chr14 | 70733185 | |||
chr14:70734429 | C | T | 1 | a0001c0013 | 1 | NA18979.hp1 | synonymous_variant | LOW | c.1983G>A | p.Arg661Arg | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/12 | 2325/11511 | 1983/3315 | 661/1104 | chr14 | 70734429 | |||
chr14:70734462 | C | G | 1 | a0005c0020 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.1950G>C | p.Ser650Ser | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/12 | 2292/11511 | 1950/3315 | 650/1104 | chr14 | 70734462 | |||
chr14:70734489 | G | A | 2 | a0001c0009 a0001c0011 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
synonymous_variant | LOW | c.1923C>T | p.Ser641Ser | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/12 | 2265/11511 | 1923/3315 | 641/1104 | chr14 | 70734489 | |||
chr14:70735975 | T | C | 2 | a0001c0006 a0001c0021 |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
synonymous_variant | LOW | c.1899A>G | p.Pro633Pro | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/12 | 2241/11511 | 1899/3315 | 633/1104 | chr14 | 70735975 | |||
chr14:70738256 | C | T | 2 | a0001c0002 a0012c0012 |
71 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
synonymous_variant | LOW | c.1833G>A | p.Ser611Ser | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/12 | 2175/11511 | 1833/3315 | 611/1104 | chr14 | 70738256 | |||
chr14:70742562 | C | G | 1 | a0001c0011 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.1356G>C | p.Thr452Thr | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/12 | 1698/11511 | 1356/3315 | 452/1104 | chr14 | 70742562 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:70722696 | AGGAAAG | A | 24 | a0001c0002t0001 a0001c0002t0008 a0001c0002t0017 others(21): Show |
80 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*7678_*7683delCTTT others(2): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 7678 | chr14 | 70722696 | ||||||
chr14:70722704 | ACCTGGT | A | 24 | a0001c0002t0001 a0001c0002t0008 a0001c0002t0017 others(21): Show |
80 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*7670_*7675delACCA others(2): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 7670 | chr14 | 70722704 | ||||||
chr14:70722705 | C | T | 2 | a0001c0001t0002 a0001c0001t0013 |
4 | HG01256.hp2 HG01258.hp2 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7675G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 7675 | chr14 | 70722705 | ||||||
chr14:70722744 | T | G | 1 | a0001c0001t0046 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7636A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 7636 | chr14 | 70722744 | ||||||
chr14:70723037 | G | T | 46 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0021 others(43): Show |
140 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*7343C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 7343 | chr14 | 70723037 | ||||||
chr14:70723199 | A | G | 118 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(115): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*7181T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 7181 | chr14 | 70723199 | ||||||
chr14:70723242 | A | C | 1 | a0001c0001t0014 | 4 | NA18950.hp1 NA18978.hp2 NA18995.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7138T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 7138 | chr14 | 70723242 | ||||||
chr14:70723385 | A | G | 1 | a0001c0001t0064 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6995T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6995 | chr14 | 70723385 | ||||||
chr14:70723412 | C | A | 6 | a0001c0001t0071 a0001c0001t0072 a0001c0001t0073 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6968G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6968 | chr14 | 70723412 | ||||||
chr14:70723435 | T | G | 1 | a0001c0001t0110 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6945A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6945 | chr14 | 70723435 | ||||||
chr14:70723557 | C | T | 2 | a0001c0009t0032 a0001c0011t0050 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6823G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6823 | chr14 | 70723557 | ||||||
chr14:70723584 | T | G | 2 | a0001c0009t0032 a0001c0011t0050 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6796A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6796 | chr14 | 70723584 | ||||||
chr14:70723744 | T | TTA | 2 | a0001c0009t0032 a0001c0011t0050 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6634_*6635dupTA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6635 | chr14 | 70723744 | ||||||
chr14:70723770 | G | A | 1 | a0001c0009t0032 | 2 | HG00099.hp2 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6610C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6610 | chr14 | 70723770 | ||||||
chr14:70723809 | T | A | 8 | a0001c0001t0007 a0001c0001t0027 a0001c0001t0111 others(5): Show |
19 | HG00733.hp1 HG01884.hp1 HG02055.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*6571A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6571 | chr14 | 70723809 | ||||||
chr14:70724366 | C | T | 1 | a0001c0001t0077 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6014G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 6014 | chr14 | 70724366 | ||||||
chr14:70724392 | C | T | 2 | a0002c0007t0063 a0002c0007t0094 |
2 | HG01109.hp2 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5988G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5988 | chr14 | 70724392 | ||||||
chr14:70724413 | A | G | 3 | a0001c0001t0071 a0001c0001t0072 a0001c0001t0073 |
3 | HG02486.hp1 HG02622.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5967T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5967 | chr14 | 70724413 | ||||||
chr14:70724415 | T | C | 1 | a0001c0002t0060 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5965A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5965 | chr14 | 70724415 | ||||||
chr14:70724469 | G | C | 1 | a0001c0002t0060 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5911C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5911 | chr14 | 70724469 | ||||||
chr14:70724499 | G | A | 2 | a0001c0003t0107 a0006c0022t0092 |
2 | HG02055.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5881C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5881 | chr14 | 70724499 | ||||||
chr14:70724540 | C | CA | 55 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(52): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*5839dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5839 | chr14 | 70724540 | ||||||
chr14:70724653 | A | G | 1 | a0001c0011t0050 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5727T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5727 | chr14 | 70724653 | ||||||
chr14:70724706 | C | T | 45 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(42): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*5674G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5674 | chr14 | 70724706 | ||||||
chr14:70724720 | C | T | 1 | a0001c0002t0028 | 2 | HG02622.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5660G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5660 | chr14 | 70724720 | ||||||
chr14:70724777 | G | A | 2 | a0001c0001t0089 a0001c0001t0102 |
2 | HG00140.hp1 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5603C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5603 | chr14 | 70724777 | ||||||
chr14:70724856 | G | A | 1 | a0001c0001t0056 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5524C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5524 | chr14 | 70724856 | ||||||
chr14:70724916 | C | G | 6 | a0001c0001t0071 a0001c0001t0072 a0001c0001t0073 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5464G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5464 | chr14 | 70724916 | ||||||
chr14:70725064 | G | A | 1 | a0001c0011t0050 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5316C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5316 | chr14 | 70725064 | ||||||
chr14:70725157 | C | A | 1 | a0001c0001t0090 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5223G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5223 | chr14 | 70725157 | ||||||
chr14:70725178 | C | G | 1 | a0001c0018t0081 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5202G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5202 | chr14 | 70725178 | ||||||
chr14:70725236 | C | A | 3 | a0001c0001t0053 a0001c0006t0018 a0001c0021t0070 |
6 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5144G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5144 | chr14 | 70725236 | ||||||
chr14:70725243 | C | T | 1 | a0001c0011t0050 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5137G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 5137 | chr14 | 70725243 | ||||||
chr14:70725424 | A | G | 3 | a0001c0002t0022 a0001c0002t0058 a0001c0002t0059 |
5 | HG02723.hp1 HG02970.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4956T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 4956 | chr14 | 70725424 | ||||||
chr14:70725722 | A | G | 3 | a0001c0001t0021 a0001c0001t0038 a0001c0001t0044 |
5 | HG00408.hp1 HG00597.hp1 NA18939.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4658T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 4658 | chr14 | 70725722 | ||||||
chr14:70725810 | C | T | 6 | a0001c0001t0007 a0001c0001t0027 a0001c0001t0111 others(3): Show |
17 | HG00733.hp1 HG01884.hp1 HG02647.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4570G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 4570 | chr14 | 70725810 | ||||||
chr14:70725823 | G | A | 59 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0012 others(56): Show |
169 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*4557C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 4557 | chr14 | 70725823 | ||||||
chr14:70725830 | T | TCA | 10 | a0001c0001t0009 a0001c0001t0051 a0001c0001t0072 others(7): Show |
19 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4548_*4549dupTG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 4549 | chr14 | 70725830 | ||||||
chr14:70725830 | TCA | T | 49 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0014 others(46): Show |
147 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*4548_*4549delTG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 4548 | chr14 | 70725830 | ||||||
chr14:70726075 | G | A | 1 | a0001c0001t0110 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4305C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 4305 | chr14 | 70726075 | ||||||
chr14:70726398 | T | C | 2 | a0001c0001t0098 a0001c0001t0108 |
2 | HG03834.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3982A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3982 | chr14 | 70726398 | ||||||
chr14:70726554 | G | T | 1 | a0001c0001t0079 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3826C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3826 | chr14 | 70726554 | ||||||
chr14:70726586 | A | G | 46 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(43): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*3794T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3794 | chr14 | 70726586 | ||||||
chr14:70726588 | T | G | 1 | a0001c0009t0032 | 2 | HG00099.hp2 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3792A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3792 | chr14 | 70726588 | ||||||
chr14:70726629 | T | C | 1 | a0001c0001t0068 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3751A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3751 | chr14 | 70726629 | ||||||
chr14:70726699 | C | T | 9 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0021 others(6): Show |
43 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3681G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3681 | chr14 | 70726699 | ||||||
chr14:70726726 | A | C | 4 | a0001c0001t0054 a0001c0002t0022 a0001c0002t0058 others(1): Show |
6 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3654T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3654 | chr14 | 70726726 | ||||||
chr14:70727081 | C | G | 1 | a0001c0001t0113 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3299G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3299 | chr14 | 70727081 | ||||||
chr14:70727156 | C | T | 2 | a0001c0001t0033 a0001c0001t0068 |
3 | HG02630.hp2 HG02897.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3224G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 3224 | chr14 | 70727156 | ||||||
chr14:70727412 | T | C | 1 | a0001c0001t0065 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2968A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2968 | chr14 | 70727412 | ||||||
chr14:70727436 | C | T | 12 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0051 others(9): Show |
26 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2944G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2944 | chr14 | 70727436 | ||||||
chr14:70727456 | C | G | 1 | a0001c0001t0083 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2924G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2924 | chr14 | 70727456 | ||||||
chr14:70727495 | C | T | 2 | a0002c0007t0063 a0002c0007t0094 |
2 | HG01109.hp2 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2885G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2885 | chr14 | 70727495 | ||||||
chr14:70727518 | T | C | 1 | a0001c0001t0110 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2862A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2862 | chr14 | 70727518 | ||||||
chr14:70727606 | T | C | 8 | a0001c0001t0016 a0001c0001t0030 a0001c0001t0056 others(5): Show |
11 | HG01074.hp1 HG01433.hp2 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2774A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2774 | chr14 | 70727606 | ||||||
chr14:70727722 | G | C | 1 | a0001c0001t0053 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2658C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2658 | chr14 | 70727722 | ||||||
chr14:70727997 | C | A | 1 | a0001c0011t0050 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2383G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2383 | chr14 | 70727997 | ||||||
chr14:70728014 | C | T | 2 | a0001c0002t0031 a0001c0002t0041 |
3 | HG02040.hp1 HG02083.hp2 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2366G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2366 | chr14 | 70728014 | ||||||
chr14:70728057 | C | T | 109 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(106): Show |
297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
3_prime_UTR_variant | MODIFIER | c.*2323G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2323 | chr14 | 70728057 | ||||||
chr14:70728088 | C | T | 1 | a0001c0002t0059 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2292G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2292 | chr14 | 70728088 | ||||||
chr14:70728104 | CAG | C | 2 | a0001c0006t0018 a0001c0021t0070 |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2274_*2275delCT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2274 | chr14 | 70728104 | ||||||
chr14:70728113 | C | CT | 15 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0021 others(12): Show |
56 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2266dupA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2266 | chr14 | 70728113 | ||||||
chr14:70728113 | C | CTT | 27 | a0001c0001t0025 a0001c0001t0044 a0001c0001t0045 others(24): Show |
72 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2265_*2266dupAA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2266 | chr14 | 70728113 | ||||||
chr14:70728113 | C | CTTT | 13 | a0001c0001t0036 a0001c0001t0073 a0001c0001t0074 others(10): Show |
22 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2264_*2266dupAAA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2266 | chr14 | 70728113 | ||||||
chr14:70728113 | C | CTTTT | 30 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(27): Show |
103 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*2263_*2266dupAAAA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2266 | chr14 | 70728113 | ||||||
chr14:70728113 | C | CTTTTT | 15 | a0001c0001t0013 a0001c0001t0030 a0001c0001t0035 others(12): Show |
20 | HG00735.hp2 HG01361.hp1 HG01433.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2262_*2266dupAAAA others(1): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2266 | chr14 | 70728113 | ||||||
chr14:70728113 | C | CTTTTTT | 3 | a0001c0001t0078 a0001c0001t0099 a0001c0006t0018 |
6 | HG00735.hp1 HG01346.hp1 HG01884.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2261_*2266dupAAAA others(2): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2266 | chr14 | 70728113 | ||||||
chr14:70728113 | CTTTTTTT others(7): Show |
C | 9 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0027 others(6): Show |
24 | HG00733.hp1 HG01106.hp2 HG01884.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2253_*2266delAAAA others(10): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2253 | chr14 | 70728113 | ||||||
chr14:70728197 | C | T | 1 | a0001c0011t0050 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2183G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2183 | chr14 | 70728197 | ||||||
chr14:70728246 | C | T | 1 | a0001c0001t0086 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2134G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 2134 | chr14 | 70728246 | ||||||
chr14:70728381 | C | T | 1 | a0001c0001t0085 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1999G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1999 | chr14 | 70728381 | ||||||
chr14:70728413 | C | T | 10 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0021 others(7): Show |
45 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1967G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1967 | chr14 | 70728413 | ||||||
chr14:70728442 | A | T | 1 | a0001c0001t0083 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1938T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1938 | chr14 | 70728442 | ||||||
chr14:70728491 | C | T | 1 | a0001c0002t0049 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1889G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1889 | chr14 | 70728491 | ||||||
chr14:70728635 | G | A | 1 | a0001c0001t0111 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1745C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1745 | chr14 | 70728635 | ||||||
chr14:70728795 | C | T | 2 | a0001c0001t0075 a0001c0001t0113 |
2 | HG01192.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1585G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1585 | chr14 | 70728795 | ||||||
chr14:70728990 | C | T | 1 | a0001c0001t0098 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1390G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1390 | chr14 | 70728990 | ||||||
chr14:70729101 | T | A | 2 | a0001c0001t0112 a0001c0005t0096 |
2 | HG03453.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1279A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1279 | chr14 | 70729101 | ||||||
chr14:70729171 | C | T | 5 | a0001c0001t0071 a0001c0001t0072 a0001c0001t0073 others(2): Show |
5 | HG01192.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1209G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1209 | chr14 | 70729171 | ||||||
chr14:70729182 | G | A | 1 | a0001c0018t0081 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1198C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1198 | chr14 | 70729182 | ||||||
chr14:70729252 | G | A | 2 | a0001c0001t0075 a0001c0001t0113 |
2 | HG01192.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1128C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1128 | chr14 | 70729252 | ||||||
chr14:70729301 | A | G | 1 | a0001c0003t0048 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1079T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1079 | chr14 | 70729301 | ||||||
chr14:70729310 | T | C | 1 | a0001c0002t0067 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1070A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1070 | chr14 | 70729310 | ||||||
chr14:70729357 | A | G | 1 | a0001c0001t0097 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1023T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 1023 | chr14 | 70729357 | ||||||
chr14:70729563 | C | T | 1 | a0001c0005t0096 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*817G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 817 | chr14 | 70729563 | ||||||
chr14:70729625 | G | A | 3 | a0001c0001t0033 a0001c0001t0068 a0001c0018t0081 |
4 | HG00609.hp1 HG02630.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*755C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 755 | chr14 | 70729625 | ||||||
chr14:70729670 | T | C | 2 | a0001c0002t0017 a0001c0002t0069 |
5 | HG02015.hp2 HG02132.hp1 NA18980.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*710A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 710 | chr14 | 70729670 | ||||||
chr14:70729710 | C | T | 10 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0021 others(7): Show |
45 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*670G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 670 | chr14 | 70729710 | ||||||
chr14:70729771 | G | C | 8 | a0001c0001t0071 a0001c0001t0072 a0001c0001t0073 others(5): Show |
11 | HG01192.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*609C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 609 | chr14 | 70729771 | ||||||
chr14:70729988 | C | T | 1 | a0001c0002t0028 | 2 | HG02622.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*392G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 392 | chr14 | 70729988 | ||||||
chr14:70730022 | G | A | 6 | a0001c0001t0071 a0001c0001t0072 a0001c0001t0073 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*358C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 358 | chr14 | 70730022 | ||||||
chr14:70730034 | G | A | 5 | a0001c0001t0025 a0001c0001t0076 a0001c0001t0077 others(2): Show |
5 | HG02145.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*346C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 12/12 | 346 | chr14 | 70730034 | ||||||
chr14:70809261 | A | AC | 20 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0038 others(17): Show |
23 | HG00597.hp1 HG01081.hp2 HG01496.hp2 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-91dupG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/12 | 91 | chr14 | 70809261 | ||||||
chr14:70809268 | C | A | 1 | a0001c0001t0019 | 4 | NA18941.hp1 NA18960.hp2 NA18998.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-97G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/12 | 97 | chr14 | 70809268 | ||||||
chr14:70809268 | C | G | 3 | a0001c0001t0010 a0001c0001t0083 a0001c0001t0084 |
11 | NA18949.hp2 NA18964.hp1 NA18968.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-97G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/12 | 97 | chr14 | 70809268 | ||||||
chr14:70809269 | C | A | 8 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0078 others(5): Show |
40 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(37): Show |
5_prime_UTR_variant | MODIFIER | c.-98G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/12 | 98 | chr14 | 70809269 | ||||||
chr14:70809269 | C | G | 4 | a0001c0001t0034 a0001c0001t0082 a0001c0002t0020 others(1): Show |
7 | HG00438.hp2 HG02083.hp1 NA18967.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-98G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/12 | 98 | chr14 | 70809269 | ||||||
chr14:70809361 | G | A | 1 | a0001c0018t0081 | 1 | HG00609.hp1 | 5_prime_UTR_variant | MODIFIER | c.-190C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/12 | 190 | chr14 | 70809361 | ||||||
chr14:70809489 | A | C | 78 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(75): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
5_prime_UTR_variant | MODIFIER | c.-318T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/12 | 318 | chr14 | 70809489 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:70731038 | T | G | 284 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(281): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2831-174A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731038 | |||||||
chr14:70731059 | T | TAAGAATA others(6079): Show |
1 | a0001c0002t0001g0104 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6088): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6058): Show |
1 | a0001c0002t0069g0093 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6067): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6052): Show |
1 | a0001c0002t0001g0082 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6061): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6087): Show |
1 | a0001c0002t0001g0073 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6096): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6045): Show |
2 | a0001c0002t0001g0097 a0001c0002t0001g0098 |
2 | NA18947.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6054): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6054): Show |
4 | a0001c0002t0001g0094 a0001c0002t0001g0099 a0001c0002t0001g0100 others(1): Show |
4 | HG00621.hp1 HG02071.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6063): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6055): Show |
1 | a0001c0002t0001g0095 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6064): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6057): Show |
4 | a0001c0002t0001g0101 a0001c0002t0020g0003 a0001c0002t0020g0014 others(1): Show |
5 | HG02683.hp1 NA18967.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6066): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6058): Show |
3 | a0001c0002t0017g0005 a0001c0002t0017g0090 a0001c0002t0017g0092 |
4 | HG02015.hp2 HG02132.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6067): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6063): Show |
1 | a0001c0002t0008g0170 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6072): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6066): Show |
2 | a0001c0002t0001g0174 a0001c0002t0008g0117 |
2 | HG02135.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6075): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6067): Show |
2 | a0001c0002t0001g0072 a0001c0002t0001g0083 |
2 | HG03710.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6076): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6068): Show |
1 | a0001c0002t0008g0081 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6077): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6070): Show |
1 | a0001c0002t0001g0118 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6079): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6076): Show |
1 | a0001c0002t0023g0106 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6085): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6077): Show |
3 | a0001c0002t0001g0007 a0001c0002t0001g0107 a0001c0002t0008g0119 |
4 | HG00639.hp1 HG01167.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6086): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6078): Show |
4 | a0001c0002t0001g0008 a0001c0002t0001g0076 a0001c0002t0001g0108 others(1): Show |
5 | HG01358.hp2 HG02273.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6087): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6079): Show |
1 | a0001c0002t0001g0105 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6088): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6080): Show |
1 | a0001c0002t0061g0080 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6089): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6083): Show |
1 | a0001c0002t0001g0004 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6092): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6084): Show |
1 | a0001c0002t0060g0096 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6093): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6085): Show |
1 | a0001c0002t0001g0175 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6094): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6092): Show |
1 | a0001c0002t0001g0089 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6101): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6093): Show |
1 | a0001c0002t0001g0176 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6102): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6078): Show |
1 | a0001c0002t0031g0177 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6087): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6079): Show |
2 | a0001c0002t0031g0079 a0001c0002t0041g0017 |
2 | HG02040.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2831-196_2831-195i others(6088): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6050): Show |
1 | a0001c0002t0008g0077 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6059): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6078): Show |
1 | a0001c0002t0001g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6087): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6077): Show |
1 | a0001c0002t0001g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6086): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6084): Show |
1 | a0001c0002t0001g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6093): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6060): Show |
1 | a0001c0002t0008g0173 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6069): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6060): Show |
1 | a0001c0002t0067g0102 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6069): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731059 | T | TAAGAATA others(6091): Show |
1 | a0001c0002t0001g0103 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2831-196_2831-195i others(6100): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731059 | |||||||
chr14:70731138 | C | T | 1 | a0001c0002t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2831-274G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731138 | |||||||
chr14:70731142 | T | C | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2831-278A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731142 | |||||||
chr14:70731355 | A | C | 76 | a0001c0001t0054g0086 a0001c0001t0093g0257 a0001c0002t0001g0004 others(73): Show |
82 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.2831-491T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731355 | |||||||
chr14:70731494 | C | T | 1 | a0001c0002t0008g0081 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2831-630G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731494 | |||||||
chr14:70731518 | C | T | 1 | a0005c0020t0106g0333 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2831-654G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731518 | |||||||
chr14:70731525 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2831-661C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731525 | |||||||
chr14:70731624 | A | C | 1 | a0001c0001t0006g0153 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2831-760T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731624 | |||||||
chr14:70731650 | T | C | 1 | a0001c0002t0008g0081 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2831-786A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731650 | |||||||
chr14:70731834 | C | T | 142 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(139): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.2830+705G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731834 | |||||||
chr14:70731953 | T | G | 4 | a0001c0002t0022g0023 a0001c0002t0022g0024 a0001c0002t0058g0025 others(1): Show |
4 | HG02723.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2830+586A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70731953 | |||||||
chr14:70732041 | T | C | 42 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(39): Show |
45 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(42): Show |
intron_variant | MODIFIER | c.2830+498A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70732041 | |||||||
chr14:70732050 | G | A | 1 | a0001c0001t0029g0167 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2830+489C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70732050 | |||||||
chr14:70732316 | G | A | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2830+223C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70732316 | |||||||
chr14:70732357 | C | A | 1 | a0006c0022t0092g0258 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2830+182G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70732357 | |||||||
chr14:70732422 | G | A | 2 | a0001c0001t0112g0320 a0001c0005t0096g0319 |
2 | HG03453.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2830+117C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | 70732422 | |||||||
chr14:70733450 | G | T | 1 | a0001c0001t0005g0314 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2027-108C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/11 | chr14 | 70733450 | |||||||
chr14:70733700 | G | A | 1 | a0001c0002t0001g0105 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2027-358C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/11 | chr14 | 70733700 | |||||||
chr14:70733724 | T | C | 1 | a0001c0001t0004g0350 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2027-382A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/11 | chr14 | 70733724 | |||||||
chr14:70733727 | G | C | 4 | a0001c0001t0040g0019 a0001c0005t0005g0322 a0001c0005t0005g0323 others(1): Show |
4 | HG01081.hp2 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2027-385C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/11 | chr14 | 70733727 | |||||||
chr14:70733960 | G | A | 1 | a0001c0004t0066g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2026+426C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/11 | chr14 | 70733960 | |||||||
chr14:70734096 | C | A | 5 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2026+290G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/11 | chr14 | 70734096 | |||||||
chr14:70734215 | T | C | 285 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(282): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2026+171A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/11 | chr14 | 70734215 | |||||||
chr14:70734373 | G | A | 2 | a0001c0002t0001g0175 a0001c0002t0008g0170 |
2 | NA18998.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2026+13C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 10/11 | chr14 | 70734373 | |||||||
chr14:70734642 | C | A | 2 | a0001c0001t0005g0012 a0001c0001t0005g0313 |
3 | NA18945.hp1 NA18970.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1914-144G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70734642 | |||||||
chr14:70734734 | A | C | 75 | a0001c0001t0054g0086 a0001c0002t0001g0004 a0001c0002t0001g0007 others(72): Show |
81 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1914-236T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70734734 | |||||||
chr14:70734924 | C | T | 24 | a0001c0001t0007g0265 a0001c0001t0007g0269 a0001c0001t0007g0273 others(21): Show |
24 | HG00733.hp1 HG01106.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1914-426G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70734924 | |||||||
chr14:70735021 | C | A | 11 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(8): Show |
11 | HG01192.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1914-523G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735021 | |||||||
chr14:70735050 | A | T | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1914-552T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735050 | |||||||
chr14:70735087 | C | T | 311 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(308): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1914-589G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735087 | |||||||
chr14:70735252 | G | T | 1 | a0001c0001t0002g0221 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1913+709C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735252 | |||||||
chr14:70735366 | CT | C | 192 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(189): Show |
204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1913+594delA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735366 | |||||||
chr14:70735376 | T | A | 1 | a0001c0001t0021g0121 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1913+585A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735376 | |||||||
chr14:70735535 | T | G | 7 | a0001c0001t0025g0026 a0001c0001t0076g0182 a0001c0001t0077g0181 others(4): Show |
7 | HG02145.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1913+426A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735535 | |||||||
chr14:70735609 | C | T | 1 | a0001c0002t0001g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1913+352G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735609 | |||||||
chr14:70735610 | G | C | 6 | a0001c0002t0001g0007 a0001c0002t0001g0105 a0001c0002t0001g0107 others(3): Show |
7 | HG00639.hp1 HG01070.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.1913+351C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735610 | |||||||
chr14:70735614 | C | T | 1 | a0001c0001t0053g0124 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1913+347G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735614 | |||||||
chr14:70735933 | C | T | 285 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(282): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1913+28G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 9/11 | chr14 | 70735933 | |||||||
chr14:70736118 | ACAC | A | 65 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(62): Show |
71 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1845-92_1845-90del others(3): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70736118 | |||||||
chr14:70736266 | C | A | 1 | a0001c0001t0090g0250 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1845-237G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70736266 | |||||||
chr14:70736352 | C | T | 1 | a0001c0002t0017g0090 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1845-323G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70736352 | |||||||
chr14:70736393 | G | A | 1 | a0001c0001t0004g0343 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1845-364C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70736393 | |||||||
chr14:70736405 | G | A | 1 | a0001c0001t0003g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1845-376C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70736405 | |||||||
chr14:70736406 | T | A | 3 | a0001c0001t0007g0265 a0001c0001t0007g0282 a0001c0001t0007g0294 |
3 | HG02895.hp1 HG02897.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1845-377A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70736406 | |||||||
chr14:70736514 | T | C | 24 | a0001c0001t0007g0265 a0001c0001t0007g0269 a0001c0001t0007g0273 others(21): Show |
24 | HG00733.hp1 HG01106.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1845-485A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70736514 | |||||||
chr14:70736786 | C | G | 24 | a0001c0001t0007g0265 a0001c0001t0007g0269 a0001c0001t0007g0273 others(21): Show |
24 | HG00733.hp1 HG01106.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1845-757G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70736786 | |||||||
chr14:70737036 | T | C | 1 | a0001c0002t0023g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1845-1007A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737036 | |||||||
chr14:70737149 | A | G | 1 | a0001c0001t0033g0129 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1844+1096T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737149 | |||||||
chr14:70737168 | G | A | 4 | a0001c0001t0007g0273 a0001c0001t0007g0284 a0001c0001t0027g0243 others(1): Show |
4 | HG00733.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1844+1077C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737168 | |||||||
chr14:70737176 | C | G | 2 | a0001c0001t0098g0339 a0001c0001t0108g0331 |
2 | HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1844+1069G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737176 | |||||||
chr14:70737448 | G | C | 119 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(116): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1844+797C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737448 | |||||||
chr14:70737545 | C | T | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1844+700G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737545 | |||||||
chr14:70737557 | G | A | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1844+688C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737557 | |||||||
chr14:70737652 | G | A | 252 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(249): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1844+593C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737652 | |||||||
chr14:70737833 | T | C | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1844+412A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 8/11 | chr14 | 70737833 | |||||||
chr14:70738412 | G | A | 1 | a0001c0002t0001g0095 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1691-14C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70738412 | |||||||
chr14:70738419 | A | G | 24 | a0001c0001t0006g0143 a0001c0001t0006g0144 a0001c0001t0006g0146 others(21): Show |
24 | HG00280.hp1 HG01256.hp1 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.1691-21T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70738419 | |||||||
chr14:70738626 | C | G | 1 | a0001c0001t0006g0155 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1691-228G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70738626 | |||||||
chr14:70738713 | T | C | 43 | a0001c0001t0002g0200 a0001c0001t0002g0222 a0001c0001t0003g0001 others(40): Show |
47 | HG00408.hp1 HG00597.hp1 HG01256.hp2 others(44): Show |
intron_variant | MODIFIER | c.1691-315A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70738713 | |||||||
chr14:70738805 | G | T | 1 | a0001c0002t0001g0103 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1691-407C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70738805 | |||||||
chr14:70738947 | C | T | 2 | a0002c0007t0063g0149 a0002c0007t0094g0256 |
2 | HG01109.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1691-549G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70738947 | |||||||
chr14:70739010 | T | C | 95 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(92): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1691-612A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739010 | |||||||
chr14:70739031 | A | G | 1 | a0001c0001t0009g0291 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1691-633T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739031 | |||||||
chr14:70739090 | C | T | 1 | a0001c0003t0001g0078 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1691-692G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739090 | |||||||
chr14:70739286 | T | C | 1 | a0001c0002t0001g0103 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1690+756A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739286 | |||||||
chr14:70739379 | C | T | 1 | a0001c0001t0009g0354 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1690+663G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739379 | |||||||
chr14:70739502 | T | TCA | 178 | a0001c0001t0002g0197 a0001c0001t0003g0001 a0001c0001t0003g0037 others(175): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1690+538_1690+539d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739502 | |||||||
chr14:70739502 | T | TCACA | 24 | a0001c0001t0005g0263 a0001c0001t0005g0300 a0001c0001t0005g0314 others(21): Show |
26 | HG00099.hp1 HG00639.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1690+536_1690+539d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739502 | |||||||
chr14:70739502 | T | TCACACA | 3 | a0001c0001t0097g0283 a0001c0002t0001g0108 a0001c0003t0055g0068 |
3 | HG01346.hp2 HG01358.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1690+534_1690+539d others(8): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739502 | |||||||
chr14:70739502 | T | TCACACAC others(11): Show |
1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1690+522_1690+539d others(20): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739502 | |||||||
chr14:70739502 | TCA | T | 17 | a0001c0001t0002g0221 a0001c0001t0004g0336 a0001c0001t0004g0337 others(14): Show |
17 | HG02572.hp1 HG03017.hp1 HG03130.hp2 others(14): Show |
intron_variant | MODIFIER | c.1690+538_1690+539d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739502 | |||||||
chr14:70739525 | C | CACTT | 5 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1690+513_1690+516d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739525 | |||||||
chr14:70739546 | A | T | 196 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(193): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1690+496T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739546 | |||||||
chr14:70739558 | C | A | 187 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(184): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1690+484G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739558 | |||||||
chr14:70739834 | G | C | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1690+208C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 7/11 | chr14 | 70739834 | |||||||
chr14:70740200 | C | T | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-36G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70740200 | |||||||
chr14:70740377 | G | A | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1568-213C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70740377 | |||||||
chr14:70740475 | T | C | 5 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1568-311A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70740475 | |||||||
chr14:70740569 | A | G | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1568-405T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70740569 | |||||||
chr14:70740577 | T | C | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1568-413A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70740577 | |||||||
chr14:70740675 | G | A | 1 | a0001c0002t0028g0006 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1568-511C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70740675 | |||||||
chr14:70740883 | C | T | 2 | a0001c0001t0002g0200 a0001c0001t0002g0222 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1568-719G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70740883 | |||||||
chr14:70741096 | C | CT | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-933dupA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741096 | |||||||
chr14:70741161 | G | A | 98 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(95): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1568-997C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741161 | |||||||
chr14:70741186 | G | A | 2 | a0001c0001t0054g0086 a0001c0002t0022g0085 |
2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1568-1022C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741186 | |||||||
chr14:70741251 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1568-1087G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741251 | |||||||
chr14:70741310 | G | A | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1567+1041C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741310 | |||||||
chr14:70741336 | C | T | 52 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0002t0001g0004 others(49): Show |
57 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1567+1015G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741336 | |||||||
chr14:70741504 | A | G | 4 | a0001c0001t0002g0002 a0001c0001t0002g0194 a0001c0001t0002g0195 others(1): Show |
6 | NA18947.hp2 NA18953.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.1567+847T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741504 | |||||||
chr14:70741505 | T | C | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1567+846A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741505 | |||||||
chr14:70741594 | T | G | 1 | a0001c0001t0003g0064 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1567+757A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741594 | |||||||
chr14:70741840 | G | A | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1567+511C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741840 | |||||||
chr14:70741870 | C | T | 1 | a0001c0002t0049g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1567+481G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741870 | |||||||
chr14:70741968 | C | A | 1 | a0009c0010t0002g0208 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1567+383G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741968 | |||||||
chr14:70741976 | T | C | 1 | a0001c0005t0005g0322 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1567+375A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741976 | |||||||
chr14:70741997 | G | A | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1567+354C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70741997 | |||||||
chr14:70742094 | G | C | 2 | a0001c0001t0054g0086 a0001c0002t0022g0085 |
2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1567+257C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70742094 | |||||||
chr14:70742210 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1567+141G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70742210 | |||||||
chr14:70742279 | A | G | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1567+72T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70742279 | |||||||
chr14:70742308 | C | A | 104 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(101): Show |
107 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1567+43G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 6/11 | chr14 | 70742308 | |||||||
chr14:70742610 | C | T | 1 | a0001c0001t0073g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1327-19G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742610 | |||||||
chr14:70742768 | G | T | 1 | a0001c0001t0005g0315 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1327-177C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742768 | |||||||
chr14:70742851 | G | C | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1327-260C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742851 | |||||||
chr14:70742901 | T | TTATATAT others(7): Show |
2 | a0001c0006t0018g0140 a0001c0006t0018g0164 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1327-311_1327-310i others(16): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742901 | |||||||
chr14:70742901 | T | TTATATAT others(13): Show |
1 | a0001c0006t0018g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1327-311_1327-310i others(22): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742901 | |||||||
chr14:70742911 | T | A | 5 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-320A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742911 | |||||||
chr14:70742911 | T | TTA | 3 | a0001c0001t0004g0343 a0001c0001t0098g0339 a0001c0003t0107g0326 |
3 | HG02895.hp2 HG03834.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1327-322_1327-321d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742911 | |||||||
chr14:70742911 | T | TTATA | 4 | a0001c0001t0108g0331 a0001c0009t0032g0122 a0001c0009t0032g0123 others(1): Show |
4 | HG00099.hp2 HG04115.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327-324_1327-321d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742911 | |||||||
chr14:70742911 | TTA | T | 93 | a0001c0001t0003g0001 a0001c0001t0003g0037 a0001c0001t0003g0038 others(90): Show |
96 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1327-322_1327-321d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742911 | |||||||
chr14:70742911 | TTATA | T | 161 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(158): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1327-324_1327-321d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742911 | |||||||
chr14:70742911 | TTATATA | T | 59 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(56): Show |
62 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.1327-326_1327-321d others(8): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70742911 | |||||||
chr14:70743233 | C | T | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1327-642G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743233 | |||||||
chr14:70743279 | C | T | 2 | a0001c0018t0081g0227 a0001c0021t0070g0141 |
2 | HG00609.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1327-688G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743279 | |||||||
chr14:70743498 | A | G | 1 | a0001c0011t0050g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1327-907T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743498 | |||||||
chr14:70743523 | A | C | 2 | a0001c0001t0007g0265 a0001c0001t0007g0282 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1327-932T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743523 | |||||||
chr14:70743699 | G | C | 6 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(3): Show |
6 | HG00609.hp1 HG01884.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1327-1108C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743699 | |||||||
chr14:70743712 | C | A | 1 | a0001c0001t0040g0019 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1327-1121G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743712 | |||||||
chr14:70743766 | A | G | 2 | a0001c0002t0001g0103 a0001c0002t0067g0102 |
2 | HG02155.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1327-1175T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743766 | |||||||
chr14:70743827 | C | T | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1327-1236G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743827 | |||||||
chr14:70743846 | C | T | 1 | a0009c0010t0002g0208 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1327-1255G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743846 | |||||||
chr14:70743854 | G | A | 1 | a0001c0002t0001g0007 | 2 | HG00639.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1327-1263C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743854 | |||||||
chr14:70743905 | C | T | 2 | a0001c0002t0069g0093 a0001c0003t0055g0068 |
2 | HG03098.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1327-1314G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70743905 | |||||||
chr14:70744039 | T | G | 5 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-1448A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744039 | |||||||
chr14:70744180 | G | A | 1 | a0001c0001t0004g0353 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1327-1589C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744180 | |||||||
chr14:70744200 | G | A | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1327-1609C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744200 | |||||||
chr14:70744289 | T | A | 1 | a0001c0002t0008g0081 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1327-1698A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744289 | |||||||
chr14:70744362 | TA | T | 7 | a0001c0001t0012g0021 a0001c0001t0012g0031 a0001c0001t0012g0032 others(4): Show |
7 | HG01891.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1327-1772delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744362 | |||||||
chr14:70744375 | A | G | 1 | a0001c0001t0004g0304 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1327-1784T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744375 | |||||||
chr14:70744421 | G | C | 1 | a0001c0001t0033g0128 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1327-1830C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744421 | |||||||
chr14:70744505 | T | G | 1 | a0001c0002t0008g0081 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1327-1914A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744505 | |||||||
chr14:70744636 | C | T | 28 | a0001c0001t0006g0143 a0001c0001t0006g0144 a0001c0001t0006g0146 others(25): Show |
28 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1327-2045G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744636 | |||||||
chr14:70744981 | AGCACTGA others(7): Show |
A | 1 | a0001c0001t0003g0054 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1327-2404_1327-239 others(18): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70744981 | |||||||
chr14:70745052 | C | T | 1 | a0001c0001t0004g0349 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1327-2461G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745052 | |||||||
chr14:70745074 | T | A | 1 | a0001c0001t0003g0054 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1327-2483A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745074 | |||||||
chr14:70745212 | C | T | 1 | a0008c0014t0016g0134 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1327-2621G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745212 | |||||||
chr14:70745212 | CT | C | 17 | a0001c0001t0006g0150 a0001c0001t0006g0151 a0001c0001t0006g0152 others(14): Show |
17 | HG01256.hp1 HG01952.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1327-2622delA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745212 | |||||||
chr14:70745299 | T | C | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1327-2708A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745299 | |||||||
chr14:70745316 | G | A | 1 | a0001c0001t0005g0316 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1327-2725C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745316 | |||||||
chr14:70745441 | A | G | 56 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(53): Show |
59 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.1327-2850T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745441 | |||||||
chr14:70745475 | C | T | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1327-2884G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745475 | |||||||
chr14:70745504 | G | A | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1327-2913C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745504 | |||||||
chr14:70745511 | G | T | 3 | a0001c0003t0008g0169 a0001c0003t0008g0178 a0001c0003t0055g0068 |
3 | HG03098.hp1 HG03540.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1327-2920C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745511 | |||||||
chr14:70745663 | G | A | 3 | a0001c0009t0032g0122 a0001c0009t0032g0123 a0001c0011t0050g0183 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1327-3072C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745663 | |||||||
chr14:70745669 | T | C | 295 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(292): Show |
310 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.1327-3078A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745669 | |||||||
chr14:70745731 | C | A | 1 | a0001c0001t0010g0231 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1326+3098G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745731 | |||||||
chr14:70745737 | C | CA | 9 | a0001c0001t0043g0020 a0001c0001t0071g0190 a0001c0001t0072g0189 others(6): Show |
9 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1326+3091dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745737 | |||||||
chr14:70745752 | T | G | 1 | a0001c0005t0096g0319 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1326+3077A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70745752 | |||||||
chr14:70746007 | A | C | 2 | a0001c0001t0007g0273 a0001c0001t0007g0284 |
2 | HG00733.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1326+2822T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746007 | |||||||
chr14:70746024 | G | A | 1 | a0001c0005t0096g0319 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1326+2805C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746024 | |||||||
chr14:70746097 | T | C | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1326+2732A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746097 | |||||||
chr14:70746352 | C | T | 1 | a0001c0001t0003g0041 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1326+2477G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746352 | |||||||
chr14:70746356 | T | C | 1 | a0001c0001t0004g0349 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1326+2473A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746356 | |||||||
chr14:70746369 | G | A | 295 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(292): Show |
310 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.1326+2460C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746369 | |||||||
chr14:70746398 | C | T | 55 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(52): Show |
58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1326+2431G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746398 | |||||||
chr14:70746403 | T | C | 1 | a0001c0001t0003g0054 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1326+2426A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746403 | |||||||
chr14:70746473 | A | G | 55 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(52): Show |
58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1326+2356T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746473 | |||||||
chr14:70746497 | A | G | 1 | a0001c0001t0002g0207 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1326+2332T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746497 | |||||||
chr14:70746777 | G | A | 1 | a0001c0002t0023g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1326+2052C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746777 | |||||||
chr14:70746790 | G | C | 1 | a0001c0005t0096g0319 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1326+2039C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746790 | |||||||
chr14:70746969 | C | T | 2 | a0001c0001t0038g0015 a0001c0001t0044g0046 |
2 | HG00597.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1326+1860G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70746969 | |||||||
chr14:70747154 | T | C | 295 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(292): Show |
310 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.1326+1675A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70747154 | |||||||
chr14:70747167 | TG | T | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1326+1661delC | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70747167 | |||||||
chr14:70747521 | T | C | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1326+1308A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70747521 | |||||||
chr14:70747550 | G | A | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1326+1279C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70747550 | |||||||
chr14:70747965 | G | T | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1326+864C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70747965 | |||||||
chr14:70747991 | C | T | 1 | a0001c0002t0001g0083 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1326+838G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70747991 | |||||||
chr14:70748061 | C | T | 1 | a0001c0011t0050g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1326+768G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748061 | |||||||
chr14:70748063 | T | C | 295 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(292): Show |
310 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.1326+766A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748063 | |||||||
chr14:70748104 | C | CA | 164 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(161): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1326+724dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748104 | |||||||
chr14:70748104 | C | CAA | 74 | a0001c0001t0005g0295 a0001c0001t0051g0172 a0001c0001t0052g0091 others(71): Show |
80 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.1326+723_1326+724d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748104 | |||||||
chr14:70748121 | T | A | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1326+708A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748121 | |||||||
chr14:70748123 | G | A | 295 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(292): Show |
310 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.1326+706C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748123 | |||||||
chr14:70748158 | TC | T | 3 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 |
3 | HG02486.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1326+670delG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748158 | |||||||
chr14:70748253 | T | C | 1 | a0001c0001t0005g0309 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1326+576A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748253 | |||||||
chr14:70748314 | C | T | 2 | a0001c0003t0008g0169 a0001c0003t0008g0178 |
2 | HG03540.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1326+515G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748314 | |||||||
chr14:70748514 | A | G | 347 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(344): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.1326+315T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748514 | |||||||
chr14:70748532 | G | A | 28 | a0001c0001t0006g0143 a0001c0001t0006g0144 a0001c0001t0006g0146 others(25): Show |
28 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1326+297C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748532 | |||||||
chr14:70748596 | T | G | 1 | a0001c0002t0028g0006 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1326+233A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748596 | |||||||
chr14:70748663 | T | G | 190 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(187): Show |
202 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1326+166A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748663 | |||||||
chr14:70748677 | T | G | 52 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0002t0001g0004 others(49): Show |
57 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1326+152A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748677 | |||||||
chr14:70748707 | T | C | 1 | a0001c0001t0098g0339 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1326+122A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748707 | |||||||
chr14:70748736 | G | A | 2 | a0001c0011t0050g0183 a0001c0013t0005g0281 |
2 | NA18979.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1326+93C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748736 | |||||||
chr14:70748809 | G | GT | 46 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(43): Show |
49 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(46): Show |
intron_variant | MODIFIER | c.1326+19dupA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 5/11 | chr14 | 70748809 | |||||||
chr14:70749012 | G | A | 104 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(101): Show |
107 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
splice_region_variant&intron_variant | LOW | c.1151-8C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 4/11 | chr14 | 70749012 | |||||||
chr14:70749050 | C | G | 1 | a0001c0006t0018g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1151-46G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 4/11 | chr14 | 70749050 | |||||||
chr14:70749105 | T | C | 52 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0002t0001g0004 others(49): Show |
57 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1151-101A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 4/11 | chr14 | 70749105 | |||||||
chr14:70749386 | T | C | 1 | a0001c0001t0003g0027 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1151-382A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 4/11 | chr14 | 70749386 | |||||||
chr14:70750146 | C | CAT | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1002-66_1002-65ins others(2): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750146 | |||||||
chr14:70750296 | C | T | 145 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(142): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1002-215G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750296 | |||||||
chr14:70750357 | C | G | 5 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002-276G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750357 | |||||||
chr14:70750502 | T | C | 102 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(99): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1002-421A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750502 | |||||||
chr14:70750504 | G | T | 145 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(142): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1002-423C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750504 | |||||||
chr14:70750541 | G | A | 1 | a0001c0001t0004g0340 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1002-460C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750541 | |||||||
chr14:70750546 | G | A | 1 | a0001c0021t0070g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1002-465C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750546 | |||||||
chr14:70750633 | C | T | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002-552G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750633 | |||||||
chr14:70750669 | G | C | 3 | a0001c0002t0020g0003 a0001c0002t0020g0014 a0001c0002t0037g0013 |
4 | NA18967.hp1 NA18972.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1002-588C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750669 | |||||||
chr14:70750717 | C | T | 1 | a0001c0005t0096g0319 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1002-636G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750717 | |||||||
chr14:70750731 | C | T | 2 | a0001c0001t0005g0311 a0001c0001t0036g0310 |
2 | NA18971.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1002-650G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750731 | |||||||
chr14:70750911 | A | T | 145 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(142): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1002-830T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750911 | |||||||
chr14:70750996 | A | T | 5 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002-915T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70750996 | |||||||
chr14:70751027 | C | T | 2 | a0003c0008t0002g0215 a0003c0008t0002g0217 |
2 | NA18964.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1002-946G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751027 | |||||||
chr14:70751035 | C | T | 2 | a0001c0002t0023g0074 a0001c0018t0081g0227 |
2 | HG00609.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1002-954G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751035 | |||||||
chr14:70751059 | C | CTCTA | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1002-982_1002-979d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751059 | |||||||
chr14:70751135 | T | C | 12 | a0001c0002t0001g0067 a0001c0002t0001g0112 a0001c0002t0008g0113 others(9): Show |
12 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1002-1054A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751135 | |||||||
chr14:70751293 | A | G | 1 | a0001c0001t0006g0143 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1002-1212T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751293 | |||||||
chr14:70751348 | T | A | 1 | a0001c0001t0012g0021 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1002-1267A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751348 | |||||||
chr14:70751404 | T | G | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(51): Show |
57 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.1002-1323A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751404 | |||||||
chr14:70751425 | G | A | 1 | a0001c0001t0005g0314 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1002-1344C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751425 | |||||||
chr14:70751460 | C | T | 4 | a0001c0003t0001g0084 a0001c0003t0008g0169 a0001c0003t0008g0178 others(1): Show |
4 | HG02257.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002-1379G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751460 | |||||||
chr14:70751462 | G | A | 5 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002-1381C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751462 | |||||||
chr14:70751466 | A | T | 4 | a0001c0003t0001g0084 a0001c0003t0008g0169 a0001c0003t0008g0178 others(1): Show |
4 | HG02257.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002-1385T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751466 | |||||||
chr14:70751514 | T | C | 1 | a0001c0005t0096g0319 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1002-1433A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751514 | |||||||
chr14:70751724 | A | T | 1 | a0001c0002t0001g0073 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1002-1643T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751724 | |||||||
chr14:70751971 | T | C | 1 | a0001c0001t0012g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1002-1890A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70751971 | |||||||
chr14:70752219 | T | A | 187 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(184): Show |
199 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1002-2138A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752219 | |||||||
chr14:70752285 | G | A | 1 | a0001c0002t0017g0090 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1002-2204C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752285 | |||||||
chr14:70752371 | T | C | 190 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(187): Show |
202 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1002-2290A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752371 | |||||||
chr14:70752427 | C | A | 1 | a0001c0021t0070g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1002-2346G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752427 | |||||||
chr14:70752447 | A | G | 2 | a0001c0001t0002g0200 a0001c0001t0002g0222 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1002-2366T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752447 | |||||||
chr14:70752457 | C | G | 4 | a0001c0002t0022g0023 a0001c0002t0022g0024 a0001c0002t0058g0025 others(1): Show |
4 | HG02723.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1002-2376G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752457 | |||||||
chr14:70752493 | G | A | 75 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(72): Show |
78 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1002-2412C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752493 | |||||||
chr14:70752792 | T | C | 1 | a0001c0001t0053g0124 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1002-2711A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752792 | |||||||
chr14:70752846 | G | A | 4 | a0001c0003t0001g0084 a0001c0003t0008g0169 a0001c0003t0008g0178 others(1): Show |
4 | HG02257.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002-2765C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752846 | |||||||
chr14:70752860 | C | T | 2 | a0001c0001t0002g0202 a0001c0005t0096g0319 |
2 | HG01069.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1002-2779G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70752860 | |||||||
chr14:70753036 | C | T | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1002-2955G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753036 | |||||||
chr14:70753116 | C | G | 3 | a0001c0009t0032g0122 a0001c0009t0032g0123 a0001c0011t0050g0183 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1002-3035G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753116 | |||||||
chr14:70753154 | C | T | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1002-3073G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753154 | |||||||
chr14:70753242 | G | C | 5 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002-3161C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753242 | |||||||
chr14:70753320 | G | A | 177 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(174): Show |
189 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1002-3239C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753320 | |||||||
chr14:70753380 | T | G | 1 | a0009c0010t0002g0208 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1002-3299A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753380 | |||||||
chr14:70753499 | G | A | 185 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(182): Show |
197 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1002-3418C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753499 | |||||||
chr14:70753634 | C | T | 1 | a0001c0001t0002g0218 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1002-3553G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753634 | |||||||
chr14:70753636 | C | T | 1 | a0001c0001t0006g0147 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1002-3555G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753636 | |||||||
chr14:70753782 | C | T | 4 | a0001c0002t0022g0023 a0001c0002t0022g0024 a0001c0002t0058g0025 others(1): Show |
4 | HG02723.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1002-3701G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753782 | |||||||
chr14:70753862 | A | G | 172 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(169): Show |
184 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1002-3781T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753862 | |||||||
chr14:70753906 | T | C | 191 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(188): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1002-3825A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70753906 | |||||||
chr14:70754137 | T | C | 1 | a0001c0001t0053g0124 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1002-4056A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754137 | |||||||
chr14:70754145 | A | G | 1 | a0001c0001t0009g0264 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1002-4064T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754145 | |||||||
chr14:70754183 | C | G | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1002-4102G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754183 | |||||||
chr14:70754378 | C | T | 1 | a0001c0003t0048g0088 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1002-4297G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754378 | |||||||
chr14:70754421 | A | G | 1 | a0001c0002t0017g0092 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1002-4340T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754421 | |||||||
chr14:70754479 | A | G | 1 | a0001c0001t0003g0064 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1002-4398T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754479 | |||||||
chr14:70754533 | G | C | 1 | a0001c0001t0011g0010 | 2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1002-4452C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754533 | |||||||
chr14:70754534 | C | T | 48 | a0001c0001t0051g0172 a0001c0002t0001g0004 a0001c0002t0001g0007 others(45): Show |
53 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1002-4453G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754534 | |||||||
chr14:70754565 | G | A | 1 | a0001c0001t0007g0325 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1002-4484C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754565 | |||||||
chr14:70754609 | C | CT | 5 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002-4529dupA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754609 | |||||||
chr14:70754760 | C | T | 2 | a0001c0003t0107g0326 a0006c0022t0092g0258 |
2 | HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1002-4679G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754760 | |||||||
chr14:70754806 | C | A | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1002-4725G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754806 | |||||||
chr14:70754895 | C | T | 1 | a0001c0001t0024g0142 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1002-4814G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754895 | |||||||
chr14:70754972 | A | G | 5 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002-4891T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70754972 | |||||||
chr14:70755011 | A | T | 1 | a0001c0003t0001g0071 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1002-4930T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755011 | |||||||
chr14:70755140 | G | T | 1 | a0001c0001t0007g0278 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1002-5059C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755140 | |||||||
chr14:70755300 | G | A | 2 | a0001c0001t0011g0011 a0001c0001t0011g0307 |
3 | HG01123.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1002-5219C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755300 | |||||||
chr14:70755348 | G | A | 281 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(278): Show |
296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.1002-5267C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755348 | |||||||
chr14:70755722 | T | C | 1 | a0001c0002t0022g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1001+5280A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755722 | |||||||
chr14:70755726 | T | C | 13 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0001c0001t0112g0320 others(10): Show |
13 | HG00099.hp2 HG00609.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1001+5276A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755726 | |||||||
chr14:70755727 | G | A | 5 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0001c0018t0081g0227 others(2): Show |
5 | HG00609.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1001+5275C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755727 | |||||||
chr14:70755746 | G | C | 1 | a0001c0011t0050g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1001+5256C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755746 | |||||||
chr14:70755795 | T | C | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1001+5207A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755795 | |||||||
chr14:70755873 | G | T | 1 | a0001c0002t0060g0096 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1001+5129C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755873 | |||||||
chr14:70755888 | C | T | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1001+5114G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70755888 | |||||||
chr14:70756035 | T | C | 1 | a0001c0002t0001g0073 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1001+4967A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70756035 | |||||||
chr14:70756271 | G | A | 1 | a0001c0011t0050g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1001+4731C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70756271 | |||||||
chr14:70756345 | C | A | 1 | a0001c0001t0005g0301 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1001+4657G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70756345 | |||||||
chr14:70756388 | A | C | 1 | a0001c0001t0002g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1001+4614T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70756388 | |||||||
chr14:70756480 | T | A | 11 | a0001c0001t0007g0265 a0001c0001t0007g0269 a0001c0001t0007g0273 others(8): Show |
11 | HG00733.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1001+4522A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70756480 | |||||||
chr14:70756551 | C | A | 1 | a0001c0001t0110g0324 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1001+4451G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70756551 | |||||||
chr14:70757098 | C | CA | 5 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001+3903dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757098 | |||||||
chr14:70757387 | G | A | 1 | a0001c0001t0029g0166 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1001+3615C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757387 | |||||||
chr14:70757438 | G | A | 4 | a0001c0001t0007g0273 a0001c0001t0007g0284 a0001c0001t0027g0243 others(1): Show |
4 | HG00733.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1001+3564C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757438 | |||||||
chr14:70757456 | G | GA | 7 | a0001c0001t0004g0341 a0001c0001t0004g0353 a0001c0001t0005g0295 others(4): Show |
7 | HG02135.hp2 HG03669.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.1001+3545dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757456 | |||||||
chr14:70757456 | GA | G | 189 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(186): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.1001+3545delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757456 | |||||||
chr14:70757503 | T | C | 190 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(187): Show |
202 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1001+3499A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757503 | |||||||
chr14:70757525 | C | A | 1 | a0001c0003t0055g0068 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1001+3477G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757525 | |||||||
chr14:70757606 | C | T | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001+3396G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757606 | |||||||
chr14:70757808 | G | A | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1001+3194C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757808 | |||||||
chr14:70757834 | T | A | 1 | a0001c0002t0049g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1001+3168A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757834 | |||||||
chr14:70757979 | A | G | 5 | a0001c0003t0001g0070 a0001c0003t0001g0071 a0001c0003t0001g0078 others(2): Show |
5 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001+3023T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757979 | |||||||
chr14:70757982 | A | G | 1 | a0001c0003t0001g0070 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1001+3020T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70757982 | |||||||
chr14:70758015 | A | T | 1 | a0001c0003t0001g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1001+2987T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758015 | |||||||
chr14:70758073 | C | T | 5 | a0001c0001t0109g0279 a0001c0004t0007g0275 a0001c0004t0007g0276 others(2): Show |
5 | HG01884.hp1 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1001+2929G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758073 | |||||||
chr14:70758282 | G | C | 5 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001+2720C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758282 | |||||||
chr14:70758319 | T | C | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1001+2683A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758319 | |||||||
chr14:70758381 | T | A | 5 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001+2621A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758381 | |||||||
chr14:70758382 | T | A | 180 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(177): Show |
192 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1001+2620A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758382 | |||||||
chr14:70758383 | A | T | 27 | a0001c0001t0006g0143 a0001c0001t0006g0144 a0001c0001t0006g0146 others(24): Show |
27 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1001+2619T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758383 | |||||||
chr14:70758394 | A | G | 1 | a0001c0003t0001g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1001+2608T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758394 | |||||||
chr14:70758440 | T | C | 3 | a0001c0002t0001g0076 a0001c0002t0008g0081 a0001c0002t0061g0080 |
3 | NA18986.hp1 NA19000.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1001+2562A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758440 | |||||||
chr14:70758448 | G | A | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1001+2554C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758448 | |||||||
chr14:70758577 | G | A | 5 | a0001c0001t0112g0320 a0001c0005t0005g0322 a0001c0005t0005g0323 others(2): Show |
5 | HG02572.hp1 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001+2425C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758577 | |||||||
chr14:70758590 | C | T | 1 | a0001c0001t0004g0329 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1001+2412G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758590 | |||||||
chr14:70758674 | A | G | 1 | a0001c0002t0049g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1001+2328T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758674 | |||||||
chr14:70758756 | C | G | 6 | a0001c0001t0012g0021 a0001c0001t0012g0031 a0001c0001t0012g0032 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001+2246G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758756 | |||||||
chr14:70758928 | A | C | 1 | a0001c0002t0028g0006 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1001+2074T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70758928 | |||||||
chr14:70759085 | T | C | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001+1917A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70759085 | |||||||
chr14:70759350 | G | A | 1 | a0001c0021t0070g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1001+1652C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70759350 | |||||||
chr14:70759381 | G | A | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1001+1621C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70759381 | |||||||
chr14:70759544 | T | C | 3 | a0001c0001t0004g0336 a0001c0001t0004g0337 a0001c0001t0004g0338 |
3 | NA18963.hp2 NA18971.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1001+1458A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70759544 | |||||||
chr14:70759586 | G | C | 99 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(96): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1001+1416C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70759586 | |||||||
chr14:70759842 | C | T | 20 | a0001c0002t0001g0067 a0001c0002t0001g0112 a0001c0002t0008g0113 others(17): Show |
21 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1001+1160G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70759842 | |||||||
chr14:70759863 | T | C | 1 | a0001c0002t0023g0075 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1001+1139A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70759863 | |||||||
chr14:70759881 | C | T | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1001+1121G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70759881 | |||||||
chr14:70760053 | GC | G | 120 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(117): Show |
127 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1001+948delG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760053 | |||||||
chr14:70760078 | CA | C | 4 | a0001c0001t0057g0133 a0001c0001t0110g0324 a0001c0003t0107g0326 others(1): Show |
4 | HG01106.hp2 HG02055.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001+923delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760078 | |||||||
chr14:70760094 | C | T | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1001+908G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760094 | |||||||
chr14:70760095 | G | A | 1 | a0001c0002t0008g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1001+907C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760095 | |||||||
chr14:70760141 | G | GCA | 18 | a0001c0001t0004g0336 a0001c0001t0004g0337 a0001c0001t0004g0338 others(15): Show |
19 | HG00733.hp1 HG01123.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.1001+859_1001+860d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760141 | |||||||
chr14:70760141 | G | GCACA | 58 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(55): Show |
62 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.1001+857_1001+860d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760141 | |||||||
chr14:70760141 | G | GCACACA | 64 | a0001c0001t0003g0066 a0001c0001t0004g0271 a0001c0001t0004g0304 others(61): Show |
65 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1001+855_1001+860d others(8): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760141 | |||||||
chr14:70760141 | G | GCACACAC others(1): Show |
64 | a0001c0001t0003g0050 a0001c0001t0005g0299 a0001c0001t0005g0300 others(61): Show |
69 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1001+853_1001+860d others(10): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760141 | |||||||
chr14:70760141 | G | GCACACAC others(3): Show |
9 | a0001c0001t0026g0245 a0001c0001t0109g0279 a0001c0002t0001g0083 others(6): Show |
9 | HG01361.hp2 HG02080.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1001+851_1001+860d others(12): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760141 | |||||||
chr14:70760141 | G | GCACACAC others(5): Show |
3 | a0001c0002t0001g0110 a0001c0002t0008g0117 a0001c0006t0018g0139 |
3 | HG02809.hp1 HG04204.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1001+849_1001+860d others(14): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760141 | |||||||
chr14:70760141 | GCACACAC others(1): Show |
G | 78 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(75): Show |
82 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.1001+853_1001+860d others(10): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760141 | |||||||
chr14:70760170 | CACAT | C | 3 | a0001c0001t0073g0187 a0001c0001t0075g0186 a0001c0001t0113g0318 |
3 | HG01192.hp1 HG02280.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1001+828_1001+831d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760170 | |||||||
chr14:70760174 | T | C | 100 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(97): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1001+828A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760174 | |||||||
chr14:70760306 | T | C | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001+696A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760306 | |||||||
chr14:70760323 | G | A | 1 | a0001c0001t0011g0292 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1001+679C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760323 | |||||||
chr14:70760560 | A | G | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1001+442T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760560 | |||||||
chr14:70760825 | G | A | 1 | a0001c0001t0112g0320 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1001+177C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 3/11 | chr14 | 70760825 | |||||||
chr14:70761196 | A | C | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.821-14T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761196 | |||||||
chr14:70761283 | G | A | 104 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(101): Show |
107 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.821-101C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761283 | |||||||
chr14:70761320 | C | A | 1 | a0001c0002t0001g0083 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.821-138G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761320 | |||||||
chr14:70761491 | A | T | 5 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.821-309T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761491 | |||||||
chr14:70761534 | G | A | 6 | a0001c0001t0012g0021 a0001c0001t0012g0031 a0001c0001t0012g0032 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.821-352C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761534 | |||||||
chr14:70761606 | T | C | 11 | a0001c0001t0007g0265 a0001c0001t0007g0269 a0001c0001t0007g0273 others(8): Show |
11 | HG00733.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.821-424A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761606 | |||||||
chr14:70761672 | G | A | 4 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(1): Show |
4 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-490C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761672 | |||||||
chr14:70761745 | T | C | 12 | a0001c0002t0001g0067 a0001c0002t0001g0112 a0001c0002t0008g0113 others(9): Show |
12 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.821-563A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761745 | |||||||
chr14:70761816 | T | C | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-634A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761816 | |||||||
chr14:70761951 | TG | T | 9 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0001c0001t0112g0320 others(6): Show |
9 | HG02145.hp2 HG02572.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.821-770delC | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761951 | |||||||
chr14:70761984 | A | C | 107 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(104): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.821-802T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70761984 | |||||||
chr14:70762065 | T | C | 4 | a0001c0001t0112g0320 a0001c0005t0005g0322 a0001c0005t0005g0323 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-883A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70762065 | |||||||
chr14:70762275 | C | T | 20 | a0001c0002t0001g0067 a0001c0002t0001g0112 a0001c0002t0008g0113 others(17): Show |
21 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.821-1093G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70762275 | |||||||
chr14:70762521 | G | A | 102 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(99): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.821-1339C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70762521 | |||||||
chr14:70762564 | C | G | 190 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(187): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.821-1382G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70762564 | |||||||
chr14:70762730 | A | G | 9 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0104 others(6): Show |
11 | HG00639.hp1 HG01070.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.821-1548T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70762730 | |||||||
chr14:70762769 | T | G | 102 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(99): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.821-1587A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70762769 | |||||||
chr14:70762995 | CACAA | C | 55 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(52): Show |
58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.821-1817_821-1814d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70762995 | |||||||
chr14:70763172 | A | C | 1 | a0001c0001t0011g0010 | 2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.821-1990T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763172 | |||||||
chr14:70763254 | C | T | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-2072G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763254 | |||||||
chr14:70763264 | C | T | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.821-2082G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763264 | |||||||
chr14:70763265 | C | T | 1 | a0001c0001t0007g0284 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.821-2083G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763265 | |||||||
chr14:70763341 | T | C | 1 | a0001c0001t0004g0341 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.821-2159A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763341 | |||||||
chr14:70763386 | C | T | 1 | a0001c0001t0103g0259 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.821-2204G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763386 | |||||||
chr14:70763422 | A | G | 1 | a0001c0005t0096g0319 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.821-2240T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763422 | |||||||
chr14:70763483 | A | ATAATACC others(1): Show |
187 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(184): Show |
199 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.821-2309_821-2302d others(10): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763483 | |||||||
chr14:70763507 | C | T | 4 | a0001c0009t0032g0122 a0001c0009t0032g0123 a0001c0011t0050g0183 others(1): Show |
4 | HG00099.hp2 HG00609.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-2325G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763507 | |||||||
chr14:70763534 | CT | C | 188 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(185): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.821-2353delA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763534 | |||||||
chr14:70763591 | T | C | 5 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.821-2409A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763591 | |||||||
chr14:70763615 | C | T | 6 | a0001c0001t0012g0021 a0001c0001t0012g0031 a0001c0001t0012g0032 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.821-2433G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763615 | |||||||
chr14:70763780 | C | T | 5 | a0001c0001t0005g0299 a0001c0001t0005g0300 a0001c0001t0005g0305 others(2): Show |
5 | NA18612.hp1 NA18948.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.821-2598G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763780 | |||||||
chr14:70763952 | G | A | 1 | a0001c0002t0001g0004 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.821-2770C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763952 | |||||||
chr14:70763981 | C | T | 3 | a0001c0001t0016g0130 a0001c0001t0016g0132 a0001c0001t0056g0131 |
3 | HG01433.hp2 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.821-2799G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70763981 | |||||||
chr14:70764012 | C | T | 1 | a0001c0001t0004g0343 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.821-2830G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764012 | |||||||
chr14:70764027 | T | C | 56 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(53): Show |
59 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.821-2845A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764027 | |||||||
chr14:70764042 | T | C | 191 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(188): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.821-2860A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764042 | |||||||
chr14:70764058 | C | T | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.821-2876G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764058 | |||||||
chr14:70764067 | A | T | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.821-2885T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764067 | |||||||
chr14:70764086 | T | C | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-2904A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764086 | |||||||
chr14:70764172 | G | A | 1 | a0001c0011t0050g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.821-2990C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764172 | |||||||
chr14:70764187 | C | T | 33 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0002t0001g0004 others(30): Show |
37 | HG00099.hp1 HG00621.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.821-3005G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764187 | |||||||
chr14:70764192 | C | CAAAAAAA | 34 | a0001c0001t0003g0001 a0001c0001t0003g0037 a0001c0001t0003g0038 others(31): Show |
37 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.821-3017_821-3011d others(9): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | |||||||
chr14:70764192 | C | CAAAAAAA others(3): Show |
1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-3020_821-3011d others(12): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | |||||||
chr14:70764192 | C | CAAAAAAA others(4): Show |
4 | a0001c0002t0001g0073 a0001c0002t0001g0118 a0001c0002t0008g0170 others(1): Show |
4 | HG01993.hp1 NA19003.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-3021_821-3011d others(13): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | |||||||
chr14:70764192 | C | CAAAAAAA others(5): Show |
45 | a0001c0001t0002g0222 a0001c0001t0004g0286 a0001c0001t0005g0277 others(42): Show |
50 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.821-3022_821-3011d others(14): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | |||||||
chr14:70764192 | C | CAAAAAAA others(6): Show |
156 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(153): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.821-3023_821-3011d others(15): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | |||||||
chr14:70764192 | C | CAAAAAAA others(7): Show |
38 | a0001c0001t0002g0194 a0001c0001t0002g0197 a0001c0001t0002g0198 others(35): Show |
38 | HG00735.hp1 HG01106.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.821-3024_821-3011d others(16): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | |||||||
chr14:70764192 | C | CAAAAAAA others(8): Show |
3 | a0001c0001t0073g0187 a0001c0001t0074g0188 a0001c0003t0008g0178 |
3 | HG02451.hp1 HG03654.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.821-3025_821-3011d others(17): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | |||||||
chr14:70764192 | C | CAAAAAAA others(9): Show |
8 | a0001c0001t0006g0156 a0001c0001t0006g0160 a0001c0001t0029g0166 others(5): Show |
8 | HG01109.hp2 HG01496.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.821-3026_821-3011d others(18): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | |||||||
chr14:70764192 | C | CAAAAAAA others(10): Show |
11 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0155 others(8): Show |
11 | HG00280.hp1 HG01256.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.821-3027_821-3011d others(19): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | |||||||
chr14:70764192 | C | CAAAAAAA others(11): Show |
7 | a0001c0001t0006g0151 a0001c0001t0006g0152 a0001c0001t0006g0153 others(4): Show |
7 | HG02004.hp1 HG02273.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.821-3011_821-3010i others(20): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | |||||||
chr14:70764192 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0006g0154 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.821-3011_821-3010i others(21): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | |||||||
chr14:70764192 | CAAAA | C | 9 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0001c0001t0112g0320 others(6): Show |
9 | HG02145.hp2 HG02572.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.821-3014_821-3011d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764192 | |||||||
chr14:70764224 | G | A | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-3042C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764224 | |||||||
chr14:70764315 | A | T | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.821-3133T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764315 | |||||||
chr14:70764346 | T | TATTG | 191 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(188): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.821-3165_821-3164i others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764346 | |||||||
chr14:70764449 | T | TA | 107 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(104): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.821-3268dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764449 | |||||||
chr14:70764467 | C | T | 121 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(118): Show |
128 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.821-3285G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764467 | |||||||
chr14:70764469 | G | T | 107 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(104): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.821-3287C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764469 | |||||||
chr14:70764482 | G | C | 2 | a0001c0002t0001g0097 a0001c0002t0001g0098 |
2 | NA18947.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.821-3300C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764482 | |||||||
chr14:70764549 | G | T | 1 | a0001c0001t0004g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.821-3367C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764549 | |||||||
chr14:70764786 | T | C | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.821-3604A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764786 | |||||||
chr14:70764808 | G | A | 1 | a0001c0001t0005g0300 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.821-3626C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764808 | |||||||
chr14:70764868 | T | C | 12 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0001c0001t0110g0324 others(9): Show |
12 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.821-3686A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764868 | |||||||
chr14:70764869 | A | G | 1 | a0001c0001t0003g0053 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.821-3687T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764869 | |||||||
chr14:70764870 | G | T | 1 | a0001c0001t0003g0053 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.821-3688C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764870 | |||||||
chr14:70764882 | T | C | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.821-3700A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764882 | |||||||
chr14:70764996 | A | G | 55 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(52): Show |
58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.821-3814T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70764996 | |||||||
chr14:70765015 | A | T | 104 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(101): Show |
107 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.821-3833T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765015 | |||||||
chr14:70765381 | A | G | 4 | a0001c0004t0007g0275 a0001c0004t0007g0276 a0001c0004t0027g0242 others(1): Show |
4 | HG01884.hp1 HG03195.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-4199T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765381 | |||||||
chr14:70765430 | C | T | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.821-4248G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765430 | |||||||
chr14:70765510 | A | T | 1 | a0001c0001t0003g0053 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.821-4328T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765510 | |||||||
chr14:70765511 | T | A | 1 | a0001c0001t0003g0053 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.821-4329A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765511 | |||||||
chr14:70765615 | C | T | 1 | a0001c0002t0062g0114 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.821-4433G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765615 | |||||||
chr14:70765623 | C | T | 3 | a0001c0009t0032g0122 a0001c0009t0032g0123 a0001c0011t0050g0183 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.821-4441G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765623 | |||||||
chr14:70765650 | C | T | 92 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(89): Show |
95 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.821-4468G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765650 | |||||||
chr14:70765672 | G | A | 1 | a0001c0001t0110g0324 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.821-4490C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765672 | |||||||
chr14:70765687 | T | C | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.821-4505A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765687 | |||||||
chr14:70765689 | T | C | 3 | a0001c0006t0018g0139 a0001c0006t0018g0140 a0001c0006t0018g0164 |
3 | HG01884.hp2 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.821-4507A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765689 | |||||||
chr14:70765735 | TA | T | 230 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(227): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.821-4554delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765735 | |||||||
chr14:70765736 | AAAAAAAA others(18): Show |
A | 11 | a0001c0002t0001g0067 a0001c0002t0001g0112 a0001c0002t0008g0113 others(8): Show |
11 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.821-4579_821-4555d others(27): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765736 | |||||||
chr14:70765737 | AAAAAAAA others(17): Show |
A | 1 | a0001c0003t0048g0088 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.821-4579_821-4556d others(26): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765737 | |||||||
chr14:70765745 | AAAAAACA others(9): Show |
A | 3 | a0001c0001t0007g0265 a0001c0001t0007g0282 a0001c0001t0007g0294 |
3 | HG02895.hp1 HG02897.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.821-4579_821-4564d others(18): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765745 | |||||||
chr14:70765746 | AAAAACAA others(8): Show |
A | 85 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(82): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.821-4579_821-4565d others(17): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765746 | |||||||
chr14:70765747 | AAAACAAA others(7): Show |
A | 19 | a0001c0001t0012g0021 a0001c0001t0012g0031 a0001c0001t0012g0032 others(16): Show |
19 | HG01192.hp1 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.821-4579_821-4566d others(16): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765747 | |||||||
chr14:70765751 | C | A | 1 | a0006c0022t0092g0258 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.821-4569G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765751 | |||||||
chr14:70765754 | A | C | 178 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(175): Show |
190 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.821-4572T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765754 | |||||||
chr14:70765761 | CA | C | 171 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(168): Show |
182 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.821-4580delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765761 | |||||||
chr14:70765763 | A | C | 5 | a0001c0001t0087g0255 a0001c0004t0007g0275 a0001c0004t0007g0276 others(2): Show |
5 | HG01884.hp1 HG03195.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.821-4581T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765763 | |||||||
chr14:70765764 | A | C | 102 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(99): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.821-4582T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765764 | |||||||
chr14:70765774 | A | C | 1 | a0001c0002t0028g0006 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.821-4592T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765774 | |||||||
chr14:70765802 | C | T | 1 | a0001c0001t0079g0209 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.821-4620G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765802 | |||||||
chr14:70765866 | A | G | 119 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(116): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.821-4684T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765866 | |||||||
chr14:70765868 | G | A | 1 | a0001c0002t0028g0006 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.821-4686C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765868 | |||||||
chr14:70765979 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.821-4797C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70765979 | |||||||
chr14:70766008 | T | C | 4 | a0001c0003t0001g0084 a0001c0003t0008g0169 a0001c0003t0008g0178 others(1): Show |
4 | HG02257.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-4826A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70766008 | |||||||
chr14:70766199 | C | T | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.821-5017G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70766199 | |||||||
chr14:70766316 | T | C | 1 | a0001c0001t0002g0213 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.821-5134A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70766316 | |||||||
chr14:70766540 | C | T | 1 | a0001c0001t0016g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.821-5358G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70766540 | |||||||
chr14:70766577 | C | T | 2 | a0001c0001t0003g0039 a0001c0001t0003g0042 |
2 | NA18955.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.821-5395G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70766577 | |||||||
chr14:70766777 | G | A | 1 | a0001c0001t0007g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.821-5595C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70766777 | |||||||
chr14:70766941 | C | T | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.821-5759G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70766941 | |||||||
chr14:70767099 | C | G | 187 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(184): Show |
199 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.821-5917G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767099 | |||||||
chr14:70767117 | C | T | 1 | a0001c0002t0001g0104 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.821-5935G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767117 | |||||||
chr14:70767279 | A | G | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.821-6097T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767279 | |||||||
chr14:70767383 | CAA | C | 18 | a0001c0001t0003g0037 a0001c0001t0003g0039 a0001c0001t0003g0040 others(15): Show |
18 | HG01993.hp1 HG02015.hp1 HG02738.hp1 others(15): Show |
intron_variant | MODIFIER | c.821-6203_821-6202d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767383 | |||||||
chr14:70767383 | CAAA | C | 270 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(267): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.821-6204_821-6202d others(5): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767383 | |||||||
chr14:70767383 | CAAAA | C | 9 | a0001c0001t0002g0222 a0001c0001t0005g0277 a0001c0001t0005g0316 others(6): Show |
9 | HG00099.hp2 HG01167.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.821-6205_821-6202d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767383 | |||||||
chr14:70767411 | C | T | 1 | a0001c0002t0001g0004 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.821-6229G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767411 | |||||||
chr14:70767653 | C | T | 1 | a0001c0003t0001g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.821-6471G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767653 | |||||||
chr14:70767661 | C | T | 86 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(83): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.821-6479G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767661 | |||||||
chr14:70767662 | G | A | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.821-6480C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767662 | |||||||
chr14:70767678 | G | A | 14 | a0001c0001t0009g0262 a0001c0001t0009g0264 a0001c0001t0009g0272 others(11): Show |
14 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.821-6496C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767678 | |||||||
chr14:70767769 | AC | A | 5 | a0001c0001t0005g0299 a0001c0001t0005g0300 a0001c0001t0005g0305 others(2): Show |
5 | NA18612.hp1 NA18948.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.821-6588delG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767769 | |||||||
chr14:70767813 | G | A | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.821-6631C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767813 | |||||||
chr14:70767876 | C | T | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-6694G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767876 | |||||||
chr14:70767879 | T | C | 187 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(184): Show |
199 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.821-6697A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767879 | |||||||
chr14:70767891 | G | A | 3 | a0001c0002t0001g0008 a0001c0002t0001g0104 a0001c0002t0001g0109 |
4 | HG01255.hp1 HG01361.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-6709C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767891 | |||||||
chr14:70767947 | T | C | 56 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(53): Show |
59 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.821-6765A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767947 | |||||||
chr14:70767961 | T | C | 40 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(37): Show |
40 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.821-6779A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70767961 | |||||||
chr14:70768084 | T | C | 4 | a0001c0002t0022g0023 a0001c0002t0022g0024 a0001c0002t0058g0025 others(1): Show |
4 | HG02723.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-6902A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768084 | |||||||
chr14:70768164 | G | A | 2 | a0001c0001t0075g0186 a0001c0001t0113g0318 |
2 | HG01192.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.821-6982C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768164 | |||||||
chr14:70768287 | C | A | 3 | a0001c0001t0004g0336 a0001c0001t0004g0337 a0001c0001t0004g0338 |
3 | NA18963.hp2 NA18971.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.821-7105G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768287 | |||||||
chr14:70768384 | T | C | 2 | a0001c0001t0005g0315 a0001c0001t0087g0255 |
2 | NA19000.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.821-7202A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768384 | |||||||
chr14:70768764 | T | C | 1 | a0001c0001t0003g0065 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.821-7582A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768764 | |||||||
chr14:70768933 | T | C | 3 | a0001c0001t0019g0356 a0001c0001t0019g0357 a0001c0001t0019g0359 |
3 | NA18941.hp1 NA18998.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.821-7751A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768933 | |||||||
chr14:70768936 | C | T | 180 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(177): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.821-7754G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768936 | |||||||
chr14:70768937 | G | A | 6 | a0001c0001t0012g0021 a0001c0001t0012g0031 a0001c0001t0012g0032 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.821-7755C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768937 | |||||||
chr14:70768941 | C | T | 3 | a0001c0009t0032g0122 a0001c0009t0032g0123 a0001c0011t0050g0183 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.821-7759G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70768941 | |||||||
chr14:70769066 | C | G | 178 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(175): Show |
190 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.821-7884G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769066 | |||||||
chr14:70769155 | AC | A | 179 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(176): Show |
191 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.821-7974delG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769155 | |||||||
chr14:70769284 | C | T | 1 | a0001c0002t0001g0007 | 2 | HG00639.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.821-8102G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769284 | |||||||
chr14:70769286 | G | A | 55 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(52): Show |
58 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.821-8104C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769286 | |||||||
chr14:70769406 | T | C | 1 | a0001c0001t0029g0166 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.821-8224A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769406 | |||||||
chr14:70769537 | G | T | 4 | a0001c0003t0001g0084 a0001c0003t0008g0169 a0001c0003t0008g0178 others(1): Show |
4 | HG02257.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-8355C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769537 | |||||||
chr14:70769618 | G | A | 7 | a0001c0001t0006g0143 a0001c0001t0006g0144 a0001c0001t0006g0146 others(4): Show |
7 | HG00280.hp1 HG01515.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.821-8436C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769618 | |||||||
chr14:70769682 | C | A | 3 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0060g0096 |
3 | NA18943.hp1 NA18947.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.821-8500G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769682 | |||||||
chr14:70769804 | G | A | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-8622C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769804 | |||||||
chr14:70769933 | G | C | 4 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(1): Show |
4 | HG02717.hp2 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-8751C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70769933 | |||||||
chr14:70770011 | C | A | 174 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(171): Show |
186 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.821-8829G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770011 | |||||||
chr14:70770158 | G | A | 1 | a0001c0005t0096g0319 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.821-8976C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770158 | |||||||
chr14:70770180 | C | T | 98 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(95): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.821-8998G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770180 | |||||||
chr14:70770283 | C | T | 2 | a0001c0002t0022g0085 a0001c0018t0081g0227 |
2 | HG00609.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.821-9101G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770283 | |||||||
chr14:70770286 | T | C | 1 | a0001c0001t0006g0159 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.821-9104A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770286 | |||||||
chr14:70770297 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.821-9115G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770297 | |||||||
chr14:70770650 | G | T | 5 | a0001c0001t0002g0193 a0001c0001t0002g0200 a0001c0001t0002g0219 others(2): Show |
5 | HG01256.hp2 HG01258.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.821-9468C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770650 | |||||||
chr14:70770833 | C | T | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-9651G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770833 | |||||||
chr14:70770844 | C | G | 2 | a0001c0001t0003g0038 a0001c0001t0003g0041 |
2 | NA18960.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.821-9662G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770844 | |||||||
chr14:70770972 | T | C | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-9790A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70770972 | |||||||
chr14:70771015 | T | C | 1 | a0001c0001t0078g0191 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.821-9833A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771015 | |||||||
chr14:70771050 | C | CT | 6 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0001c0002t0017g0090 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.821-9869dupA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771050 | |||||||
chr14:70771050 | C | T | 4 | a0001c0001t0112g0320 a0001c0005t0005g0322 a0001c0005t0005g0323 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-9868G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771050 | |||||||
chr14:70771067 | C | T | 1 | a0001c0001t0004g0271 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.821-9885G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771067 | |||||||
chr14:70771106 | G | A | 92 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(89): Show |
95 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.821-9924C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771106 | |||||||
chr14:70771193 | G | A | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.821-10011C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771193 | |||||||
chr14:70771348 | C | T | 3 | a0001c0005t0005g0322 a0001c0005t0005g0323 a0001c0005t0035g0321 |
3 | HG02572.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.821-10166G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771348 | |||||||
chr14:70771349 | C | T | 9 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0001c0001t0112g0320 others(6): Show |
9 | HG02145.hp2 HG02572.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.821-10167G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771349 | |||||||
chr14:70771428 | T | C | 1 | a0001c0001t0003g0050 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.821-10246A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771428 | |||||||
chr14:70771446 | C | G | 6 | a0001c0001t0002g0002 a0001c0001t0002g0194 a0001c0001t0002g0195 others(3): Show |
8 | NA18940.hp2 NA18947.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.821-10264G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771446 | |||||||
chr14:70771485 | C | T | 1 | a0001c0001t0005g0295 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.821-10303G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771485 | |||||||
chr14:70771581 | G | A | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-10399C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771581 | |||||||
chr14:70771625 | T | G | 4 | a0001c0003t0001g0084 a0001c0003t0008g0169 a0001c0003t0008g0178 others(1): Show |
4 | HG02257.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-10443A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771625 | |||||||
chr14:70771726 | T | C | 56 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(53): Show |
59 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.821-10544A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771726 | |||||||
chr14:70771780 | A | C | 1 | a0001c0003t0107g0326 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.821-10598T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771780 | |||||||
chr14:70771818 | G | A | 1 | a0001c0002t0001g0176 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.821-10636C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771818 | |||||||
chr14:70771887 | T | G | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.821-10705A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771887 | |||||||
chr14:70771897 | CCTGTTGT others(1): Show |
C | 11 | a0001c0001t0010g0231 a0001c0001t0010g0232 a0001c0001t0010g0233 others(8): Show |
11 | NA18949.hp2 NA18964.hp1 NA18968.hp2 others(8): Show |
intron_variant | MODIFIER | c.821-10723_821-1071 others(12): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771897 | |||||||
chr14:70771969 | C | T | 178 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(175): Show |
190 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.821-10787G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70771969 | |||||||
chr14:70772041 | A | G | 1 | a0001c0001t0024g0142 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.821-10859T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772041 | |||||||
chr14:70772181 | A | G | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.821-10999T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772181 | |||||||
chr14:70772195 | G | A | 1 | a0001c0001t0006g0160 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.821-11013C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772195 | |||||||
chr14:70772197 | G | A | 2 | a0001c0001t0004g0352 a0001c0001t0004g0353 |
2 | NA19009.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.821-11015C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772197 | |||||||
chr14:70772250 | G | A | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-11068C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772250 | |||||||
chr14:70772501 | C | T | 1 | a0001c0001t0012g0021 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.821-11319G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772501 | |||||||
chr14:70772544 | G | C | 1 | a0001c0001t0104g0260 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.821-11362C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772544 | |||||||
chr14:70772688 | C | T | 1 | a0001c0002t0042g0018 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.821-11506G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772688 | |||||||
chr14:70772733 | C | T | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.821-11551G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70772733 | |||||||
chr14:70773052 | C | T | 1 | a0009c0010t0002g0208 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.821-11870G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773052 | |||||||
chr14:70773148 | A | G | 1 | a0001c0001t0009g0287 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.821-11966T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773148 | |||||||
chr14:70773167 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.821-11985C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773167 | |||||||
chr14:70773171 | T | C | 2 | a0003c0008t0002g0215 a0003c0008t0002g0217 |
2 | NA18964.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.821-11989A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773171 | |||||||
chr14:70773210 | A | G | 1 | a0001c0021t0070g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.821-12028T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773210 | |||||||
chr14:70773364 | T | C | 1 | a0001c0002t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.821-12182A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773364 | |||||||
chr14:70773432 | C | G | 1 | a0009c0010t0002g0208 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.821-12250G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773432 | |||||||
chr14:70773513 | C | A | 1 | a0001c0009t0032g0122 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.821-12331G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773513 | |||||||
chr14:70773600 | T | C | 1 | a0001c0002t0028g0006 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.821-12418A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773600 | |||||||
chr14:70773975 | C | A | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-12793G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70773975 | |||||||
chr14:70774091 | C | G | 177 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(174): Show |
189 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.821-12909G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774091 | |||||||
chr14:70774288 | A | G | 1 | a0001c0002t0017g0090 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.821-13106T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774288 | |||||||
chr14:70774319 | T | C | 2 | a0001c0003t0107g0326 a0006c0022t0092g0258 |
2 | HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.821-13137A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774319 | |||||||
chr14:70774403 | C | T | 1 | a0001c0001t0002g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.821-13221G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774403 | |||||||
chr14:70774643 | T | C | 1 | a0001c0001t0005g0296 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.821-13461A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774643 | |||||||
chr14:70774664 | A | G | 1 | a0001c0001t0012g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.821-13482T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774664 | |||||||
chr14:70774725 | G | A | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-13543C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774725 | |||||||
chr14:70774726 | C | G | 1 | a0001c0001t0016g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.821-13544G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774726 | |||||||
chr14:70774853 | C | T | 3 | a0001c0001t0007g0265 a0001c0001t0007g0282 a0001c0001t0007g0294 |
3 | HG02895.hp1 HG02897.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.821-13671G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774853 | |||||||
chr14:70774897 | T | C | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-13715A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774897 | |||||||
chr14:70774943 | C | T | 1 | a0001c0001t0004g0337 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.821-13761G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774943 | |||||||
chr14:70774946 | T | C | 4 | a0001c0001t0004g0344 a0001c0001t0004g0345 a0001c0001t0004g0346 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-13764A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774946 | |||||||
chr14:70774949 | A | C | 193 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(190): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.821-13767T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774949 | |||||||
chr14:70774974 | C | T | 1 | a0001c0001t0007g0294 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.821-13792G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774974 | |||||||
chr14:70774983 | C | CA | 12 | a0001c0001t0004g0330 a0001c0001t0004g0334 a0001c0001t0004g0335 others(9): Show |
12 | HG00621.hp2 HG00673.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.821-13802dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70774983 | C | CAAAAAAA others(2): Show |
14 | a0001c0001t0003g0027 a0001c0001t0003g0037 a0001c0001t0003g0039 others(11): Show |
14 | HG00408.hp1 HG02015.hp1 HG03471.hp1 others(11): Show |
intron_variant | MODIFIER | c.821-13810_821-1380 others(13): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70774983 | C | CAAAAAAA others(3): Show |
11 | a0001c0001t0003g0038 a0001c0001t0003g0051 a0001c0001t0003g0056 others(8): Show |
11 | HG00597.hp1 HG02056.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.821-13811_821-1380 others(14): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70774983 | C | CAAAAAAA others(4): Show |
8 | a0001c0001t0003g0001 a0001c0001t0003g0048 a0001c0001t0003g0049 others(5): Show |
11 | NA18945.hp2 NA18953.hp2 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.821-13812_821-1380 others(15): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70774983 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0003g0055 a0001c0001t0021g0052 |
2 | NA18939.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.821-13813_821-1380 others(16): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70774983 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0003g0029 a0001c0001t0003g0042 |
2 | HG02280.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.821-13816_821-1380 others(19): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70774983 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0003g0030 a0001c0001t0025g0026 |
2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.821-13817_821-1380 others(20): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70774983 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0003g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.821-13818_821-1380 others(21): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70774983 | C | CAAAAAAA others(17): Show |
1 | a0001c0003t0001g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.821-13825_821-1380 others(28): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70774983 | CA | C | 8 | a0001c0001t0004g0327 a0001c0001t0006g0151 a0001c0001t0006g0153 others(5): Show |
8 | HG02300.hp1 HG03579.hp1 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.821-13802delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70774983 | CAA | C | 19 | a0001c0001t0006g0143 a0001c0001t0006g0144 a0001c0001t0006g0146 others(16): Show |
19 | HG00280.hp1 HG01256.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.821-13803_821-1380 others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70774983 | CAAA | C | 38 | a0001c0001t0002g0009 a0001c0001t0002g0197 a0001c0001t0002g0198 others(35): Show |
39 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.821-13804_821-1380 others(7): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70774983 | CAAAA | C | 119 | a0001c0001t0002g0002 a0001c0001t0002g0193 a0001c0001t0002g0194 others(116): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.821-13805_821-1380 others(8): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70774983 | CAAAAA | C | 22 | a0001c0001t0005g0296 a0001c0001t0012g0021 a0001c0001t0012g0031 others(19): Show |
22 | HG00099.hp2 HG01106.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.821-13806_821-1380 others(9): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70774983 | CAAAAAA | C | 9 | a0001c0002t0001g0089 a0001c0002t0001g0099 a0001c0002t0008g0077 others(6): Show |
9 | HG01168.hp1 HG02040.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.821-13807_821-1380 others(10): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70774983 | CAAAAAAA | C | 60 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0002t0001g0004 others(57): Show |
66 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.821-13808_821-1380 others(11): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70774983 | CAAAAAAA others(5): Show |
C | 2 | a0001c0003t0008g0178 a0001c0003t0055g0068 |
2 | HG03098.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.821-13813_821-1380 others(16): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70774983 | CAAAAAAA others(6): Show |
C | 1 | a0001c0003t0008g0169 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.821-13814_821-1380 others(17): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70774983 | |||||||
chr14:70775245 | T | G | 13 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0001c0001t0110g0324 others(10): Show |
13 | HG01106.hp2 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.821-14063A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70775245 | |||||||
chr14:70775741 | G | T | 14 | a0001c0001t0009g0262 a0001c0001t0009g0264 a0001c0001t0009g0272 others(11): Show |
14 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.821-14559C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70775741 | |||||||
chr14:70775937 | C | T | 10 | a0001c0001t0007g0265 a0001c0001t0007g0269 a0001c0001t0007g0273 others(7): Show |
10 | HG00733.hp1 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.821-14755G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70775937 | |||||||
chr14:70775989 | G | A | 1 | a0001c0011t0050g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.821-14807C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70775989 | |||||||
chr14:70776047 | A | T | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-14865T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776047 | |||||||
chr14:70776065 | T | C | 52 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0002t0001g0004 others(49): Show |
57 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.821-14883A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776065 | |||||||
chr14:70776158 | C | T | 4 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(1): Show |
4 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-14976G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776158 | |||||||
chr14:70776183 | C | G | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.821-15001G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776183 | |||||||
chr14:70776285 | C | T | 1 | a0001c0005t0096g0319 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.821-15103G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776285 | |||||||
chr14:70776325 | T | C | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-15143A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776325 | |||||||
chr14:70776398 | C | A | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-15216G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776398 | |||||||
chr14:70776503 | T | C | 1 | a0001c0002t0049g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.821-15321A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776503 | |||||||
chr14:70776626 | T | A | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(51): Show |
57 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.821-15444A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776626 | |||||||
chr14:70776631 | G | A | 1 | a0001c0001t0009g0303 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.821-15449C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776631 | |||||||
chr14:70776707 | G | A | 2 | a0001c0001t0029g0166 a0001c0001t0029g0167 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.821-15525C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776707 | |||||||
chr14:70776769 | C | T | 1 | a0001c0001t0005g0306 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.821-15587G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776769 | |||||||
chr14:70776833 | CT | C | 287 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(284): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.821-15652delA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776833 | |||||||
chr14:70776900 | C | A | 3 | a0001c0005t0005g0322 a0001c0005t0005g0323 a0001c0005t0035g0321 |
3 | HG02572.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.821-15718G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70776900 | |||||||
chr14:70777073 | T | C | 1 | a0001c0001t0004g0335 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.821-15891A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777073 | |||||||
chr14:70777111 | G | A | 1 | a0001c0011t0050g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.821-15929C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777111 | |||||||
chr14:70777117 | C | T | 1 | a0001c0002t0008g0081 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.821-15935G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777117 | |||||||
chr14:70777233 | C | T | 3 | a0001c0009t0032g0122 a0001c0009t0032g0123 a0001c0011t0050g0183 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.821-16051G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777233 | |||||||
chr14:70777328 | T | C | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.821-16146A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777328 | |||||||
chr14:70777358 | A | G | 1 | a0001c0001t0013g0223 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.821-16176T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777358 | |||||||
chr14:70777471 | C | T | 2 | a0001c0001t0002g0219 a0001c0001t0013g0220 |
2 | HG01361.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.821-16289G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777471 | |||||||
chr14:70777476 | G | A | 1 | a0001c0002t0028g0006 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.821-16294C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777476 | |||||||
chr14:70777492 | A | C | 1 | a0001c0001t0003g0061 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.821-16310T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777492 | |||||||
chr14:70777757 | C | T | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-16575G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777757 | |||||||
chr14:70777761 | C | G | 1 | a0001c0001t0003g0056 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.821-16579G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777761 | |||||||
chr14:70777794 | G | A | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-16612C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777794 | |||||||
chr14:70777808 | A | C | 1 | a0001c0001t0083g0241 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.821-16626T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70777808 | |||||||
chr14:70778032 | T | A | 2 | a0001c0001t0009g0262 a0001c0001t0009g0272 |
2 | HG01257.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.821-16850A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778032 | |||||||
chr14:70778077 | T | C | 172 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(169): Show |
184 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.821-16895A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778077 | |||||||
chr14:70778086 | T | TTTG | 93 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(90): Show |
96 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.821-16907_821-1690 others(7): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778086 | |||||||
chr14:70778146 | A | G | 53 | a0001c0001t0007g0308 a0001c0001t0051g0172 a0001c0001t0052g0091 others(50): Show |
58 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.821-16964T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778146 | |||||||
chr14:70778276 | AT | A | 232 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(229): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.821-17095delA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778276 | |||||||
chr14:70778276 | ATT | A | 11 | a0001c0001t0005g0268 a0001c0001t0005g0277 a0001c0001t0005g0295 others(8): Show |
11 | HG01070.hp2 HG01106.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.821-17096_821-1709 others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778276 | |||||||
chr14:70778294 | T | G | 1 | a0001c0001t0002g0218 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.821-17112A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778294 | |||||||
chr14:70778299 | C | T | 44 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(41): Show |
47 | HG00408.hp1 HG00597.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.821-17117G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778299 | |||||||
chr14:70778348 | C | T | 98 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(95): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.821-17166G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778348 | |||||||
chr14:70778422 | T | C | 1 | a0001c0005t0005g0322 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.821-17240A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778422 | |||||||
chr14:70778457 | G | A | 176 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(173): Show |
188 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.821-17275C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778457 | |||||||
chr14:70778477 | T | C | 5 | a0001c0001t0021g0052 a0001c0001t0021g0120 a0001c0001t0021g0121 others(2): Show |
5 | HG00408.hp1 HG00597.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.821-17295A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778477 | |||||||
chr14:70778501 | C | G | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-17319G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778501 | |||||||
chr14:70778505 | A | C | 92 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(89): Show |
95 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.821-17323T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778505 | |||||||
chr14:70778507 | C | T | 1 | a0001c0001t0004g0350 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.821-17325G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778507 | |||||||
chr14:70778560 | G | A | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.821-17378C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778560 | |||||||
chr14:70778565 | T | C | 1 | a0001c0011t0050g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.821-17383A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778565 | |||||||
chr14:70778596 | A | G | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-17414T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778596 | |||||||
chr14:70778685 | C | T | 1 | a0001c0001t0086g0253 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.821-17503G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778685 | |||||||
chr14:70778731 | T | C | 4 | a0001c0003t0001g0084 a0001c0003t0008g0169 a0001c0003t0008g0178 others(1): Show |
4 | HG02257.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-17549A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778731 | |||||||
chr14:70778826 | A | G | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821-17644T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778826 | |||||||
chr14:70778880 | G | A | 1 | a0001c0009t0032g0122 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.821-17698C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70778880 | |||||||
chr14:70779023 | GA | G | 182 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(179): Show |
194 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.821-17842delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779023 | |||||||
chr14:70779115 | C | T | 5 | a0001c0001t0021g0052 a0001c0001t0021g0120 a0001c0001t0021g0121 others(2): Show |
5 | HG00408.hp1 HG00597.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.821-17933G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779115 | |||||||
chr14:70779145 | A | G | 185 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(182): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.821-17963T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779145 | |||||||
chr14:70779151 | G | A | 1 | a0001c0002t0008g0117 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.821-17969C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779151 | |||||||
chr14:70779165 | C | T | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.821-17983G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779165 | |||||||
chr14:70779177 | C | T | 1 | a0001c0002t0061g0080 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.821-17995G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779177 | |||||||
chr14:70779234 | G | A | 4 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(1): Show |
4 | HG02717.hp2 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-18052C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779234 | |||||||
chr14:70779324 | A | C | 177 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(174): Show |
189 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.821-18142T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779324 | |||||||
chr14:70779360 | C | A | 1 | a0001c0005t0096g0319 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.821-18178G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779360 | |||||||
chr14:70779480 | G | T | 1 | a0001c0002t0008g0117 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.821-18298C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779480 | |||||||
chr14:70779537 | T | C | 1 | a0001c0002t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.821-18355A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779537 | |||||||
chr14:70779581 | C | T | 176 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(173): Show |
188 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.821-18399G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779581 | |||||||
chr14:70779610 | T | A | 2 | a0001c0001t0013g0192 a0001c0001t0078g0191 |
2 | HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.821-18428A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779610 | |||||||
chr14:70779669 | C | T | 182 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(179): Show |
194 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.821-18487G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779669 | |||||||
chr14:70779945 | C | T | 2 | a0001c0001t0075g0186 a0001c0001t0113g0318 |
2 | HG01192.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.821-18763G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779945 | |||||||
chr14:70779990 | G | C | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821-18808C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70779990 | |||||||
chr14:70780111 | A | G | 1 | a0001c0006t0018g0164 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.821-18929T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70780111 | |||||||
chr14:70780190 | G | C | 298 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.821-19008C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70780190 | |||||||
chr14:70780251 | T | C | 99 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(96): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.821-19069A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70780251 | |||||||
chr14:70780278 | T | C | 99 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(96): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.821-19096A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70780278 | |||||||
chr14:70780322 | G | A | 1 | a0001c0002t0049g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.821-19140C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70780322 | |||||||
chr14:70780382 | T | C | 4 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(1): Show |
4 | HG02717.hp2 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-19200A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70780382 | |||||||
chr14:70780553 | T | C | 1 | a0001c0011t0050g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.821-19371A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70780553 | |||||||
chr14:70781078 | T | G | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+19589A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70781078 | |||||||
chr14:70781196 | G | T | 3 | a0001c0001t0004g0336 a0001c0001t0004g0337 a0001c0001t0004g0338 |
3 | NA18963.hp2 NA18971.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.820+19471C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70781196 | |||||||
chr14:70781512 | T | C | 77 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0001t0054g0086 others(74): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.820+19155A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70781512 | |||||||
chr14:70781549 | A | G | 1 | a0001c0005t0096g0319 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.820+19118T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70781549 | |||||||
chr14:70781674 | T | C | 180 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(177): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.820+18993A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70781674 | |||||||
chr14:70781790 | T | G | 1 | a0001c0001t0073g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.820+18877A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70781790 | |||||||
chr14:70781873 | A | C | 2 | a0001c0001t0054g0086 a0001c0002t0022g0085 |
2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.820+18794T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70781873 | |||||||
chr14:70781964 | G | T | 4 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(1): Show |
4 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+18703C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70781964 | |||||||
chr14:70782046 | C | T | 1 | a0001c0001t0090g0250 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.820+18621G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782046 | |||||||
chr14:70782312 | A | G | 2 | a0001c0001t0003g0038 a0001c0001t0003g0041 |
2 | NA18960.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.820+18355T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782312 | |||||||
chr14:70782376 | A | G | 3 | a0001c0009t0032g0122 a0001c0009t0032g0123 a0001c0011t0050g0183 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.820+18291T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782376 | |||||||
chr14:70782377 | T | C | 170 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(167): Show |
181 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.820+18290A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782377 | |||||||
chr14:70782387 | T | C | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.820+18280A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782387 | |||||||
chr14:70782473 | C | A | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.820+18194G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782473 | |||||||
chr14:70782513 | C | T | 93 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(90): Show |
96 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.820+18154G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782513 | |||||||
chr14:70782754 | C | G | 121 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(118): Show |
127 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.820+17913G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782754 | |||||||
chr14:70782781 | C | G | 1 | a0001c0001t0101g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.820+17886G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782781 | |||||||
chr14:70782981 | G | A | 3 | a0001c0001t0110g0324 a0001c0003t0107g0326 a0006c0022t0092g0258 |
3 | HG01106.hp2 HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.820+17686C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782981 | |||||||
chr14:70782999 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.820+17668G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70782999 | |||||||
chr14:70783000 | G | A | 2 | a0001c0001t0003g0065 a0001c0001t0004g0347 |
2 | NA19088.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.820+17667C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783000 | |||||||
chr14:70783085 | C | T | 26 | a0001c0001t0054g0086 a0001c0002t0001g0067 a0001c0002t0001g0112 others(23): Show |
27 | HG00323.hp1 HG00609.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.820+17582G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783085 | |||||||
chr14:70783260 | G | A | 1 | a0001c0001t0015g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.820+17407C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783260 | |||||||
chr14:70783317 | T | A | 1 | a0001c0001t0007g0317 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.820+17350A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783317 | |||||||
chr14:70783360 | C | T | 1 | a0001c0001t0004g0329 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.820+17307G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783360 | |||||||
chr14:70783461 | C | CT | 173 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(170): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.820+17205_820+1720 others(5): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783461 | |||||||
chr14:70783547 | C | T | 1 | a0001c0002t0020g0014 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.820+17120G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783547 | |||||||
chr14:70783560 | C | T | 4 | a0001c0001t0007g0273 a0001c0001t0007g0284 a0001c0001t0027g0243 others(1): Show |
4 | HG00733.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+17107G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783560 | |||||||
chr14:70783561 | G | A | 1 | a0001c0021t0070g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.820+17106C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70783561 | |||||||
chr14:70784031 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.820+16636G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784031 | |||||||
chr14:70784042 | G | C | 147 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(144): Show |
158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.820+16625C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784042 | |||||||
chr14:70784140 | G | C | 5 | a0001c0001t0109g0279 a0001c0004t0007g0275 a0001c0004t0007g0276 others(2): Show |
5 | HG01884.hp1 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.820+16527C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784140 | |||||||
chr14:70784247 | C | G | 26 | a0001c0001t0054g0086 a0001c0002t0001g0067 a0001c0002t0001g0112 others(23): Show |
27 | HG00323.hp1 HG00609.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.820+16420G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784247 | |||||||
chr14:70784295 | A | G | 2 | a0001c0001t0002g0205 a0004c0016t0002g0204 |
2 | HG01081.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.820+16372T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784295 | |||||||
chr14:70784311 | A | T | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+16356T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784311 | |||||||
chr14:70784323 | A | T | 78 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0001t0054g0086 others(75): Show |
84 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.820+16344T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784323 | |||||||
chr14:70784466 | G | A | 99 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(96): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.820+16201C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784466 | |||||||
chr14:70784485 | G | A | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(51): Show |
57 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.820+16182C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784485 | |||||||
chr14:70784507 | C | G | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+16160G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784507 | |||||||
chr14:70784509 | G | A | 3 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 |
3 | HG02717.hp2 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.820+16158C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784509 | |||||||
chr14:70784616 | G | A | 1 | a0001c0001t0003g0066 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.820+16051C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784616 | |||||||
chr14:70784666 | C | T | 1 | a0001c0006t0018g0164 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.820+16001G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784666 | |||||||
chr14:70784705 | G | C | 93 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(90): Show |
96 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.820+15962C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784705 | |||||||
chr14:70784726 | A | C | 1 | a0001c0002t0031g0079 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.820+15941T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784726 | |||||||
chr14:70784749 | G | C | 37 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(34): Show |
40 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.820+15918C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784749 | |||||||
chr14:70784769 | T | C | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.820+15898A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784769 | |||||||
chr14:70784877 | A | G | 2 | a0001c0001t0002g0009 a0001c0001t0013g0203 |
3 | HG00642.hp1 HG00735.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.820+15790T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784877 | |||||||
chr14:70784916 | A | C | 1 | a0001c0001t0009g0262 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.820+15751T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70784916 | |||||||
chr14:70785506 | T | G | 1 | a0001c0001t0085g0249 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.820+15161A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785506 | |||||||
chr14:70785576 | G | A | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+15091C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785576 | |||||||
chr14:70785655 | G | A | 1 | a0001c0021t0070g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.820+15012C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785655 | |||||||
chr14:70785680 | T | C | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(51): Show |
57 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.820+14987A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785680 | |||||||
chr14:70785694 | T | C | 6 | a0001c0001t0012g0021 a0001c0001t0012g0031 a0001c0001t0012g0032 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.820+14973A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785694 | |||||||
chr14:70785742 | G | C | 1 | a0001c0002t0001g0089 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.820+14925C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785742 | |||||||
chr14:70785846 | C | T | 1 | a0001c0002t0008g0117 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.820+14821G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785846 | |||||||
chr14:70785901 | C | T | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(51): Show |
57 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.820+14766G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785901 | |||||||
chr14:70785905 | A | C | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+14762T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785905 | |||||||
chr14:70785938 | G | C | 157 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(154): Show |
168 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.820+14729C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70785938 | |||||||
chr14:70786040 | A | C | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+14627T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786040 | |||||||
chr14:70786069 | A | C | 157 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(154): Show |
168 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.820+14598T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786069 | |||||||
chr14:70786070 | G | A | 105 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(102): Show |
111 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.820+14597C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786070 | |||||||
chr14:70786105 | T | C | 1 | a0001c0021t0070g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.820+14562A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786105 | |||||||
chr14:70786305 | A | G | 1 | a0001c0001t0006g0155 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.820+14362T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786305 | |||||||
chr14:70786352 | C | T | 95 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(92): Show |
101 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.820+14315G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786352 | |||||||
chr14:70786486 | C | T | 2 | a0001c0001t0015g0184 a0001c0001t0015g0185 |
2 | HG03654.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.820+14181G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786486 | |||||||
chr14:70786505 | A | C | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+14162T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786505 | |||||||
chr14:70786558 | G | C | 1 | a0001c0005t0096g0319 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.820+14109C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786558 | |||||||
chr14:70786784 | T | C | 76 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(73): Show |
79 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.820+13883A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786784 | |||||||
chr14:70786794 | A | G | 1 | a0001c0011t0050g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.820+13873T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786794 | |||||||
chr14:70786918 | T | C | 1 | a0001c0001t0074g0188 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.820+13749A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70786918 | |||||||
chr14:70787041 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.820+13626T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787041 | |||||||
chr14:70787042 | T | C | 1 | a0001c0003t0001g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.820+13625A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787042 | |||||||
chr14:70787070 | A | C | 4 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(1): Show |
4 | HG02717.hp2 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+13597T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787070 | |||||||
chr14:70787226 | T | C | 1 | a0001c0003t0008g0178 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.820+13441A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787226 | |||||||
chr14:70787275 | A | G | 4 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(1): Show |
4 | HG02717.hp2 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+13392T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787275 | |||||||
chr14:70787336 | G | A | 1 | a0001c0001t0005g0315 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.820+13331C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787336 | |||||||
chr14:70787398 | C | T | 99 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(96): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.820+13269G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787398 | |||||||
chr14:70787401 | G | A | 53 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(50): Show |
56 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.820+13266C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787401 | |||||||
chr14:70787409 | G | A | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(51): Show |
57 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.820+13258C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787409 | |||||||
chr14:70787451 | C | G | 1 | a0001c0001t0104g0260 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.820+13216G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787451 | |||||||
chr14:70787454 | G | A | 1 | a0001c0001t0003g0041 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.820+13213C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787454 | |||||||
chr14:70787507 | C | CA | 37 | a0001c0001t0003g0060 a0001c0001t0004g0348 a0001c0001t0005g0315 others(34): Show |
37 | HG00280.hp1 HG01109.hp2 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.820+13159dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787507 | |||||||
chr14:70787507 | CA | C | 132 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(129): Show |
141 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.820+13159delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787507 | |||||||
chr14:70787544 | C | A | 77 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0001t0054g0086 others(74): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.820+13123G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787544 | |||||||
chr14:70787777 | GT | G | 10 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(7): Show |
10 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.820+12889delA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787777 | |||||||
chr14:70787817 | A | C | 3 | a0001c0001t0014g0036 a0001c0001t0014g0044 a0001c0001t0014g0045 |
3 | NA18950.hp1 NA18995.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.820+12850T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787817 | |||||||
chr14:70787947 | C | T | 4 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(1): Show |
4 | HG02717.hp2 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+12720G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787947 | |||||||
chr14:70787981 | C | A | 286 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(283): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.820+12686G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70787981 | |||||||
chr14:70788065 | A | G | 1 | a0001c0006t0018g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.820+12602T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788065 | |||||||
chr14:70788217 | T | C | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.820+12450A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788217 | |||||||
chr14:70788237 | C | T | 147 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(144): Show |
158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.820+12430G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788237 | |||||||
chr14:70788270 | A | G | 2 | a0001c0001t0054g0086 a0001c0002t0022g0085 |
2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.820+12397T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788270 | |||||||
chr14:70788395 | C | A | 1 | a0001c0003t0048g0088 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.820+12272G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788395 | |||||||
chr14:70788426 | C | T | 10 | a0001c0001t0007g0265 a0001c0001t0007g0269 a0001c0001t0007g0273 others(7): Show |
10 | HG00733.hp1 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.820+12241G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788426 | |||||||
chr14:70788527 | A | G | 1 | a0001c0006t0018g0164 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.820+12140T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788527 | |||||||
chr14:70788573 | C | T | 3 | a0001c0001t0033g0128 a0001c0001t0033g0129 a0001c0001t0068g0127 |
3 | HG02630.hp2 HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.820+12094G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788573 | |||||||
chr14:70788718 | A | G | 77 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0001t0054g0086 others(74): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.820+11949T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788718 | |||||||
chr14:70788739 | G | T | 1 | a0001c0003t0055g0068 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.820+11928C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788739 | |||||||
chr14:70788779 | G | C | 21 | a0001c0001t0054g0086 a0001c0002t0001g0067 a0001c0002t0001g0112 others(18): Show |
22 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.820+11888C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788779 | |||||||
chr14:70788859 | A | T | 1 | a0001c0001t0097g0283 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.820+11808T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70788859 | |||||||
chr14:70789189 | G | T | 156 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(153): Show |
167 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.820+11478C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789189 | |||||||
chr14:70789233 | G | A | 25 | a0001c0001t0054g0086 a0001c0002t0001g0067 a0001c0002t0001g0112 others(22): Show |
26 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.820+11434C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789233 | |||||||
chr14:70789512 | C | A | 3 | a0001c0003t0008g0169 a0001c0003t0008g0178 a0001c0003t0055g0068 |
3 | HG03098.hp1 HG03540.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.820+11155G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789512 | |||||||
chr14:70789598 | T | C | 1 | a0001c0002t0001g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.820+11069A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789598 | |||||||
chr14:70789604 | G | C | 1 | a0001c0001t0012g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.820+11063C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789604 | |||||||
chr14:70789608 | T | C | 1 | a0001c0001t0005g0314 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.820+11059A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789608 | |||||||
chr14:70789650 | G | A | 105 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(102): Show |
111 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.820+11017C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789650 | |||||||
chr14:70789672 | G | T | 1 | a0001c0002t0008g0077 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.820+10995C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789672 | |||||||
chr14:70789717 | G | A | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+10950C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789717 | |||||||
chr14:70789834 | T | C | 1 | a0001c0006t0018g0164 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.820+10833A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789834 | |||||||
chr14:70789912 | G | A | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+10755C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789912 | |||||||
chr14:70789944 | C | A | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.820+10723G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70789944 | |||||||
chr14:70790007 | G | A | 1 | a0001c0002t0001g0100 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.820+10660C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790007 | |||||||
chr14:70790055 | G | A | 5 | a0001c0001t0002g0193 a0001c0001t0002g0200 a0001c0001t0002g0219 others(2): Show |
5 | HG01256.hp2 HG01258.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+10612C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790055 | |||||||
chr14:70790085 | G | A | 1 | a0001c0001t0005g0309 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.820+10582C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790085 | |||||||
chr14:70790219 | T | C | 3 | a0001c0009t0032g0122 a0001c0009t0032g0123 a0001c0011t0050g0183 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.820+10448A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790219 | |||||||
chr14:70790281 | C | G | 1 | a0001c0001t0038g0015 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.820+10386G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790281 | |||||||
chr14:70790478 | G | A | 99 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(96): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.820+10189C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790478 | |||||||
chr14:70790689 | A | G | 170 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(167): Show |
181 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.820+9978T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790689 | |||||||
chr14:70790690 | T | C | 2 | a0001c0001t0019g0356 a0001c0001t0019g0357 |
2 | NA18998.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.820+9977A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790690 | |||||||
chr14:70790701 | A | C | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | NA18747.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.820+9966T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790701 | |||||||
chr14:70790869 | C | A | 1 | a0001c0001t0003g0042 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.820+9798G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790869 | |||||||
chr14:70790883 | C | G | 52 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0002t0001g0004 others(49): Show |
57 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.820+9784G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70790883 | |||||||
chr14:70791442 | A | G | 121 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(118): Show |
127 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.820+9225T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70791442 | |||||||
chr14:70791476 | T | C | 3 | a0001c0001t0004g0344 a0001c0001t0004g0345 a0001c0001t0004g0346 |
3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.820+9191A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70791476 | |||||||
chr14:70791588 | C | T | 1 | a0001c0001t0026g0244 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.820+9079G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70791588 | |||||||
chr14:70791589 | G | A | 3 | a0001c0009t0032g0122 a0001c0009t0032g0123 a0001c0011t0050g0183 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.820+9078C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70791589 | |||||||
chr14:70791683 | C | T | 1 | a0001c0002t0001g0089 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.820+8984G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70791683 | |||||||
chr14:70791724 | C | T | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(51): Show |
57 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.820+8943G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70791724 | |||||||
chr14:70791951 | G | A | 6 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(3): Show |
6 | HG01192.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+8716C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70791951 | |||||||
chr14:70792577 | C | T | 1 | a0001c0001t0004g0337 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.820+8090G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70792577 | |||||||
chr14:70792680 | C | T | 7 | a0001c0001t0054g0086 a0001c0001t0075g0186 a0001c0002t0022g0023 others(4): Show |
7 | HG01192.hp1 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.820+7987G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70792680 | |||||||
chr14:70792902 | G | A | 1 | a0001c0002t0001g0101 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.820+7765C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70792902 | |||||||
chr14:70792955 | C | T | 326 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(323): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.820+7712G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70792955 | |||||||
chr14:70792987 | G | A | 5 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+7680C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70792987 | |||||||
chr14:70793111 | T | C | 1 | a0001c0001t0007g0325 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.820+7556A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793111 | |||||||
chr14:70793149 | C | T | 8 | a0001c0001t0010g0231 a0001c0001t0010g0232 a0001c0001t0010g0233 others(5): Show |
8 | NA18949.hp2 NA18964.hp1 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.820+7518G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793149 | |||||||
chr14:70793164 | G | T | 168 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(165): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.820+7503C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793164 | |||||||
chr14:70793179 | T | C | 5 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(2): Show |
5 | HG01192.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+7488A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793179 | |||||||
chr14:70793374 | C | T | 168 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(165): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.820+7293G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793374 | |||||||
chr14:70793536 | AAAAT | A | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.820+7127_820+7130d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793536 | |||||||
chr14:70793585 | A | G | 3 | a0001c0005t0005g0322 a0001c0005t0005g0323 a0001c0005t0035g0321 |
3 | HG02572.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.820+7082T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793585 | |||||||
chr14:70793590 | T | C | 52 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0002t0001g0004 others(49): Show |
57 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.820+7077A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793590 | |||||||
chr14:70793591 | G | A | 4 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(1): Show |
4 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+7076C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793591 | |||||||
chr14:70793652 | T | TTTCA | 218 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(215): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.820+7011_820+7014d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793652 | |||||||
chr14:70793652 | T | TTTCATTC others(1): Show |
35 | a0001c0001t0002g0201 a0001c0001t0003g0028 a0001c0001t0005g0295 others(32): Show |
35 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.820+7007_820+7014d others(10): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793652 | |||||||
chr14:70793652 | T | TTTCATTC others(5): Show |
1 | a0001c0001t0024g0142 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.820+7003_820+7014d others(14): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793652 | |||||||
chr14:70793781 | T | C | 1 | a0001c0001t0002g0225 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.820+6886A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793781 | |||||||
chr14:70793846 | G | A | 12 | a0001c0002t0001g0067 a0001c0002t0001g0112 a0001c0002t0008g0113 others(9): Show |
12 | HG00323.hp1 HG00741.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.820+6821C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793846 | |||||||
chr14:70793912 | T | C | 4 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 others(1): Show |
4 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+6755A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70793912 | |||||||
chr14:70794038 | T | C | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.820+6629A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794038 | |||||||
chr14:70794119 | G | A | 2 | a0001c0002t0001g0103 a0001c0002t0067g0102 |
2 | HG02155.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.820+6548C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794119 | |||||||
chr14:70794132 | C | A | 1 | a0001c0001t0005g0301 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.820+6535G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794132 | |||||||
chr14:70794149 | G | C | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.820+6518C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794149 | |||||||
chr14:70794193 | A | C | 1 | a0001c0001t0006g0152 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.820+6474T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794193 | |||||||
chr14:70794291 | G | C | 1 | a0002c0007t0094g0256 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.820+6376C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794291 | |||||||
chr14:70794295 | T | C | 21 | a0001c0001t0005g0263 a0001c0001t0005g0268 a0001c0001t0005g0277 others(18): Show |
21 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.820+6372A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794295 | |||||||
chr14:70794308 | G | C | 1 | a0001c0001t0002g0221 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.820+6359C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794308 | |||||||
chr14:70794325 | T | C | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.820+6342A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794325 | |||||||
chr14:70794420 | T | A | 2 | a0001c0001t0033g0129 a0001c0001t0068g0127 |
2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.820+6247A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794420 | |||||||
chr14:70794591 | TA | T | 3 | a0001c0009t0032g0122 a0001c0009t0032g0123 a0001c0011t0050g0183 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.820+6075delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794591 | |||||||
chr14:70794660 | G | A | 3 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 |
3 | HG02486.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.820+6007C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794660 | |||||||
chr14:70794693 | T | TC | 93 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(90): Show |
96 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.820+5973dupG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794693 | |||||||
chr14:70794747 | G | A | 36 | a0001c0001t0006g0143 a0001c0001t0006g0144 a0001c0001t0006g0146 others(33): Show |
36 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.820+5920C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794747 | |||||||
chr14:70794913 | G | A | 326 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(323): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.820+5754C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794913 | |||||||
chr14:70794935 | C | T | 77 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0001t0054g0086 others(74): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.820+5732G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794935 | |||||||
chr14:70794938 | A | G | 1 | a0001c0001t0003g0037 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.820+5729T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794938 | |||||||
chr14:70794966 | C | T | 1 | a0001c0001t0005g0277 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.820+5701G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794966 | |||||||
chr14:70794967 | G | A | 1 | a0001c0001t0013g0223 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.820+5700C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794967 | |||||||
chr14:70794989 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0083g0241 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.820+5677_820+5678i others(14): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794989 | |||||||
chr14:70794990 | C | CT | 65 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(62): Show |
68 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.820+5676dupA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | |||||||
chr14:70794990 | C | CTTT | 33 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(30): Show |
36 | HG00408.hp1 HG02015.hp1 HG02056.hp2 others(33): Show |
intron_variant | MODIFIER | c.820+5674_820+5676d others(5): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | |||||||
chr14:70794990 | C | CTTTT | 6 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0060 others(3): Show |
6 | HG00597.hp1 HG00609.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+5673_820+5676d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | |||||||
chr14:70794990 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0005g0302 a0001c0001t0005g0306 a0001c0001t0009g0303 |
3 | HG00323.hp2 NA18946.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.820+5667_820+5676d others(12): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | |||||||
chr14:70794990 | C | CTTTTTTT others(4): Show |
53 | a0001c0001t0004g0286 a0001c0001t0005g0012 a0001c0001t0005g0263 others(50): Show |
56 | HG00140.hp1 HG00280.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.820+5666_820+5676d others(13): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | |||||||
chr14:70794990 | C | CTTTTTTT others(5): Show |
36 | a0001c0001t0004g0271 a0001c0001t0005g0277 a0001c0001t0005g0305 others(33): Show |
36 | HG00438.hp2 HG00597.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.820+5665_820+5676d others(14): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | |||||||
chr14:70794990 | C | CTTTTTTT others(6): Show |
6 | a0001c0001t0007g0269 a0001c0001t0012g0032 a0001c0001t0086g0253 others(3): Show |
6 | HG01891.hp1 HG02074.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.820+5664_820+5676d others(15): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | |||||||
chr14:70794990 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0012g0033 a0001c0001t0110g0324 |
2 | HG01106.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.820+5663_820+5676d others(16): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | |||||||
chr14:70794990 | C | T | 1 | a0001c0001t0083g0241 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.820+5677G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70794990 | |||||||
chr14:70795031 | T | C | 77 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0001t0054g0086 others(74): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.820+5636A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795031 | |||||||
chr14:70795037 | G | A | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(51): Show |
57 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.820+5630C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795037 | |||||||
chr14:70795075 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.820+5592G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795075 | |||||||
chr14:70795137 | G | A | 1 | a0001c0001t0005g0305 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.820+5530C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795137 | |||||||
chr14:70795164 | T | G | 3 | a0001c0009t0032g0122 a0001c0009t0032g0123 a0001c0011t0050g0183 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.820+5503A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795164 | |||||||
chr14:70795187 | G | A | 1 | a0001c0001t0012g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.820+5480C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795187 | |||||||
chr14:70795310 | A | C | 4 | a0001c0004t0007g0275 a0001c0004t0007g0276 a0001c0004t0027g0242 others(1): Show |
4 | HG01884.hp1 HG03195.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+5357T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795310 | |||||||
chr14:70795348 | G | A | 2 | a0001c0001t0073g0187 a0001c0011t0050g0183 |
2 | NA20129.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.820+5319C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795348 | |||||||
chr14:70795411 | C | T | 27 | a0001c0001t0006g0143 a0001c0001t0006g0144 a0001c0001t0006g0146 others(24): Show |
27 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.820+5256G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795411 | |||||||
chr14:70795505 | T | C | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(51): Show |
57 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.820+5162A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795505 | |||||||
chr14:70795578 | C | T | 1 | a0001c0003t0008g0178 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.820+5089G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795578 | |||||||
chr14:70795620 | C | T | 95 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(92): Show |
98 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.820+5047G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795620 | |||||||
chr14:70795767 | C | CT | 100 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(97): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.820+4899dupA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795767 | |||||||
chr14:70795852 | G | A | 1 | a0001c0009t0032g0122 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.820+4815C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70795852 | |||||||
chr14:70796142 | T | TC | 139 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(136): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.820+4524dupG | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796142 | |||||||
chr14:70796215 | T | C | 139 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(136): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.820+4452A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796215 | |||||||
chr14:70796277 | G | A | 52 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0002t0001g0004 others(49): Show |
57 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.820+4390C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796277 | |||||||
chr14:70796348 | T | C | 1 | a0001c0006t0018g0164 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.820+4319A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796348 | |||||||
chr14:70796420 | T | C | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.820+4247A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796420 | |||||||
chr14:70796452 | T | C | 1 | a0001c0021t0070g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.820+4215A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796452 | |||||||
chr14:70796481 | G | A | 3 | a0001c0009t0032g0122 a0001c0009t0032g0123 a0001c0011t0050g0183 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.820+4186C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796481 | |||||||
chr14:70796485 | C | A | 1 | a0001c0001t0029g0167 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.820+4182G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796485 | |||||||
chr14:70796519 | C | G | 95 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(92): Show |
98 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.820+4148G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796519 | |||||||
chr14:70796555 | G | A | 5 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+4112C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796555 | |||||||
chr14:70796578 | T | C | 1 | a0001c0002t0023g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.820+4089A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796578 | |||||||
chr14:70796606 | G | A | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.820+4061C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796606 | |||||||
chr14:70796710 | C | T | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.820+3957G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796710 | |||||||
chr14:70796721 | C | T | 5 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(2): Show |
5 | HG01192.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+3946G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796721 | |||||||
chr14:70796795 | G | A | 1 | a0001c0009t0032g0122 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.820+3872C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796795 | |||||||
chr14:70796926 | A | C | 1 | a0001c0003t0001g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.820+3741T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70796926 | |||||||
chr14:70797136 | C | T | 27 | a0001c0001t0006g0143 a0001c0001t0006g0144 a0001c0001t0006g0146 others(24): Show |
27 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.820+3531G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797136 | |||||||
chr14:70797233 | C | A | 1 | a0001c0001t0003g0050 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.820+3434G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797233 | |||||||
chr14:70797260 | C | T | 3 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 |
3 | HG02717.hp2 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.820+3407G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797260 | |||||||
chr14:70797341 | A | G | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.820+3326T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797341 | |||||||
chr14:70797389 | C | T | 73 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0001t0054g0086 others(70): Show |
79 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.820+3278G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797389 | |||||||
chr14:70797404 | C | T | 4 | a0001c0003t0001g0084 a0001c0003t0008g0169 a0001c0003t0008g0178 others(1): Show |
4 | HG02257.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.820+3263G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797404 | |||||||
chr14:70797407 | A | G | 139 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(136): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.820+3260T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797407 | |||||||
chr14:70797417 | A | AAAT | 136 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(133): Show |
142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.820+3247_820+3249d others(5): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797417 | |||||||
chr14:70797442 | A | C | 1 | a0001c0002t0008g0077 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.820+3225T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797442 | |||||||
chr14:70797536 | G | A | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.820+3131C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797536 | |||||||
chr14:70797638 | C | T | 1 | a0001c0006t0018g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.820+3029G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797638 | |||||||
chr14:70797891 | A | C | 3 | a0001c0009t0032g0122 a0001c0009t0032g0123 a0001c0011t0050g0183 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.820+2776T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797891 | |||||||
chr14:70797956 | G | C | 95 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(92): Show |
98 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.820+2711C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70797956 | |||||||
chr14:70798165 | C | G | 1 | a0001c0001t0006g0150 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.820+2502G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798165 | |||||||
chr14:70798194 | A | C | 1 | a0001c0011t0050g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.820+2473T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798194 | |||||||
chr14:70798201 | A | G | 78 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0001t0054g0086 others(75): Show |
84 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.820+2466T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798201 | |||||||
chr14:70798313 | G | A | 1 | a0001c0002t0028g0006 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.820+2354C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798313 | |||||||
chr14:70798425 | T | TATCTGCT others(20): Show |
216 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(213): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.820+2241_820+2242i others(29): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798425 | |||||||
chr14:70798425 | T | TTTTCCAG others(33): Show |
1 | a0001c0002t0001g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.820+2241_820+2242i others(42): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798425 | |||||||
chr14:70798435 | C | G | 2 | a0001c0003t0008g0169 a0001c0003t0008g0178 |
2 | HG03540.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.820+2232G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798435 | |||||||
chr14:70798461 | G | A | 1 | a0001c0003t0008g0178 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.820+2206C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798461 | |||||||
chr14:70798471 | G | GT | 54 | a0001c0001t0003g0042 a0001c0001t0004g0271 a0001c0001t0004g0330 others(51): Show |
55 | HG00099.hp2 HG00408.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.820+2195dupA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798471 | |||||||
chr14:70798471 | G | GTT | 27 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(24): Show |
30 | HG00408.hp1 HG01192.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.820+2194_820+2195d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798471 | |||||||
chr14:70798471 | G | GTTT | 19 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(16): Show |
19 | HG00597.hp1 HG01109.hp2 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.820+2193_820+2195d others(5): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798471 | |||||||
chr14:70798471 | G | GTTTT | 25 | a0001c0001t0006g0143 a0001c0001t0006g0144 a0001c0001t0006g0146 others(22): Show |
25 | HG00280.hp1 HG01515.hp1 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.820+2192_820+2195d others(6): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798471 | |||||||
chr14:70798471 | G | GTTTTTT | 10 | a0001c0001t0002g0222 a0001c0001t0016g0132 a0001c0001t0016g0136 others(7): Show |
10 | HG01074.hp1 HG01081.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.820+2190_820+2195d others(8): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798471 | |||||||
chr14:70798471 | G | GTTTTTTT | 32 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(29): Show |
35 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.820+2189_820+2195d others(9): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798471 | |||||||
chr14:70798471 | G | GTTTTTTT others(1): Show |
11 | a0001c0001t0002g0194 a0001c0001t0002g0195 a0001c0001t0002g0196 others(8): Show |
11 | HG01258.hp2 HG01346.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.820+2188_820+2195d others(10): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798471 | |||||||
chr14:70798471 | GT | G | 8 | a0001c0001t0004g0328 a0001c0001t0005g0306 a0001c0001t0007g0317 others(5): Show |
8 | HG00609.hp1 HG01496.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.820+2195delA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798471 | |||||||
chr14:70798501 | C | T | 1 | a0001c0002t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.820+2166G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798501 | |||||||
chr14:70798536 | T | C | 95 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(92): Show |
98 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.820+2131A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798536 | |||||||
chr14:70798603 | C | T | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.820+2064G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798603 | |||||||
chr14:70798639 | CG | C | 7 | a0001c0001t0005g0012 a0001c0001t0005g0311 a0001c0001t0005g0312 others(4): Show |
8 | HG03654.hp2 NA18945.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.820+2027delC | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798639 | |||||||
chr14:70798695 | G | T | 18 | a0001c0001t0003g0001 a0001c0001t0003g0048 a0001c0001t0003g0049 others(15): Show |
21 | HG00408.hp1 HG00597.hp1 NA18939.hp1 others(18): Show |
intron_variant | MODIFIER | c.820+1972C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798695 | |||||||
chr14:70798699 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.820+1968G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798699 | |||||||
chr14:70798783 | G | C | 5 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(2): Show |
5 | HG01192.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+1884C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798783 | |||||||
chr14:70798911 | C | T | 5 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(2): Show |
5 | HG01192.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+1756G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70798911 | |||||||
chr14:70799056 | C | T | 36 | a0001c0001t0006g0143 a0001c0001t0006g0144 a0001c0001t0006g0146 others(33): Show |
36 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.820+1611G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799056 | |||||||
chr14:70799080 | A | G | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.820+1587T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799080 | |||||||
chr14:70799101 | A | G | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(51): Show |
57 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.820+1566T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799101 | |||||||
chr14:70799132 | C | G | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.820+1535G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799132 | |||||||
chr14:70799176 | AT | A | 52 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(49): Show |
55 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.820+1490delA | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799176 | |||||||
chr14:70799204 | T | C | 9 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0104 others(6): Show |
11 | HG00639.hp1 HG01070.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.820+1463A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799204 | |||||||
chr14:70799233 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.820+1434C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799233 | |||||||
chr14:70799346 | G | T | 36 | a0001c0001t0006g0143 a0001c0001t0006g0144 a0001c0001t0006g0146 others(33): Show |
36 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.820+1321C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799346 | |||||||
chr14:70799408 | C | T | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.820+1259G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799408 | |||||||
chr14:70799433 | G | A | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.820+1234C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799433 | |||||||
chr14:70799501 | G | A | 1 | a0001c0001t0074g0188 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.820+1166C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799501 | |||||||
chr14:70799540 | C | T | 1 | a0001c0001t0006g0150 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.820+1127G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799540 | |||||||
chr14:70799628 | C | T | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.820+1039G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799628 | |||||||
chr14:70799631 | G | A | 59 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(56): Show |
62 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.820+1036C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799631 | |||||||
chr14:70799726 | G | A | 7 | a0001c0002t0001g0067 a0001c0002t0001g0112 a0001c0002t0008g0113 others(4): Show |
7 | HG01255.hp2 HG02155.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.820+941C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799726 | |||||||
chr14:70799999 | CATTTAAT | C | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.820+661_820+667del others(7): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70799999 | |||||||
chr14:70800062 | A | G | 217 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.820+605T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70800062 | |||||||
chr14:70800205 | A | G | 100 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(97): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.820+462T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70800205 | |||||||
chr14:70800225 | C | T | 59 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(56): Show |
62 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.820+442G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70800225 | |||||||
chr14:70800252 | G | T | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.820+415C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70800252 | |||||||
chr14:70800530 | C | T | 1 | a0001c0001t0021g0120 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.820+137G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70800530 | |||||||
chr14:70800600 | C | T | 3 | a0001c0009t0032g0122 a0001c0009t0032g0123 a0001c0011t0050g0183 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.820+67G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70800600 | |||||||
chr14:70800628 | C | T | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(51): Show |
57 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.820+39G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70800628 | |||||||
chr14:70800634 | T | C | 1 | a0001c0001t0004g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.820+33A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | 70800634 | |||||||
chr14:70801247 | TATTTTCC others(5): Show |
T | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.407-179_407-168del others(12): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70801247 | |||||||
chr14:70801330 | A | G | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.407-250T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70801330 | |||||||
chr14:70801382 | G | A | 2 | a0001c0002t0001g0115 a0001c0002t0001g0116 |
2 | HG01106.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.407-302C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70801382 | |||||||
chr14:70801543 | C | T | 3 | a0001c0001t0006g0143 a0001c0001t0006g0144 a0001c0001t0065g0145 |
3 | HG02523.hp1 NA18984.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.407-463G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70801543 | |||||||
chr14:70801729 | G | C | 47 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(44): Show |
50 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.407-649C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70801729 | |||||||
chr14:70802157 | A | G | 1 | a0007c0017t0025g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.407-1077T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802157 | |||||||
chr14:70802235 | C | G | 2 | a0001c0001t0071g0190 a0001c0001t0072g0189 |
2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.407-1155G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802235 | |||||||
chr14:70802260 | G | T | 1 | a0001c0001t0110g0324 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.407-1180C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802260 | |||||||
chr14:70802394 | A | G | 217 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.407-1314T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802394 | |||||||
chr14:70802415 | T | C | 1 | a0001c0001t0005g0314 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.407-1335A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802415 | |||||||
chr14:70802715 | T | C | 2 | a0001c0001t0004g0348 a0001c0001t0004g0349 |
2 | HG00673.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.407-1635A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802715 | |||||||
chr14:70802847 | T | A | 3 | a0001c0006t0018g0138 a0001c0006t0018g0139 a0001c0006t0018g0140 |
3 | HG02717.hp2 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.407-1767A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802847 | |||||||
chr14:70802852 | G | C | 1 | a0001c0001t0002g0225 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.407-1772C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802852 | |||||||
chr14:70802899 | A | C | 217 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.407-1819T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802899 | |||||||
chr14:70802946 | G | A | 17 | a0001c0001t0006g0150 a0001c0001t0006g0151 a0001c0001t0006g0152 others(14): Show |
17 | HG01256.hp1 HG01952.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.407-1866C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802946 | |||||||
chr14:70802978 | C | T | 59 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(56): Show |
62 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.407-1898G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70802978 | |||||||
chr14:70803044 | A | G | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.407-1964T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803044 | |||||||
chr14:70803149 | T | A | 3 | a0001c0009t0032g0122 a0001c0009t0032g0123 a0001c0011t0050g0183 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.407-2069A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803149 | |||||||
chr14:70803221 | G | A | 1 | a0001c0001t0007g0317 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.407-2141C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803221 | |||||||
chr14:70803305 | A | G | 1 | a0001c0002t0001g0067 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.407-2225T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803305 | |||||||
chr14:70803336 | T | TC | 3 | a0001c0001t0024g0168 a0001c0001t0029g0166 a0001c0001t0029g0167 |
3 | HG03209.hp1 HG03579.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.407-2257_407-2256i others(3): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803336 | |||||||
chr14:70803337 | T | A | 4 | a0001c0001t0006g0165 a0001c0001t0024g0168 a0001c0001t0029g0166 others(1): Show |
4 | HG03209.hp1 HG03579.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.407-2257A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | |||||||
chr14:70803337 | T | C | 22 | a0001c0001t0006g0143 a0001c0001t0006g0144 a0001c0001t0006g0146 others(19): Show |
22 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.407-2257A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | |||||||
chr14:70803337 | T | TA | 25 | a0001c0001t0004g0350 a0001c0001t0004g0352 a0001c0001t0004g0353 others(22): Show |
27 | HG00609.hp2 HG00673.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.407-2258dupT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | |||||||
chr14:70803337 | T | TAA | 9 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(6): Show |
9 | HG02015.hp1 HG02145.hp2 NA18906.hp2 others(6): Show |
intron_variant | MODIFIER | c.407-2259_407-2258d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | |||||||
chr14:70803337 | T | TAAA | 33 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(30): Show |
36 | HG00408.hp1 HG00597.hp1 HG02056.hp2 others(33): Show |
intron_variant | MODIFIER | c.407-2260_407-2258d others(5): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | |||||||
chr14:70803337 | TA | T | 24 | a0001c0001t0004g0329 a0001c0001t0005g0268 a0001c0001t0007g0265 others(21): Show |
24 | HG01070.hp2 HG01891.hp1 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.407-2258delT | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | |||||||
chr14:70803337 | TAA | T | 64 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0001t0054g0086 others(61): Show |
70 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.407-2259_407-2258d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | |||||||
chr14:70803337 | TAAA | T | 9 | a0001c0002t0001g0067 a0001c0002t0001g0072 a0001c0002t0001g0073 others(6): Show |
9 | HG01167.hp1 HG01168.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.407-2260_407-2258d others(5): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | |||||||
chr14:70803337 | TAAAAAA | T | 50 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(47): Show |
53 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.407-2263_407-2258d others(8): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803337 | |||||||
chr14:70803338 | A | C | 1 | a0001c0001t0024g0142 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.407-2258T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803338 | |||||||
chr14:70803349 | A | C | 2 | a0001c0001t0004g0327 a0001c0001t0004g0328 |
2 | NA18939.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.407-2269T>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803349 | |||||||
chr14:70803614 | A | G | 1 | a0001c0003t0008g0169 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.407-2534T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803614 | |||||||
chr14:70803774 | T | A | 1 | a0001c0009t0032g0123 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.407-2694A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803774 | |||||||
chr14:70803786 | C | A | 41 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(38): Show |
44 | HG00408.hp1 HG00597.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.407-2706G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803786 | |||||||
chr14:70803848 | C | T | 1 | a0001c0001t0009g0264 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.407-2768G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803848 | |||||||
chr14:70803974 | G | C | 5 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(2): Show |
5 | HG01192.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.407-2894C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803974 | |||||||
chr14:70803990 | T | C | 3 | a0001c0009t0032g0122 a0001c0009t0032g0123 a0001c0011t0050g0183 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.407-2910A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70803990 | |||||||
chr14:70804014 | C | T | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.407-2934G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804014 | |||||||
chr14:70804063 | G | A | 2 | a0001c0002t0001g0118 a0001c0002t0008g0117 |
2 | NA19011.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.407-2983C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804063 | |||||||
chr14:70804151 | T | C | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.407-3071A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804151 | |||||||
chr14:70804194 | C | G | 5 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.407-3114G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804194 | |||||||
chr14:70804223 | G | C | 1 | a0001c0001t0007g0325 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.407-3143C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804223 | |||||||
chr14:70804279 | A | G | 36 | a0001c0001t0006g0143 a0001c0001t0006g0144 a0001c0001t0006g0146 others(33): Show |
36 | HG00280.hp1 HG01109.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.407-3199T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804279 | |||||||
chr14:70804296 | A | G | 1 | a0001c0005t0096g0319 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.407-3216T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804296 | |||||||
chr14:70804338 | T | G | 327 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(324): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.407-3258A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804338 | |||||||
chr14:70804544 | C | T | 1 | a0001c0001t0053g0124 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.407-3464G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804544 | |||||||
chr14:70804632 | T | C | 77 | a0001c0001t0051g0172 a0001c0001t0052g0091 a0001c0001t0054g0086 others(74): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.407-3552A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804632 | |||||||
chr14:70804659 | A | G | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(51): Show |
57 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.407-3579T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804659 | |||||||
chr14:70804692 | TAA | T | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(51): Show |
57 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.407-3614_407-3613d others(4): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804692 | |||||||
chr14:70804729 | A | G | 1 | a0001c0001t0005g0263 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.407-3649T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804729 | |||||||
chr14:70804731 | G | A | 1 | a0001c0003t0107g0326 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.407-3651C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804731 | |||||||
chr14:70804759 | C | T | 1 | a0001c0001t0009g0262 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.407-3679G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804759 | |||||||
chr14:70804800 | A | T | 3 | a0001c0009t0032g0122 a0001c0009t0032g0123 a0001c0011t0050g0183 |
3 | HG00099.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.407-3720T>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804800 | |||||||
chr14:70804823 | C | T | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.407-3743G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70804823 | |||||||
chr14:70805275 | CCTT | C | 4 | a0001c0005t0005g0322 a0001c0005t0005g0323 a0001c0005t0035g0321 others(1): Show |
4 | HG01496.hp2 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+3488_406+3490d others(5): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70805275 | |||||||
chr14:70805587 | C | A | 1 | a0001c0001t0005g0316 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.406+3179G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70805587 | |||||||
chr14:70805906 | G | A | 1 | a0001c0002t0008g0119 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.406+2860C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70805906 | |||||||
chr14:70806075 | G | A | 59 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(56): Show |
62 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.406+2691C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806075 | |||||||
chr14:70806084 | A | G | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.406+2682T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806084 | |||||||
chr14:70806108 | C | T | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(51): Show |
57 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.406+2658G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806108 | |||||||
chr14:70806146 | C | T | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.406+2620G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806146 | |||||||
chr14:70806244 | T | C | 1 | a0001c0001t0010g0240 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.406+2522A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806244 | |||||||
chr14:70806458 | A | G | 4 | a0001c0002t0022g0023 a0001c0002t0022g0024 a0001c0002t0058g0025 others(1): Show |
4 | HG02723.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.406+2308T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806458 | |||||||
chr14:70806650 | T | G | 1 | a0001c0001t0083g0241 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.406+2116A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806650 | |||||||
chr14:70806692 | T | C | 1 | a0001c0001t0072g0189 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.406+2074A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806692 | |||||||
chr14:70806710 | C | G | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+2056G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806710 | |||||||
chr14:70806742 | C | T | 6 | a0001c0001t0112g0320 a0001c0005t0005g0322 a0001c0005t0005g0323 others(3): Show |
6 | HG01496.hp2 HG02572.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.406+2024G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806742 | |||||||
chr14:70806894 | C | T | 1 | a0001c0001t0113g0318 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.406+1872G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70806894 | |||||||
chr14:70807058 | T | C | 1 | a0001c0001t0007g0317 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.406+1708A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807058 | |||||||
chr14:70807155 | G | A | 1 | a0001c0001t0026g0254 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.406+1611C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807155 | |||||||
chr14:70807220 | G | A | 1 | a0001c0018t0081g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.406+1546C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807220 | |||||||
chr14:70807232 | C | A | 2 | a0001c0001t0004g0352 a0001c0001t0004g0353 |
2 | NA19009.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.406+1534G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807232 | |||||||
chr14:70807267 | G | A | 1 | a0001c0001t0113g0318 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.406+1499C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807267 | |||||||
chr14:70807327 | T | C | 1 | a0001c0011t0050g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.406+1439A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807327 | |||||||
chr14:70807363 | G | A | 1 | a0001c0001t0087g0255 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.406+1403C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807363 | |||||||
chr14:70807483 | C | T | 2 | a0001c0009t0032g0122 a0001c0009t0032g0123 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.406+1283G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807483 | |||||||
chr14:70807608 | T | G | 1 | a0001c0002t0020g0014 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.406+1158A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807608 | |||||||
chr14:70807862 | T | A | 92 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(89): Show |
95 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.406+904A>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807862 | |||||||
chr14:70807960 | G | T | 326 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(323): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.406+806C>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807960 | |||||||
chr14:70807972 | T | G | 4 | a0001c0001t0076g0182 a0001c0001t0077g0181 a0007c0017t0025g0179 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+794A>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70807972 | |||||||
chr14:70808005 | C | G | 95 | a0001c0001t0004g0271 a0001c0001t0004g0286 a0001c0001t0004g0304 others(92): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.406+761G>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808005 | |||||||
chr14:70808013 | C | T | 1 | a0001c0001t0012g0021 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.406+753G>A | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808013 | |||||||
chr14:70808157 | T | C | 2 | a0001c0001t0021g0120 a0001c0001t0021g0121 |
2 | HG00408.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.406+609A>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808157 | |||||||
chr14:70808432 | G | C | 1 | a0001c0001t0080g0226 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.406+334C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808432 | |||||||
chr14:70808439 | C | CG | 115 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0028 others(112): Show |
124 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.406+326dupC | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808439 | |||||||
chr14:70808441 | G | C | 1 | a0001c0001t0009g0354 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.406+325C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808441 | |||||||
chr14:70808443 | G | C | 1 | a0001c0011t0050g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.406+323C>G | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808443 | |||||||
chr14:70808541 | G | A | 1 | a0001c0001t0111g0355 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.406+225C>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808541 | |||||||
chr14:70808606 | A | G | 221 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0193 others(218): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.406+160T>C | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808606 | |||||||
chr14:70808662 | C | A | 5 | a0001c0001t0071g0190 a0001c0001t0072g0189 a0001c0001t0073g0187 others(2): Show |
5 | HG01192.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.406+104G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808662 | |||||||
chr14:70808758 | C | A | 1 | a0001c0001t0071g0190 | 1 | HG02486.hp1 | splice_region_variant&intron_variant | LOW | c.406+8G>T | MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 1/11 | chr14 | 70808758 |