Item | Value |
---|---|
geneid | 9020 |
ensemblid | ENSG00000006062.18 |
hgncid | 6853 |
symbol | MAP3K14 |
name | mitogen-activated protein kinase kinase kinase 14 |
refseq_nuc | NM_003954.5 |
refseq_prot | NP_003945.2 |
ensembl_nuc | ENST00000344686.8 |
ensembl_prot | ENSP00000478552.1 |
mane_status | MANE Select |
chr | chr17 |
start | 45263119 |
end | 45317020 |
strand | - |
ver | v1.2 |
region | chr17:45263119-45317020 |
region5000 | chr17:45258119-45322020 |
regionname0 | MAP3K14_chr17_45263119_45317020 |
regionname5000 | MAP3K14_chr17_45258119_45322020 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 947 | 327 | 89 | 55 | 139 | 14 | 28 | 103 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | MAVME others(942): Show |
chr17 | 45258119 | 45322020 |
a0002 | 0/0 | 947 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | MAVME others(942): Show |
chr17 | 45258119 | 45322020 |
a0003 | 0/0 | 947 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | MAVME others(942): Show |
chr17 | 45258119 | 45322020 |
a0004 | 0/0 | 947 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | MAVME others(942): Show |
chr17 | 45258119 | 45322020 |
a0005 | 0/0 | 947 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | MAVME others(942): Show |
chr17 | 45258119 | 45322020 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2841 | 242 | 77 | 39 | 95 | 8 | 22 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | ATGGC others(2836): Show |
chr17 | 45258119 | 45322020 | ||
a0001c0002 | 1/0 | 2841 | 81 | 10 | 15 | 43 | 6 | 6 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | ATGGC others(2836): Show |
chr17 | 45258119 | 45322020 | ||
a0001c0006 | 0/0 | 2841 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | ATGGC others(2836): Show |
chr17 | 45258119 | 45322020 | ||
a0001c0008 | 0/0 | 2841 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | ATGGC others(2836): Show |
chr17 | 45258119 | 45322020 | ||
a0001c0009 | 0/0 | 2841 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | ATGGC others(2836): Show |
chr17 | 45258119 | 45322020 | ||
a0001c0010 | 0/0 | 2841 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | ATGGC others(2836): Show |
chr17 | 45258119 | 45322020 | ||
a0002c0003 | 0/0 | 2841 | 3 | 0 | 3 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | ATGGC others(2836): Show |
chr17 | 45258119 | 45322020 | ||
a0003c0004 | 0/0 | 2841 | 3 | 1 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | ATGGC others(2836): Show |
chr17 | 45258119 | 45322020 | ||
a0004c0005 | 0/0 | 2841 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | ATGGC others(2836): Show |
chr17 | 45258119 | 45322020 | ||
a0005c0007 | 0/0 | 2841 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | ATGGC others(2836): Show |
chr17 | 45258119 | 45322020 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4442 | 69 | 33 | 11 | 22 | 0 | 2 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0001t0002 | 0/0 | 4442 | 115 | 21 | 21 | 52 | 5 | 16 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0001t0003 | 0/0 | 4442 | 20 | 0 | 2 | 17 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0001t0004 | 0/0 | 4442 | 16 | 13 | 1 | 0 | 0 | 2 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0001t0005 | 0/0 | 4442 | 7 | 1 | 4 | 0 | 2 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0001t0007 | 0/0 | 4442 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0001t0008 | 0/0 | 4442 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0001t0010 | 0/0 | 4442 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0001t0011 | 0/0 | 4442 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0001t0012 | 0/0 | 4442 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0001t0013 | 0/0 | 4442 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0001t0015 | 0/0 | 4442 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0001t0017 | 0/0 | 4442 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0001t0018 | 0/0 | 4442 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0001t0019 | 0/0 | 4442 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0002t0001 | 1/0 | 4442 | 75 | 8 | 15 | 39 | 6 | 6 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0002t0006 | 0/0 | 4442 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0002t0009 | 0/0 | 4442 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0002t0014 | 0/0 | 4442 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0002t0016 | 0/0 | 4442 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0006t0001 | 0/0 | 4442 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0008t0002 | 0/0 | 4442 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0009t0001 | 0/0 | 4442 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0001c0010t0009 | 0/0 | 4442 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0002c0003t0001 | 0/0 | 4442 | 3 | 0 | 3 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0003c0004t0001 | 0/0 | 4442 | 3 | 1 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0004c0005t0002 | 0/0 | 4442 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
a0005c0007t0002 | 0/0 | 4442 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | GGGAG others(4437): Show |
chr17 | 45258119 | 45322020 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0001 | 0/0 | 13 | 2 | 1 | 9 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0002 | 0/0 | 7 | 0 | 3 | 3 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0004g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0004g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0005g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0007g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0007g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0007g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0010g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0010g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0011g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0011g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0012g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0013g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0015g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0017g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0018g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0001t0019g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0075 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0009g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0014g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0002t0016g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0006t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0008t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0009t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0001c0010t0009g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0002c0003t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0002c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0002c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0003c0004t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0003c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0003c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0004c0005t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0004c0005t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
a0005c0007t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | GBR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0167 | EUR | GBR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0228 | EUR | GBR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0169 | EUR | GBR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | FIN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0007 | EUR | FIN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0239 | EUR | FIN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0251 | EUR | FIN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00597 | hp2 | a0001 | c0001 | t0011 | g0084 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0168 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0240 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0108 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0207 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01167 | hp2 | a0004 | c0005 | t0002 | g0138 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0238 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0181 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01169 | hp1 | a0001 | c0001 | t0005 | g0182 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01169 | hp2 | a0004 | c0005 | t0002 | g0137 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01192 | hp1 | a0001 | c0001 | t0005 | g0156 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01256 | hp2 | a0002 | c0003 | t0001 | g0222 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0219 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01358 | hp2 | a0002 | c0003 | t0001 | g0223 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01361 | hp1 | a0001 | c0006 | t0001 | g0225 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0229 | EUR | IBS | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0252 | EUR | IBS | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0288 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02004 | hp2 | a0002 | c0003 | t0001 | g0224 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0143 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | CDX | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | CDX | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02258 | hp2 | a0001 | c0001 | t0008 | g0197 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | KHV | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0286 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0266 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0271 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02647 | hp1 | a0001 | c0008 | t0002 | g0275 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02647 | hp2 | a0001 | c0001 | t0007 | g0234 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0106 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0235 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0274 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02723 | hp2 | a0001 | c0001 | t0010 | g0278 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0236 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02886 | hp1 | a0001 | c0001 | t0015 | g0187 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0289 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0291 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0220 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0292 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0293 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03209 | hp2 | a0001 | c0001 | t0008 | g0215 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0227 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0287 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03516 | hp2 | a0003 | c0004 | t0001 | g0026 | AFR | ESN | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0116 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03669 | hp2 | a0001 | c0001 | t0017 | g0157 | SAS | PJL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | BEB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | BEB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | BEB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0209 | SAS | STU | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | STU | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0087 | SAS | STU | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | STU | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0237 | SAS | STU | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0290 | AFR | YRI | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | CHB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | CHB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | YRI | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | YRI | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18948 | hp2 | a0001 | c0001 | t0011 | g0092 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18949 | hp2 | a0001 | c0001 | t0018 | g0090 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18956 | hp1 | a0001 | c0002 | t0006 | g0183 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18974 | hp1 | a0001 | c0001 | t0013 | g0093 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18998 | hp1 | a0003 | c0004 | t0001 | g0052 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19002 | hp2 | a0001 | c0002 | t0006 | g0056 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19004 | hp1 | a0001 | c0002 | t0006 | g0055 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19011 | hp1 | a0001 | c0009 | t0001 | g0217 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0294 | AFR | LWK | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19030 | hp2 | a0001 | c0002 | t0009 | g0263 | AFR | LWK | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19043 | hp1 | a0001 | c0002 | t0016 | g0150 | AFR | LWK | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | LWK | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19065 | hp2 | a0005 | c0007 | t0002 | g0195 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19081 | hp2 | a0001 | c0002 | t0014 | g0060 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19085 | hp2 | a0003 | c0004 | t0001 | g0053 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | YRI | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | YRI | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | ASW | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ASW | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0006 | EUR | TSI | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0149 | EUR | TSI | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA20805 | hp2 | a0001 | c0001 | t0012 | g0107 | EUR | TSI | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | GIH | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0202 | SAS | GIH | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0277 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0231 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
HG03471 | hp2 | a0001 | c0010 | t0009 | g0253 | AFR | MSL | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | USA | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | LWK | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
NA21309 | hp2 | a0001 | c0001 | t0019 | g0214 | AFR | LWK | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0152 | REF | REF | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0075 | REF | REF | MAP3K14_chr17_45258119_45322020 | MAP3K14 | chr17 | 45258119 | 45322020 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:45267660 | C | G | 1 | a0005 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.2072G>C | p.Arg691Thr | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 12/16 | 2153/4442 | 2072/2844 | 691/947 | chr17 | 45267660 | |||
chr17:45286809 | G | C | 1 | a0004 | 2 | HG01167.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.774C>G | p.Phe258Leu | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/16 | 855/4442 | 774/2844 | 258/947 | chr17 | 45286809 | |||
chr17:45286819 | G | A | 1 | a0003 | 3 | HG03516.hp2 NA18998.hp1 NA19085.hp2 |
missense_variant | MODERATE | c.764C>T | p.Thr255Met | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/16 | 845/4442 | 764/2844 | 255/947 | chr17 | 45286819 | |||
chr17:45287272 | C | T | 1 | a0002 | 3 | HG01256.hp2 HG01358.hp2 HG02004.hp2 |
missense_variant | MODERATE | c.419G>A | p.Ser140Asn | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 4/16 | 500/4442 | 419/2844 | 140/947 | chr17 | 45287272 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:45264774 | G | C | 4 | a0001c0001 a0001c0008 a0004c0005 others(1): Show |
245 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(242): Show |
synonymous_variant | LOW | c.2706C>G | p.Val902Val | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 2787/4442 | 2706/2844 | 902/947 | chr17 | 45264774 | |||
chr17:45267425 | T | C | 1 | a0001c0010 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.2307A>G | p.Glu769Glu | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 12/16 | 2388/4442 | 2307/2844 | 769/947 | chr17 | 45267425 | |||
chr17:45267434 | C | T | 1 | a0001c0009 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.2298G>A | p.Pro766Pro | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 12/16 | 2379/4442 | 2298/2844 | 766/947 | chr17 | 45267434 | |||
chr17:45267629 | C | T | 1 | a0001c0008 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.2103G>A | p.Arg701Arg | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 12/16 | 2184/4442 | 2103/2844 | 701/947 | chr17 | 45267629 | |||
chr17:45290578 | C | T | 1 | a0001c0006 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.168G>A | p.Glu56Glu | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/16 | 249/4442 | 168/2844 | 56/947 | chr17 | 45290578 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:45263226 | G | A | 2 | a0001c0001t0007 a0001c0001t0010 |
5 | HG02486.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1410C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 1410 | chr17 | 45263226 | ||||||
chr17:45263239 | C | T | 1 | a0001c0001t0018 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1397G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 1397 | chr17 | 45263239 | ||||||
chr17:45263264 | C | T | 1 | a0001c0001t0005 | 7 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1372G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 1372 | chr17 | 45263264 | ||||||
chr17:45263342 | G | A | 2 | a0001c0002t0009 a0001c0010t0009 |
2 | HG03471.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1294C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 1294 | chr17 | 45263342 | ||||||
chr17:45263460 | T | C | 1 | a0001c0001t0010 | 2 | HG02486.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1176A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 1176 | chr17 | 45263460 | ||||||
chr17:45263569 | G | A | 9 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(6): Show |
141 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1067C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 1067 | chr17 | 45263569 | ||||||
chr17:45263743 | C | T | 2 | a0001c0001t0003 a0001c0001t0012 |
21 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*893G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 893 | chr17 | 45263743 | ||||||
chr17:45263758 | C | T | 1 | a0001c0001t0017 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*878G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 878 | chr17 | 45263758 | ||||||
chr17:45263951 | A | G | 1 | a0001c0002t0016 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*685T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 685 | chr17 | 45263951 | ||||||
chr17:45263992 | A | G | 1 | a0001c0001t0004 | 16 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*644T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 644 | chr17 | 45263992 | ||||||
chr17:45264099 | G | T | 1 | a0001c0001t0015 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*537C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 537 | chr17 | 45264099 | ||||||
chr17:45264174 | C | T | 1 | a0001c0002t0014 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*462G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 462 | chr17 | 45264174 | ||||||
chr17:45264248 | C | T | 1 | a0001c0002t0006 | 3 | NA18956.hp1 NA19002.hp2 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*388G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 388 | chr17 | 45264248 | ||||||
chr17:45264526 | C | T | 1 | a0001c0001t0013 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*110G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 110 | chr17 | 45264526 | ||||||
chr17:45264535 | G | A | 1 | a0001c0001t0012 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 101 | chr17 | 45264535 | ||||||
chr17:45264546 | G | T | 2 | a0001c0001t0003 a0001c0001t0012 |
21 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*90C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 90 | chr17 | 45264546 | ||||||
chr17:45264585 | C | T | 1 | a0001c0001t0008 | 2 | HG02258.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*51G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 51 | chr17 | 45264585 | ||||||
chr17:45264605 | G | A | 1 | a0001c0001t0019 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*31C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 31 | chr17 | 45264605 | ||||||
chr17:45264610 | T | C | 1 | a0001c0001t0011 | 2 | HG00597.hp2 NA18948.hp2 |
3_prime_UTR_variant | MODIFIER | c.*26A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 16/16 | 26 | chr17 | 45264610 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:45264939 | C | A | 109 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(106): Show |
136 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.2680-139G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 15/15 | chr17 | 45264939 | |||||||
chr17:45265033 | C | T | 1 | a0001c0001t0002g0210 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2679+130G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 15/15 | chr17 | 45265033 | |||||||
chr17:45265293 | G | C | 2 | a0001c0001t0005g0143 a0001c0001t0005g0169 |
2 | HG00140.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.2579-30C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45265293 | |||||||
chr17:45265531 | G | A | 1 | a0001c0001t0015g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2579-268C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45265531 | |||||||
chr17:45265626 | C | CG | 72 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(69): Show |
74 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.2579-364dupC | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45265626 | |||||||
chr17:45265752 | T | C | 1 | a0001c0001t0003g0108 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2579-489A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45265752 | |||||||
chr17:45265799 | C | T | 17 | a0001c0001t0001g0023 a0001c0001t0001g0188 a0001c0001t0001g0189 others(14): Show |
17 | HG01891.hp2 HG02280.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.2579-536G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45265799 | |||||||
chr17:45265882 | T | C | 18 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0043 others(15): Show |
21 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.2579-619A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45265882 | |||||||
chr17:45265950 | A | G | 2 | a0001c0001t0005g0143 a0001c0001t0005g0169 |
2 | HG00140.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.2578+587T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45265950 | |||||||
chr17:45266016 | C | T | 2 | a0003c0004t0001g0052 a0003c0004t0001g0053 |
2 | NA18998.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2578+521G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45266016 | |||||||
chr17:45266310 | A | G | 1 | a0001c0002t0001g0050 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2578+227T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45266310 | |||||||
chr17:45266314 | G | A | 1 | a0001c0001t0002g0129 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2578+223C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45266314 | |||||||
chr17:45266480 | G | A | 18 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(15): Show |
18 | HG02145.hp1 HG02145.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.2578+57C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 14/15 | chr17 | 45266480 | |||||||
chr17:45266691 | C | T | 2 | a0001c0001t0002g0184 a0001c0001t0002g0185 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2434-10G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 13/15 | chr17 | 45266691 | |||||||
chr17:45266706 | G | A | 127 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0256 others(124): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2434-25C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 13/15 | chr17 | 45266706 | |||||||
chr17:45266737 | C | T | 1 | a0001c0001t0002g0283 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2434-56G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 13/15 | chr17 | 45266737 | |||||||
chr17:45266766 | C | T | 1 | a0001c0001t0017g0157 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2434-85G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 13/15 | chr17 | 45266766 | |||||||
chr17:45268090 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1973-331C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268090 | |||||||
chr17:45268099 | C | T | 3 | a0001c0001t0002g0111 a0001c0001t0002g0136 a0001c0001t0002g0205 |
3 | HG01109.hp1 HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1973-340G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268099 | |||||||
chr17:45268174 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1973-415G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268174 | |||||||
chr17:45268183 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1973-424G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268183 | |||||||
chr17:45268187 | T | C | 1 | a0001c0001t0002g0213 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1973-428A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268187 | |||||||
chr17:45268328 | C | A | 1 | a0001c0001t0002g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1973-569G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268328 | |||||||
chr17:45268491 | G | A | 14 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0059 others(11): Show |
16 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1973-732C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268491 | |||||||
chr17:45268593 | G | T | 6 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
6 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1973-834C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268593 | |||||||
chr17:45268706 | C | T | 1 | a0001c0002t0001g0202 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1973-947G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45268706 | |||||||
chr17:45269057 | C | T | 1 | a0001c0001t0019g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1973-1298G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269057 | |||||||
chr17:45269102 | G | A | 1 | a0001c0001t0015g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1972+1311C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269102 | |||||||
chr17:45269126 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1972+1287G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269126 | |||||||
chr17:45269256 | C | T | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1972+1157G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269256 | |||||||
chr17:45269264 | A | C | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1972+1149T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269264 | |||||||
chr17:45269265 | G | C | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1972+1148C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269265 | |||||||
chr17:45269266 | C | T | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1972+1147G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269266 | |||||||
chr17:45269268 | T | C | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1972+1145A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269268 | |||||||
chr17:45269542 | C | T | 1 | a0001c0002t0001g0070 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1972+871G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269542 | |||||||
chr17:45269611 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1972+802C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269611 | |||||||
chr17:45269613 | G | T | 256 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(253): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.1972+800C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269613 | |||||||
chr17:45269617 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1972+796G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269617 | |||||||
chr17:45269632 | A | G | 1 | a0001c0001t0004g0290 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1972+781T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269632 | |||||||
chr17:45269699 | T | C | 34 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0031 others(31): Show |
39 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1972+714A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269699 | |||||||
chr17:45269969 | C | G | 255 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(252): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.1972+444G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45269969 | |||||||
chr17:45270243 | C | T | 72 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(69): Show |
74 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1972+170G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 11/15 | chr17 | 45270243 | |||||||
chr17:45270598 | T | A | 1 | a0001c0001t0002g0206 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1822-35A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 10/15 | chr17 | 45270598 | |||||||
chr17:45270618 | G | C | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1822-55C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 10/15 | chr17 | 45270618 | |||||||
chr17:45270975 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1821+83C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 10/15 | chr17 | 45270975 | |||||||
chr17:45271028 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1821+30G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 10/15 | chr17 | 45271028 | |||||||
chr17:45271041 | T | G | 13 | a0001c0001t0001g0191 a0001c0001t0001g0260 a0001c0001t0001g0264 others(10): Show |
13 | HG02280.hp1 HG02486.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1821+17A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 10/15 | chr17 | 45271041 | |||||||
chr17:45271045 | T | G | 13 | a0001c0001t0001g0191 a0001c0001t0001g0260 a0001c0001t0001g0264 others(10): Show |
13 | HG02280.hp1 HG02486.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1821+13A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 10/15 | chr17 | 45271045 | |||||||
chr17:45271367 | A | G | 2 | a0001c0001t0002g0051 a0001c0001t0002g0127 |
2 | NA18994.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1658-146T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45271367 | |||||||
chr17:45271407 | G | A | 7 | a0001c0001t0001g0255 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG02145.hp2 HG02559.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1658-186C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45271407 | |||||||
chr17:45271520 | G | A | 257 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(254): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1658-299C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45271520 | |||||||
chr17:45271751 | A | G | 1 | a0001c0001t0002g0126 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1658-530T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45271751 | |||||||
chr17:45271809 | G | A | 86 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(83): Show |
88 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1658-588C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45271809 | |||||||
chr17:45271830 | G | T | 8 | a0001c0002t0001g0015 a0001c0002t0001g0192 a0001c0002t0001g0193 others(5): Show |
9 | HG00673.hp1 HG02083.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1658-609C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45271830 | |||||||
chr17:45272362 | A | AT | 42 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(39): Show |
44 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1657+1140dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45272362 | |||||||
chr17:45272515 | T | C | 34 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0031 others(31): Show |
39 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1657+988A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45272515 | |||||||
chr17:45272553 | G | T | 257 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(254): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1657+950C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45272553 | |||||||
chr17:45272714 | C | T | 34 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0031 others(31): Show |
39 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1657+789G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45272714 | |||||||
chr17:45273109 | C | T | 1 | a0001c0001t0004g0274 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1657+394G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45273109 | |||||||
chr17:45273147 | G | A | 86 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(83): Show |
88 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1657+356C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45273147 | |||||||
chr17:45273299 | A | G | 115 | a0001c0001t0001g0023 a0001c0001t0001g0198 a0001c0001t0001g0199 others(112): Show |
142 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1657+204T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45273299 | |||||||
chr17:45273396 | C | T | 3 | a0001c0002t0001g0024 a0001c0002t0001g0025 a0003c0004t0001g0026 |
3 | HG01069.hp1 HG01071.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1657+107G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45273396 | |||||||
chr17:45273403 | G | T | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1657+100C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45273403 | |||||||
chr17:45273470 | T | C | 8 | a0001c0001t0001g0191 a0001c0001t0001g0260 a0001c0001t0001g0264 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1657+33A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 9/15 | chr17 | 45273470 | |||||||
chr17:45273634 | G | A | 2 | a0001c0002t0001g0266 a0001c0002t0001g0271 |
2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1553-27C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 8/15 | chr17 | 45273634 | |||||||
chr17:45273672 | C | G | 34 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0031 others(31): Show |
39 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1553-65G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 8/15 | chr17 | 45273672 | |||||||
chr17:45273707 | T | C | 1 | a0001c0001t0003g0004 | 3 | NA18955.hp1 NA18962.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1553-100A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 8/15 | chr17 | 45273707 | |||||||
chr17:45273760 | G | C | 115 | a0001c0001t0001g0023 a0001c0001t0001g0198 a0001c0001t0001g0199 others(112): Show |
142 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1553-153C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 8/15 | chr17 | 45273760 | |||||||
chr17:45273867 | C | T | 1 | a0001c0001t0002g0261 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1552+256G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 8/15 | chr17 | 45273867 | |||||||
chr17:45274290 | G | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0153 a0001c0001t0001g0170 others(1): Show |
4 | HG01106.hp1 HG02056.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.1421-36C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 7/15 | chr17 | 45274290 | |||||||
chr17:45274682 | C | T | 41 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(38): Show |
43 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.1291-89G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45274682 | |||||||
chr17:45274714 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1291-121G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45274714 | |||||||
chr17:45274764 | G | T | 1 | a0001c0001t0002g0125 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1291-171C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45274764 | |||||||
chr17:45274854 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1291-261G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45274854 | |||||||
chr17:45274953 | C | T | 1 | a0001c0002t0001g0293 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1291-360G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45274953 | |||||||
chr17:45275090 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1291-497C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275090 | |||||||
chr17:45275100 | G | C | 1 | a0001c0001t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1291-507C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275100 | |||||||
chr17:45275103 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1291-510G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275103 | |||||||
chr17:45275260 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1291-667C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275260 | |||||||
chr17:45275275 | T | C | 144 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(141): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1291-682A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275275 | |||||||
chr17:45275356 | T | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1291-763A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275356 | |||||||
chr17:45275386 | T | C | 2 | a0004c0005t0002g0137 a0004c0005t0002g0138 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1291-793A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275386 | |||||||
chr17:45275482 | CA | C | 111 | a0001c0001t0001g0023 a0001c0001t0001g0198 a0001c0001t0001g0199 others(108): Show |
138 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1291-890delT | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275482 | |||||||
chr17:45275489 | AAAAAAC | A | 125 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(122): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1291-902_1291-897d others(8): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275489 | |||||||
chr17:45275490 | AAAAAC | A | 19 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(16): Show |
19 | HG00621.hp1 HG00741.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1291-902_1291-898d others(7): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275490 | |||||||
chr17:45275536 | C | A | 1 | a0001c0001t0019g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1291-943G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275536 | |||||||
chr17:45275752 | TTTC | T | 41 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(38): Show |
43 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.1291-1162_1291-116 others(7): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275752 | |||||||
chr17:45275760 | CT | C | 141 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(138): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1291-1168delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275760 | |||||||
chr17:45275765 | T | C | 13 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0043 others(10): Show |
16 | HG00438.hp2 HG00621.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1291-1172A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275765 | |||||||
chr17:45275868 | T | TCTCCTGC others(16): Show |
1 | a0001c0002t0001g0193 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1291-1298_1291-127 others(27): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275868 | |||||||
chr17:45275902 | C | T | 74 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(71): Show |
76 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.1291-1309G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275902 | |||||||
chr17:45275936 | A | G | 1 | a0001c0001t0013g0093 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1291-1343T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45275936 | |||||||
chr17:45276041 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1291-1448C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276041 | |||||||
chr17:45276056 | C | T | 144 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(141): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1291-1463G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276056 | |||||||
chr17:45276204 | C | A | 3 | a0001c0001t0002g0254 a0001c0002t0009g0263 a0001c0010t0009g0253 |
3 | HG01243.hp1 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1291-1611G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276204 | |||||||
chr17:45276279 | T | A | 13 | a0001c0001t0001g0191 a0001c0001t0001g0260 a0001c0001t0001g0264 others(10): Show |
13 | HG02280.hp1 HG02486.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1291-1686A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276279 | |||||||
chr17:45276310 | G | A | 112 | a0001c0001t0001g0023 a0001c0001t0001g0198 a0001c0001t0001g0199 others(109): Show |
139 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1291-1717C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276310 | |||||||
chr17:45276359 | A | G | 1 | a0001c0001t0002g0261 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1291-1766T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276359 | |||||||
chr17:45276396 | C | T | 76 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(73): Show |
78 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1291-1803G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276396 | |||||||
chr17:45276517 | CT | C | 74 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(71): Show |
76 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.1291-1925delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276517 | |||||||
chr17:45276551 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1291-1958C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276551 | |||||||
chr17:45276823 | C | CT | 39 | a0001c0001t0001g0021 a0001c0001t0001g0191 a0001c0001t0001g0256 others(36): Show |
42 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1291-2231dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276823 | |||||||
chr17:45276823 | C | CTT | 51 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0044 others(48): Show |
53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1291-2232_1291-223 others(6): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276823 | |||||||
chr17:45276823 | C | CTTT | 16 | a0001c0001t0001g0027 a0001c0001t0001g0142 a0001c0001t0001g0145 others(13): Show |
16 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1291-2233_1291-223 others(7): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276823 | |||||||
chr17:45276823 | CT | C | 99 | a0001c0001t0001g0023 a0001c0001t0001g0198 a0001c0001t0001g0232 others(96): Show |
126 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1291-2231delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276823 | |||||||
chr17:45276823 | CTT | C | 6 | a0001c0001t0002g0078 a0001c0001t0002g0091 a0001c0001t0002g0094 others(3): Show |
6 | HG02896.hp2 NA18747.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291-2232_1291-223 others(6): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276823 | |||||||
chr17:45276932 | C | T | 4 | a0001c0001t0002g0076 a0001c0001t0002g0091 a0001c0001t0002g0134 others(1): Show |
4 | NA18939.hp1 NA18943.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291-2339G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276932 | |||||||
chr17:45276992 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1291-2399C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45276992 | |||||||
chr17:45277152 | T | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0165 |
2 | NA18969.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1291-2559A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45277152 | |||||||
chr17:45277153 | A | C | 2 | a0001c0001t0002g0123 a0001c0001t0002g0130 |
2 | HG03654.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1291-2560T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45277153 | |||||||
chr17:45277250 | C | T | 32 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0031 others(29): Show |
37 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1291-2657G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45277250 | |||||||
chr17:45277314 | G | A | 132 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(129): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1291-2721C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45277314 | |||||||
chr17:45277501 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1291-2908C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45277501 | |||||||
chr17:45277563 | G | A | 78 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(75): Show |
80 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1291-2970C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45277563 | |||||||
chr17:45277729 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1291-3136G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45277729 | |||||||
chr17:45277795 | G | A | 2 | a0001c0002t0001g0029 a0001c0002t0001g0030 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1291-3202C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45277795 | |||||||
chr17:45278360 | G | C | 1 | a0001c0001t0002g0122 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1291-3767C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45278360 | |||||||
chr17:45278679 | C | CT | 23 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(20): Show |
23 | HG00642.hp2 HG02145.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1291-4087dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45278679 | |||||||
chr17:45278679 | C | CTTT | 11 | a0001c0001t0001g0256 a0001c0001t0002g0254 a0001c0002t0001g0024 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1291-4089_1291-408 others(7): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45278679 | |||||||
chr17:45278679 | CT | C | 17 | a0001c0001t0001g0175 a0001c0001t0001g0191 a0001c0001t0001g0260 others(14): Show |
17 | HG01256.hp1 HG02109.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1291-4087delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45278679 | |||||||
chr17:45279407 | G | A | 10 | a0001c0001t0001g0256 a0001c0001t0002g0254 a0001c0002t0001g0024 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1291-4814C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45279407 | |||||||
chr17:45279425 | C | G | 1 | a0001c0001t0001g0166 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1291-4832G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45279425 | |||||||
chr17:45279494 | A | G | 1 | a0001c0002t0001g0192 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1291-4901T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45279494 | |||||||
chr17:45279525 | C | T | 2 | a0003c0004t0001g0052 a0003c0004t0001g0053 |
2 | NA18998.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1291-4932G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45279525 | |||||||
chr17:45279536 | G | A | 2 | a0001c0001t0008g0197 a0001c0001t0008g0215 |
2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1291-4943C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45279536 | |||||||
chr17:45279675 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1291-5082C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45279675 | |||||||
chr17:45279797 | A | G | 1 | a0001c0001t0017g0157 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1290+5015T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45279797 | |||||||
chr17:45280299 | C | CT | 47 | a0001c0001t0001g0021 a0001c0001t0001g0065 a0001c0001t0001g0066 others(44): Show |
47 | HG00558.hp2 HG00642.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1290+4512dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280299 | |||||||
chr17:45280299 | C | CTT | 33 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(30): Show |
35 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.1290+4511_1290+451 others(6): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280299 | |||||||
chr17:45280299 | C | CTTT | 15 | a0001c0001t0001g0151 a0001c0001t0001g0158 a0001c0001t0001g0160 others(12): Show |
15 | HG01433.hp1 HG02055.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1290+4510_1290+451 others(7): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280299 | |||||||
chr17:45280299 | C | CTTTT | 6 | a0001c0001t0001g0142 a0001c0001t0001g0170 a0001c0001t0001g0176 others(3): Show |
6 | HG00741.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1290+4509_1290+451 others(8): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280299 | |||||||
chr17:45280299 | CT | C | 13 | a0001c0001t0001g0279 a0001c0001t0002g0129 a0001c0001t0002g0203 others(10): Show |
14 | HG00673.hp1 HG02083.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.1290+4512delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280299 | |||||||
chr17:45280342 | C | T | 10 | a0001c0001t0001g0256 a0001c0001t0002g0254 a0001c0002t0001g0024 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1290+4470G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280342 | |||||||
chr17:45280437 | G | C | 35 | a0001c0001t0003g0043 a0001c0002t0001g0003 a0001c0002t0001g0007 others(32): Show |
40 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1290+4375C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280437 | |||||||
chr17:45280452 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1290+4360G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280452 | |||||||
chr17:45280503 | C | T | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4309G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280503 | |||||||
chr17:45280533 | G | A | 13 | a0001c0001t0001g0191 a0001c0001t0001g0260 a0001c0001t0001g0264 others(10): Show |
13 | HG02280.hp1 HG02486.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1290+4279C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280533 | |||||||
chr17:45280535 | C | G | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4277G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280535 | |||||||
chr17:45280536 | C | A | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4276G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280536 | |||||||
chr17:45280538 | C | A | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4274G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280538 | |||||||
chr17:45280544 | A | G | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4268T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280544 | |||||||
chr17:45280546 | T | A | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4266A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280546 | |||||||
chr17:45280547 | CACCCGCC others(3): Show |
C | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4255_1290+426 others(14): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280547 | |||||||
chr17:45280559 | C | T | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4253G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280559 | |||||||
chr17:45280560 | C | G | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4252G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280560 | |||||||
chr17:45280562 | C | G | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4250G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280562 | |||||||
chr17:45280563 | T | G | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4249A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280563 | |||||||
chr17:45280564 | C | T | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1290+4248G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280564 | |||||||
chr17:45280571 | C | T | 18 | a0001c0001t0002g0081 a0001c0001t0003g0004 a0001c0001t0003g0008 others(15): Show |
21 | HG00408.hp1 HG00621.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1290+4241G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280571 | |||||||
chr17:45280799 | C | T | 109 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(106): Show |
114 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1290+4013G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280799 | |||||||
chr17:45280812 | T | C | 1 | a0001c0002t0001g0202 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1290+4000A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280812 | |||||||
chr17:45280857 | C | T | 2 | a0001c0001t0002g0273 a0001c0001t0015g0187 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1290+3955G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280857 | |||||||
chr17:45280858 | G | A | 2 | a0004c0005t0002g0137 a0004c0005t0002g0138 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1290+3954C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280858 | |||||||
chr17:45280887 | A | G | 11 | a0001c0001t0001g0256 a0001c0001t0002g0254 a0001c0002t0001g0024 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1290+3925T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280887 | |||||||
chr17:45280936 | C | T | 2 | a0004c0005t0002g0137 a0004c0005t0002g0138 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1290+3876G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45280936 | |||||||
chr17:45281051 | T | C | 18 | a0001c0001t0002g0081 a0001c0001t0003g0004 a0001c0001t0003g0008 others(15): Show |
21 | HG00408.hp1 HG00621.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1290+3761A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281051 | |||||||
chr17:45281314 | A | T | 1 | a0001c0001t0005g0156 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1290+3498T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281314 | |||||||
chr17:45281324 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1290+3488C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281324 | |||||||
chr17:45281504 | G | C | 1 | a0001c0002t0001g0116 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1290+3308C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281504 | |||||||
chr17:45281640 | C | CT | 55 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0044 others(52): Show |
56 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1290+3171dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281640 | |||||||
chr17:45281640 | C | CTT | 6 | a0001c0001t0001g0014 a0001c0001t0001g0147 a0001c0001t0001g0170 others(3): Show |
7 | HG02486.hp1 HG03516.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.1290+3170_1290+317 others(6): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281640 | |||||||
chr17:45281640 | CT | C | 8 | a0001c0001t0001g0160 a0001c0001t0002g0130 a0001c0001t0002g0248 others(5): Show |
8 | HG00323.hp2 HG02004.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.1290+3171delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281640 | |||||||
chr17:45281640 | CTTT | C | 19 | a0001c0001t0002g0081 a0001c0001t0003g0004 a0001c0001t0003g0008 others(16): Show |
22 | HG00408.hp1 HG00621.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.1290+3169_1290+317 others(7): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281640 | |||||||
chr17:45281671 | G | A | 3 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 |
3 | HG03209.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1290+3141C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281671 | |||||||
chr17:45281731 | G | A | 1 | a0001c0001t0010g0277 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1290+3081C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281731 | |||||||
chr17:45281758 | C | G | 1 | a0001c0001t0001g0022 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1290+3054G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281758 | |||||||
chr17:45281874 | A | G | 257 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(254): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1290+2938T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281874 | |||||||
chr17:45281933 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1290+2879G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45281933 | |||||||
chr17:45282105 | T | G | 1 | a0001c0002t0001g0040 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1290+2707A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282105 | |||||||
chr17:45282217 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1290+2595C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282217 | |||||||
chr17:45282465 | G | C | 1 | a0001c0009t0001g0217 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1290+2347C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282465 | |||||||
chr17:45282524 | T | C | 144 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(141): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1290+2288A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282524 | |||||||
chr17:45282538 | G | C | 3 | a0001c0001t0002g0190 a0001c0001t0002g0208 a0001c0001t0002g0216 |
3 | HG01109.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1290+2274C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282538 | |||||||
chr17:45282554 | C | CA | 109 | a0001c0001t0001g0023 a0001c0001t0001g0198 a0001c0001t0001g0199 others(106): Show |
135 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1290+2257dupT | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282554 | |||||||
chr17:45282554 | CA | C | 141 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(138): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1290+2257delT | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282554 | |||||||
chr17:45282559 | A | G | 1 | a0002c0003t0001g0222 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1290+2253T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282559 | |||||||
chr17:45282690 | G | A | 113 | a0001c0001t0001g0023 a0001c0001t0001g0198 a0001c0001t0001g0199 others(110): Show |
140 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1290+2122C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282690 | |||||||
chr17:45282753 | C | T | 6 | a0001c0001t0001g0232 a0001c0001t0002g0017 a0001c0001t0002g0186 others(3): Show |
7 | HG01884.hp2 HG02109.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1290+2059G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282753 | |||||||
chr17:45282761 | A | G | 257 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(254): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1290+2051T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282761 | |||||||
chr17:45282881 | C | T | 1 | a0001c0001t0002g0085 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1290+1931G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282881 | |||||||
chr17:45282971 | GGCAGCTC others(15): Show |
G | 1 | a0001c0001t0001g0067 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1290+1819_1290+184 others(26): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45282971 | |||||||
chr17:45283260 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1290+1552G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283260 | |||||||
chr17:45283340 | C | T | 2 | a0001c0001t0002g0184 a0001c0001t0002g0185 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1290+1472G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283340 | |||||||
chr17:45283463 | A | G | 2 | a0001c0001t0002g0273 a0001c0001t0015g0187 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1290+1349T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283463 | |||||||
chr17:45283573 | G | T | 37 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0003g0043 others(34): Show |
42 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.1290+1239C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283573 | |||||||
chr17:45283627 | G | A | 72 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(69): Show |
74 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1290+1185C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283627 | |||||||
chr17:45283846 | G | A | 39 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(36): Show |
41 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.1290+966C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283846 | |||||||
chr17:45283880 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1290+932C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283880 | |||||||
chr17:45283931 | G | A | 2 | a0001c0001t0005g0143 a0001c0001t0005g0169 |
2 | HG00140.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1290+881C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283931 | |||||||
chr17:45283983 | C | G | 257 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(254): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1290+829G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45283983 | |||||||
chr17:45284124 | G | A | 112 | a0001c0001t0001g0023 a0001c0001t0001g0198 a0001c0001t0001g0199 others(109): Show |
139 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1290+688C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45284124 | |||||||
chr17:45284421 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0004c0005t0002g0137 others(1): Show |
4 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1290+391G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45284421 | |||||||
chr17:45284522 | C | A | 112 | a0001c0001t0001g0023 a0001c0001t0001g0198 a0001c0001t0001g0199 others(109): Show |
139 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1290+290G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 6/15 | chr17 | 45284522 | |||||||
chr17:45285050 | G | A | 1 | a0001c0001t0002g0283 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1153-101C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285050 | |||||||
chr17:45285089 | C | T | 7 | a0001c0001t0002g0071 a0001c0001t0002g0077 a0001c0001t0002g0088 others(4): Show |
7 | HG00558.hp1 HG02080.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.1153-140G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285089 | |||||||
chr17:45285108 | C | T | 58 | a0001c0001t0001g0023 a0001c0001t0001g0064 a0001c0001t0001g0065 others(55): Show |
62 | HG01109.hp2 HG01243.hp2 HG01358.hp1 others(59): Show |
intron_variant | MODIFIER | c.1153-159G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285108 | |||||||
chr17:45285127 | G | A | 1 | a0001c0001t0002g0149 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1153-178C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285127 | |||||||
chr17:45285148 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1153-199G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285148 | |||||||
chr17:45285554 | A | G | 9 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(6): Show |
9 | HG02145.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1153-605T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285554 | |||||||
chr17:45285579 | T | C | 2 | a0001c0001t0002g0184 a0001c0001t0002g0185 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1153-630A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285579 | |||||||
chr17:45285632 | A | G | 3 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0178 |
3 | HG01256.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1153-683T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285632 | |||||||
chr17:45285705 | G | A | 1 | a0001c0001t0004g0288 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1152+726C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285705 | |||||||
chr17:45285800 | A | T | 15 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0255 others(12): Show |
15 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1152+631T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285800 | |||||||
chr17:45285967 | TA | T | 46 | a0001c0001t0001g0023 a0001c0001t0001g0064 a0001c0001t0001g0065 others(43): Show |
51 | HG00099.hp2 HG01109.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.1152+463delT | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45285967 | |||||||
chr17:45286005 | C | G | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0004c0005t0002g0137 others(1): Show |
4 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152+426G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45286005 | |||||||
chr17:45286006 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1152+425G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45286006 | |||||||
chr17:45286092 | G | A | 1 | a0001c0001t0003g0104 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1152+339C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45286092 | |||||||
chr17:45286337 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1152+94C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 5/15 | chr17 | 45286337 | |||||||
chr17:45287111 | G | A | 7 | a0001c0001t0004g0019 a0001c0001t0004g0231 a0001c0001t0004g0288 others(4): Show |
8 | HG01891.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.537+43C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 4/15 | chr17 | 45287111 | |||||||
chr17:45287127 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.537+27C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 4/15 | chr17 | 45287127 | |||||||
chr17:45287371 | C | A | 16 | a0001c0001t0002g0081 a0001c0001t0003g0004 a0001c0001t0003g0008 others(13): Show |
19 | HG00621.hp2 HG01069.hp2 HG01175.hp2 others(16): Show |
splice_region_variant&intron_variant | LOW | c.327-7G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287371 | |||||||
chr17:45287399 | C | T | 2 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
2 | NA18974.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.327-35G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287399 | |||||||
chr17:45287407 | C | T | 2 | a0001c0002t0001g0024 a0001c0002t0001g0025 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.327-43G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287407 | |||||||
chr17:45287474 | G | T | 4 | a0001c0001t0001g0256 a0001c0002t0001g0028 a0001c0002t0001g0029 others(1): Show |
4 | HG02257.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.327-110C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287474 | |||||||
chr17:45287499 | G | A | 9 | a0001c0001t0001g0255 a0001c0001t0002g0254 a0001c0001t0015g0187 others(6): Show |
9 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-135C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287499 | |||||||
chr17:45287516 | G | GA | 18 | a0001c0001t0002g0081 a0001c0001t0002g0273 a0001c0001t0003g0004 others(15): Show |
21 | HG00621.hp2 HG01069.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.327-153dupT | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287516 | |||||||
chr17:45287548 | A | G | 59 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0044 others(56): Show |
65 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.327-184T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287548 | |||||||
chr17:45287637 | A | G | 2 | a0001c0001t0001g0262 a0001c0002t0009g0263 |
2 | HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.327-273T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287637 | |||||||
chr17:45287649 | G | A | 18 | a0001c0001t0002g0081 a0001c0001t0003g0004 a0001c0001t0003g0008 others(15): Show |
21 | HG00408.hp1 HG00621.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.327-285C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287649 | |||||||
chr17:45287723 | C | T | 48 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(45): Show |
50 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.327-359G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287723 | |||||||
chr17:45287818 | G | A | 7 | a0001c0001t0005g0143 a0001c0001t0005g0156 a0001c0001t0005g0167 others(4): Show |
7 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(4): Show |
intron_variant | MODIFIER | c.327-454C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287818 | |||||||
chr17:45287889 | T | G | 1 | a0001c0001t0002g0096 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.327-525A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287889 | |||||||
chr17:45287895 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.327-531C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287895 | |||||||
chr17:45287964 | C | T | 4 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0004c0005t0002g0137 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.327-600G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45287964 | |||||||
chr17:45288026 | G | A | 39 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(36): Show |
41 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.327-662C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45288026 | |||||||
chr17:45288075 | A | G | 39 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(36): Show |
41 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.327-711T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45288075 | |||||||
chr17:45288360 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG01106.hp1 NA18960.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.326+876C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45288360 | |||||||
chr17:45288379 | G | GT | 169 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0044 others(166): Show |
200 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.326+856dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45288379 | |||||||
chr17:45288379 | G | GTT | 46 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(43): Show |
48 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.326+855_326+856dup others(2): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45288379 | |||||||
chr17:45288597 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.326+639G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45288597 | |||||||
chr17:45289181 | G | T | 23 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0002g0254 others(20): Show |
25 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.326+55C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 3/15 | chr17 | 45289181 | |||||||
chr17:45289336 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.257-31C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45289336 | |||||||
chr17:45289488 | A | G | 2 | a0001c0001t0002g0273 a0001c0001t0015g0187 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.257-183T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45289488 | |||||||
chr17:45289708 | A | C | 1 | a0001c0002t0016g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.257-403T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45289708 | |||||||
chr17:45289786 | G | A | 74 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(71): Show |
97 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.257-481C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45289786 | |||||||
chr17:45289790 | C | T | 1 | a0001c0002t0001g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.257-485G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45289790 | |||||||
chr17:45289919 | C | T | 1 | a0001c0001t0003g0102 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.256+571G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45289919 | |||||||
chr17:45289941 | G | A | 1 | a0001c0001t0002g0133 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.256+549C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45289941 | |||||||
chr17:45289965 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.256+525A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45289965 | |||||||
chr17:45290058 | C | T | 15 | a0001c0002t0001g0006 a0001c0002t0001g0226 a0001c0002t0001g0227 others(12): Show |
17 | HG00140.hp1 HG00323.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.256+432G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45290058 | |||||||
chr17:45290117 | G | C | 1 | a0001c0002t0001g0054 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.256+373C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45290117 | |||||||
chr17:45290287 | T | C | 224 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(221): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.256+203A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 2/15 | chr17 | 45290287 | |||||||
chr17:45290896 | T | C | 8 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0002t0001g0007 others(5): Show |
9 | HG00099.hp1 HG00280.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20-131A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45290896 | |||||||
chr17:45290949 | C | T | 5 | a0001c0001t0007g0234 a0001c0001t0007g0235 a0001c0001t0007g0236 others(2): Show |
5 | HG02486.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-184G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45290949 | |||||||
chr17:45290951 | C | A | 3 | a0001c0002t0001g0024 a0001c0002t0001g0025 a0003c0004t0001g0026 |
3 | HG01069.hp1 HG01071.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-20-186G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45290951 | |||||||
chr17:45290973 | C | T | 7 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0002g0254 others(4): Show |
7 | HG01243.hp1 HG02257.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20-208G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45290973 | |||||||
chr17:45291024 | G | A | 1 | a0001c0002t0009g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-20-259C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291024 | |||||||
chr17:45291234 | C | T | 5 | a0001c0002t0001g0005 a0001c0002t0001g0207 a0001c0002t0001g0219 others(2): Show |
7 | HG00733.hp1 HG00735.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20-469G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291234 | |||||||
chr17:45291296 | C | CTG | 24 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0285 others(21): Show |
26 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-20-533_-20-532dup others(2): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291296 | |||||||
chr17:45291296 | CTG | C | 201 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(198): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.-20-533_-20-532del others(2): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291296 | |||||||
chr17:45291500 | T | C | 2 | a0001c0001t0002g0273 a0001c0001t0015g0187 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-20-735A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291500 | |||||||
chr17:45291515 | C | T | 3 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 |
3 | HG03209.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-20-750G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291515 | |||||||
chr17:45291541 | G | T | 5 | a0001c0001t0007g0234 a0001c0001t0007g0235 a0001c0001t0007g0236 others(2): Show |
5 | HG02486.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-776C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291541 | |||||||
chr17:45291561 | C | T | 2 | a0004c0005t0002g0137 a0004c0005t0002g0138 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-20-796G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291561 | |||||||
chr17:45291820 | G | A | 1 | a0001c0002t0001g0057 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-20-1055C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45291820 | |||||||
chr17:45292241 | GGTGGCCT others(6): Show |
G | 44 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(41): Show |
46 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.-20-1489_-20-1477d others(15): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292241 | |||||||
chr17:45292286 | C | T | 11 | a0001c0001t0001g0191 a0001c0001t0001g0232 a0001c0001t0001g0264 others(8): Show |
12 | HG01243.hp2 HG01884.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-1521G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292286 | |||||||
chr17:45292287 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-20-1522C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292287 | |||||||
chr17:45292411 | C | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-20-1646G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292411 | |||||||
chr17:45292427 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0147 a0001c0001t0001g0177 |
4 | NA18963.hp2 NA18964.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-1662C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292427 | |||||||
chr17:45292538 | G | C | 44 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(41): Show |
46 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.-20-1773C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292538 | |||||||
chr17:45292614 | C | G | 5 | a0001c0002t0001g0005 a0001c0002t0001g0207 a0001c0002t0001g0219 others(2): Show |
7 | HG00733.hp1 HG00735.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20-1849G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292614 | |||||||
chr17:45292903 | C | T | 2 | a0001c0001t0002g0086 a0001c0001t0002g0117 |
2 | HG02027.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-20-2138G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292903 | |||||||
chr17:45292938 | G | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-20-2173C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292938 | |||||||
chr17:45292993 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-20-2228C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45292993 | |||||||
chr17:45293115 | C | T | 68 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(65): Show |
90 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.-20-2350G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45293115 | |||||||
chr17:45293172 | C | T | 11 | a0001c0001t0001g0191 a0001c0001t0001g0232 a0001c0001t0001g0264 others(8): Show |
12 | HG01243.hp2 HG01884.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-2407G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45293172 | |||||||
chr17:45293184 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-20-2419T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45293184 | |||||||
chr17:45293447 | A | G | 2 | a0001c0001t0002g0273 a0001c0001t0015g0187 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-20-2682T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45293447 | |||||||
chr17:45293846 | G | T | 1 | a0001c0001t0015g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-20-3081C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45293846 | |||||||
chr17:45293847 | A | G | 1 | a0001c0001t0015g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-20-3082T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45293847 | |||||||
chr17:45293908 | G | A | 12 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(9): Show |
12 | HG02145.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-3143C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45293908 | |||||||
chr17:45293929 | G | T | 18 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0198 others(15): Show |
18 | HG01099.hp1 HG02145.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-20-3164C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45293929 | |||||||
chr17:45294251 | G | A | 1 | a0001c0001t0002g0094 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-20-3486C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45294251 | |||||||
chr17:45294263 | G | A | 1 | a0001c0001t0003g0072 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-20-3498C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45294263 | |||||||
chr17:45294479 | C | T | 1 | a0001c0001t0008g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-20-3714G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45294479 | |||||||
chr17:45294521 | T | C | 5 | a0001c0001t0007g0234 a0001c0001t0007g0235 a0001c0001t0007g0236 others(2): Show |
5 | HG02486.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-3756A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45294521 | |||||||
chr17:45295156 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-20-4391A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45295156 | |||||||
chr17:45295202 | C | T | 10 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0002g0254 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20-4437G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45295202 | |||||||
chr17:45295223 | A | AT | 157 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(154): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.-20-4459dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45295223 | |||||||
chr17:45295496 | T | C | 1 | a0001c0002t0001g0058 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-20-4731A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45295496 | |||||||
chr17:45295766 | A | T | 1 | a0001c0002t0001g0046 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-20-5001T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45295766 | |||||||
chr17:45296034 | C | T | 10 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0002g0254 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20-5269G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296034 | |||||||
chr17:45296089 | G | C | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0003g0073 |
3 | HG01099.hp1 HG01175.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-20-5324C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296089 | |||||||
chr17:45296179 | C | T | 1 | a0001c0001t0007g0234 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-20-5414G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296179 | |||||||
chr17:45296262 | C | T | 1 | a0001c0001t0015g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-20-5497G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296262 | |||||||
chr17:45296396 | A | G | 11 | a0001c0001t0001g0191 a0001c0001t0001g0232 a0001c0001t0001g0264 others(8): Show |
12 | HG01243.hp2 HG01884.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-5631T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296396 | |||||||
chr17:45296410 | A | G | 2 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
2 | NA18974.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-20-5645T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296410 | |||||||
chr17:45296689 | T | C | 36 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0002g0051 others(33): Show |
41 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.-20-5924A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296689 | |||||||
chr17:45296737 | A | T | 11 | a0001c0001t0001g0191 a0001c0001t0001g0232 a0001c0001t0001g0264 others(8): Show |
12 | HG01243.hp2 HG01884.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-5972T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296737 | |||||||
chr17:45296812 | C | T | 2 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
2 | NA18974.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-20-6047G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45296812 | |||||||
chr17:45297286 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-20-6521T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297286 | |||||||
chr17:45297357 | G | A | 11 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0231 others(8): Show |
13 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-20-6592C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297357 | |||||||
chr17:45297436 | C | T | 1 | a0001c0001t0015g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-20-6671G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297436 | |||||||
chr17:45297494 | G | A | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.-20-6729C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297494 | |||||||
chr17:45297572 | A | T | 1 | a0001c0001t0002g0085 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-20-6807T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297572 | |||||||
chr17:45297716 | C | CT | 12 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0002g0254 others(9): Show |
12 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-6952dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297716 | |||||||
chr17:45297716 | CT | C | 161 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(158): Show |
190 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.-20-6952delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297716 | |||||||
chr17:45297716 | CTT | C | 36 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0002g0051 others(33): Show |
41 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.-20-6953_-20-6952d others(4): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297716 | |||||||
chr17:45297746 | G | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0145 a0001c0001t0001g0147 others(10): Show |
14 | HG00735.hp1 HG00741.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20-6981C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297746 | |||||||
chr17:45297814 | G | A | 5 | a0001c0001t0007g0234 a0001c0001t0007g0235 a0001c0001t0007g0236 others(2): Show |
5 | HG02486.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-7049C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297814 | |||||||
chr17:45297873 | C | T | 35 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0002g0051 others(32): Show |
40 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-20-7108G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297873 | |||||||
chr17:45297987 | G | A | 2 | a0001c0001t0002g0273 a0001c0001t0004g0274 |
2 | HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20-7222C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45297987 | |||||||
chr17:45298128 | C | A | 1 | a0001c0001t0002g0098 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-20-7363G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45298128 | |||||||
chr17:45298202 | C | T | 1 | a0001c0002t0016g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-20-7437G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45298202 | |||||||
chr17:45298744 | C | T | 80 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(77): Show |
86 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.-20-7979G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45298744 | |||||||
chr17:45298777 | G | C | 12 | a0001c0001t0001g0285 a0001c0001t0004g0019 a0001c0001t0004g0020 others(9): Show |
14 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-20-8012C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45298777 | |||||||
chr17:45298817 | C | G | 11 | a0001c0001t0001g0191 a0001c0001t0001g0232 a0001c0001t0001g0264 others(8): Show |
12 | HG01243.hp2 HG01884.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-8052G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45298817 | |||||||
chr17:45298829 | C | T | 2 | a0001c0001t0002g0111 a0001c0001t0002g0136 |
2 | HG01109.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.-20-8064G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45298829 | |||||||
chr17:45298833 | A | G | 1 | a0001c0001t0004g0020 | 2 | HG01358.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-20-8068T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45298833 | |||||||
chr17:45298848 | A | T | 1 | a0001c0002t0001g0116 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-20-8083T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45298848 | |||||||
chr17:45299032 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-20-8267T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299032 | |||||||
chr17:45299062 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-20-8297G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299062 | |||||||
chr17:45299075 | G | GTA | 5 | a0001c0001t0007g0234 a0001c0001t0007g0235 a0001c0001t0007g0236 others(2): Show |
5 | HG02486.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-8312_-20-8311d others(4): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299075 | |||||||
chr17:45299081 | C | T | 117 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(114): Show |
143 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.-20-8316G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299081 | |||||||
chr17:45299140 | G | A | 1 | a0001c0002t0001g0227 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-20-8375C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299140 | |||||||
chr17:45299180 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-20-8415C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299180 | |||||||
chr17:45299244 | A | G | 1 | a0001c0001t0004g0286 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-20-8479T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299244 | |||||||
chr17:45299395 | T | G | 118 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(115): Show |
144 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.-20-8630A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299395 | |||||||
chr17:45299595 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-20-8830G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299595 | |||||||
chr17:45299954 | G | A | 38 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(35): Show |
40 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.-20-9189C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45299954 | |||||||
chr17:45300138 | G | T | 4 | a0001c0001t0001g0256 a0001c0002t0001g0028 a0001c0002t0001g0029 others(1): Show |
4 | HG02257.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-9373C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300138 | |||||||
chr17:45300153 | T | A | 1 | a0001c0002t0001g0228 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-20-9388A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300153 | |||||||
chr17:45300185 | CA | C | 38 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(35): Show |
40 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.-20-9421delT | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300185 | |||||||
chr17:45300224 | C | T | 1 | a0001c0002t0001g0238 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-20-9459G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300224 | |||||||
chr17:45300267 | T | C | 1 | a0001c0002t0001g0293 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-20-9502A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300267 | |||||||
chr17:45300357 | TC | T | 11 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0002g0254 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20-9593delG | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300357 | |||||||
chr17:45300801 | T | C | 1 | a0001c0002t0001g0293 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-20-10036A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300801 | |||||||
chr17:45300846 | T | TA | 116 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(113): Show |
142 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-10082_-20-1008 others(5): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300846 | |||||||
chr17:45300847 | T | A | 180 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(177): Show |
210 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.-20-10082A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45300847 | |||||||
chr17:45301032 | G | C | 38 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(35): Show |
40 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.-20-10267C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45301032 | |||||||
chr17:45301124 | C | T | 3 | a0001c0001t0001g0276 a0001c0001t0001g0279 a0001c0008t0002g0275 |
3 | HG02572.hp1 HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-20-10359G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45301124 | |||||||
chr17:45301167 | C | CA | 18 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0002g0011 others(15): Show |
19 | HG00673.hp2 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-20-10403dupT | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45301167 | |||||||
chr17:45301271 | C | T | 2 | a0001c0002t0001g0194 a0005c0007t0002g0195 |
2 | NA19065.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-20-10506G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45301271 | |||||||
chr17:45301335 | T | C | 2 | a0001c0001t0002g0246 a0001c0001t0002g0249 |
2 | HG00642.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.-20-10570A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45301335 | |||||||
chr17:45301687 | A | G | 1 | a0001c0001t0002g0113 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-20-10922T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45301687 | |||||||
chr17:45301833 | CT | C | 68 | a0001c0001t0001g0161 a0001c0001t0001g0191 a0001c0001t0001g0232 others(65): Show |
74 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.-20-11069delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45301833 | |||||||
chr17:45302122 | C | T | 38 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(35): Show |
40 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.-20-11357G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302122 | |||||||
chr17:45302167 | GT | G | 115 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(112): Show |
141 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.-20-11403delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302167 | |||||||
chr17:45302221 | C | T | 8 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(5): Show |
8 | HG02145.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20-11456G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302221 | |||||||
chr17:45302383 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0002t0001g0045 |
3 | NA19058.hp1 NA19074.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-20-11618G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302383 | |||||||
chr17:45302399 | T | C | 38 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(35): Show |
40 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.-20-11634A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302399 | |||||||
chr17:45302697 | T | C | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-20-11932A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302697 | |||||||
chr17:45302749 | C | T | 38 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(35): Show |
40 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.-20-11984G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302749 | |||||||
chr17:45302854 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-20-12089T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302854 | |||||||
chr17:45302975 | G | A | 38 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(35): Show |
40 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.-20-12210C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45302975 | |||||||
chr17:45303300 | A | C | 213 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(210): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.-20-12535T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303300 | |||||||
chr17:45303326 | C | T | 11 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0002g0254 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20-12561G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303326 | |||||||
chr17:45303443 | C | T | 13 | a0001c0001t0001g0191 a0001c0001t0001g0232 a0001c0001t0001g0264 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-20-12678G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303443 | |||||||
chr17:45303465 | G | A | 1 | a0001c0001t0004g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-20-12700C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303465 | |||||||
chr17:45303741 | C | CT | 15 | a0001c0001t0001g0142 a0001c0001t0001g0257 a0001c0001t0001g0258 others(12): Show |
15 | HG02145.hp1 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20-12977dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303741 | |||||||
chr17:45303817 | C | T | 2 | a0001c0001t0007g0235 a0001c0001t0007g0236 |
2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-20-13052G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303817 | |||||||
chr17:45303867 | C | T | 7 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0002g0254 others(4): Show |
7 | HG01243.hp1 HG02257.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21+13093G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303867 | |||||||
chr17:45303884 | G | A | 3 | a0001c0001t0002g0273 a0001c0001t0004g0274 a0001c0001t0015g0187 |
3 | HG02615.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-21+13076C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303884 | |||||||
chr17:45303935 | C | T | 1 | a0001c0001t0008g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-21+13025G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45303935 | |||||||
chr17:45304010 | C | CT | 37 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0151 others(34): Show |
42 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.-21+12949dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45304010 | |||||||
chr17:45304010 | CT | C | 21 | a0001c0001t0001g0178 a0001c0001t0002g0099 a0001c0001t0002g0135 others(18): Show |
23 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.-21+12949delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45304010 | |||||||
chr17:45304015 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-21+12945A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45304015 | |||||||
chr17:45304105 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-21+12855G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45304105 | |||||||
chr17:45304106 | G | A | 19 | a0001c0001t0002g0081 a0001c0001t0002g0110 a0001c0001t0003g0004 others(16): Show |
22 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.-21+12854C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45304106 | |||||||
chr17:45304193 | G | A | 2 | a0001c0001t0002g0111 a0001c0001t0002g0136 |
2 | HG01109.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.-21+12767C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45304193 | |||||||
chr17:45304642 | G | A | 12 | a0001c0001t0001g0285 a0001c0001t0004g0019 a0001c0001t0004g0020 others(9): Show |
14 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21+12318C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45304642 | |||||||
chr17:45305010 | C | A | 1 | a0001c0002t0001g0058 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-21+11950G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45305010 | |||||||
chr17:45305125 | T | A | 1 | a0001c0001t0004g0292 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-21+11835A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45305125 | |||||||
chr17:45305136 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-21+11824G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45305136 | |||||||
chr17:45305396 | G | GT | 122 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0064 others(119): Show |
138 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.-21+11563dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45305396 | |||||||
chr17:45305396 | G | GTT | 19 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(16): Show |
19 | HG01175.hp2 HG01243.hp1 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-21+11562_-21+1156 others(6): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45305396 | |||||||
chr17:45305498 | C | T | 1 | a0001c0001t0002g0079 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-21+11462G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45305498 | |||||||
chr17:45305569 | T | A | 13 | a0001c0001t0001g0191 a0001c0001t0001g0232 a0001c0001t0001g0264 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21+11391A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45305569 | |||||||
chr17:45305734 | A | G | 180 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(177): Show |
210 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.-21+11226T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45305734 | |||||||
chr17:45306073 | A | C | 1 | a0001c0002t0001g0293 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-21+10887T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306073 | |||||||
chr17:45306118 | G | A | 214 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.-21+10842C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306118 | |||||||
chr17:45306158 | G | A | 11 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0002g0254 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21+10802C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306158 | |||||||
chr17:45306229 | C | T | 38 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(35): Show |
40 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.-21+10731G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306229 | |||||||
chr17:45306230 | A | G | 180 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(177): Show |
210 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.-21+10730T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306230 | |||||||
chr17:45306333 | T | TAAAAATT others(251): Show |
2 | a0001c0002t0001g0028 a0001c0002t0001g0029 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-21+10626_-21+1062 others(262): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306333 | |||||||
chr17:45306333 | T | TAAAAATT others(252): Show |
1 | a0001c0002t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-21+10626_-21+1062 others(263): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306333 | |||||||
chr17:45306333 | T | TAAAAATT others(265): Show |
1 | a0001c0002t0001g0024 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-21+10626_-21+1062 others(276): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306333 | |||||||
chr17:45306333 | T | TAAAAATT others(266): Show |
2 | a0001c0002t0001g0025 a0003c0004t0001g0026 |
2 | HG01071.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-21+10626_-21+1062 others(277): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306333 | |||||||
chr17:45306333 | T | TAAAAATT others(273): Show |
2 | a0001c0001t0002g0254 a0001c0010t0009g0253 |
2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-21+10626_-21+1062 others(284): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306333 | |||||||
chr17:45306333 | T | TAAAAATT others(274): Show |
1 | a0001c0001t0001g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-21+10626_-21+1062 others(285): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306333 | |||||||
chr17:45306333 | T | TAAAAATT others(275): Show |
1 | a0001c0001t0001g0256 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-21+10626_-21+1062 others(286): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306333 | |||||||
chr17:45306696 | T | C | 1 | a0001c0001t0002g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-21+10264A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306696 | |||||||
chr17:45306874 | C | G | 13 | a0001c0001t0001g0285 a0001c0001t0004g0019 a0001c0001t0004g0020 others(10): Show |
15 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-21+10086G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306874 | |||||||
chr17:45306906 | A | C | 1 | a0001c0001t0002g0140 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-21+10054T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306906 | |||||||
chr17:45306907 | C | A | 1 | a0001c0001t0002g0140 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-21+10053G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306907 | |||||||
chr17:45306979 | C | T | 35 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0002g0051 others(32): Show |
40 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-21+9981G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45306979 | |||||||
chr17:45307073 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-21+9887G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45307073 | |||||||
chr17:45307199 | A | C | 1 | a0001c0001t0002g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-21+9761T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45307199 | |||||||
chr17:45307266 | A | T | 111 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(108): Show |
137 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.-21+9694T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45307266 | |||||||
chr17:45307564 | T | C | 1 | a0003c0004t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-21+9396A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45307564 | |||||||
chr17:45307720 | C | T | 13 | a0001c0001t0001g0285 a0001c0001t0004g0019 a0001c0001t0004g0020 others(10): Show |
15 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-21+9240G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45307720 | |||||||
chr17:45307897 | C | A | 38 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(35): Show |
40 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.-21+9063G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45307897 | |||||||
chr17:45307983 | G | A | 163 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(160): Show |
191 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.-21+8977C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45307983 | |||||||
chr17:45308109 | T | C | 2 | a0001c0001t0002g0017 a0001c0001t0002g0233 |
3 | HG01243.hp2 HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-21+8851A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308109 | |||||||
chr17:45308148 | G | A | 3 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 |
3 | HG03209.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-21+8812C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308148 | |||||||
chr17:45308254 | G | T | 38 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(35): Show |
40 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.-21+8706C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308254 | |||||||
chr17:45308487 | T | G | 1 | a0001c0001t0002g0141 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-21+8473A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308487 | |||||||
chr17:45308563 | G | A | 3 | a0001c0002t0001g0024 a0001c0002t0001g0025 a0003c0004t0001g0026 |
3 | HG01069.hp1 HG01071.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-21+8397C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308563 | |||||||
chr17:45308569 | C | T | 1 | a0001c0001t0002g0077 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-21+8391G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308569 | |||||||
chr17:45308671 | CT | C | 12 | a0001c0001t0001g0191 a0001c0001t0001g0232 a0001c0001t0001g0264 others(9): Show |
13 | HG01169.hp1 HG01243.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-21+8288delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308671 | |||||||
chr17:45308744 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-21+8216A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308744 | |||||||
chr17:45308792 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-21+8168G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308792 | |||||||
chr17:45308793 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-21+8167C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308793 | |||||||
chr17:45308958 | C | T | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | HG02040.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.-21+8002G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308958 | |||||||
chr17:45308988 | AT | A | 178 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(175): Show |
208 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.-21+7971delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45308988 | |||||||
chr17:45309021 | T | G | 3 | a0001c0001t0002g0273 a0001c0001t0004g0274 a0001c0001t0015g0187 |
3 | HG02615.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-21+7939A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309021 | |||||||
chr17:45309175 | C | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0002t0016g0150 |
3 | HG03041.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-21+7785G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309175 | |||||||
chr17:45309232 | G | A | 1 | a0001c0002t0016g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-21+7728C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309232 | |||||||
chr17:45309257 | T | C | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0002t0016g0150 |
3 | HG03041.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-21+7703A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309257 | |||||||
chr17:45309343 | C | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0002g0184 others(2): Show |
5 | HG01099.hp1 HG01175.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+7617G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309343 | |||||||
chr17:45309361 | C | A | 1 | a0001c0002t0001g0272 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-21+7599G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309361 | |||||||
chr17:45309738 | T | G | 178 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(175): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.-21+7222A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309738 | |||||||
chr17:45309807 | C | T | 1 | a0001c0001t0008g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-21+7153G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309807 | |||||||
chr17:45309878 | A | C | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0015g0187 |
3 | HG02886.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-21+7082T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45309878 | |||||||
chr17:45310027 | C | CT | 11 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0280 others(8): Show |
11 | HG01243.hp1 HG01261.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21+6932dupA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310027 | |||||||
chr17:45310027 | C | CTT | 7 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0267 others(4): Show |
7 | HG02622.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-21+6931_-21+6932d others(4): Show |
MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310027 | |||||||
chr17:45310027 | CT | C | 59 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(56): Show |
63 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.-21+6932delA | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310027 | |||||||
chr17:45310065 | G | A | 1 | a0001c0001t0003g0179 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-21+6895C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310065 | |||||||
chr17:45310071 | G | C | 1 | a0001c0002t0001g0240 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-21+6889C>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310071 | |||||||
chr17:45310074 | G | A | 7 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0267 others(4): Show |
7 | HG02622.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-21+6886C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310074 | |||||||
chr17:45310091 | A | T | 10 | a0001c0001t0001g0285 a0001c0001t0004g0019 a0001c0001t0004g0286 others(7): Show |
11 | HG01891.hp1 HG02280.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21+6869T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310091 | |||||||
chr17:45310369 | T | C | 3 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 |
3 | HG03209.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-21+6591A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310369 | |||||||
chr17:45310515 | T | A | 1 | a0001c0001t0003g0180 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-21+6445A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310515 | |||||||
chr17:45310521 | C | T | 8 | a0001c0002t0001g0015 a0001c0002t0001g0192 a0001c0002t0001g0193 others(5): Show |
9 | HG00673.hp1 HG02083.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21+6439G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310521 | |||||||
chr17:45310623 | C | T | 2 | a0001c0001t0001g0191 a0001c0001t0002g0190 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-21+6337G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45310623 | |||||||
chr17:45311023 | T | C | 4 | a0001c0002t0001g0241 a0001c0002t0001g0242 a0001c0002t0001g0243 others(1): Show |
4 | HG02523.hp2 NA18948.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+5937A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45311023 | |||||||
chr17:45311047 | G | A | 9 | a0001c0001t0002g0018 a0001c0001t0002g0245 a0001c0001t0002g0246 others(6): Show |
10 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.-21+5913C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45311047 | |||||||
chr17:45311078 | T | A | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-21+5882A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45311078 | |||||||
chr17:45311258 | T | C | 2 | a0001c0001t0005g0181 a0001c0001t0005g0182 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-21+5702A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45311258 | |||||||
chr17:45311494 | G | A | 6 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
6 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21+5466C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45311494 | |||||||
chr17:45312126 | G | A | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-21+4834C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45312126 | |||||||
chr17:45312171 | A | T | 1 | a0001c0001t0001g0269 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-21+4789T>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45312171 | |||||||
chr17:45312360 | T | A | 83 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(80): Show |
91 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.-21+4600A>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45312360 | |||||||
chr17:45312514 | A | G | 1 | a0001c0001t0003g0073 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-21+4446T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45312514 | |||||||
chr17:45312636 | G | T | 1 | a0001c0001t0003g0072 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-21+4324C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45312636 | |||||||
chr17:45312755 | G | A | 35 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0002g0051 others(32): Show |
40 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-21+4205C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45312755 | |||||||
chr17:45312977 | G | A | 47 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0285 others(44): Show |
54 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-21+3983C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45312977 | |||||||
chr17:45313013 | G | A | 10 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0002g0254 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.-21+3947C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313013 | |||||||
chr17:45313022 | G | T | 1 | a0001c0001t0002g0071 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-21+3938C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313022 | |||||||
chr17:45313118 | C | T | 1 | a0001c0002t0001g0070 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-21+3842G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313118 | |||||||
chr17:45313245 | G | A | 2 | a0001c0001t0002g0273 a0001c0001t0004g0274 |
2 | HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-21+3715C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313245 | |||||||
chr17:45313252 | T | C | 12 | a0001c0001t0001g0285 a0001c0001t0004g0019 a0001c0001t0004g0020 others(9): Show |
14 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21+3708A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313252 | |||||||
chr17:45313323 | A | C | 6 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
6 | HG02559.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21+3637T>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313323 | |||||||
chr17:45313397 | A | G | 47 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0285 others(44): Show |
54 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-21+3563T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313397 | |||||||
chr17:45313431 | A | G | 1 | a0001c0001t0002g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-21+3529T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313431 | |||||||
chr17:45313962 | G | T | 47 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0285 others(44): Show |
54 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-21+2998C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45313962 | |||||||
chr17:45314116 | A | G | 7 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0002g0254 others(4): Show |
7 | HG01243.hp1 HG02257.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21+2844T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45314116 | |||||||
chr17:45314173 | A | G | 2 | a0001c0001t0002g0184 a0001c0001t0002g0185 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-21+2787T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45314173 | |||||||
chr17:45314229 | C | T | 12 | a0001c0001t0001g0285 a0001c0001t0004g0019 a0001c0001t0004g0020 others(9): Show |
14 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21+2731G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45314229 | |||||||
chr17:45314379 | T | G | 3 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0002t0001g0271 |
3 | HG02622.hp1 HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-21+2581A>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45314379 | |||||||
chr17:45314456 | A | G | 10 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0002g0254 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.-21+2504T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45314456 | |||||||
chr17:45314842 | G | A | 87 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(84): Show |
95 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.-21+2118C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45314842 | |||||||
chr17:45314905 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-21+2055G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45314905 | |||||||
chr17:45315015 | C | CA | 40 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(37): Show |
42 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.-21+1944dupT | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45315015 | |||||||
chr17:45315278 | A | G | 3 | a0001c0002t0001g0024 a0001c0002t0001g0025 a0003c0004t0001g0026 |
3 | HG01069.hp1 HG01071.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-21+1682T>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45315278 | |||||||
chr17:45316050 | G | A | 5 | a0001c0001t0001g0276 a0001c0001t0001g0279 a0001c0001t0010g0277 others(2): Show |
5 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21+910C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316050 | |||||||
chr17:45316172 | G | A | 1 | a0001c0001t0004g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-21+788C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316172 | |||||||
chr17:45316177 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-21+783G>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316177 | |||||||
chr17:45316201 | G | A | 3 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
3 | HG02145.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-21+759C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316201 | |||||||
chr17:45316344 | T | C | 1 | a0001c0001t0002g0283 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-21+616A>G | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316344 | |||||||
chr17:45316651 | G | A | 1 | a0001c0001t0002g0284 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-21+309C>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316651 | |||||||
chr17:45316697 | C | A | 12 | a0001c0001t0001g0285 a0001c0001t0004g0019 a0001c0001t0004g0020 others(9): Show |
14 | HG01358.hp1 HG01891.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21+263G>T | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316697 | |||||||
chr17:45316702 | C | G | 1 | a0001c0001t0001g0023 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-21+258G>C | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316702 | |||||||
chr17:45316746 | G | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-21+214C>A | MAP3K14 | ENSG00000006062.18 | transcript | ENST00000344686.8 | protein_coding | 1/15 | chr17 | 45316746 |