Item | Value |
---|---|
geneid | 4216 |
ensemblid | ENSG00000085511.20 |
hgncid | 6856 |
symbol | MAP3K4 |
name | mitogen-activated protein kinase kinase kinase 4 |
refseq_nuc | NM_005922.4 |
refseq_prot | NP_005913.3 |
ensembl_nuc | ENST00000392142.9 |
ensembl_prot | ENSP00000375986.4 |
mane_status | MANE Select |
chr | chr6 |
start | 160991769 |
end | 161117380 |
strand | + |
ver | v1.2 |
region | chr6:160991769-161117380 |
region5000 | chr6:160986769-161122380 |
regionname0 | MAP3K4_chr6_160991769_161117380 |
regionname5000 | MAP3K4_chr6_160986769_161122380 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1607 | 296 | 73 | 56 | 130 | 10 | 27 | 94 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | MREAA others(1602): Show |
chr6 | 160986769 | 161122380 |
a0002 | 0/0 | 1608 | 16 | 3 | 2 | 6 | 0 | 5 | 6 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | MREAA others(1603): Show |
chr6 | 160986769 | 161122380 |
a0003 | 1/0 | 1608 | 10 | 0 | 3 | 4 | 2 | 0 | 4 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | MREAA others(1603): Show |
chr6 | 160986769 | 161122380 |
a0004 | 0/0 | 1607 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | MREAA others(1602): Show |
chr6 | 160986769 | 161122380 |
a0005 | 0/0 | 1607 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | MREAA others(1602): Show |
chr6 | 160986769 | 161122380 |
a0006 | 0/0 | 1607 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | MREAA others(1602): Show |
chr6 | 160986769 | 161122380 |
a0007 | 0/0 | 1604 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | MREAA others(1599): Show |
chr6 | 160986769 | 161122380 |
a0008 | 0/0 | 1613 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | MREAA others(1608): Show |
chr6 | 160986769 | 161122380 |
a0009 | 0/0 | 1607 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | MREAA others(1602): Show |
chr6 | 160986769 | 161122380 |
a0010 | 0/0 | 1607 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | MREAA others(1602): Show |
chr6 | 160986769 | 161122380 |
a0011 | 0/0 | 1586 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | MREAA others(1581): Show |
chr6 | 160986769 | 161122380 |
a0012 | 0/0 | 1608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | MRETA others(1603): Show |
chr6 | 160986769 | 161122380 |
a0013 | 0/0 | 1607 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | MREAA others(1602): Show |
chr6 | 160986769 | 161122380 |
a0014 | 0/1 | 1607 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | MREAA others(1602): Show |
chr6 | 160986769 | 161122380 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4821 | 287 | 73 | 51 | 126 | 10 | 27 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4816): Show |
chr6 | 160986769 | 161122380 | ||
a0001c0005 | 0/0 | 4821 | 4 | 0 | 4 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4816): Show |
chr6 | 160986769 | 161122380 | ||
a0001c0007 | 0/0 | 4821 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4816): Show |
chr6 | 160986769 | 161122380 | ||
a0001c0014 | 0/0 | 4821 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4816): Show |
chr6 | 160986769 | 161122380 | ||
a0001c0016 | 0/0 | 4821 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4816): Show |
chr6 | 160986769 | 161122380 | ||
a0001c0018 | 0/0 | 4821 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4816): Show |
chr6 | 160986769 | 161122380 | ||
a0002c0002 | 0/0 | 4824 | 13 | 2 | 1 | 6 | 0 | 4 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4819): Show |
chr6 | 160986769 | 161122380 | ||
a0002c0010 | 0/0 | 4824 | 2 | 0 | 1 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4819): Show |
chr6 | 160986769 | 161122380 | ||
a0002c0012 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4819): Show |
chr6 | 160986769 | 161122380 | ||
a0003c0003 | 1/0 | 4824 | 10 | 0 | 3 | 4 | 2 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4819): Show |
chr6 | 160986769 | 161122380 | ||
a0004c0004 | 0/0 | 4821 | 6 | 6 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4816): Show |
chr6 | 160986769 | 161122380 | ||
a0005c0006 | 0/0 | 4821 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4816): Show |
chr6 | 160986769 | 161122380 | ||
a0006c0009 | 0/0 | 4821 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4816): Show |
chr6 | 160986769 | 161122380 | ||
a0007c0008 | 0/0 | 4812 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4807): Show |
chr6 | 160986769 | 161122380 | ||
a0008c0021 | 0/0 | 4839 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4834): Show |
chr6 | 160986769 | 161122380 | ||
a0009c0020 | 0/0 | 4821 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4816): Show |
chr6 | 160986769 | 161122380 | ||
a0010c0017 | 0/0 | 4821 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4816): Show |
chr6 | 160986769 | 161122380 | ||
a0011c0015 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4826): Show |
chr6 | 160986769 | 161122380 | ||
a0012c0011 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4819): Show |
chr6 | 160986769 | 161122380 | ||
a0013c0013 | 0/0 | 4821 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4816): Show |
chr6 | 160986769 | 161122380 | ||
a0014c0019 | 0/1 | 4821 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | ATGAG others(4816): Show |
chr6 | 160986769 | 161122380 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5497 | 196 | 46 | 27 | 92 | 8 | 23 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
a0001c0001t0002 | 0/0 | 5497 | 84 | 23 | 24 | 32 | 2 | 3 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
a0001c0001t0003 | 0/0 | 5497 | 4 | 4 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
a0001c0001t0005 | 0/0 | 5497 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
a0001c0001t0006 | 0/0 | 5497 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
a0001c0001t0007 | 0/0 | 5497 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
a0001c0005t0002 | 0/0 | 5497 | 4 | 0 | 4 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
a0001c0007t0001 | 0/0 | 5497 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
a0001c0014t0001 | 0/0 | 5497 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
a0001c0016t0001 | 0/0 | 5497 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
a0001c0018t0002 | 0/0 | 5497 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
a0002c0002t0002 | 0/0 | 5500 | 13 | 2 | 1 | 6 | 0 | 4 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5495): Show |
chr6 | 160986769 | 161122380 |
a0002c0010t0002 | 0/0 | 5500 | 2 | 0 | 1 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5495): Show |
chr6 | 160986769 | 161122380 |
a0002c0012t0004 | 0/0 | 5500 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5495): Show |
chr6 | 160986769 | 161122380 |
a0003c0003t0002 | 1/0 | 5500 | 9 | 0 | 3 | 3 | 2 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5495): Show |
chr6 | 160986769 | 161122380 |
a0003c0003t0008 | 0/0 | 5500 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5495): Show |
chr6 | 160986769 | 161122380 |
a0004c0004t0002 | 0/0 | 5497 | 6 | 6 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
a0005c0006t0001 | 0/0 | 5497 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
a0006c0009t0002 | 0/0 | 5497 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
a0007c0008t0002 | 0/0 | 5488 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5483): Show |
chr6 | 160986769 | 161122380 |
a0008c0021t0001 | 0/0 | 5515 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5510): Show |
chr6 | 160986769 | 161122380 |
a0009c0020t0001 | 0/0 | 5497 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
a0010c0017t0002 | 0/0 | 5497 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
a0011c0015t0002 | 0/0 | 5507 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5502): Show |
chr6 | 160986769 | 161122380 |
a0012c0011t0004 | 0/0 | 5500 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5495): Show |
chr6 | 160986769 | 161122380 |
a0013c0013t0001 | 0/0 | 5497 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
a0014c0019t0001 | 0/1 | 5497 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | GCTCG others(5492): Show |
chr6 | 160986769 | 161122380 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0001 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0001t0007g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0005t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0005t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0005t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0005t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0007t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0007t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0014t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0016t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0001c0018t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0002c0002t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0002c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0002c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0002c0010t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0002c0010t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0002c0012t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0003c0003t0002g0264 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0003c0003t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0003c0003t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0003c0003t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0003c0003t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0003c0003t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0003c0003t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0003c0003t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0003c0003t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0003c0003t0008g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0004c0004t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0004c0004t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0004c0004t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0004c0004t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0004c0004t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0005c0006t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0005c0006t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0005c0006t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0006c0009t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0006c0009t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0007c0008t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0008c0021t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0009c0020t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0010c0017t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0011c0015t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0012c0011t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0013c0013t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
a0014c0019t0001g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | GBR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0330 | EUR | GBR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00140 | hp1 | a0003 | c0003 | t0002 | g0316 | EUR | GBR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | GBR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00280 | hp1 | a0003 | c0003 | t0002 | g0323 | EUR | FIN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | FIN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0096 | EUR | FIN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | FIN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00423 | hp1 | a0001 | c0007 | t0001 | g0252 | EAS | CHS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00639 | hp1 | a0008 | c0021 | t0001 | g0127 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | CHS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0317 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00738 | hp1 | a0002 | c0010 | t0002 | g0022 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0325 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01070 | hp2 | a0009 | c0020 | t0001 | g0179 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01168 | hp2 | a0003 | c0003 | t0002 | g0310 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01169 | hp2 | a0003 | c0003 | t0002 | g0321 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0327 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01361 | hp1 | a0002 | c0002 | t0002 | g0013 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0326 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | IBS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | IBS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | IBS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0117 | EUR | IBS | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01928 | hp2 | a0001 | c0005 | t0002 | g0329 | AMR | PEL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01934 | hp1 | a0001 | c0018 | t0002 | g0320 | AMR | PEL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | PEL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01952 | hp1 | a0001 | c0005 | t0002 | g0314 | AMR | PEL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01978 | hp1 | a0003 | c0003 | t0002 | g0318 | AMR | PEL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01978 | hp2 | a0010 | c0017 | t0002 | g0206 | AMR | PEL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG01981 | hp2 | a0001 | c0005 | t0002 | g0328 | AMR | PEL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02004 | hp1 | a0001 | c0005 | t0002 | g0322 | AMR | PEL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02055 | hp1 | a0002 | c0012 | t0004 | g0285 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02145 | hp2 | a0004 | c0004 | t0002 | g0291 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CDX | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | CDX | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CDX | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CDX | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02257 | hp1 | a0011 | c0015 | t0002 | g0305 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0293 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02647 | hp1 | a0006 | c0009 | t0002 | g0286 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0324 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0015 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0294 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02738 | hp1 | a0001 | c0001 | t0007 | g0295 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03041 | hp1 | a0004 | c0004 | t0002 | g0006 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | MSL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03098 | hp2 | a0012 | c0011 | t0004 | g0284 | AFR | MSL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0298 | AFR | ESN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | MSL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | MSL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | MSL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0018 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03453 | hp1 | a0006 | c0009 | t0002 | g0287 | AFR | MSL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03453 | hp2 | a0004 | c0004 | t0002 | g0006 | AFR | MSL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0302 | AFR | MSL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03486 | hp2 | a0004 | c0004 | t0002 | g0304 | AFR | MSL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03490 | hp2 | a0002 | c0010 | t0002 | g0016 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0289 | AFR | ESN | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0312 | SAS | STU | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | STU | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0023 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0025 | SAS | BEB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | STU | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | STU | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | YRI | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | YRI | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18906 | hp1 | a0007 | c0008 | t0002 | g0007 | AFR | YRI | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18954 | hp1 | a0003 | c0003 | t0002 | g0307 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18956 | hp2 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18968 | hp1 | a0001 | c0001 | t0005 | g0161 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18970 | hp1 | a0003 | c0003 | t0002 | g0315 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18977 | hp2 | a0001 | c0007 | t0001 | g0248 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18988 | hp1 | a0001 | c0014 | t0001 | g0154 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19002 | hp2 | a0001 | c0001 | t0006 | g0039 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19003 | hp2 | a0001 | c0016 | t0001 | g0011 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19005 | hp2 | a0003 | c0003 | t0008 | g0313 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | LWK | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19043 | hp1 | a0007 | c0008 | t0002 | g0007 | AFR | LWK | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | LWK | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19057 | hp2 | a0005 | c0006 | t0001 | g0031 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19060 | hp2 | a0013 | c0013 | t0001 | g0269 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19062 | hp2 | a0005 | c0006 | t0001 | g0040 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19076 | hp2 | a0003 | c0003 | t0002 | g0319 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19091 | hp2 | a0005 | c0006 | t0001 | g0038 | EAS | JPT | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | YRI | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ASW | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ASW | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02486 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | MSL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | USA | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
HG06807 | hp2 | a0004 | c0004 | t0002 | g0303 | AFR | USA | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | USA | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | LWK | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
NA21309 | hp2 | a0004 | c0004 | t0002 | g0306 | AFR | LWK | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
homoSapiens | chm13v2 | a0014 | c0019 | t0001 | g0125 | REF | REF | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
homoSapiens | grch38p0 | a0003 | c0003 | t0002 | g0264 | REF | REF | MAP3K4_chr6_160986769_161122380 | MAP3K4 | chr6 | 160986769 | 161122380 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:160991941 | G | A | 1 | a0012 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.10G>A | p.Ala4Thr | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/27 | 173/5500 | 10/4827 | 4/1608 | chr6 | 160991941 | |||
chr6:160992012 | A | ACCG | 2 | a0002 a0012 |
17 | HG00738.hp1 HG01361.hp1 HG02055.hp1 others(14): Show |
disruptive_inframe_insertion | MODERATE | c.93_95dupGCC | p.Pro32dup | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/27 | 259/5500 | 96/4827 | 32/1608 | INFO_REALIGN_3_PRIME | chr6 | 160992012 | ||
chr6:160992037 | C | CCGGAACC others(11): Show |
1 | a0008 | 1 | HG00639.hp1 | disruptive_inframe_insertion | MODERATE | c.108_125dupGGAACCCG others(10): Show |
p.Ser42_Glu43insGluP others(14): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/27 | 289/5500 | 126/4827 | 42/1608 | INFO_REALIGN_3_PRIME | chr6 | 160992037 | ||
chr6:161034296 | C | T | 1 | a0006 | 2 | HG02647.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.190C>T | p.Pro64Ser | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/27 | 353/5500 | 190/4827 | 64/1608 | chr6 | 161034296 | |||
chr6:161048742 | G | A | 12 | a0001 a0002 a0004 others(9): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
missense_variant | MODERATE | c.470G>A | p.Arg157His | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/27 | 633/5500 | 470/4827 | 157/1608 | chr6 | 161048742 | |||
chr6:161048855 | A | C | 1 | a0005 | 3 | NA19057.hp2 NA19062.hp2 NA19091.hp2 |
missense_variant | MODERATE | c.583A>C | p.Asn195His | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/27 | 746/5500 | 583/4827 | 195/1608 | chr6 | 161048855 | |||
chr6:161049275 | G | A | 1 | a0004 | 6 | HG02145.hp2 HG03041.hp1 HG03453.hp2 others(3): Show |
missense_variant | MODERATE | c.1003G>A | p.Val335Ile | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/27 | 1166/5500 | 1003/4827 | 335/1608 | chr6 | 161049275 | |||
chr6:161070652 | G | T | 1 | a0009 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.1752G>T | p.Gln584His | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/27 | 1915/5500 | 1752/4827 | 584/1608 | chr6 | 161070652 | |||
chr6:161087848 | A | C | 2 | a0002 a0010 |
3 | HG00738.hp1 HG01978.hp2 HG03490.hp2 |
missense_variant | MODERATE | c.2717A>C | p.His906Pro | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 10/27 | 2880/5500 | 2717/4827 | 906/1608 | chr6 | 161087848 | |||
chr6:161092086 | G | A | 1 | a0013 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.3212G>A | p.Arg1071Gln | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 13/27 | 3375/5500 | 3212/4827 | 1071/1608 | chr6 | 161092086 | |||
chr6:161098318 | CCTG | C | 11 | a0001 a0002 a0004 others(8): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(326): Show |
disruptive_inframe_deletion | MODERATE | c.3596_3598delCTG | p.Ala1199del | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/27 | 3759/5500 | 3596/4827 | 1199/1608 | INFO_REALIGN_3_PRIME | chr6 | 161098318 | ||
chr6:161098318 | CCTGCTGC others(5): Show |
C | 1 | a0007 | 2 | NA18906.hp1 NA19043.hp1 |
disruptive_inframe_deletion | MODERATE | c.3587_3598delCTGCTG others(6): Show |
p.Ala1196_Ala1199del | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/27 | 3750/5500 | 3587/4827 | 1196/1608 | INFO_REALIGN_3_PRIME | chr6 | 161098318 | ||
chr6:161115245 | G | GAGTGACC others(3): Show |
1 | a0011 | 1 | HG02257.hp1 | frameshift_variant&stop_gained | HIGH | c.4752_4761dupTGACCC others(4): Show |
p.Met1588fs | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 26/27 | 4925/5500 | 4762/4827 | 1588/1608 | INFO_REALIGN_3_PRIME | chr6 | 161115245 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:160992009 | G | A | 2 | a0002c0012 a0012c0011 |
2 | HG02055.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.78G>A | p.Pro26Pro | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/27 | 241/5500 | 78/4827 | 26/1608 | chr6 | 160992009 | |||
chr6:161081024 | C | T | 1 | a0001c0018 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.2241C>T | p.Ala747Ala | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/27 | 2404/5500 | 2241/4827 | 747/1608 | chr6 | 161081024 | |||
chr6:161086586 | C | T | 2 | a0001c0005 a0001c0018 |
5 | HG01928.hp2 HG01934.hp1 HG01952.hp1 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.2475C>T | p.Asp825Asp | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 9/27 | 2638/5500 | 2475/4827 | 825/1608 | chr6 | 161086586 | |||
chr6:161098389 | T | C | 1 | a0001c0014 | 1 | NA18988.hp1 | synonymous_variant | LOW | c.3636T>C | p.Ser1212Ser | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/27 | 3799/5500 | 3636/4827 | 1212/1608 | chr6 | 161098389 | |||
chr6:161098392 | G | A | 1 | a0001c0007 | 2 | HG00423.hp1 NA18977.hp2 |
synonymous_variant | LOW | c.3639G>A | p.Val1213Val | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/27 | 3802/5500 | 3639/4827 | 1213/1608 | chr6 | 161098392 | |||
chr6:161112726 | C | T | 1 | a0001c0016 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.4578C>T | p.Ala1526Ala | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/27 | 4741/5500 | 4578/4827 | 1526/1608 | chr6 | 161112726 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:160991811 | G | C | 1 | a0001c0001t0005 | 1 | NA18968.hp1 | 5_prime_UTR_variant | MODIFIER | c.-121G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/27 | 121 | chr6 | 160991811 | ||||||
chr6:160991825 | G | A | 1 | a0001c0001t0006 | 1 | NA19002.hp2 | 5_prime_UTR_variant | MODIFIER | c.-107G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/27 | 107 | chr6 | 160991825 | ||||||
chr6:160991873 | T | C | 2 | a0002c0012t0004 a0012c0011t0004 |
2 | HG02055.hp1 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-59T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/27 | 59 | chr6 | 160991873 | ||||||
chr6:160991906 | G | T | 1 | a0001c0001t0003 | 4 | HG01891.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-26G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/27 | 26 | chr6 | 160991906 | ||||||
chr6:161116937 | C | T | 1 | a0003c0003t0008 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*67C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 27/27 | 67 | chr6 | 161116937 | ||||||
chr6:161117218 | G | A | 12 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(9): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*348G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 27/27 | 348 | chr6 | 161117218 | ||||||
chr6:161117223 | A | G | 1 | a0001c0001t0007 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*353A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 27/27 | 353 | chr6 | 161117223 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:160992179 | G | T | 26 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0312 others(23): Show |
29 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.152+96G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160992179 | |||||||
chr6:160992212 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152+129G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160992212 | |||||||
chr6:160992247 | G | C | 2 | a0001c0001t0001g0010 a0001c0016t0001g0011 |
2 | NA18946.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.152+164G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160992247 | |||||||
chr6:160992359 | A | G | 6 | a0004c0004t0002g0006 a0004c0004t0002g0303 a0004c0004t0002g0304 others(3): Show |
8 | HG02257.hp1 HG03041.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.152+276A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160992359 | |||||||
chr6:160992401 | C | T | 6 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+318C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160992401 | |||||||
chr6:160992410 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.152+327C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160992410 | |||||||
chr6:160992607 | A | G | 1 | a0001c0001t0007g0295 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.152+524A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160992607 | |||||||
chr6:160992620 | C | G | 11 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(8): Show |
11 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.152+537C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160992620 | |||||||
chr6:160992839 | C | G | 1 | a0001c0001t0001g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.152+756C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160992839 | |||||||
chr6:160992999 | T | A | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+916T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160992999 | |||||||
chr6:160993013 | A | T | 26 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0312 others(23): Show |
29 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.152+930A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993013 | |||||||
chr6:160993015 | G | A | 280 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(277): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.152+932G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993015 | |||||||
chr6:160993107 | T | C | 2 | a0001c0001t0001g0239 a0001c0001t0002g0297 |
2 | HG02056.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.152+1024T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993107 | |||||||
chr6:160993210 | A | G | 2 | a0002c0002t0002g0237 a0002c0002t0002g0238 |
2 | NA18956.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.152+1127A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993210 | |||||||
chr6:160993216 | A | G | 6 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(3): Show |
6 | HG00621.hp2 HG02155.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+1133A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993216 | |||||||
chr6:160993359 | C | G | 7 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(4): Show |
7 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+1276C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993359 | |||||||
chr6:160993360 | C | G | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.152+1277C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993360 | |||||||
chr6:160993463 | C | G | 26 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0312 others(23): Show |
29 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.152+1380C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993463 | |||||||
chr6:160993509 | T | G | 280 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(277): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.152+1426T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993509 | |||||||
chr6:160993537 | C | G | 9 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(6): Show |
9 | HG01109.hp2 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.152+1454C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993537 | |||||||
chr6:160993646 | G | A | 15 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0015 others(12): Show |
15 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.152+1563G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993646 | |||||||
chr6:160993735 | T | TA | 9 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(6): Show |
9 | HG00408.hp1 HG01361.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.152+1667dupA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 160993735 | ||||||
chr6:160993735 | TA | T | 229 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(226): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.152+1667delA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 160993735 | ||||||
chr6:160993813 | C | T | 12 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(9): Show |
12 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+1730C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993813 | |||||||
chr6:160993831 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.152+1748C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993831 | |||||||
chr6:160993839 | T | A | 1 | a0001c0001t0003g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.152+1756T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993839 | |||||||
chr6:160993852 | G | T | 1 | a0001c0001t0003g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.152+1769G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993852 | |||||||
chr6:160993856 | T | TGAC | 254 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(251): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.152+1773_152+1774i others(5): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993856 | |||||||
chr6:160993857 | C | A | 254 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(251): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.152+1774C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993857 | |||||||
chr6:160993894 | A | G | 1 | a0001c0001t0001g0281 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.152+1811A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993894 | |||||||
chr6:160993979 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152+1896A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160993979 | |||||||
chr6:160994034 | G | C | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152+1951G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160994034 | |||||||
chr6:160994122 | C | CT | 6 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+2051dupT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 160994122 | ||||||
chr6:160994138 | ATTTTC | A | 4 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(1): Show |
4 | HG02615.hp1 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+2060_152+2064d others(7): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 160994138 | ||||||
chr6:160994307 | C | T | 1 | a0007c0008t0002g0007 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.152+2224C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160994307 | |||||||
chr6:160994313 | T | C | 9 | a0001c0001t0002g0012 a0001c0001t0002g0222 a0001c0001t0002g0223 others(6): Show |
9 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.152+2230T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160994313 | |||||||
chr6:160994314 | T | C | 255 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(252): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.152+2231T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160994314 | |||||||
chr6:160994422 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.152+2339T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160994422 | |||||||
chr6:160994580 | C | T | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.152+2497C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160994580 | |||||||
chr6:160994598 | G | C | 26 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0033 others(23): Show |
26 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.152+2515G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160994598 | |||||||
chr6:160994661 | G | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0136 a0001c0001t0001g0137 others(93): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.152+2578G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160994661 | |||||||
chr6:160994727 | G | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0054 others(210): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.152+2644G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160994727 | |||||||
chr6:160994762 | G | A | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+2679G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160994762 | |||||||
chr6:160994825 | C | G | 9 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(6): Show |
9 | HG01109.hp2 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.152+2742C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160994825 | |||||||
chr6:160994825 | C | T | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152+2742C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160994825 | |||||||
chr6:160994906 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.152+2823G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160994906 | |||||||
chr6:160994915 | T | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(278): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.152+2832T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160994915 | |||||||
chr6:160995064 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02738.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.152+2981G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160995064 | |||||||
chr6:160995243 | A | T | 1 | a0001c0001t0001g0280 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.152+3160A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160995243 | |||||||
chr6:160995357 | A | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+3274A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160995357 | |||||||
chr6:160995662 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152+3579T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160995662 | |||||||
chr6:160995779 | A | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+3696A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160995779 | |||||||
chr6:160995961 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.152+3878T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160995961 | |||||||
chr6:160995962 | A | T | 1 | a0001c0001t0002g0135 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.152+3879A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160995962 | |||||||
chr6:160996117 | CT | C | 32 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0033 others(29): Show |
34 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.152+4036delT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 160996117 | ||||||
chr6:160996121 | T | A | 32 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0033 others(29): Show |
34 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.152+4038T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160996121 | |||||||
chr6:160996122 | ATGT | A | 32 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0033 others(29): Show |
34 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.152+4040_152+4042d others(5): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160996122 | |||||||
chr6:160996284 | C | G | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.152+4201C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160996284 | |||||||
chr6:160996399 | C | A | 15 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0015 others(12): Show |
15 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.152+4316C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160996399 | |||||||
chr6:160996428 | C | T | 32 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0033 others(29): Show |
34 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.152+4345C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160996428 | |||||||
chr6:160996589 | T | C | 15 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0015 others(12): Show |
15 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.152+4506T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160996589 | |||||||
chr6:160996594 | C | T | 20 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0033 others(17): Show |
20 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.152+4511C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160996594 | |||||||
chr6:160996608 | A | T | 2 | a0001c0001t0001g0133 a0001c0001t0002g0134 |
2 | HG02027.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.152+4525A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160996608 | |||||||
chr6:160996619 | A | G | 12 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(9): Show |
12 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.152+4536A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160996619 | |||||||
chr6:160996622 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(275): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.152+4539G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160996622 | |||||||
chr6:160997102 | C | T | 1 | a0001c0001t0002g0279 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.152+5019C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160997102 | |||||||
chr6:160997171 | C | T | 12 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(9): Show |
12 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+5088C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160997171 | |||||||
chr6:160997247 | A | C | 32 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0033 others(29): Show |
34 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.152+5164A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160997247 | |||||||
chr6:160997610 | T | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0054 others(210): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.152+5527T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160997610 | |||||||
chr6:160997652 | G | A | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+5569G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160997652 | |||||||
chr6:160997683 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.152+5600G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160997683 | |||||||
chr6:160997819 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.152+5736G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160997819 | |||||||
chr6:160997863 | G | A | 3 | a0004c0004t0002g0303 a0004c0004t0002g0304 a0011c0015t0002g0305 |
3 | HG02257.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.152+5780G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160997863 | |||||||
chr6:160997881 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152+5798G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160997881 | |||||||
chr6:160998048 | A | G | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.152+5965A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160998048 | |||||||
chr6:160998281 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0209 |
4 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+6198A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160998281 | |||||||
chr6:160998461 | G | A | 1 | a0001c0001t0002g0297 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.152+6378G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160998461 | |||||||
chr6:160998520 | T | C | 26 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0033 others(23): Show |
26 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.152+6437T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160998520 | |||||||
chr6:160998789 | A | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+6706A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160998789 | |||||||
chr6:160999015 | G | A | 1 | a0001c0001t0002g0288 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152+6932G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160999015 | |||||||
chr6:160999021 | A | C | 3 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 |
3 | HG01433.hp1 HG01516.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.152+6938A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160999021 | |||||||
chr6:160999382 | A | C | 1 | a0001c0001t0001g0028 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.152+7299A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160999382 | |||||||
chr6:160999396 | T | C | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.152+7313T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160999396 | |||||||
chr6:160999416 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.152+7333T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160999416 | |||||||
chr6:160999429 | C | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+7346C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160999429 | |||||||
chr6:160999535 | A | C | 7 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(4): Show |
7 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+7452A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160999535 | |||||||
chr6:160999578 | TG | T | 12 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(9): Show |
12 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+7498delG | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 160999578 | ||||||
chr6:160999660 | T | C | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | NA18941.hp1 NA18970.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.152+7577T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160999660 | |||||||
chr6:160999736 | A | G | 2 | a0001c0001t0002g0278 a0001c0001t0002g0279 |
2 | HG02155.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.152+7653A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160999736 | |||||||
chr6:160999838 | C | T | 6 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+7755C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 160999838 | |||||||
chr6:161000003 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152+7920C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000003 | |||||||
chr6:161000026 | C | T | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152+7943C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000026 | |||||||
chr6:161000373 | C | G | 9 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(6): Show |
9 | HG01109.hp2 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.152+8290C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000373 | |||||||
chr6:161000440 | C | G | 1 | a0001c0001t0002g0116 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.152+8357C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000440 | |||||||
chr6:161000617 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.152+8534A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000617 | |||||||
chr6:161000706 | G | A | 2 | a0001c0001t0002g0052 a0001c0001t0002g0116 |
2 | NA18948.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.152+8623G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000706 | |||||||
chr6:161000795 | A | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+8712A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000795 | |||||||
chr6:161000799 | G | A | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+8716G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000799 | |||||||
chr6:161000801 | A | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+8718A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000801 | |||||||
chr6:161000804 | C | T | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.152+8721C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000804 | |||||||
chr6:161000805 | C | A | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+8722C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000805 | |||||||
chr6:161000805 | C | G | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.152+8722C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000805 | |||||||
chr6:161000808 | T | C | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.152+8725T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000808 | |||||||
chr6:161000808 | TATATAC | T | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+8727_152+8732d others(8): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161000808 | ||||||
chr6:161000810 | T | C | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.152+8727T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000810 | |||||||
chr6:161000814 | CACACATG others(33): Show |
C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0185 a0001c0001t0001g0189 others(6): Show |
11 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.152+8743_152+8782d others(42): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161000814 | ||||||
chr6:161000818 | CAT | C | 9 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(6): Show |
9 | HG01109.hp2 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.152+8736_152+8737d others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000818 | |||||||
chr6:161000846 | C | T | 1 | a0001c0001t0002g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.152+8763C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000846 | |||||||
chr6:161000852 | T | C | 1 | a0001c0001t0002g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.152+8769T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000852 | |||||||
chr6:161000915 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.152+8832A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000915 | |||||||
chr6:161000930 | C | CAT | 9 | a0001c0001t0002g0012 a0001c0001t0002g0222 a0001c0001t0002g0223 others(6): Show |
9 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.152+8854_152+8855d others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161000930 | ||||||
chr6:161000944 | CAT | C | 4 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(1): Show |
4 | HG02615.hp1 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+8863_152+8864d others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161000944 | ||||||
chr6:161000959 | A | ATATAATA others(31): Show |
1 | a0001c0001t0001g0277 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.152+8983_152+9020d others(40): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161000959 | ||||||
chr6:161000959 | ATATAATA others(31): Show |
A | 24 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0312 others(21): Show |
27 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.152+8983_152+9020d others(40): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161000959 | ||||||
chr6:161000959 | ATATAATA others(69): Show |
A | 254 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(251): Show |
262 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.152+8945_152+9020d others(78): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161000959 | ||||||
chr6:161000987 | ATATTATA others(73): Show |
A | 1 | a0002c0002t0002g0025 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.152+8905_152+8984d others(82): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161000987 | |||||||
chr6:161001160 | A | G | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152+9077A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161001160 | |||||||
chr6:161001358 | T | C | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152+9275T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161001358 | |||||||
chr6:161001772 | C | T | 1 | a0001c0001t0002g0115 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.152+9689C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161001772 | |||||||
chr6:161001784 | G | A | 1 | a0002c0002t0002g0015 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.152+9701G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161001784 | |||||||
chr6:161001966 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.152+9883T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161001966 | |||||||
chr6:161002016 | C | T | 7 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(4): Show |
7 | HG01109.hp2 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+9933C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161002016 | |||||||
chr6:161002017 | A | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(278): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.152+9934A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161002017 | |||||||
chr6:161002050 | G | GT | 43 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0042 others(40): Show |
43 | HG00544.hp2 HG00621.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.152+9988dupT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161002050 | ||||||
chr6:161002100 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.152+10017T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161002100 | |||||||
chr6:161002124 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.152+10041A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161002124 | |||||||
chr6:161002198 | T | G | 12 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(9): Show |
12 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.152+10115T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161002198 | |||||||
chr6:161002589 | C | CT | 236 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0055 others(233): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.152+10526dupT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161002589 | ||||||
chr6:161002589 | C | CTT | 30 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0033 others(27): Show |
30 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.152+10525_152+1052 others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161002589 | ||||||
chr6:161002589 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0247 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.152+10517_152+1052 others(14): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161002589 | ||||||
chr6:161002622 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.152+10539C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161002622 | |||||||
chr6:161003033 | CATGAT | C | 73 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0133 others(70): Show |
76 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.152+10953_152+1095 others(9): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161003033 | ||||||
chr6:161003090 | C | G | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152+11007C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161003090 | |||||||
chr6:161003208 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.152+11125A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161003208 | |||||||
chr6:161003277 | T | TCTC | 281 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(278): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.152+11196_152+1119 others(7): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161003277 | ||||||
chr6:161003451 | G | A | 2 | a0002c0002t0002g0013 a0002c0002t0002g0014 |
2 | HG01361.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.152+11368G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161003451 | |||||||
chr6:161003650 | A | G | 214 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0054 others(211): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.152+11567A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161003650 | |||||||
chr6:161003660 | T | C | 1 | a0001c0001t0002g0289 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.152+11577T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161003660 | |||||||
chr6:161003884 | A | T | 9 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(6): Show |
9 | HG01109.hp2 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.152+11801A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161003884 | |||||||
chr6:161003941 | TAA | T | 213 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0054 others(210): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.152+11859_152+1186 others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161003941 | |||||||
chr6:161004113 | GA | G | 213 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0054 others(210): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.152+12032delA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161004113 | ||||||
chr6:161004214 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.152+12131G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161004214 | |||||||
chr6:161004240 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(275): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.152+12157G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161004240 | |||||||
chr6:161004375 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.152+12292G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161004375 | |||||||
chr6:161004748 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.152+12665C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161004748 | |||||||
chr6:161004879 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.152+12796A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161004879 | |||||||
chr6:161004933 | C | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0105 a0001c0001t0001g0106 others(1): Show |
4 | NA18957.hp2 NA19085.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+12850C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161004933 | |||||||
chr6:161005096 | T | C | 1 | a0012c0011t0004g0284 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.152+13013T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005096 | |||||||
chr6:161005139 | CT | C | 8 | a0001c0001t0001g0054 a0001c0001t0001g0059 a0001c0001t0001g0185 others(5): Show |
8 | HG01069.hp2 HG02630.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.152+13073delT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161005139 | ||||||
chr6:161005175 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.152+13092G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005175 | |||||||
chr6:161005194 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152+13111G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005194 | |||||||
chr6:161005233 | G | A | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.152+13150G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005233 | |||||||
chr6:161005262 | C | A | 38 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(35): Show |
38 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.152+13179C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005262 | |||||||
chr6:161005272 | G | A | 1 | a0002c0002t0002g0017 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.152+13189G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005272 | |||||||
chr6:161005286 | A | T | 9 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(6): Show |
9 | HG01109.hp2 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.152+13203A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005286 | |||||||
chr6:161005351 | A | G | 280 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(277): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.152+13268A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005351 | |||||||
chr6:161005435 | C | G | 6 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+13352C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005435 | |||||||
chr6:161005436 | A | C | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.152+13353A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005436 | |||||||
chr6:161005512 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.152+13429T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005512 | |||||||
chr6:161005513 | T | A | 219 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0054 others(216): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.152+13430T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005513 | |||||||
chr6:161005549 | C | T | 26 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0312 others(23): Show |
29 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.152+13466C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005549 | |||||||
chr6:161005574 | A | G | 1 | a0001c0001t0003g0045 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.152+13491A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005574 | |||||||
chr6:161005745 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.152+13662C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005745 | |||||||
chr6:161005746 | G | A | 16 | a0001c0001t0001g0033 a0002c0002t0002g0013 a0002c0002t0002g0014 others(13): Show |
16 | HG00738.hp1 HG01361.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.152+13663G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005746 | |||||||
chr6:161005868 | A | G | 9 | a0001c0001t0001g0002 a0001c0001t0001g0185 a0001c0001t0001g0189 others(6): Show |
11 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.152+13785A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005868 | |||||||
chr6:161005869 | CCTCTGCC others(9): Show |
C | 26 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0033 others(23): Show |
26 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.152+13788_152+1380 others(20): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161005869 | ||||||
chr6:161005893 | T | TTC | 11 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(8): Show |
11 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.152+13813_152+1381 others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161005893 | ||||||
chr6:161005895 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.152+13812C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005895 | |||||||
chr6:161005977 | G | A | 15 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0015 others(12): Show |
15 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.152+13894G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161005977 | |||||||
chr6:161006008 | G | C | 26 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0312 others(23): Show |
29 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.152+13925G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161006008 | |||||||
chr6:161006030 | C | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0041 |
2 | HG00733.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.152+13947C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161006030 | |||||||
chr6:161006163 | A | G | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152+14080A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161006163 | |||||||
chr6:161006388 | T | A | 1 | a0001c0001t0002g0327 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.152+14305T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161006388 | |||||||
chr6:161006585 | C | T | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+14502C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161006585 | |||||||
chr6:161006689 | A | G | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(1): Show |
4 | NA18950.hp2 NA18988.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+14606A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161006689 | |||||||
chr6:161006754 | A | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+14671A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161006754 | |||||||
chr6:161006780 | C | T | 32 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0033 others(29): Show |
34 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.152+14697C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161006780 | |||||||
chr6:161007374 | G | T | 6 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0308 others(3): Show |
9 | HG00741.hp1 HG01069.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.152+15291G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161007374 | |||||||
chr6:161007395 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.152+15312A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161007395 | |||||||
chr6:161007480 | T | C | 32 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0033 others(29): Show |
34 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.152+15397T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161007480 | |||||||
chr6:161007658 | G | A | 26 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0312 others(23): Show |
29 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.152+15575G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161007658 | |||||||
chr6:161007701 | T | C | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+15618T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161007701 | |||||||
chr6:161007719 | G | T | 1 | a0001c0001t0002g0293 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.152+15636G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161007719 | |||||||
chr6:161007787 | A | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.152+15704A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161007787 | |||||||
chr6:161007791 | A | C | 1 | a0001c0001t0002g0052 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.152+15708A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161007791 | |||||||
chr6:161007821 | G | A | 280 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(277): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.152+15738G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161007821 | |||||||
chr6:161007940 | T | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+15857T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161007940 | |||||||
chr6:161008013 | G | A | 9 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(6): Show |
9 | HG01109.hp2 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.152+15930G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161008013 | |||||||
chr6:161008252 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.152+16169C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161008252 | |||||||
chr6:161008259 | C | A | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.152+16176C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161008259 | |||||||
chr6:161008259 | C | T | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+16176C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161008259 | |||||||
chr6:161008270 | G | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02735.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.152+16187G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161008270 | |||||||
chr6:161008384 | A | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+16301A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161008384 | |||||||
chr6:161008457 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0271 |
2 | HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.152+16374C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161008457 | |||||||
chr6:161008603 | A | G | 12 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(9): Show |
12 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.152+16520A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161008603 | |||||||
chr6:161008613 | A | G | 26 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(23): Show |
26 | HG00738.hp1 HG01109.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.152+16530A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161008613 | |||||||
chr6:161008673 | T | C | 279 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(276): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.152+16590T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161008673 | |||||||
chr6:161008714 | G | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0185 a0001c0001t0001g0189 others(6): Show |
11 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.152+16631G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161008714 | |||||||
chr6:161008795 | A | G | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.152+16712A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161008795 | |||||||
chr6:161008923 | G | A | 15 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0015 others(12): Show |
15 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.152+16840G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161008923 | |||||||
chr6:161008978 | C | T | 26 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(23): Show |
26 | HG00738.hp1 HG01109.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.152+16895C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161008978 | |||||||
chr6:161008988 | C | CT | 41 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0033 others(38): Show |
43 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.152+16920dupT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161008988 | ||||||
chr6:161009070 | C | T | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+16987C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161009070 | |||||||
chr6:161009122 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.152+17039C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161009122 | |||||||
chr6:161009131 | C | T | 6 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+17048C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161009131 | |||||||
chr6:161009174 | G | T | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.152+17091G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161009174 | |||||||
chr6:161009314 | G | A | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.152+17231G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161009314 | |||||||
chr6:161009436 | G | T | 271 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(268): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.152+17353G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161009436 | |||||||
chr6:161009490 | G | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0054 others(210): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.152+17407G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161009490 | |||||||
chr6:161009554 | A | G | 12 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(9): Show |
12 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+17471A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161009554 | |||||||
chr6:161009605 | G | A | 6 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG01243.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+17522G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161009605 | |||||||
chr6:161009724 | C | T | 271 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(268): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.152+17641C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161009724 | |||||||
chr6:161009727 | A | G | 1 | a0001c0001t0002g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.152+17644A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161009727 | |||||||
chr6:161009810 | T | C | 271 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(268): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.152+17727T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161009810 | |||||||
chr6:161009861 | C | T | 2 | a0001c0001t0001g0282 a0001c0001t0002g0292 |
2 | HG02818.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.152+17778C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161009861 | |||||||
chr6:161009907 | G | A | 5 | a0001c0001t0002g0001 a0001c0001t0002g0144 a0001c0001t0002g0145 others(2): Show |
8 | HG00735.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.152+17824G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161009907 | |||||||
chr6:161009952 | G | A | 277 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(274): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.152+17869G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161009952 | |||||||
chr6:161010008 | C | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0054 others(206): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.152+17925C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161010008 | |||||||
chr6:161010162 | A | G | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.152+18079A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161010162 | |||||||
chr6:161010175 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.152+18092A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161010175 | |||||||
chr6:161010226 | C | T | 271 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(268): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.152+18143C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161010226 | |||||||
chr6:161010237 | A | G | 1 | a0007c0008t0002g0007 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.152+18154A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161010237 | |||||||
chr6:161010248 | G | A | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.152+18165G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161010248 | |||||||
chr6:161010360 | A | G | 1 | a0001c0001t0002g0115 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.152+18277A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161010360 | |||||||
chr6:161010498 | GT | G | 271 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(268): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.152+18422delT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161010498 | ||||||
chr6:161010671 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.152+18588A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161010671 | |||||||
chr6:161010713 | A | G | 1 | a0001c0001t0002g0103 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.152+18630A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161010713 | |||||||
chr6:161010856 | T | C | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+18773T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161010856 | |||||||
chr6:161011176 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.152+19093G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161011176 | |||||||
chr6:161011330 | T | C | 8 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(5): Show |
8 | HG01109.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.152+19247T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161011330 | |||||||
chr6:161011360 | T | A | 1 | a0001c0001t0002g0294 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.152+19277T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161011360 | |||||||
chr6:161011434 | C | T | 1 | a0010c0017t0002g0206 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.152+19351C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161011434 | |||||||
chr6:161011435 | G | A | 91 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(88): Show |
92 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.152+19352G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161011435 | |||||||
chr6:161011599 | C | T | 2 | a0002c0002t0002g0237 a0002c0002t0002g0238 |
2 | NA18956.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.152+19516C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161011599 | |||||||
chr6:161011835 | C | T | 280 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(277): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.152+19752C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161011835 | |||||||
chr6:161011952 | C | T | 280 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(277): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.152+19869C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161011952 | |||||||
chr6:161012002 | C | G | 280 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(277): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.152+19919C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161012002 | |||||||
chr6:161012051 | G | A | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG01109.hp1 HG04184.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.152+19968G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161012051 | |||||||
chr6:161012198 | G | C | 12 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(9): Show |
12 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.152+20115G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161012198 | |||||||
chr6:161012220 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.152+20137G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161012220 | |||||||
chr6:161012442 | G | A | 281 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(278): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.152+20359G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161012442 | |||||||
chr6:161012841 | T | TA | 26 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0312 others(23): Show |
29 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.152+20759dupA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161012841 | ||||||
chr6:161012849 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.152+20766T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161012849 | |||||||
chr6:161012853 | T | C | 1 | a0002c0002t0002g0238 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.152+20770T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161012853 | |||||||
chr6:161012924 | A | T | 1 | a0001c0001t0001g0280 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.152+20841A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161012924 | |||||||
chr6:161012929 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.152+20846C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161012929 | |||||||
chr6:161012949 | T | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(201): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.152+20866T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161012949 | |||||||
chr6:161013090 | A | G | 1 | a0001c0001t0002g0289 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.152+21007A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161013090 | |||||||
chr6:161013142 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.152+21059A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161013142 | |||||||
chr6:161013229 | A | G | 254 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(251): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.153-21030A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161013229 | |||||||
chr6:161013256 | C | T | 254 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(251): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.153-21003C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161013256 | |||||||
chr6:161013304 | G | A | 235 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(232): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.153-20955G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161013304 | |||||||
chr6:161013309 | C | G | 16 | a0001c0001t0001g0010 a0001c0001t0001g0242 a0001c0001t0001g0247 others(13): Show |
16 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.153-20950C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161013309 | |||||||
chr6:161013555 | T | C | 279 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(276): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.153-20704T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161013555 | |||||||
chr6:161013556 | G | A | 272 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(269): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.153-20703G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161013556 | |||||||
chr6:161013570 | GGT | G | 8 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(5): Show |
8 | HG01109.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.153-20688_153-2068 others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161013570 | |||||||
chr6:161013620 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.153-20639A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161013620 | |||||||
chr6:161013668 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.153-20591C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161013668 | |||||||
chr6:161013687 | C | T | 1 | a0002c0002t0002g0015 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.153-20572C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161013687 | |||||||
chr6:161013780 | A | G | 1 | a0002c0002t0002g0017 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153-20479A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161013780 | |||||||
chr6:161013855 | G | A | 78 | a0001c0001t0001g0056 a0001c0001t0001g0133 a0001c0001t0001g0136 others(75): Show |
81 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.153-20404G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161013855 | |||||||
chr6:161013975 | G | T | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0221 |
3 | HG01243.hp1 HG02280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.153-20284G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161013975 | |||||||
chr6:161013987 | T | A | 14 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0015 others(11): Show |
14 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.153-20272T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161013987 | |||||||
chr6:161014005 | C | A | 6 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(3): Show |
6 | HG00621.hp2 HG02155.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-20254C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161014005 | |||||||
chr6:161014050 | T | C | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-20209T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161014050 | |||||||
chr6:161014300 | TC | T | 4 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(1): Show |
4 | HG01891.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-19958delC | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161014300 | |||||||
chr6:161014334 | G | A | 6 | a0004c0004t0002g0006 a0004c0004t0002g0291 a0004c0004t0002g0303 others(3): Show |
8 | HG02145.hp2 HG03041.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.153-19925G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161014334 | |||||||
chr6:161014536 | C | T | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-19723C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161014536 | |||||||
chr6:161014609 | C | T | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.153-19650C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161014609 | |||||||
chr6:161014610 | A | G | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.153-19649A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161014610 | |||||||
chr6:161014766 | C | G | 1 | a0001c0001t0002g0279 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.153-19493C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161014766 | |||||||
chr6:161014845 | CA | C | 26 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0312 others(23): Show |
29 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.153-19412delA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161014845 | ||||||
chr6:161015018 | G | T | 6 | a0004c0004t0002g0006 a0004c0004t0002g0291 a0004c0004t0002g0303 others(3): Show |
8 | HG02145.hp2 HG03041.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.153-19241G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161015018 | |||||||
chr6:161015094 | A | G | 1 | a0001c0001t0002g0293 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.153-19165A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161015094 | |||||||
chr6:161015249 | C | T | 265 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(262): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.153-19010C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161015249 | |||||||
chr6:161015276 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG02040.hp1 NA18945.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.153-18983G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161015276 | |||||||
chr6:161015565 | G | C | 280 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(277): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.153-18694G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161015565 | |||||||
chr6:161015698 | C | T | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-18561C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161015698 | |||||||
chr6:161015728 | A | G | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.153-18531A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161015728 | |||||||
chr6:161016047 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.153-18212C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161016047 | |||||||
chr6:161016058 | G | A | 16 | a0001c0001t0002g0051 a0001c0001t0002g0060 a0001c0001t0002g0061 others(13): Show |
16 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.153-18201G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161016058 | |||||||
chr6:161016246 | A | C | 3 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 |
3 | HG01891.hp1 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.153-18013A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161016246 | |||||||
chr6:161016260 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.153-17999T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161016260 | |||||||
chr6:161016431 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.153-17828A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161016431 | |||||||
chr6:161016724 | A | C | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-17535A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161016724 | |||||||
chr6:161016724 | A | G | 7 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(4): Show |
7 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-17535A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161016724 | |||||||
chr6:161016743 | T | C | 327 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0026 others(324): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.153-17516T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161016743 | |||||||
chr6:161017045 | G | A | 4 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(1): Show |
4 | HG01891.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-17214G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161017045 | |||||||
chr6:161017094 | T | A | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-17165T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161017094 | |||||||
chr6:161017232 | C | T | 1 | a0003c0003t0002g0323 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.153-17027C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161017232 | |||||||
chr6:161017326 | C | G | 6 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-16933C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161017326 | |||||||
chr6:161017526 | T | C | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-16733T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161017526 | |||||||
chr6:161017625 | G | T | 15 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0015 others(12): Show |
15 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.153-16634G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161017625 | |||||||
chr6:161017774 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0002g0079 |
2 | NA18971.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.153-16485A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161017774 | |||||||
chr6:161017921 | A | G | 1 | a0002c0002t0002g0017 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153-16338A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161017921 | |||||||
chr6:161017963 | C | T | 26 | a0001c0001t0001g0136 a0001c0001t0001g0174 a0001c0001t0001g0175 others(23): Show |
26 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.153-16296C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161017963 | |||||||
chr6:161018076 | A | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-16183A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161018076 | |||||||
chr6:161018254 | A | G | 1 | a0007c0008t0002g0007 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.153-16005A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161018254 | |||||||
chr6:161018296 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.153-15963G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161018296 | |||||||
chr6:161018375 | G | T | 26 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0312 others(23): Show |
29 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.153-15884G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161018375 | |||||||
chr6:161018376 | G | C | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-15883G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161018376 | |||||||
chr6:161018639 | G | A | 95 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0239 others(92): Show |
98 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.153-15620G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161018639 | |||||||
chr6:161018651 | G | A | 6 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0308 others(3): Show |
9 | HG00741.hp1 HG01069.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-15608G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161018651 | |||||||
chr6:161018748 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.153-15511A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161018748 | |||||||
chr6:161018968 | G | T | 1 | a0001c0005t0002g0322 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.153-15291G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161018968 | |||||||
chr6:161019334 | T | C | 13 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(10): Show |
15 | HG02145.hp2 HG02257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.153-14925T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161019334 | |||||||
chr6:161019422 | C | T | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-14837C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161019422 | |||||||
chr6:161019446 | C | T | 1 | a0005c0006t0001g0040 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.153-14813C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161019446 | |||||||
chr6:161019520 | C | T | 5 | a0001c0001t0002g0001 a0001c0001t0002g0144 a0001c0001t0002g0145 others(2): Show |
8 | HG00735.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.153-14739C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161019520 | |||||||
chr6:161019531 | C | T | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 |
3 | NA18747.hp1 NA19000.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.153-14728C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161019531 | |||||||
chr6:161019617 | T | C | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-14642T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161019617 | |||||||
chr6:161019618 | T | A | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-14641T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161019618 | |||||||
chr6:161019619 | G | A | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-14640G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161019619 | |||||||
chr6:161019623 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-14636G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161019623 | |||||||
chr6:161019850 | A | T | 19 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(16): Show |
19 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.153-14409A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161019850 | |||||||
chr6:161020029 | T | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(189): Show |
198 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.153-14230T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161020029 | |||||||
chr6:161020077 | T | C | 87 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0239 others(84): Show |
88 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.153-14182T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161020077 | |||||||
chr6:161020265 | C | CTTTG | 29 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0312 others(26): Show |
32 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.153-13969_153-1396 others(8): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161020265 | ||||||
chr6:161020265 | CTTTG | C | 34 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0207 others(31): Show |
36 | HG00738.hp1 HG01109.hp2 HG01361.hp1 others(33): Show |
intron_variant | MODIFIER | c.153-13969_153-1396 others(8): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161020265 | ||||||
chr6:161020265 | CTTTGTTT others(1): Show |
C | 49 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0239 others(46): Show |
50 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.153-13973_153-1396 others(12): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161020265 | ||||||
chr6:161020317 | C | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-13942C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161020317 | |||||||
chr6:161020433 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.153-13826G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161020433 | |||||||
chr6:161020556 | G | T | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.153-13703G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161020556 | |||||||
chr6:161020656 | T | TA | 16 | a0001c0001t0001g0036 a0001c0001t0001g0087 a0001c0001t0001g0150 others(13): Show |
16 | HG00597.hp1 HG01168.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.153-13585dupA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161020656 | ||||||
chr6:161020656 | T | TAA | 11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0002g0003 others(8): Show |
14 | HG00741.hp1 HG01069.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.153-13586_153-1358 others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161020656 | ||||||
chr6:161020656 | TA | T | 17 | a0001c0001t0002g0223 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01169.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.153-13585delA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161020656 | ||||||
chr6:161020674 | A | AAACAAG | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-13585_153-1358 others(10): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161020674 | |||||||
chr6:161020675 | C | A | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-13584C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161020675 | |||||||
chr6:161020717 | C | T | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-13542C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161020717 | |||||||
chr6:161020801 | T | C | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-13458T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161020801 | |||||||
chr6:161020893 | G | C | 1 | a0001c0001t0003g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.153-13366G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161020893 | |||||||
chr6:161020896 | C | T | 1 | a0001c0001t0003g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.153-13363C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161020896 | |||||||
chr6:161021246 | A | G | 12 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(9): Show |
14 | HG02145.hp2 HG02615.hp1 HG03041.hp1 others(11): Show |
intron_variant | MODIFIER | c.153-13013A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161021246 | |||||||
chr6:161021393 | C | G | 14 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(11): Show |
14 | HG01109.hp2 HG02451.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.153-12866C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161021393 | |||||||
chr6:161021575 | G | A | 6 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG01243.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-12684G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161021575 | |||||||
chr6:161021734 | C | G | 1 | a0001c0001t0002g0078 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.153-12525C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161021734 | |||||||
chr6:161021841 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.153-12418A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161021841 | |||||||
chr6:161021932 | CA | C | 8 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(5): Show |
8 | HG01109.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.153-12318delA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161021932 | ||||||
chr6:161022051 | T | G | 2 | a0002c0002t0002g0018 a0002c0002t0002g0025 |
2 | HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.153-12208T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161022051 | |||||||
chr6:161022424 | A | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(189): Show |
198 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.153-11835A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161022424 | |||||||
chr6:161022534 | C | G | 1 | a0001c0001t0001g0198 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.153-11725C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161022534 | |||||||
chr6:161022707 | T | C | 302 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(299): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.153-11552T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161022707 | |||||||
chr6:161022907 | G | C | 1 | a0001c0001t0002g0117 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.153-11352G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161022907 | |||||||
chr6:161022975 | G | C | 81 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0239 others(78): Show |
82 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.153-11284G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161022975 | |||||||
chr6:161023120 | A | G | 302 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(299): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.153-11139A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161023120 | |||||||
chr6:161023404 | A | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(189): Show |
198 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.153-10855A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161023404 | |||||||
chr6:161023754 | C | T | 1 | a0001c0001t0003g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.153-10505C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161023754 | |||||||
chr6:161024028 | G | A | 302 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(299): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.153-10231G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161024028 | |||||||
chr6:161024227 | C | G | 1 | a0001c0001t0002g0046 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-10032C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161024227 | |||||||
chr6:161024251 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.153-10008G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161024251 | |||||||
chr6:161024255 | C | T | 8 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(5): Show |
8 | HG01109.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.153-10004C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161024255 | |||||||
chr6:161024519 | C | G | 15 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0015 others(12): Show |
15 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.153-9740C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161024519 | |||||||
chr6:161024716 | G | A | 8 | a0001c0001t0001g0175 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
8 | HG01074.hp1 HG01106.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.153-9543G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161024716 | |||||||
chr6:161024725 | A | G | 15 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0015 others(12): Show |
15 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.153-9534A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161024725 | |||||||
chr6:161024739 | T | G | 1 | a0002c0012t0004g0285 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.153-9520T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161024739 | |||||||
chr6:161024820 | G | A | 294 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(291): Show |
303 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.153-9439G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161024820 | |||||||
chr6:161024912 | G | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(190): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.153-9347G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161024912 | |||||||
chr6:161024931 | G | T | 15 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0015 others(12): Show |
15 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.153-9328G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161024931 | |||||||
chr6:161025002 | T | G | 15 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0015 others(12): Show |
15 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.153-9257T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161025002 | |||||||
chr6:161025413 | G | T | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-8846G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161025413 | |||||||
chr6:161025515 | G | A | 1 | a0002c0002t0002g0025 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.153-8744G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161025515 | |||||||
chr6:161025597 | G | T | 1 | a0001c0001t0001g0247 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.153-8662G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161025597 | |||||||
chr6:161025775 | C | G | 1 | a0001c0001t0003g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.153-8484C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161025775 | |||||||
chr6:161026014 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0099 |
2 | HG00609.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.153-8245A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026014 | |||||||
chr6:161026015 | G | A | 16 | a0001c0001t0001g0197 a0002c0002t0002g0013 a0002c0002t0002g0014 others(13): Show |
16 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.153-8244G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026015 | |||||||
chr6:161026101 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.153-8158C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026101 | |||||||
chr6:161026161 | T | C | 1 | a0007c0008t0002g0007 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.153-8098T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026161 | |||||||
chr6:161026169 | G | C | 1 | a0007c0008t0002g0007 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.153-8090G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026169 | |||||||
chr6:161026170 | G | T | 1 | a0007c0008t0002g0007 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.153-8089G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026170 | |||||||
chr6:161026189 | G | A | 6 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-8070G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026189 | |||||||
chr6:161026191 | C | T | 14 | a0001c0001t0001g0197 a0002c0002t0002g0015 a0002c0002t0002g0017 others(11): Show |
14 | HG00738.hp1 HG02683.hp2 HG03239.hp2 others(11): Show |
intron_variant | MODIFIER | c.153-8068C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026191 | |||||||
chr6:161026193 | C | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0098 others(38): Show |
42 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.153-8066C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026193 | |||||||
chr6:161026217 | G | T | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.153-8042G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026217 | |||||||
chr6:161026223 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.153-8036T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026223 | |||||||
chr6:161026226 | G | A | 11 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(8): Show |
11 | HG01109.hp2 HG02451.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.153-8033G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026226 | |||||||
chr6:161026231 | T | C | 4 | a0001c0001t0001g0152 a0001c0001t0002g0009 a0001c0001t0003g0043 others(1): Show |
4 | HG02976.hp1 HG03579.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-8028T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026231 | |||||||
chr6:161026279 | C | T | 1 | a0001c0018t0002g0320 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.153-7980C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026279 | |||||||
chr6:161026290 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.153-7969G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026290 | |||||||
chr6:161026297 | A | AT | 204 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(201): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.153-7951dupT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161026297 | ||||||
chr6:161026321 | A | G | 1 | a0007c0008t0002g0007 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.153-7938A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026321 | |||||||
chr6:161026337 | A | G | 27 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0120 others(24): Show |
27 | HG00140.hp2 HG00323.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.153-7922A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026337 | |||||||
chr6:161026356 | T | C | 5 | a0001c0001t0001g0149 a0001c0001t0001g0250 a0001c0001t0001g0251 others(2): Show |
5 | HG02132.hp1 HG02145.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-7903T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026356 | |||||||
chr6:161026362 | T | C | 286 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(283): Show |
295 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.153-7897T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026362 | |||||||
chr6:161026377 | T | C | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.153-7882T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026377 | |||||||
chr6:161026382 | T | G | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.153-7877T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026382 | |||||||
chr6:161026407 | T | C | 3 | a0002c0002t0002g0019 a0002c0002t0002g0020 a0002c0002t0002g0024 |
3 | NA18952.hp1 NA19058.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.153-7852T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026407 | |||||||
chr6:161026414 | C | T | 2 | a0001c0001t0001g0330 a0001c0001t0002g0327 |
2 | HG00099.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.153-7845C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026414 | |||||||
chr6:161026415 | A | G | 4 | a0001c0001t0001g0272 a0001c0001t0001g0330 a0001c0001t0002g0327 others(1): Show |
4 | HG00099.hp2 HG01346.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-7844A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026415 | |||||||
chr6:161026415 | A | T | 1 | a0001c0001t0001g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.153-7844A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026415 | |||||||
chr6:161026425 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.153-7834G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026425 | |||||||
chr6:161026426 | T | C | 12 | a0001c0001t0001g0137 a0001c0001t0001g0150 a0001c0001t0001g0155 others(9): Show |
12 | HG00423.hp1 HG02004.hp1 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.153-7833T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026426 | |||||||
chr6:161026433 | T | C | 1 | a0007c0008t0002g0007 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.153-7826T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026433 | |||||||
chr6:161026440 | G | A | 3 | a0002c0002t0002g0019 a0002c0002t0002g0020 a0002c0002t0002g0024 |
3 | NA18952.hp1 NA19058.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.153-7819G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026440 | |||||||
chr6:161026476 | A | G | 42 | a0001c0001t0001g0054 a0001c0001t0001g0071 a0001c0001t0001g0072 others(39): Show |
42 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.153-7783A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026476 | |||||||
chr6:161026606 | T | C | 4 | a0002c0002t0002g0019 a0002c0002t0002g0020 a0002c0002t0002g0021 others(1): Show |
4 | NA18945.hp2 NA18952.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-7653T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161026606 | |||||||
chr6:161026733 | C | CT | 42 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0083 others(39): Show |
42 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.153-7502dupT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161026733 | ||||||
chr6:161026733 | CT | C | 20 | a0001c0001t0001g0240 a0001c0001t0001g0253 a0001c0001t0001g0267 others(17): Show |
20 | HG00673.hp2 HG00738.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.153-7502delT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161026733 | ||||||
chr6:161027135 | T | G | 15 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0015 others(12): Show |
15 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.153-7124T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161027135 | |||||||
chr6:161027175 | G | A | 14 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(11): Show |
14 | HG01109.hp2 HG02451.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.153-7084G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161027175 | |||||||
chr6:161027259 | C | G | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.153-7000C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161027259 | |||||||
chr6:161027333 | A | T | 16 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(13): Show |
16 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.153-6926A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161027333 | |||||||
chr6:161027419 | T | C | 6 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0089 others(3): Show |
6 | HG02165.hp2 NA18747.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-6840T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161027419 | |||||||
chr6:161027464 | G | C | 1 | a0001c0001t0002g0057 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.153-6795G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161027464 | |||||||
chr6:161027483 | A | G | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.153-6776A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161027483 | |||||||
chr6:161027677 | T | G | 6 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-6582T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161027677 | |||||||
chr6:161027763 | C | T | 5 | a0004c0004t0002g0006 a0004c0004t0002g0291 a0004c0004t0002g0303 others(2): Show |
7 | HG02145.hp2 HG03041.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-6496C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161027763 | |||||||
chr6:161028018 | C | T | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.153-6241C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161028018 | |||||||
chr6:161028085 | T | A | 90 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0098 others(87): Show |
93 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.153-6174T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161028085 | |||||||
chr6:161028123 | C | T | 6 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-6136C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161028123 | |||||||
chr6:161028153 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.153-6106G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161028153 | |||||||
chr6:161028269 | TC | T | 10 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.153-5988delC | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161028269 | ||||||
chr6:161028292 | CTAAAT | C | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0098 others(38): Show |
42 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.153-5962_153-5958d others(7): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161028292 | ||||||
chr6:161028356 | T | TG | 32 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0055 others(29): Show |
33 | HG00323.hp1 HG00609.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.153-5898dupG | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161028356 | ||||||
chr6:161028544 | A | G | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0098 others(38): Show |
42 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.153-5715A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161028544 | |||||||
chr6:161028629 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.153-5630A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161028629 | |||||||
chr6:161028638 | T | C | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-5621T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161028638 | |||||||
chr6:161028658 | C | CT | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-5590dupT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161028658 | ||||||
chr6:161028670 | A | T | 1 | a0001c0001t0002g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.153-5589A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161028670 | |||||||
chr6:161028938 | C | G | 1 | a0001c0001t0003g0045 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.153-5321C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161028938 | |||||||
chr6:161029007 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.153-5252G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161029007 | |||||||
chr6:161029008 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.153-5251C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161029008 | |||||||
chr6:161029010 | A | G | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0003g0043 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-5249A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161029010 | |||||||
chr6:161029055 | C | G | 9 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(6): Show |
9 | HG01109.hp2 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-5204C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161029055 | |||||||
chr6:161029158 | C | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG00099.hp1 HG00280.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.153-5101C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161029158 | |||||||
chr6:161029311 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.153-4948C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161029311 | |||||||
chr6:161029496 | C | T | 90 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0098 others(87): Show |
93 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.153-4763C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161029496 | |||||||
chr6:161029635 | C | A | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-4624C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161029635 | |||||||
chr6:161029657 | A | T | 1 | a0001c0001t0001g0088 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.153-4602A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161029657 | |||||||
chr6:161029735 | G | T | 6 | a0004c0004t0002g0006 a0004c0004t0002g0291 a0004c0004t0002g0303 others(3): Show |
8 | HG02145.hp2 HG03041.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.153-4524G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161029735 | |||||||
chr6:161029767 | C | T | 1 | a0001c0001t0002g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.153-4492C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161029767 | |||||||
chr6:161029810 | CT | C | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0098 others(38): Show |
42 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.153-4448delT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161029810 | |||||||
chr6:161029841 | T | TTTTG | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-4398_153-4395d others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161029841 | ||||||
chr6:161030066 | G | A | 16 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(13): Show |
16 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.153-4193G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161030066 | |||||||
chr6:161030123 | A | G | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.153-4136A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161030123 | |||||||
chr6:161030525 | G | A | 17 | a0001c0001t0002g0208 a0001c0007t0001g0248 a0002c0002t0002g0013 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.153-3734G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161030525 | |||||||
chr6:161030834 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.153-3425A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161030834 | |||||||
chr6:161030932 | T | A | 2 | a0006c0009t0002g0286 a0006c0009t0002g0287 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.153-3327T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161030932 | |||||||
chr6:161031044 | T | C | 16 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(13): Show |
16 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.153-3215T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161031044 | |||||||
chr6:161031113 | T | C | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.153-3146T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161031113 | |||||||
chr6:161031182 | A | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG00738.hp2 HG01081.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.153-3077A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161031182 | |||||||
chr6:161031242 | T | C | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.153-3017T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161031242 | |||||||
chr6:161031279 | T | C | 1 | a0006c0009t0002g0286 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.153-2980T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161031279 | |||||||
chr6:161031301 | A | C | 1 | a0001c0001t0002g0069 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.153-2958A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161031301 | |||||||
chr6:161031361 | T | C | 13 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG02040.hp2 NA18941.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.153-2898T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161031361 | |||||||
chr6:161031377 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.153-2882A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161031377 | |||||||
chr6:161031602 | C | T | 90 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0098 others(87): Show |
93 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.153-2657C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161031602 | |||||||
chr6:161031673 | T | G | 16 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(13): Show |
16 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.153-2586T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161031673 | |||||||
chr6:161031711 | G | A | 302 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(299): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.153-2548G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161031711 | |||||||
chr6:161031764 | G | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0001g0185 others(7): Show |
12 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.153-2495G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161031764 | |||||||
chr6:161032124 | A | G | 1 | a0001c0001t0002g0069 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.153-2135A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161032124 | |||||||
chr6:161032140 | G | A | 1 | a0001c0005t0002g0322 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.153-2119G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161032140 | |||||||
chr6:161032173 | A | G | 2 | a0001c0001t0001g0267 a0001c0001t0001g0281 |
2 | HG02083.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.153-2086A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161032173 | |||||||
chr6:161032362 | A | G | 302 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(299): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.153-1897A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161032362 | |||||||
chr6:161032475 | C | T | 16 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(13): Show |
16 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.153-1784C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161032475 | |||||||
chr6:161032493 | C | T | 1 | a0010c0017t0002g0206 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.153-1766C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161032493 | |||||||
chr6:161032577 | G | C | 286 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(283): Show |
295 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.153-1682G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161032577 | |||||||
chr6:161032606 | T | A | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-1653T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161032606 | |||||||
chr6:161032881 | CAT | C | 12 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(9): Show |
14 | HG02145.hp2 HG02615.hp1 HG03041.hp1 others(11): Show |
intron_variant | MODIFIER | c.153-1375_153-1374d others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161032881 | ||||||
chr6:161033033 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.153-1226A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161033033 | |||||||
chr6:161033073 | G | A | 302 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(299): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.153-1186G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161033073 | |||||||
chr6:161033137 | T | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-1122T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161033137 | |||||||
chr6:161033430 | G | A | 234 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(231): Show |
241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.153-829G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161033430 | |||||||
chr6:161033550 | C | CCTTG | 285 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(282): Show |
294 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.153-708_153-705dup others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr6 | 161033550 | ||||||
chr6:161033589 | T | G | 13 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(10): Show |
15 | HG02145.hp2 HG02257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.153-670T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161033589 | |||||||
chr6:161033630 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.153-629A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161033630 | |||||||
chr6:161033961 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.153-298A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161033961 | |||||||
chr6:161034088 | A | T | 1 | a0001c0001t0001g0136 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.153-171A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1/26 | chr6 | 161034088 | |||||||
chr6:161034459 | G | A | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+10G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161034459 | |||||||
chr6:161034572 | A | AT | 279 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(276): Show |
288 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.343+132dupT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161034572 | ||||||
chr6:161034572 | A | ATT | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.343+131_343+132dup others(2): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161034572 | ||||||
chr6:161034572 | A | ATTT | 16 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(13): Show |
16 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.343+130_343+132dup others(3): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161034572 | ||||||
chr6:161034703 | T | C | 2 | a0001c0001t0002g0062 a0001c0001t0002g0063 |
2 | NA18944.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.343+254T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161034703 | |||||||
chr6:161034846 | G | A | 9 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(6): Show |
9 | HG01109.hp2 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.343+397G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161034846 | |||||||
chr6:161034969 | G | C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0231 others(4): Show |
7 | HG00621.hp2 HG02155.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.343+520G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161034969 | |||||||
chr6:161034997 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.343+548C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161034997 | |||||||
chr6:161035085 | C | CT | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.343+643dupT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161035085 | ||||||
chr6:161035176 | C | T | 16 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(13): Show |
16 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.343+727C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161035176 | |||||||
chr6:161035235 | T | A | 3 | a0001c0001t0002g0090 a0001c0001t0002g0103 a0001c0001t0002g0115 |
3 | HG02056.hp1 NA18999.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.343+786T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161035235 | |||||||
chr6:161035636 | T | C | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(268): Show |
278 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.343+1187T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161035636 | |||||||
chr6:161035727 | T | C | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | NA18950.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.343+1278T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161035727 | |||||||
chr6:161035735 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0283 |
2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.343+1286A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161035735 | |||||||
chr6:161035790 | C | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.343+1341C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161035790 | |||||||
chr6:161035830 | T | C | 9 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(6): Show |
9 | HG01109.hp2 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.343+1381T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161035830 | |||||||
chr6:161036031 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG00741.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.343+1582C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161036031 | |||||||
chr6:161036032 | G | A | 16 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(13): Show |
16 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.343+1583G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161036032 | |||||||
chr6:161036040 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.343+1591G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161036040 | |||||||
chr6:161036093 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.343+1644A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161036093 | |||||||
chr6:161036151 | G | A | 13 | a0001c0001t0002g0053 a0001c0001t0002g0222 a0001c0001t0002g0223 others(10): Show |
13 | HG01109.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.343+1702G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161036151 | |||||||
chr6:161036197 | T | C | 1 | a0001c0001t0002g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.343+1748T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161036197 | |||||||
chr6:161036203 | A | G | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.343+1754A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161036203 | |||||||
chr6:161036604 | T | G | 1 | a0001c0001t0001g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.343+2155T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161036604 | |||||||
chr6:161036742 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.343+2293G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161036742 | |||||||
chr6:161037011 | C | T | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.343+2562C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161037011 | |||||||
chr6:161037204 | G | A | 16 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(13): Show |
16 | HG00738.hp1 HG01361.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.343+2755G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161037204 | |||||||
chr6:161037307 | C | T | 2 | a0001c0001t0001g0253 a0001c0001t0001g0257 |
2 | HG00673.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.343+2858C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161037307 | |||||||
chr6:161037504 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0041 |
2 | HG00733.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.343+3055C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161037504 | |||||||
chr6:161037579 | C | T | 13 | a0001c0001t0002g0053 a0001c0001t0002g0222 a0001c0001t0002g0223 others(10): Show |
13 | HG01109.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.343+3130C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161037579 | |||||||
chr6:161037645 | T | A | 1 | a0001c0001t0001g0027 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.343+3196T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161037645 | |||||||
chr6:161037659 | C | CCA | 19 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0033 others(16): Show |
19 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.343+3212_343+3213d others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161037659 | ||||||
chr6:161037713 | C | T | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.343+3264C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161037713 | |||||||
chr6:161037723 | G | C | 286 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(283): Show |
295 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.343+3274G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161037723 | |||||||
chr6:161037899 | G | A | 19 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0033 others(16): Show |
19 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.343+3450G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161037899 | |||||||
chr6:161037944 | T | C | 11 | a0001c0001t0002g0053 a0001c0001t0002g0222 a0001c0001t0002g0223 others(8): Show |
11 | HG01109.hp2 HG02451.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.343+3495T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161037944 | |||||||
chr6:161037971 | A | AT | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.343+3530dupT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161037971 | ||||||
chr6:161038035 | C | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0098 others(35): Show |
39 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.343+3586C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161038035 | |||||||
chr6:161038231 | A | G | 1 | a0001c0001t0002g0057 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.343+3782A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161038231 | |||||||
chr6:161038258 | A | C | 1 | a0001c0001t0001g0282 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.343+3809A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161038258 | |||||||
chr6:161038633 | A | G | 302 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(299): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.343+4184A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161038633 | |||||||
chr6:161038830 | A | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+4381A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161038830 | |||||||
chr6:161038838 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.343+4389C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161038838 | |||||||
chr6:161038901 | G | A | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.343+4452G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161038901 | |||||||
chr6:161039261 | C | T | 7 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(4): Show |
7 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.343+4812C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161039261 | |||||||
chr6:161039279 | C | CA | 138 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0027 others(135): Show |
139 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.343+4851dupA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161039279 | ||||||
chr6:161039279 | C | CAA | 61 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0036 others(58): Show |
64 | HG00323.hp1 HG00423.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.343+4850_343+4851d others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161039279 | ||||||
chr6:161039279 | C | CAAA | 10 | a0001c0001t0001g0100 a0001c0001t0001g0190 a0001c0001t0001g0194 others(7): Show |
10 | HG00621.hp2 HG01884.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.343+4849_343+4851d others(5): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161039279 | ||||||
chr6:161039480 | A | G | 196 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(193): Show |
202 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.343+5031A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161039480 | |||||||
chr6:161039484 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.343+5035T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161039484 | |||||||
chr6:161039563 | A | G | 1 | a0001c0001t0003g0045 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.343+5114A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161039563 | |||||||
chr6:161039729 | A | T | 1 | a0007c0008t0002g0007 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.343+5280A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161039729 | |||||||
chr6:161039845 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.343+5396C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161039845 | |||||||
chr6:161039901 | A | G | 3 | a0001c0001t0001g0247 a0001c0001t0001g0270 a0001c0001t0001g0274 |
3 | HG00621.hp1 NA19060.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.343+5452A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161039901 | |||||||
chr6:161039905 | T | C | 285 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(282): Show |
294 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.343+5456T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161039905 | |||||||
chr6:161040037 | G | T | 29 | a0001c0001t0002g0053 a0001c0001t0002g0208 a0001c0001t0002g0222 others(26): Show |
29 | HG00738.hp1 HG01109.hp2 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.343+5588G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161040037 | |||||||
chr6:161040420 | CAAAG | C | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.343+5976_343+5979d others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161040420 | ||||||
chr6:161040744 | A | C | 6 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.343+6295A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161040744 | |||||||
chr6:161040832 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0150 |
2 | NA18942.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.343+6383G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161040832 | |||||||
chr6:161040842 | A | G | 1 | a0001c0001t0002g0116 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.343+6393A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161040842 | |||||||
chr6:161040922 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.343+6473A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161040922 | |||||||
chr6:161040982 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.343+6533A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161040982 | |||||||
chr6:161041124 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.343+6675T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161041124 | |||||||
chr6:161041173 | G | T | 1 | a0001c0001t0003g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.343+6724G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161041173 | |||||||
chr6:161041204 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.343+6755A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161041204 | |||||||
chr6:161041235 | A | T | 82 | a0001c0001t0001g0056 a0001c0001t0001g0133 a0001c0001t0001g0136 others(79): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.343+6786A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161041235 | |||||||
chr6:161041319 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.343+6870A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161041319 | |||||||
chr6:161041679 | G | A | 4 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(1): Show |
4 | HG01891.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-6937G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161041679 | |||||||
chr6:161041715 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.344-6901C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161041715 | |||||||
chr6:161041784 | G | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(263): Show |
273 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.344-6832G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161041784 | |||||||
chr6:161041805 | C | T | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-6811C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161041805 | |||||||
chr6:161041811 | G | T | 29 | a0001c0001t0002g0053 a0001c0001t0002g0208 a0001c0001t0002g0222 others(26): Show |
29 | HG00738.hp1 HG01109.hp2 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.344-6805G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161041811 | |||||||
chr6:161041912 | C | CTTGTTTT others(5): Show |
1 | a0001c0001t0002g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.344-6702_344-6701i others(14): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161041912 | ||||||
chr6:161041912 | C | CTTT | 25 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0080 others(22): Show |
26 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.344-6693_344-6691d others(5): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161041912 | ||||||
chr6:161041912 | C | CTTTT | 13 | a0001c0001t0001g0098 a0001c0001t0001g0104 a0001c0001t0001g0168 others(10): Show |
14 | HG00423.hp1 HG00621.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.344-6694_344-6691d others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161041912 | ||||||
chr6:161041912 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0002g0297 a0001c0001t0002g0298 |
2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.344-6701_344-6691d others(13): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161041912 | ||||||
chr6:161041912 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0002g0299 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.344-6702_344-6691d others(14): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161041912 | ||||||
chr6:161041912 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0002g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.344-6691_344-6690i others(19): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161041912 | ||||||
chr6:161041912 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0002g0301 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.344-6691_344-6690i others(20): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161041912 | ||||||
chr6:161041923 | TTTC | T | 25 | a0001c0001t0002g0053 a0001c0001t0002g0222 a0001c0001t0002g0223 others(22): Show |
25 | HG00738.hp1 HG01109.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.344-6690_344-6688d others(5): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161041923 | ||||||
chr6:161041924 | TTC | T | 10 | a0001c0001t0001g0055 a0001c0001t0001g0071 a0001c0001t0001g0072 others(7): Show |
10 | HG01257.hp1 HG02083.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.344-6690_344-6689d others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161041924 | ||||||
chr6:161041925 | TC | T | 148 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(145): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.344-6690delC | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161041925 | |||||||
chr6:161041926 | C | T | 112 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0027 others(109): Show |
115 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.344-6690C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161041926 | |||||||
chr6:161041928 | T | TTTTTTTT others(3): Show |
1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.344-6679_344-6678i others(12): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161041928 | ||||||
chr6:161041932 | T | C | 1 | a0001c0001t0003g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.344-6684T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161041932 | |||||||
chr6:161041932 | T | TC | 12 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(9): Show |
12 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.344-6684_344-6683i others(3): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161041932 | |||||||
chr6:161041946 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.344-6670T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161041946 | |||||||
chr6:161041979 | A | C | 13 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(10): Show |
15 | HG02145.hp2 HG02257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.344-6637A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161041979 | |||||||
chr6:161042005 | G | A | 12 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(9): Show |
12 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.344-6611G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161042005 | |||||||
chr6:161042036 | G | T | 1 | a0001c0001t0001g0242 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.344-6580G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161042036 | |||||||
chr6:161042040 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.344-6576G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161042040 | |||||||
chr6:161042112 | A | G | 1 | a0007c0008t0002g0007 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.344-6504A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161042112 | |||||||
chr6:161042148 | G | A | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.344-6468G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161042148 | |||||||
chr6:161042166 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.344-6450C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161042166 | |||||||
chr6:161042209 | A | G | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.344-6407A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161042209 | |||||||
chr6:161042218 | A | C | 1 | a0003c0003t0002g0318 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.344-6398A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161042218 | |||||||
chr6:161042227 | T | C | 19 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(16): Show |
21 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.344-6389T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161042227 | |||||||
chr6:161042560 | C | T | 13 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(10): Show |
15 | HG02145.hp2 HG02257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.344-6056C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161042560 | |||||||
chr6:161042627 | T | C | 7 | a0004c0004t0002g0006 a0004c0004t0002g0291 a0004c0004t0002g0303 others(4): Show |
9 | HG02145.hp2 HG02257.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.344-5989T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161042627 | |||||||
chr6:161042830 | C | T | 7 | a0004c0004t0002g0006 a0004c0004t0002g0291 a0004c0004t0002g0303 others(4): Show |
9 | HG02145.hp2 HG02257.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.344-5786C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161042830 | |||||||
chr6:161042908 | GCA | G | 30 | a0001c0001t0001g0010 a0001c0001t0001g0080 a0001c0001t0001g0242 others(27): Show |
30 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.344-5675_344-5674d others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161042908 | ||||||
chr6:161042908 | GCACA | G | 23 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0104 others(20): Show |
23 | HG00733.hp1 HG00735.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.344-5677_344-5674d others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161042908 | ||||||
chr6:161042908 | GCACACA | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(207): Show |
217 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.344-5679_344-5674d others(8): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161042908 | ||||||
chr6:161042908 | GCACACAC others(1): Show |
G | 20 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(17): Show |
20 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.344-5681_344-5674d others(10): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161042908 | ||||||
chr6:161042908 | GCACACAC others(3): Show |
G | 5 | a0001c0001t0001g0196 a0001c0001t0001g0254 a0001c0001t0001g0255 others(2): Show |
5 | HG01433.hp1 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.344-5683_344-5674d others(12): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161042908 | ||||||
chr6:161042908 | GCACACAC others(5): Show |
G | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.344-5685_344-5674d others(14): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161042908 | ||||||
chr6:161042908 | GCACACAC others(7): Show |
G | 13 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(10): Show |
15 | HG01109.hp2 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.344-5687_344-5674d others(16): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161042908 | ||||||
chr6:161043001 | T | G | 6 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0168 others(3): Show |
6 | NA18952.hp2 NA18956.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-5615T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161043001 | |||||||
chr6:161043022 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.344-5594A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161043022 | |||||||
chr6:161043307 | T | C | 7 | a0001c0001t0001g0186 a0001c0001t0001g0239 a0001c0001t0001g0258 others(4): Show |
7 | HG02056.hp2 HG02132.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-5309T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161043307 | |||||||
chr6:161043591 | C | T | 283 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(280): Show |
292 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.344-5025C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161043591 | |||||||
chr6:161043600 | T | C | 283 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(280): Show |
292 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.344-5016T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161043600 | |||||||
chr6:161043624 | C | G | 1 | a0001c0001t0002g0077 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.344-4992C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161043624 | |||||||
chr6:161043692 | G | A | 1 | a0002c0002t0002g0017 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.344-4924G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161043692 | |||||||
chr6:161043720 | C | T | 1 | a0013c0013t0001g0269 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.344-4896C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161043720 | |||||||
chr6:161043937 | G | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0098 others(38): Show |
42 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.344-4679G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161043937 | |||||||
chr6:161043958 | A | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-4658A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161043958 | |||||||
chr6:161044265 | A | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0091 others(101): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.344-4351A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161044265 | |||||||
chr6:161044286 | A | G | 2 | a0001c0001t0002g0062 a0001c0001t0002g0063 |
2 | NA18944.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.344-4330A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161044286 | |||||||
chr6:161044392 | A | G | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.344-4224A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161044392 | |||||||
chr6:161044523 | C | G | 1 | a0001c0001t0002g0067 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.344-4093C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161044523 | |||||||
chr6:161044580 | A | T | 1 | a0001c0001t0002g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.344-4036A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161044580 | |||||||
chr6:161044892 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.344-3724G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161044892 | |||||||
chr6:161045022 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.344-3594A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161045022 | |||||||
chr6:161045065 | A | G | 4 | a0001c0001t0002g0003 a0001c0001t0002g0308 a0001c0001t0002g0325 others(1): Show |
6 | HG00741.hp1 HG01069.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.344-3551A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161045065 | |||||||
chr6:161045148 | G | A | 78 | a0001c0001t0001g0056 a0001c0001t0001g0136 a0001c0001t0001g0137 others(75): Show |
81 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.344-3468G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161045148 | |||||||
chr6:161045225 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.344-3391G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161045225 | |||||||
chr6:161045226 | T | TG | 11 | a0001c0001t0001g0186 a0001c0001t0001g0243 a0001c0001t0001g0253 others(8): Show |
11 | HG00673.hp2 HG02040.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.344-3383dupG | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161045226 | ||||||
chr6:161045233 | G | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.344-3383G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161045233 | |||||||
chr6:161045270 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.344-3346C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161045270 | |||||||
chr6:161045298 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.344-3318T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161045298 | |||||||
chr6:161045339 | T | G | 15 | a0001c0001t0001g0194 a0001c0001t0001g0218 a0001c0001t0001g0219 others(12): Show |
17 | HG02145.hp2 HG02896.hp2 HG02897.hp2 others(14): Show |
intron_variant | MODIFIER | c.344-3277T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161045339 | |||||||
chr6:161045357 | T | C | 1 | a0012c0011t0004g0284 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.344-3259T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161045357 | |||||||
chr6:161045404 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.344-3212A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161045404 | |||||||
chr6:161045499 | G | A | 1 | a0001c0001t0002g0048 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.344-3117G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161045499 | |||||||
chr6:161045500 | T | A | 1 | a0001c0001t0002g0048 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.344-3116T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161045500 | |||||||
chr6:161045711 | C | G | 6 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-2905C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161045711 | |||||||
chr6:161045724 | C | T | 1 | a0001c0001t0002g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.344-2892C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161045724 | |||||||
chr6:161045983 | T | A | 1 | a0001c0001t0001g0162 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.344-2633T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161045983 | |||||||
chr6:161046031 | T | C | 232 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(229): Show |
239 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.344-2585T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161046031 | |||||||
chr6:161046043 | G | A | 1 | a0002c0002t0002g0238 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.344-2573G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161046043 | |||||||
chr6:161046048 | T | G | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.344-2568T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161046048 | |||||||
chr6:161046053 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.344-2563T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161046053 | |||||||
chr6:161046055 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.344-2561A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161046055 | |||||||
chr6:161046150 | C | CAGTG | 6 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(3): Show |
6 | HG02647.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.344-2464_344-2461d others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161046150 | ||||||
chr6:161046525 | AAAT | A | 5 | a0004c0004t0002g0006 a0004c0004t0002g0291 a0004c0004t0002g0303 others(2): Show |
6 | HG02145.hp2 HG03041.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.344-2080_344-2078d others(5): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161046525 | ||||||
chr6:161046533 | A | AT | 261 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(258): Show |
268 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.344-2082dupT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161046533 | ||||||
chr6:161046672 | A | G | 1 | a0001c0001t0002g0117 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.344-1944A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161046672 | |||||||
chr6:161046862 | T | C | 6 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0308 others(3): Show |
9 | HG00741.hp1 HG01069.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.344-1754T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161046862 | |||||||
chr6:161046957 | A | G | 1 | a0001c0001t0002g0289 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.344-1659A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161046957 | |||||||
chr6:161047117 | C | CAT | 20 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(17): Show |
22 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.344-1472_344-1471d others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161047117 | ||||||
chr6:161047117 | C | CATAT | 4 | a0002c0012t0004g0285 a0006c0009t0002g0286 a0006c0009t0002g0287 others(1): Show |
4 | HG02055.hp1 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.344-1474_344-1471d others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161047117 | ||||||
chr6:161047117 | C | CATATAT | 6 | a0001c0001t0003g0044 a0004c0004t0002g0006 a0004c0004t0002g0291 others(3): Show |
7 | HG02145.hp2 HG02976.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.344-1476_344-1471d others(8): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161047117 | ||||||
chr6:161047117 | C | CATATATA others(3): Show |
1 | a0001c0001t0001g0121 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.344-1480_344-1471d others(12): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161047117 | ||||||
chr6:161047117 | C | CATATATA others(5): Show |
3 | a0001c0001t0002g0012 a0001c0001t0002g0046 a0001c0001t0002g0049 |
3 | HG02615.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.344-1482_344-1471d others(14): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161047117 | ||||||
chr6:161047117 | C | CATATATA others(7): Show |
1 | a0001c0001t0001g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.344-1484_344-1471d others(16): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161047117 | ||||||
chr6:161047117 | C | CATATATA others(9): Show |
5 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG02723.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.344-1486_344-1471d others(18): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161047117 | ||||||
chr6:161047117 | C | CATATATA others(11): Show |
4 | a0001c0001t0002g0009 a0001c0001t0002g0029 a0001c0001t0002g0030 others(1): Show |
4 | HG03225.hp1 HG03471.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.344-1488_344-1471d others(20): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161047117 | ||||||
chr6:161047117 | CAT | C | 25 | a0001c0001t0001g0175 a0001c0001t0001g0180 a0001c0001t0001g0181 others(22): Show |
25 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.344-1472_344-1471d others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161047117 | ||||||
chr6:161047117 | CATAT | C | 54 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0082 others(51): Show |
57 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.344-1474_344-1471d others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161047117 | ||||||
chr6:161047117 | CATATAT | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(174): Show |
181 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.344-1476_344-1471d others(8): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161047117 | ||||||
chr6:161047117 | CATATATA others(9): Show |
C | 1 | a0001c0001t0001g0253 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.344-1486_344-1471d others(18): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161047117 | ||||||
chr6:161047270 | G | A | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.344-1346G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161047270 | |||||||
chr6:161047279 | C | CA | 236 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(233): Show |
243 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.344-1326dupA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161047279 | ||||||
chr6:161047391 | G | A | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.344-1225G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161047391 | |||||||
chr6:161047478 | G | A | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.344-1138G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161047478 | |||||||
chr6:161047550 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.344-1066G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161047550 | |||||||
chr6:161047594 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.344-1022C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161047594 | |||||||
chr6:161047710 | G | T | 1 | a0001c0001t0001g0168 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.344-906G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161047710 | |||||||
chr6:161047722 | T | C | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.344-894T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161047722 | |||||||
chr6:161047746 | G | A | 12 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(9): Show |
12 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.344-870G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161047746 | |||||||
chr6:161047785 | A | G | 236 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(233): Show |
243 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.344-831A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161047785 | |||||||
chr6:161047802 | A | T | 3 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 |
3 | HG01891.hp1 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.344-814A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161047802 | |||||||
chr6:161047862 | A | G | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.344-754A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161047862 | |||||||
chr6:161047953 | A | G | 52 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0072 others(49): Show |
53 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.344-663A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161047953 | |||||||
chr6:161048085 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.344-531T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161048085 | |||||||
chr6:161048262 | C | T | 1 | a0002c0010t0002g0016 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.344-354C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161048262 | |||||||
chr6:161048423 | T | A | 301 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(298): Show |
310 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.344-193T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161048423 | |||||||
chr6:161048480 | A | C | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.344-136A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161048480 | |||||||
chr6:161048572 | A | G | 7 | a0004c0004t0002g0006 a0004c0004t0002g0291 a0004c0004t0002g0303 others(4): Show |
9 | HG02145.hp2 HG02257.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.344-44A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161048572 | |||||||
chr6:161048579 | A | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0105 a0001c0001t0001g0106 others(1): Show |
4 | NA18957.hp2 NA19085.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.344-37A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | chr6 | 161048579 | |||||||
chr6:161048599 | AT | A | 13 | a0001c0001t0001g0133 a0001c0001t0001g0163 a0001c0001t0001g0277 others(10): Show |
13 | HG01109.hp2 HG01243.hp2 HG02027.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.344-6delT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr6 | 161048599 | ||||||
chr6:161050006 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0104 |
2 | NA18978.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1707+27A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161050006 | |||||||
chr6:161050050 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1707+71G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161050050 | |||||||
chr6:161050056 | T | C | 1 | a0011c0015t0002g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1707+77T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161050056 | |||||||
chr6:161050473 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1707+494C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161050473 | |||||||
chr6:161050704 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1707+725A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161050704 | |||||||
chr6:161050836 | G | A | 6 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG01243.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1707+857G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161050836 | |||||||
chr6:161050864 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1707+885T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161050864 | |||||||
chr6:161050955 | A | C | 1 | a0001c0001t0002g0068 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1707+976A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161050955 | |||||||
chr6:161051026 | A | G | 1 | a0001c0001t0002g0144 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1707+1047A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161051026 | |||||||
chr6:161051154 | T | C | 327 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(324): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.1707+1175T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161051154 | |||||||
chr6:161051167 | G | A | 1 | a0001c0001t0002g0288 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1707+1188G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161051167 | |||||||
chr6:161051574 | A | C | 1 | a0001c0001t0001g0220 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1707+1595A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161051574 | |||||||
chr6:161051576 | T | C | 7 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(4): Show |
7 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.1707+1597T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161051576 | |||||||
chr6:161051985 | T | C | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.1707+2006T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161051985 | |||||||
chr6:161052045 | G | A | 3 | a0001c0001t0002g0090 a0001c0001t0002g0103 a0001c0001t0002g0115 |
3 | HG02056.hp1 NA18999.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1707+2066G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161052045 | |||||||
chr6:161052110 | G | A | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.1707+2131G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161052110 | |||||||
chr6:161052263 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1707+2284A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161052263 | |||||||
chr6:161052508 | A | G | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1707+2529A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161052508 | |||||||
chr6:161052731 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1707+2752G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161052731 | |||||||
chr6:161052787 | A | G | 4 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(1): Show |
4 | HG02615.hp1 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1707+2808A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161052787 | |||||||
chr6:161052918 | C | T | 4 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(1): Show |
4 | HG02451.hp2 NA18941.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1707+2939C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161052918 | |||||||
chr6:161053210 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1707+3231G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161053210 | |||||||
chr6:161053499 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1707+3520A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161053499 | |||||||
chr6:161053542 | A | G | 1 | a0001c0005t0002g0322 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1707+3563A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161053542 | |||||||
chr6:161053546 | G | C | 6 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0003g0043 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1707+3567G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161053546 | |||||||
chr6:161053563 | T | G | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1707+3584T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161053563 | |||||||
chr6:161053628 | G | A | 26 | a0001c0001t0002g0053 a0001c0001t0002g0208 a0001c0001t0002g0222 others(23): Show |
26 | HG00738.hp1 HG01109.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.1707+3649G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161053628 | |||||||
chr6:161053671 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1707+3692A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161053671 | |||||||
chr6:161053678 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1707+3699G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161053678 | |||||||
chr6:161053847 | G | T | 1 | a0001c0001t0002g0008 | 2 | HG01106.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1707+3868G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161053847 | |||||||
chr6:161053934 | A | C | 76 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0080 others(73): Show |
77 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1707+3955A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161053934 | |||||||
chr6:161053951 | C | T | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1707+3972C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161053951 | |||||||
chr6:161053967 | C | T | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1707+3988C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161053967 | |||||||
chr6:161054155 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1707+4176C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161054155 | |||||||
chr6:161054211 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1707+4232A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161054211 | |||||||
chr6:161054216 | G | A | 6 | a0004c0004t0002g0006 a0004c0004t0002g0291 a0004c0004t0002g0303 others(3): Show |
8 | HG02145.hp2 HG03041.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.1707+4237G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161054216 | |||||||
chr6:161054231 | T | G | 9 | a0001c0001t0002g0053 a0001c0001t0002g0222 a0001c0001t0002g0223 others(6): Show |
9 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1707+4252T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161054231 | |||||||
chr6:161054278 | C | T | 4 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(1): Show |
4 | HG02615.hp1 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1707+4299C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161054278 | |||||||
chr6:161054300 | A | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1707+4321A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161054300 | |||||||
chr6:161054303 | C | T | 3 | a0001c0001t0001g0136 a0001c0001t0001g0178 a0009c0020t0001g0179 |
3 | HG01070.hp2 HG01258.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1707+4324C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161054303 | |||||||
chr6:161054391 | A | G | 2 | a0002c0002t0002g0013 a0002c0002t0002g0014 |
2 | HG01361.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1707+4412A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161054391 | |||||||
chr6:161054402 | G | A | 10 | a0001c0001t0001g0058 a0001c0001t0001g0216 a0001c0001t0001g0217 others(7): Show |
10 | HG01934.hp2 HG02145.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1707+4423G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161054402 | |||||||
chr6:161054444 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1707+4465C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161054444 | |||||||
chr6:161054450 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1707+4471C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161054450 | |||||||
chr6:161054452 | GCCCAAA | G | 3 | a0002c0002t0002g0019 a0002c0002t0002g0020 a0002c0002t0002g0024 |
3 | NA18952.hp1 NA19058.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1707+4475_1707+448 others(10): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161054452 | ||||||
chr6:161054496 | A | C | 82 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0098 others(79): Show |
83 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1707+4517A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161054496 | |||||||
chr6:161054660 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1707+4681T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161054660 | |||||||
chr6:161054787 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1707+4808A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161054787 | |||||||
chr6:161054808 | G | T | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1707+4829G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161054808 | |||||||
chr6:161054868 | G | GA | 6 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(3): Show |
6 | HG02647.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1707+4895dupA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161054868 | ||||||
chr6:161055213 | A | C | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1707+5234A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161055213 | |||||||
chr6:161055564 | C | T | 1 | a0002c0012t0004g0285 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1707+5585C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161055564 | |||||||
chr6:161055609 | C | T | 7 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(4): Show |
7 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1707+5630C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161055609 | |||||||
chr6:161055648 | A | G | 95 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0098 others(92): Show |
98 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.1707+5669A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161055648 | |||||||
chr6:161055831 | T | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1707+5852T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161055831 | |||||||
chr6:161055899 | A | G | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.1707+5920A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161055899 | |||||||
chr6:161056047 | T | C | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1707+6068T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161056047 | |||||||
chr6:161056354 | C | T | 1 | a0001c0001t0002g0052 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1707+6375C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161056354 | |||||||
chr6:161056391 | G | A | 6 | a0004c0004t0002g0006 a0004c0004t0002g0291 a0004c0004t0002g0303 others(3): Show |
8 | HG02145.hp2 HG03041.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.1707+6412G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161056391 | |||||||
chr6:161056488 | G | C | 1 | a0001c0001t0001g0271 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1707+6509G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161056488 | |||||||
chr6:161056632 | A | G | 89 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0098 others(86): Show |
92 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.1707+6653A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161056632 | |||||||
chr6:161056718 | A | G | 9 | a0001c0001t0002g0053 a0001c0001t0002g0222 a0001c0001t0002g0223 others(6): Show |
9 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1707+6739A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161056718 | |||||||
chr6:161056848 | C | G | 6 | a0004c0004t0002g0006 a0004c0004t0002g0291 a0004c0004t0002g0303 others(3): Show |
8 | HG02145.hp2 HG03041.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.1707+6869C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161056848 | |||||||
chr6:161056928 | G | A | 11 | a0001c0001t0002g0053 a0001c0001t0002g0222 a0001c0001t0002g0223 others(8): Show |
11 | HG01109.hp2 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1707+6949G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161056928 | |||||||
chr6:161056969 | C | G | 4 | a0003c0003t0002g0307 a0003c0003t0002g0315 a0003c0003t0002g0319 others(1): Show |
4 | NA18954.hp1 NA18970.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1707+6990C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161056969 | |||||||
chr6:161057200 | T | C | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.1707+7221T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161057200 | |||||||
chr6:161057406 | A | G | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1707+7427A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161057406 | |||||||
chr6:161057414 | A | G | 214 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0026 others(211): Show |
220 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1707+7435A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161057414 | |||||||
chr6:161057478 | G | C | 302 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(299): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.1707+7499G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161057478 | |||||||
chr6:161057773 | C | T | 6 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1707+7794C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161057773 | |||||||
chr6:161057901 | T | G | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1707+7922T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161057901 | |||||||
chr6:161057967 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1707+7988A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161057967 | |||||||
chr6:161058016 | A | G | 1 | a0002c0002t0002g0023 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1707+8037A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161058016 | |||||||
chr6:161058052 | C | T | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.1707+8073C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161058052 | |||||||
chr6:161058058 | A | G | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1707+8079A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161058058 | |||||||
chr6:161058063 | G | A | 6 | a0004c0004t0002g0006 a0004c0004t0002g0291 a0004c0004t0002g0303 others(3): Show |
8 | HG02145.hp2 HG03041.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.1707+8084G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161058063 | |||||||
chr6:161058137 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1707+8158G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161058137 | |||||||
chr6:161058315 | C | T | 6 | a0004c0004t0002g0006 a0004c0004t0002g0291 a0004c0004t0002g0303 others(3): Show |
8 | HG02145.hp2 HG03041.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.1707+8336C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161058315 | |||||||
chr6:161058547 | G | C | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1707+8568G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161058547 | |||||||
chr6:161058728 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1707+8749G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161058728 | |||||||
chr6:161058757 | G | GAT | 10 | a0001c0001t0001g0177 a0001c0001t0002g0012 a0001c0001t0002g0135 others(7): Show |
10 | HG01361.hp2 HG01934.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1707+8796_1707+879 others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161058757 | ||||||
chr6:161058803 | A | G | 7 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(4): Show |
7 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1707+8824A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161058803 | |||||||
chr6:161058875 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1707+8896T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161058875 | |||||||
chr6:161058969 | A | G | 12 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(9): Show |
12 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.1707+8990A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161058969 | |||||||
chr6:161059088 | T | G | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1707+9109T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161059088 | |||||||
chr6:161059100 | A | G | 80 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0104 others(77): Show |
83 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1707+9121A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161059100 | |||||||
chr6:161059142 | A | ATT | 218 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0026 others(215): Show |
224 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.1707+9173_1707+917 others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161059142 | ||||||
chr6:161059257 | T | G | 1 | a0001c0001t0001g0138 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1707+9278T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161059257 | |||||||
chr6:161059260 | T | C | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1707+9281T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161059260 | |||||||
chr6:161059340 | T | C | 1 | a0011c0015t0002g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1707+9361T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161059340 | |||||||
chr6:161059538 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1707+9559G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161059538 | |||||||
chr6:161059599 | A | G | 33 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0104 others(30): Show |
34 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1707+9620A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161059599 | |||||||
chr6:161059862 | C | CT | 167 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(164): Show |
169 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.1707+9894dupT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161059862 | ||||||
chr6:161059862 | C | CTT | 60 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0072 others(57): Show |
64 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1707+9893_1707+989 others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161059862 | ||||||
chr6:161059955 | A | G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1707+9976A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161059955 | |||||||
chr6:161060316 | A | G | 50 | a0001c0001t0001g0010 a0001c0001t0001g0080 a0001c0001t0001g0082 others(47): Show |
54 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.1708-10292A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161060316 | |||||||
chr6:161060618 | C | CT | 22 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0106 others(19): Show |
22 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.1708-9971dupT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161060618 | ||||||
chr6:161060618 | CT | C | 13 | a0001c0001t0001g0122 a0001c0001t0001g0174 a0001c0001t0002g0009 others(10): Show |
13 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1708-9971delT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161060618 | ||||||
chr6:161060618 | CTT | C | 71 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0104 others(68): Show |
74 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1708-9972_1708-997 others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161060618 | ||||||
chr6:161060637 | T | TG | 6 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0003g0043 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1708-9970dupG | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161060637 | ||||||
chr6:161060958 | C | T | 83 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0104 others(80): Show |
86 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1708-9650C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161060958 | |||||||
chr6:161060999 | C | A | 1 | a0001c0001t0003g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1708-9609C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161060999 | |||||||
chr6:161061019 | C | T | 6 | a0004c0004t0002g0006 a0004c0004t0002g0291 a0004c0004t0002g0303 others(3): Show |
8 | HG02145.hp2 HG03041.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.1708-9589C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161061019 | |||||||
chr6:161061091 | G | A | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1708-9517G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161061091 | |||||||
chr6:161061436 | A | G | 6 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG01243.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1708-9172A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161061436 | |||||||
chr6:161061462 | T | C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0104 others(31): Show |
35 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.1708-9146T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161061462 | |||||||
chr6:161061788 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1708-8820G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161061788 | |||||||
chr6:161062191 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1708-8417A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161062191 | |||||||
chr6:161062338 | G | T | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1708-8270G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161062338 | |||||||
chr6:161062350 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1708-8258T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161062350 | |||||||
chr6:161062456 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1708-8152T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161062456 | |||||||
chr6:161062555 | C | A | 33 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0104 others(30): Show |
34 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1708-8053C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161062555 | |||||||
chr6:161062674 | C | T | 9 | a0001c0001t0002g0053 a0001c0001t0002g0222 a0001c0001t0002g0223 others(6): Show |
9 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1708-7934C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161062674 | |||||||
chr6:161062867 | AGTTT | A | 4 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0134 others(1): Show |
4 | HG02040.hp2 NA18941.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.1708-7730_1708-772 others(8): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161062867 | ||||||
chr6:161062917 | C | CT | 202 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0026 others(199): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1708-7689dupT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161062917 | ||||||
chr6:161062977 | A | G | 9 | a0001c0001t0002g0053 a0001c0001t0002g0222 a0001c0001t0002g0223 others(6): Show |
9 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1708-7631A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161062977 | |||||||
chr6:161062985 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0041 |
2 | HG00733.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.1708-7623T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161062985 | |||||||
chr6:161063021 | A | G | 1 | a0002c0012t0004g0285 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1708-7587A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161063021 | |||||||
chr6:161063054 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1708-7554T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161063054 | |||||||
chr6:161063183 | A | C | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1708-7425A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161063183 | |||||||
chr6:161063341 | C | G | 40 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0098 others(37): Show |
41 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.1708-7267C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161063341 | |||||||
chr6:161063431 | A | G | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1708-7177A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161063431 | |||||||
chr6:161063479 | G | A | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1708-7129G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161063479 | |||||||
chr6:161064476 | C | A | 39 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0098 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1708-6132C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161064476 | |||||||
chr6:161064564 | G | A | 7 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(4): Show |
7 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1708-6044G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161064564 | |||||||
chr6:161064686 | A | G | 10 | a0001c0001t0001g0080 a0001c0001t0002g0052 a0001c0001t0002g0075 others(7): Show |
10 | HG02040.hp2 NA18941.hp2 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.1708-5922A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161064686 | |||||||
chr6:161064828 | G | A | 1 | a0002c0002t0002g0025 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1708-5780G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161064828 | |||||||
chr6:161064848 | A | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1708-5760A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161064848 | |||||||
chr6:161064911 | G | T | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.1708-5697G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161064911 | |||||||
chr6:161065011 | G | A | 4 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(1): Show |
4 | HG02615.hp1 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1708-5597G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065011 | |||||||
chr6:161065104 | C | T | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1708-5504C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065104 | |||||||
chr6:161065130 | G | A | 11 | a0001c0001t0002g0053 a0001c0001t0002g0222 a0001c0001t0002g0223 others(8): Show |
11 | HG01109.hp2 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1708-5478G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065130 | |||||||
chr6:161065221 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1708-5387G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065221 | |||||||
chr6:161065278 | A | C | 1 | a0001c0001t0001g0282 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1708-5330A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065278 | |||||||
chr6:161065425 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1708-5183C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065425 | |||||||
chr6:161065555 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1708-5053A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065555 | |||||||
chr6:161065567 | G | T | 1 | a0001c0001t0002g0030 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1708-5041G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065567 | |||||||
chr6:161065665 | A | G | 90 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0098 others(87): Show |
93 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1708-4943A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065665 | |||||||
chr6:161065720 | T | C | 6 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1708-4888T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065720 | |||||||
chr6:161065798 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0171 |
2 | HG02735.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1708-4810C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065798 | |||||||
chr6:161065862 | C | T | 2 | a0001c0001t0002g0046 a0001c0001t0002g0047 |
2 | HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1708-4746C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065862 | |||||||
chr6:161065870 | G | A | 7 | a0004c0004t0002g0006 a0004c0004t0002g0291 a0004c0004t0002g0303 others(4): Show |
9 | HG02145.hp2 HG02257.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1708-4738G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065870 | |||||||
chr6:161065887 | G | A | 200 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(197): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1708-4721G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065887 | |||||||
chr6:161065892 | C | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(197): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1708-4716C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065892 | |||||||
chr6:161065919 | A | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(197): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1708-4689A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065919 | |||||||
chr6:161065921 | G | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(197): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1708-4687G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065921 | |||||||
chr6:161065925 | A | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(197): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1708-4683A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161065925 | |||||||
chr6:161065937 | C | CA | 146 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(143): Show |
149 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.1708-4651dupA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161065937 | ||||||
chr6:161065937 | C | CAA | 86 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0055 others(83): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1708-4652_1708-465 others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161065937 | ||||||
chr6:161065937 | C | CAAA | 24 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0034 others(21): Show |
24 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.1708-4653_1708-465 others(7): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161065937 | ||||||
chr6:161065937 | CA | C | 17 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0002g0009 others(14): Show |
19 | HG01934.hp2 HG02257.hp1 HG02647.hp1 others(16): Show |
intron_variant | MODIFIER | c.1708-4651delA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161065937 | ||||||
chr6:161066121 | T | C | 6 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(3): Show |
6 | HG02647.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1708-4487T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161066121 | |||||||
chr6:161066345 | G | A | 42 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0098 others(39): Show |
43 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.1708-4263G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161066345 | |||||||
chr6:161066762 | G | T | 142 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0026 others(139): Show |
145 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1708-3846G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161066762 | |||||||
chr6:161066862 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1708-3746C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161066862 | |||||||
chr6:161066863 | G | A | 3 | a0001c0001t0001g0182 a0002c0012t0004g0285 a0012c0011t0004g0284 |
3 | HG01515.hp1 HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1708-3745G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161066863 | |||||||
chr6:161067051 | T | G | 92 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0080 others(89): Show |
95 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1708-3557T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161067051 | |||||||
chr6:161067167 | G | T | 1 | a0001c0001t0001g0272 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1708-3441G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161067167 | |||||||
chr6:161067301 | G | C | 1 | a0001c0001t0001g0155 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1708-3307G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161067301 | |||||||
chr6:161067528 | G | A | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1708-3080G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161067528 | |||||||
chr6:161067594 | AAATT | A | 9 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(6): Show |
9 | HG00738.hp2 HG00741.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1708-3010_1708-300 others(8): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161067594 | ||||||
chr6:161067643 | G | A | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1708-2965G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161067643 | |||||||
chr6:161067717 | C | T | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.1708-2891C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161067717 | |||||||
chr6:161068106 | C | T | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1708-2502C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161068106 | |||||||
chr6:161068300 | A | T | 203 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(200): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1708-2308A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161068300 | |||||||
chr6:161068456 | G | A | 302 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(299): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.1708-2152G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161068456 | |||||||
chr6:161068602 | T | G | 1 | a0001c0001t0002g0301 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1708-2006T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161068602 | |||||||
chr6:161068817 | G | A | 5 | a0001c0005t0002g0314 a0001c0005t0002g0322 a0001c0005t0002g0328 others(2): Show |
5 | HG01928.hp2 HG01934.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1708-1791G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161068817 | |||||||
chr6:161069155 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1708-1453C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161069155 | |||||||
chr6:161069188 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0002g0075 |
2 | HG01515.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1708-1420C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161069188 | |||||||
chr6:161069227 | A | C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0026 others(220): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.1708-1381A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161069227 | |||||||
chr6:161069450 | G | A | 1 | a0007c0008t0002g0007 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1708-1158G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161069450 | |||||||
chr6:161069518 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1708-1090G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161069518 | |||||||
chr6:161069957 | T | G | 6 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0003g0043 others(3): Show |
7 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1708-651T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161069957 | |||||||
chr6:161070014 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0152 |
2 | HG02738.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1708-594C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161070014 | |||||||
chr6:161070091 | A | G | 11 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(8): Show |
11 | HG01934.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1708-517A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161070091 | |||||||
chr6:161070182 | G | A | 7 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(4): Show |
7 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1708-426G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161070182 | |||||||
chr6:161070230 | G | GT | 18 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(15): Show |
18 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.1708-371dupT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr6 | 161070230 | ||||||
chr6:161070377 | A | G | 4 | a0003c0003t0002g0307 a0003c0003t0002g0315 a0003c0003t0002g0319 others(1): Show |
4 | NA18954.hp1 NA18970.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1708-231A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161070377 | |||||||
chr6:161070564 | C | T | 6 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG01243.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1708-44C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 3/26 | chr6 | 161070564 | |||||||
chr6:161070874 | A | T | 6 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG01243.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+24A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/26 | chr6 | 161070874 | |||||||
chr6:161070949 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1950+99C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/26 | chr6 | 161070949 | |||||||
chr6:161070957 | G | C | 1 | a0001c0001t0001g0027 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1950+107G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/26 | chr6 | 161070957 | |||||||
chr6:161071028 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1950+178G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/26 | chr6 | 161071028 | |||||||
chr6:161071159 | A | T | 1 | a0001c0001t0001g0162 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1950+309A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/26 | chr6 | 161071159 | |||||||
chr6:161071208 | G | T | 9 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1950+358G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/26 | chr6 | 161071208 | |||||||
chr6:161071211 | T | A | 9 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(6): Show |
9 | HG02040.hp1 HG02040.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.1950+361T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/26 | chr6 | 161071211 | |||||||
chr6:161071804 | C | T | 1 | a0001c0001t0002g0063 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1950+954C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/26 | chr6 | 161071804 | |||||||
chr6:161071848 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1950+998G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/26 | chr6 | 161071848 | |||||||
chr6:161071984 | G | A | 1 | a0001c0001t0002g0077 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1950+1134G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/26 | chr6 | 161071984 | |||||||
chr6:161072145 | C | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0106 a0001c0001t0001g0266 |
3 | NA19085.hp1 NA19086.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1950+1295C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/26 | chr6 | 161072145 | |||||||
chr6:161072323 | C | T | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1951-1143C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/26 | chr6 | 161072323 | |||||||
chr6:161072857 | C | T | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1951-609C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/26 | chr6 | 161072857 | |||||||
chr6:161072858 | C | T | 9 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0004c0004t0002g0006 others(6): Show |
11 | HG02145.hp2 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1951-608C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/26 | chr6 | 161072858 | |||||||
chr6:161072867 | C | G | 1 | a0001c0001t0003g0045 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1951-599C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/26 | chr6 | 161072867 | |||||||
chr6:161072947 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1951-519C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/26 | chr6 | 161072947 | |||||||
chr6:161073056 | A | G | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0221 |
3 | HG01243.hp1 HG02280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1951-410A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 4/26 | chr6 | 161073056 | |||||||
chr6:161073683 | C | G | 1 | a0001c0001t0001g0260 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2097+71C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161073683 | |||||||
chr6:161073691 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2097+79T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161073691 | |||||||
chr6:161073734 | A | T | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2097+122A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161073734 | |||||||
chr6:161074061 | G | A | 6 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2097+449G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161074061 | |||||||
chr6:161074088 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2097+476G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161074088 | |||||||
chr6:161074137 | G | A | 66 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0104 others(63): Show |
67 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.2097+525G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161074137 | |||||||
chr6:161074400 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2097+788A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161074400 | |||||||
chr6:161074626 | A | G | 88 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0098 others(85): Show |
91 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.2097+1014A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161074626 | |||||||
chr6:161074734 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2097+1122G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161074734 | |||||||
chr6:161075258 | G | A | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2097+1646G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161075258 | |||||||
chr6:161075304 | G | A | 1 | a0001c0001t0002g0317 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2097+1692G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161075304 | |||||||
chr6:161075609 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2097+1997C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161075609 | |||||||
chr6:161075703 | C | T | 1 | a0001c0001t0003g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2097+2091C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161075703 | |||||||
chr6:161075753 | G | A | 301 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(298): Show |
310 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.2097+2141G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161075753 | |||||||
chr6:161075871 | G | A | 36 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0104 others(33): Show |
37 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.2097+2259G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161075871 | |||||||
chr6:161075879 | A | C | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2097+2267A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161075879 | |||||||
chr6:161075931 | G | A | 36 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0104 others(33): Show |
37 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.2097+2319G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161075931 | |||||||
chr6:161076150 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2097+2538A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161076150 | |||||||
chr6:161076162 | G | T | 302 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(299): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.2097+2550G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161076162 | |||||||
chr6:161076262 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | NA18964.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.2097+2650G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161076262 | |||||||
chr6:161076667 | A | G | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.2097+3055A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161076667 | |||||||
chr6:161076682 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2097+3070G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161076682 | |||||||
chr6:161076708 | C | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0080 a0001c0001t0001g0098 others(32): Show |
36 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.2097+3096C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161076708 | |||||||
chr6:161076747 | A | C | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2097+3135A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161076747 | |||||||
chr6:161076861 | G | A | 11 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(8): Show |
11 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.2097+3249G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161076861 | |||||||
chr6:161076894 | G | C | 1 | a0001c0001t0001g0280 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2097+3282G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161076894 | |||||||
chr6:161076934 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0041 |
2 | HG00733.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.2097+3322G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161076934 | |||||||
chr6:161077032 | T | C | 3 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0312 |
3 | HG03491.hp1 HG03492.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2097+3420T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161077032 | |||||||
chr6:161077080 | A | C | 16 | a0001c0001t0001g0187 a0001c0001t0002g0029 a0001c0001t0002g0030 others(13): Show |
18 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.2097+3468A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161077080 | |||||||
chr6:161077185 | A | G | 1 | a0001c0001t0002g0297 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2097+3573A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161077185 | |||||||
chr6:161077279 | T | C | 319 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(316): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.2098-3602T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161077279 | |||||||
chr6:161077295 | G | A | 39 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0051 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.2098-3586G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161077295 | |||||||
chr6:161077440 | G | C | 49 | a0001c0001t0001g0005 a0001c0001t0001g0080 a0001c0001t0001g0098 others(46): Show |
50 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.2098-3441G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161077440 | |||||||
chr6:161077876 | T | A | 33 | a0001c0001t0001g0005 a0001c0001t0001g0080 a0001c0001t0001g0098 others(30): Show |
34 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.2098-3005T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161077876 | |||||||
chr6:161077893 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2098-2988A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161077893 | |||||||
chr6:161077902 | C | T | 1 | a0003c0003t0002g0307 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2098-2979C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161077902 | |||||||
chr6:161078138 | G | T | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2098-2743G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161078138 | |||||||
chr6:161078230 | A | G | 9 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0004c0004t0002g0006 others(6): Show |
11 | HG02145.hp2 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2098-2651A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161078230 | |||||||
chr6:161078283 | G | T | 1 | a0001c0001t0001g0105 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2098-2598G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161078283 | |||||||
chr6:161078299 | C | T | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2098-2582C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161078299 | |||||||
chr6:161078304 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0257 |
2 | HG00673.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.2098-2577G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161078304 | |||||||
chr6:161078403 | A | T | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2098-2478A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161078403 | |||||||
chr6:161078461 | G | A | 285 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(282): Show |
292 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.2098-2420G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161078461 | |||||||
chr6:161078727 | C | T | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2098-2154C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161078727 | |||||||
chr6:161078850 | G | A | 189 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(186): Show |
195 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.2098-2031G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161078850 | |||||||
chr6:161078866 | T | C | 302 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(299): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.2098-2015T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161078866 | |||||||
chr6:161078948 | T | C | 1 | a0002c0002t0002g0023 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2098-1933T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161078948 | |||||||
chr6:161078970 | T | C | 7 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(4): Show |
7 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2098-1911T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161078970 | |||||||
chr6:161078979 | C | T | 1 | a0004c0004t0002g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2098-1902C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161078979 | |||||||
chr6:161079010 | T | C | 1 | a0001c0001t0002g0110 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2098-1871T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161079010 | |||||||
chr6:161079133 | G | A | 17 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(14): Show |
17 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.2098-1748G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161079133 | |||||||
chr6:161079216 | G | GA | 73 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0080 others(70): Show |
76 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.2098-1647dupA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr6 | 161079216 | ||||||
chr6:161079216 | G | GAA | 207 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0026 others(204): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.2098-1648_2098-164 others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr6 | 161079216 | ||||||
chr6:161079216 | G | GAAA | 6 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0197 others(3): Show |
6 | HG01358.hp2 HG01928.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2098-1649_2098-164 others(7): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr6 | 161079216 | ||||||
chr6:161079216 | G | GAAAA | 13 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(10): Show |
13 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.2098-1650_2098-164 others(8): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr6 | 161079216 | ||||||
chr6:161079244 | A | G | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2098-1637A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161079244 | |||||||
chr6:161079299 | C | T | 1 | a0002c0012t0004g0285 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2098-1582C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161079299 | |||||||
chr6:161079316 | G | C | 1 | a0001c0001t0002g0090 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2098-1565G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161079316 | |||||||
chr6:161079424 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0026 others(134): Show |
143 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.2098-1457G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161079424 | |||||||
chr6:161079492 | G | A | 2 | a0006c0009t0002g0286 a0006c0009t0002g0287 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2098-1389G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161079492 | |||||||
chr6:161079499 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2098-1382C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161079499 | |||||||
chr6:161079624 | C | T | 1 | a0001c0001t0003g0045 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2098-1257C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161079624 | |||||||
chr6:161079718 | T | G | 319 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(316): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.2098-1163T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161079718 | |||||||
chr6:161079842 | C | G | 319 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(316): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.2098-1039C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161079842 | |||||||
chr6:161080008 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2098-873C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161080008 | |||||||
chr6:161080287 | T | C | 302 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(299): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.2098-594T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161080287 | |||||||
chr6:161080506 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2098-375G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161080506 | |||||||
chr6:161080546 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2098-335A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161080546 | |||||||
chr6:161080709 | C | T | 3 | a0001c0001t0002g0003 a0001c0001t0002g0308 a0001c0001t0002g0326 |
5 | HG01069.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2098-172C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161080709 | |||||||
chr6:161080787 | C | A | 1 | a0012c0011t0004g0284 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2098-94C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 5/26 | chr6 | 161080787 | |||||||
chr6:161081062 | C | T | 284 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(281): Show |
293 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.2255+24C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161081062 | |||||||
chr6:161081295 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2255+257G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161081295 | |||||||
chr6:161081306 | G | T | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2255+268G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161081306 | |||||||
chr6:161081413 | C | T | 2 | a0001c0001t0001g0330 a0001c0001t0002g0327 |
2 | HG00099.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.2255+375C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161081413 | |||||||
chr6:161081679 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2255+641G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161081679 | |||||||
chr6:161081738 | A | G | 9 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2255+700A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161081738 | |||||||
chr6:161081741 | G | A | 1 | a0001c0001t0002g0062 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2255+703G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161081741 | |||||||
chr6:161081748 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2255+710G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161081748 | |||||||
chr6:161081938 | A | C | 1 | a0001c0001t0002g0116 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2255+900A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161081938 | |||||||
chr6:161081984 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2255+946G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161081984 | |||||||
chr6:161081992 | T | C | 2 | a0001c0001t0001g0159 a0001c0001t0007g0295 |
2 | HG02738.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2255+954T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161081992 | |||||||
chr6:161082052 | G | A | 6 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2255+1014G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161082052 | |||||||
chr6:161082306 | A | G | 1 | a0002c0002t0002g0025 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2255+1268A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161082306 | |||||||
chr6:161082438 | CT | C | 299 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(296): Show |
308 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.2255+1404delT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr6 | 161082438 | ||||||
chr6:161082720 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2255+1682C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161082720 | |||||||
chr6:161082892 | C | T | 293 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(290): Show |
302 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.2256-1609C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161082892 | |||||||
chr6:161082968 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2256-1533C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161082968 | |||||||
chr6:161082974 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2256-1527G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161082974 | |||||||
chr6:161083307 | G | A | 6 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG01243.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2256-1194G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161083307 | |||||||
chr6:161083603 | A | G | 10 | a0001c0001t0001g0137 a0001c0001t0001g0150 a0001c0001t0001g0155 others(7): Show |
10 | HG02148.hp1 NA18940.hp1 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.2256-898A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161083603 | |||||||
chr6:161083665 | A | G | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.2256-836A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161083665 | |||||||
chr6:161083816 | A | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0297 a0001c0001t0002g0298 others(4): Show |
7 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2256-685A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161083816 | |||||||
chr6:161083837 | C | G | 1 | a0001c0001t0001g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2256-664C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161083837 | |||||||
chr6:161084035 | A | C | 7 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(4): Show |
7 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.2256-466A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161084035 | |||||||
chr6:161084171 | A | G | 19 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0222 others(16): Show |
21 | HG01934.hp2 HG02145.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.2256-330A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161084171 | |||||||
chr6:161084259 | G | A | 7 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(4): Show |
7 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2256-242G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 6/26 | chr6 | 161084259 | |||||||
chr6:161084623 | A | G | 1 | a0001c0001t0001g0002 | 3 | HG02258.hp2 HG02559.hp2 HG03130.hp2 |
splice_region_variant&intron_variant | LOW | c.2372+6A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 7/26 | chr6 | 161084623 | |||||||
chr6:161084666 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2372+49C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 7/26 | chr6 | 161084666 | |||||||
chr6:161084879 | G | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0104 |
2 | NA18978.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2372+262G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 7/26 | chr6 | 161084879 | |||||||
chr6:161084884 | C | A | 1 | a0001c0001t0001g0259 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2372+267C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 7/26 | chr6 | 161084884 | |||||||
chr6:161084926 | C | T | 7 | a0001c0001t0002g0051 a0001c0001t0002g0060 a0001c0001t0002g0068 others(4): Show |
7 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(4): Show |
intron_variant | MODIFIER | c.2372+309C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 7/26 | chr6 | 161084926 | |||||||
chr6:161084990 | C | CA | 8 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0082 others(5): Show |
8 | HG02015.hp2 HG02451.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.2372+381dupA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr6 | 161084990 | ||||||
chr6:161085024 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0105 a0001c0001t0001g0106 others(1): Show |
4 | NA18957.hp2 NA19085.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.2372+407G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 7/26 | chr6 | 161085024 | |||||||
chr6:161085097 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2372+480G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 7/26 | chr6 | 161085097 | |||||||
chr6:161085145 | CA | C | 279 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(276): Show |
288 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.2372+542delA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr6 | 161085145 | ||||||
chr6:161085195 | G | T | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2372+578G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 7/26 | chr6 | 161085195 | |||||||
chr6:161085202 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2372+585A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 7/26 | chr6 | 161085202 | |||||||
chr6:161085509 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2373-870G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 7/26 | chr6 | 161085509 | |||||||
chr6:161085807 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2373-572C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 7/26 | chr6 | 161085807 | |||||||
chr6:161085907 | G | T | 290 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(287): Show |
299 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.2373-472G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 7/26 | chr6 | 161085907 | |||||||
chr6:161085938 | T | C | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2373-441T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 7/26 | chr6 | 161085938 | |||||||
chr6:161086198 | A | G | 1 | a0002c0002t0002g0023 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2373-181A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 7/26 | chr6 | 161086198 | |||||||
chr6:161086256 | A | G | 6 | a0001c0001t0002g0032 a0001c0001t0002g0061 a0001c0001t0002g0064 others(3): Show |
6 | HG00423.hp2 NA18947.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.2373-123A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 7/26 | chr6 | 161086256 | |||||||
chr6:161086522 | T | G | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2472+44T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 8/26 | chr6 | 161086522 | |||||||
chr6:161086752 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2556+85A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 9/26 | chr6 | 161086752 | |||||||
chr6:161086788 | A | G | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2556+121A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 9/26 | chr6 | 161086788 | |||||||
chr6:161086872 | G | C | 1 | a0001c0001t0001g0140 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2556+205G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 9/26 | chr6 | 161086872 | |||||||
chr6:161086874 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2556+207G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 9/26 | chr6 | 161086874 | |||||||
chr6:161087217 | C | A | 3 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 |
3 | HG01891.hp1 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2557-471C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 9/26 | chr6 | 161087217 | |||||||
chr6:161087373 | G | T | 4 | a0001c0001t0006g0039 a0005c0006t0001g0031 a0005c0006t0001g0038 others(1): Show |
4 | NA19002.hp2 NA19057.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.2557-315G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 9/26 | chr6 | 161087373 | |||||||
chr6:161087404 | C | G | 2 | a0006c0009t0002g0286 a0006c0009t0002g0287 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2557-284C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 9/26 | chr6 | 161087404 | |||||||
chr6:161087406 | G | A | 208 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(205): Show |
214 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.2557-282G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 9/26 | chr6 | 161087406 | |||||||
chr6:161087971 | T | A | 305 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(302): Show |
314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.2823+17T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 10/26 | chr6 | 161087971 | |||||||
chr6:161088396 | T | A | 1 | a0001c0001t0001g0236 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2823+442T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 10/26 | chr6 | 161088396 | |||||||
chr6:161088445 | C | T | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2823+491C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 10/26 | chr6 | 161088445 | |||||||
chr6:161088511 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(257): Show |
267 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.2823+557T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 10/26 | chr6 | 161088511 | |||||||
chr6:161088566 | G | A | 4 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0006c0009t0002g0286 others(1): Show |
4 | HG02647.hp1 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2823+612G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 10/26 | chr6 | 161088566 | |||||||
chr6:161088689 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2824-633C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 10/26 | chr6 | 161088689 | |||||||
chr6:161088690 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2824-632C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 10/26 | chr6 | 161088690 | |||||||
chr6:161088815 | T | A | 9 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0004c0004t0002g0006 others(6): Show |
11 | HG02145.hp2 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2824-507T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 10/26 | chr6 | 161088815 | |||||||
chr6:161089015 | TACAC | T | 9 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0004c0004t0002g0006 others(6): Show |
11 | HG02145.hp2 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2824-298_2824-295d others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr6 | 161089015 | ||||||
chr6:161089083 | A | G | 1 | a0001c0001t0002g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2824-239A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 10/26 | chr6 | 161089083 | |||||||
chr6:161089163 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2824-159T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 10/26 | chr6 | 161089163 | |||||||
chr6:161089814 | A | G | 44 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0035 others(41): Show |
45 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.2973+343A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161089814 | |||||||
chr6:161089942 | A | G | 44 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0035 others(41): Show |
45 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.2973+471A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161089942 | |||||||
chr6:161090183 | A | G | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2973+712A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161090183 | |||||||
chr6:161090196 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2973+725T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161090196 | |||||||
chr6:161090214 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2973+743T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161090214 | |||||||
chr6:161090360 | CAGGGCAG others(88): Show |
C | 1 | a0001c0001t0002g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2974-953_2974-859d others(97): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr6 | 161090360 | ||||||
chr6:161090393 | C | T | 179 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(176): Show |
186 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.2973+922C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161090393 | |||||||
chr6:161090434 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2974-945G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161090434 | |||||||
chr6:161090461 | A | C | 1 | a0001c0001t0002g0317 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2974-918A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161090461 | |||||||
chr6:161090498 | C | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2974-881C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161090498 | |||||||
chr6:161090521 | T | C | 1 | a0001c0001t0003g0045 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2974-858T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161090521 | |||||||
chr6:161090526 | T | G | 44 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0035 others(41): Show |
45 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.2974-853T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161090526 | |||||||
chr6:161090607 | ATGGAGGG others(183): Show |
A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(230): Show |
240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.2974-737_2974-548d others(2): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr6 | 161090607 | ||||||
chr6:161090730 | T | A | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2974-649T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161090730 | |||||||
chr6:161090733 | T | A | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2974-646T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161090733 | |||||||
chr6:161090964 | C | A | 12 | a0001c0001t0002g0009 a0001c0001t0002g0222 a0001c0001t0002g0223 others(9): Show |
14 | HG02145.hp2 HG02257.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.2974-415C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161090964 | |||||||
chr6:161091003 | G | A | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.2974-376G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161091003 | |||||||
chr6:161091067 | T | A | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2974-312T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161091067 | |||||||
chr6:161091327 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2974-52A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161091327 | |||||||
chr6:161091360 | C | G | 9 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0004c0004t0002g0006 others(6): Show |
11 | HG02145.hp2 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2974-19C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 11/26 | chr6 | 161091360 | |||||||
chr6:161092335 | T | A | 1 | a0001c0001t0002g0117 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3269+192T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 13/26 | chr6 | 161092335 | |||||||
chr6:161092363 | T | C | 1 | a0001c0001t0002g0288 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3269+220T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 13/26 | chr6 | 161092363 | |||||||
chr6:161092371 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02040.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.3269+228C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 13/26 | chr6 | 161092371 | |||||||
chr6:161092632 | G | A | 7 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(4): Show |
7 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.3270-346G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 13/26 | chr6 | 161092632 | |||||||
chr6:161092639 | C | CTTGGTTT others(17): Show |
6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.3270-339_3270-338i others(26): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 13/26 | chr6 | 161092639 | |||||||
chr6:161092640 | A | G | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.3270-338A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 13/26 | chr6 | 161092640 | |||||||
chr6:161093141 | G | A | 32 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0080 others(29): Show |
33 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.3348+85G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 14/26 | chr6 | 161093141 | |||||||
chr6:161094006 | A | G | 12 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0053 others(9): Show |
12 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3427+155A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161094006 | |||||||
chr6:161094351 | A | C | 21 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0208 others(18): Show |
21 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.3427+500A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161094351 | |||||||
chr6:161094457 | T | C | 1 | a0002c0002t0002g0018 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3427+606T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161094457 | |||||||
chr6:161094478 | A | G | 7 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(4): Show |
7 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.3427+627A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161094478 | |||||||
chr6:161094774 | A | G | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3427+923A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161094774 | |||||||
chr6:161094795 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3427+944A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161094795 | |||||||
chr6:161095043 | A | G | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3427+1192A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161095043 | |||||||
chr6:161095082 | C | T | 1 | a0012c0011t0004g0284 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3427+1231C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161095082 | |||||||
chr6:161095134 | A | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02735.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3427+1283A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161095134 | |||||||
chr6:161095271 | G | A | 6 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3427+1420G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161095271 | |||||||
chr6:161095308 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3427+1457G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161095308 | |||||||
chr6:161095356 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3427+1505A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161095356 | |||||||
chr6:161095416 | G | A | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.3427+1565G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161095416 | |||||||
chr6:161095795 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3428-1285A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161095795 | |||||||
chr6:161095799 | T | G | 52 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(49): Show |
56 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.3428-1281T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161095799 | |||||||
chr6:161095893 | A | G | 2 | a0001c0007t0001g0248 a0001c0007t0001g0252 |
2 | HG00423.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.3428-1187A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161095893 | |||||||
chr6:161096087 | A | G | 7 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(4): Show |
7 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.3428-993A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161096087 | |||||||
chr6:161096109 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3428-971A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161096109 | |||||||
chr6:161096127 | T | C | 2 | a0001c0001t0001g0249 a0001c0001t0001g0256 |
2 | HG00597.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.3428-953T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161096127 | |||||||
chr6:161096258 | AT | A | 9 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0004c0004t0002g0006 others(6): Show |
11 | HG02145.hp2 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.3428-819delT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr6 | 161096258 | ||||||
chr6:161096431 | T | C | 1 | a0001c0001t0001g0010 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3428-649T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161096431 | |||||||
chr6:161096437 | C | G | 1 | a0001c0001t0001g0268 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3428-643C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161096437 | |||||||
chr6:161096689 | C | T | 1 | a0001c0001t0005g0161 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3428-391C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161096689 | |||||||
chr6:161096748 | C | G | 2 | a0001c0001t0002g0081 a0001c0001t0002g0107 |
2 | NA18950.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.3428-332C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161096748 | |||||||
chr6:161096816 | AT | A | 9 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0004c0004t0002g0006 others(6): Show |
11 | HG02145.hp2 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.3428-262delT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr6 | 161096816 | ||||||
chr6:161096886 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3428-194G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161096886 | |||||||
chr6:161096928 | T | C | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.3428-152T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161096928 | |||||||
chr6:161096932 | T | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(251): Show |
261 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.3428-148T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 15/26 | chr6 | 161096932 | |||||||
chr6:161097349 | A | G | 254 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(251): Show |
261 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.3524+173A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 16/26 | chr6 | 161097349 | |||||||
chr6:161097413 | C | G | 9 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3524+237C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 16/26 | chr6 | 161097413 | |||||||
chr6:161097482 | A | G | 290 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(287): Show |
299 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.3524+306A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 16/26 | chr6 | 161097482 | |||||||
chr6:161097781 | G | GT | 247 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(244): Show |
254 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.3525-487dupT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr6 | 161097781 | ||||||
chr6:161098023 | G | C | 1 | a0001c0001t0002g0145 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3525-255G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 16/26 | chr6 | 161098023 | |||||||
chr6:161098053 | C | G | 9 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0004c0004t0002g0006 others(6): Show |
11 | HG02145.hp2 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.3525-225C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 16/26 | chr6 | 161098053 | |||||||
chr6:161098154 | A | G | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3525-124A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 16/26 | chr6 | 161098154 | |||||||
chr6:161098216 | A | G | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.3525-62A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 16/26 | chr6 | 161098216 | |||||||
chr6:161098261 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0099 |
2 | HG00609.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.3525-17T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 16/26 | chr6 | 161098261 | |||||||
chr6:161098467 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3674+40C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161098467 | |||||||
chr6:161098505 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3674+78T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161098505 | |||||||
chr6:161098543 | G | A | 7 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(4): Show |
7 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.3674+116G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161098543 | |||||||
chr6:161098576 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3674+149C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161098576 | |||||||
chr6:161098768 | A | G | 36 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0029 others(33): Show |
38 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(35): Show |
intron_variant | MODIFIER | c.3674+341A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161098768 | |||||||
chr6:161098994 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3674+567C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161098994 | |||||||
chr6:161099081 | A | G | 4 | a0003c0003t0002g0307 a0003c0003t0002g0315 a0003c0003t0002g0319 others(1): Show |
4 | NA18954.hp1 NA18970.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.3674+654A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161099081 | |||||||
chr6:161099116 | A | G | 19 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0029 others(16): Show |
21 | HG02145.hp2 HG02257.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.3674+689A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161099116 | |||||||
chr6:161099194 | A | G | 305 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(302): Show |
314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.3674+767A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161099194 | |||||||
chr6:161099318 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3674+891T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161099318 | |||||||
chr6:161099528 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3674+1101T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161099528 | |||||||
chr6:161099576 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3674+1149G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161099576 | |||||||
chr6:161099711 | T | C | 25 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0029 others(22): Show |
27 | HG01934.hp2 HG02145.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.3674+1284T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161099711 | |||||||
chr6:161099739 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.3674+1312A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161099739 | |||||||
chr6:161099777 | C | T | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.3674+1350C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161099777 | |||||||
chr6:161099805 | G | A | 319 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(316): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.3674+1378G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161099805 | |||||||
chr6:161099878 | T | C | 1 | a0002c0002t0002g0025 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3674+1451T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161099878 | |||||||
chr6:161099912 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3674+1485G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161099912 | |||||||
chr6:161100007 | A | G | 46 | a0001c0001t0001g0281 a0001c0001t0002g0001 a0001c0001t0002g0004 others(43): Show |
50 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.3674+1580A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161100007 | |||||||
chr6:161100039 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3674+1612G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161100039 | |||||||
chr6:161100208 | G | A | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3675-1684G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161100208 | |||||||
chr6:161100274 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3675-1618G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161100274 | |||||||
chr6:161100300 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0097 |
3 | NA18954.hp2 NA18964.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.3675-1592G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161100300 | |||||||
chr6:161100330 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3675-1562A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161100330 | |||||||
chr6:161100510 | C | T | 8 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0231 others(5): Show |
8 | HG00621.hp2 HG02155.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.3675-1382C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161100510 | |||||||
chr6:161100639 | A | C | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3675-1253A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161100639 | |||||||
chr6:161100648 | A | G | 23 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(20): Show |
23 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.3675-1244A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161100648 | |||||||
chr6:161100688 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3675-1204G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161100688 | |||||||
chr6:161100741 | G | A | 3 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 |
3 | HG01891.hp1 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3675-1151G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161100741 | |||||||
chr6:161100747 | AT | A | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.3675-1143delT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr6 | 161100747 | ||||||
chr6:161100832 | A | G | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.3675-1060A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161100832 | |||||||
chr6:161101131 | C | T | 7 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(4): Show |
7 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.3675-761C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161101131 | |||||||
chr6:161101333 | G | A | 289 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(286): Show |
298 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.3675-559G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161101333 | |||||||
chr6:161101364 | G | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(240): Show |
250 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.3675-528G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161101364 | |||||||
chr6:161101376 | TTAAATG | T | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3675-512_3675-507d others(8): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr6 | 161101376 | ||||||
chr6:161101446 | A | G | 30 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0208 others(27): Show |
32 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(29): Show |
intron_variant | MODIFIER | c.3675-446A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161101446 | |||||||
chr6:161101563 | T | A | 1 | a0001c0001t0002g0004 | 2 | HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.3675-329T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161101563 | |||||||
chr6:161101645 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3675-247C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161101645 | |||||||
chr6:161101703 | C | T | 6 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3675-189C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 17/26 | chr6 | 161101703 | |||||||
chr6:161102067 | A | G | 9 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0004c0004t0002g0006 others(6): Show |
11 | HG02145.hp2 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.3775+75A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 18/26 | chr6 | 161102067 | |||||||
chr6:161102209 | G | C | 1 | a0001c0001t0003g0045 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3775+217G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 18/26 | chr6 | 161102209 | |||||||
chr6:161102802 | T | TA | 16 | a0001c0001t0001g0054 a0001c0001t0001g0082 a0001c0001t0001g0083 others(13): Show |
16 | HG01243.hp1 HG03098.hp1 NA18940.hp1 others(13): Show |
intron_variant | MODIFIER | c.3856+45dupA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr6 | 161102802 | ||||||
chr6:161102802 | TA | T | 54 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(51): Show |
56 | HG00639.hp1 HG00738.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.3856+45delA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr6 | 161102802 | ||||||
chr6:161102802 | TAA | T | 8 | a0001c0001t0001g0121 a0001c0001t0001g0126 a0001c0001t0002g0009 others(5): Show |
8 | HG01515.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.3856+44_3856+45del others(2): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr6 | 161102802 | ||||||
chr6:161102816 | A | C | 12 | a0001c0001t0002g0009 a0001c0001t0002g0222 a0001c0001t0002g0223 others(9): Show |
14 | HG02145.hp2 HG02257.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.3856+37A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161102816 | |||||||
chr6:161103002 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3856+223A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161103002 | |||||||
chr6:161103035 | A | T | 7 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(4): Show |
7 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.3856+256A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161103035 | |||||||
chr6:161103328 | G | A | 6 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3856+549G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161103328 | |||||||
chr6:161103512 | G | A | 2 | a0001c0001t0001g0126 a0008c0021t0001g0127 |
2 | HG00639.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.3856+733G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161103512 | |||||||
chr6:161103524 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3856+745C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161103524 | |||||||
chr6:161103678 | G | A | 6 | a0001c0001t0001g0058 a0001c0001t0001g0216 a0001c0001t0001g0217 others(3): Show |
6 | HG02145.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3856+899G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161103678 | |||||||
chr6:161103817 | A | G | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.3856+1038A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161103817 | |||||||
chr6:161103955 | A | G | 300 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(297): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.3856+1176A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161103955 | |||||||
chr6:161104057 | A | T | 9 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.3856+1278A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161104057 | |||||||
chr6:161104085 | G | A | 1 | a0001c0001t0002g0075 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3856+1306G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161104085 | |||||||
chr6:161104213 | A | G | 305 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(302): Show |
314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.3856+1434A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161104213 | |||||||
chr6:161104299 | G | A | 14 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0222 others(11): Show |
16 | HG02145.hp2 HG02257.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.3856+1520G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161104299 | |||||||
chr6:161104355 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0273 |
2 | HG00544.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3856+1576G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161104355 | |||||||
chr6:161104415 | C | CA | 12 | a0001c0001t0001g0150 a0001c0001t0001g0187 a0001c0001t0001g0243 others(9): Show |
12 | HG00544.hp2 HG00558.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.3856+1654dupA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr6 | 161104415 | ||||||
chr6:161104415 | C | CAA | 10 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0222 others(7): Show |
11 | HG02145.hp2 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.3856+1653_3856+165 others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr6 | 161104415 | ||||||
chr6:161104415 | CA | C | 9 | a0001c0001t0001g0084 a0001c0001t0001g0149 a0001c0001t0001g0186 others(6): Show |
10 | HG02056.hp2 HG02132.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.3856+1654delA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr6 | 161104415 | ||||||
chr6:161104451 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3856+1672C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161104451 | |||||||
chr6:161104495 | C | T | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3856+1716C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161104495 | |||||||
chr6:161104510 | G | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
4 | NA18747.hp1 NA19000.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.3856+1731G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161104510 | |||||||
chr6:161104630 | A | G | 305 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(302): Show |
314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.3856+1851A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161104630 | |||||||
chr6:161104674 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3857-1840G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161104674 | |||||||
chr6:161104709 | C | CA | 79 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(76): Show |
84 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.3857-1789dupA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr6 | 161104709 | ||||||
chr6:161104709 | C | CAA | 172 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(169): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.3857-1790_3857-178 others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr6 | 161104709 | ||||||
chr6:161104709 | C | CAAA | 17 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0055 others(14): Show |
17 | HG00609.hp2 HG02040.hp1 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.3857-1791_3857-178 others(7): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr6 | 161104709 | ||||||
chr6:161104820 | G | T | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3857-1694G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161104820 | |||||||
chr6:161104855 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3857-1659A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161104855 | |||||||
chr6:161105146 | A | G | 6 | a0001c0001t0001g0058 a0001c0001t0001g0216 a0001c0001t0001g0217 others(3): Show |
6 | HG02145.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3857-1368A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161105146 | |||||||
chr6:161105409 | A | G | 7 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(4): Show |
7 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.3857-1105A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161105409 | |||||||
chr6:161105424 | A | T | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.3857-1090A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161105424 | |||||||
chr6:161105454 | T | C | 1 | a0001c0001t0002g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3857-1060T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161105454 | |||||||
chr6:161105475 | G | A | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.3857-1039G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161105475 | |||||||
chr6:161105477 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3857-1037G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161105477 | |||||||
chr6:161105598 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.3857-916C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161105598 | |||||||
chr6:161105641 | G | T | 263 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(260): Show |
270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.3857-873G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161105641 | |||||||
chr6:161105793 | G | A | 7 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(4): Show |
7 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.3857-721G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161105793 | |||||||
chr6:161105800 | G | C | 11 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(8): Show |
11 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.3857-714G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161105800 | |||||||
chr6:161105838 | GT | G | 275 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(272): Show |
282 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.3857-661delT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr6 | 161105838 | ||||||
chr6:161105840 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3857-674T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161105840 | |||||||
chr6:161105842 | T | G | 1 | a0001c0001t0001g0112 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3857-672T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161105842 | |||||||
chr6:161105856 | G | C | 1 | a0001c0007t0001g0248 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.3857-658G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161105856 | |||||||
chr6:161106280 | A | G | 1 | a0001c0001t0002g0317 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3857-234A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161106280 | |||||||
chr6:161106362 | A | G | 9 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0004c0004t0002g0006 others(6): Show |
11 | HG02145.hp2 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.3857-152A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161106362 | |||||||
chr6:161106380 | G | T | 1 | a0001c0001t0001g0203 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3857-134G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 19/26 | chr6 | 161106380 | |||||||
chr6:161106752 | T | C | 15 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(12): Show |
17 | HG02145.hp2 HG02257.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.4048+47T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | chr6 | 161106752 | |||||||
chr6:161106805 | T | C | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.4048+100T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | chr6 | 161106805 | |||||||
chr6:161106826 | A | G | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4048+121A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | chr6 | 161106826 | |||||||
chr6:161106956 | C | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(296): Show |
308 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.4048+251C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | chr6 | 161106956 | |||||||
chr6:161107008 | C | G | 1 | a0001c0001t0001g0209 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4048+303C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | chr6 | 161107008 | |||||||
chr6:161107042 | A | ACG | 3 | a0001c0001t0002g0003 a0001c0001t0002g0308 a0001c0001t0002g0326 |
5 | HG01069.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.4048+345_4048+346d others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr6 | 161107042 | ||||||
chr6:161107042 | ACG | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(149): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.4048+345_4048+346d others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr6 | 161107042 | ||||||
chr6:161107043 | C | T | 6 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.4048+338C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | chr6 | 161107043 | |||||||
chr6:161107046 | G | A | 1 | a0001c0001t0002g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4048+341G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | chr6 | 161107046 | |||||||
chr6:161107048 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4048+343G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | chr6 | 161107048 | |||||||
chr6:161107048 | G | GCA | 22 | a0001c0001t0001g0056 a0001c0001t0001g0114 a0001c0001t0001g0128 others(19): Show |
22 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.4048+344_4048+345i others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr6 | 161107048 | ||||||
chr6:161107048 | G | GCACACA | 3 | a0002c0012t0004g0285 a0004c0004t0002g0303 a0012c0011t0004g0284 |
3 | HG02055.hp1 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4048+344_4048+345i others(8): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr6 | 161107048 | ||||||
chr6:161107048 | G | GCACACAC others(1): Show |
7 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0004c0004t0002g0006 others(4): Show |
9 | HG02145.hp2 HG02257.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.4048+344_4048+345i others(10): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr6 | 161107048 | ||||||
chr6:161107048 | G | GCACACAC others(3): Show |
1 | a0004c0004t0002g0304 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4048+344_4048+345i others(12): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr6 | 161107048 | ||||||
chr6:161107048 | GCGCA | G | 13 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(10): Show |
13 | HG00408.hp1 HG01258.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.4048+345_4048+348d others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr6 | 161107048 | ||||||
chr6:161107048 | GCGCACA | G | 39 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0051 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.4048+345_4048+350d others(8): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr6 | 161107048 | ||||||
chr6:161107050 | G | A | 105 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0055 others(102): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.4048+345G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | chr6 | 161107050 | |||||||
chr6:161107050 | G | GCA | 8 | a0001c0001t0001g0330 a0001c0001t0002g0008 a0001c0001t0002g0317 others(5): Show |
9 | HG00099.hp2 HG00733.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.4048+373_4048+374d others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr6 | 161107050 | ||||||
chr6:161107050 | G | GCACA | 4 | a0001c0005t0002g0322 a0001c0005t0002g0328 a0001c0005t0002g0329 others(1): Show |
4 | HG01928.hp2 HG01934.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.4048+371_4048+374d others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr6 | 161107050 | ||||||
chr6:161107050 | G | GCACACAC others(1): Show |
3 | a0001c0001t0002g0029 a0001c0001t0002g0048 a0001c0001t0002g0049 |
3 | HG03225.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4048+367_4048+374d others(10): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr6 | 161107050 | ||||||
chr6:161107050 | G | GCACACAC others(3): Show |
1 | a0001c0001t0002g0046 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4048+365_4048+374d others(12): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr6 | 161107050 | ||||||
chr6:161107050 | G | GCGCACAC others(3): Show |
1 | a0001c0001t0002g0030 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4048+346_4048+347i others(12): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr6 | 161107050 | ||||||
chr6:161107073 | CACACACG others(5): Show |
C | 2 | a0006c0009t0002g0286 a0006c0009t0002g0287 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4048+369_4048+380d others(14): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | chr6 | 161107073 | |||||||
chr6:161107075 | CACACGCA others(3): Show |
C | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4048+371_4048+380d others(12): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | chr6 | 161107075 | |||||||
chr6:161107535 | C | G | 1 | a0001c0001t0001g0148 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4049-364C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | chr6 | 161107535 | |||||||
chr6:161107537 | G | A | 7 | a0001c0001t0002g0053 a0001c0001t0002g0288 a0001c0001t0002g0289 others(4): Show |
7 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.4049-362G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | chr6 | 161107537 | |||||||
chr6:161107545 | T | G | 3 | a0001c0001t0002g0004 a0001c0001t0002g0096 a0001c0001t0002g0111 |
4 | HG00323.hp1 HG01074.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.4049-354T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | chr6 | 161107545 | |||||||
chr6:161107547 | T | C | 1 | a0001c0001t0002g0118 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4049-352T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | chr6 | 161107547 | |||||||
chr6:161107615 | C | G | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.4049-284C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | chr6 | 161107615 | |||||||
chr6:161107703 | A | C | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.4049-196A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 20/26 | chr6 | 161107703 | |||||||
chr6:161108044 | G | T | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.4119+75G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 21/26 | chr6 | 161108044 | |||||||
chr6:161108154 | G | A | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4119+185G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 21/26 | chr6 | 161108154 | |||||||
chr6:161108285 | A | G | 42 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(39): Show |
42 | HG00639.hp1 HG00738.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.4119+316A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 21/26 | chr6 | 161108285 | |||||||
chr6:161108370 | G | C | 14 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(11): Show |
16 | HG02145.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.4120-373G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 21/26 | chr6 | 161108370 | |||||||
chr6:161108486 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4120-257G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 21/26 | chr6 | 161108486 | |||||||
chr6:161108503 | G | A | 4 | a0001c0001t0001g0196 a0001c0001t0001g0283 a0001c0001t0002g0029 others(1): Show |
4 | HG01891.hp1 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.4120-240G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 21/26 | chr6 | 161108503 | |||||||
chr6:161108526 | G | C | 134 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0120 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.4120-217G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 21/26 | chr6 | 161108526 | |||||||
chr6:161108646 | A | C | 51 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0033 others(48): Show |
52 | HG00323.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.4120-97A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 21/26 | chr6 | 161108646 | |||||||
chr6:161108648 | A | C | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.4120-95A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 21/26 | chr6 | 161108648 | |||||||
chr6:161108866 | C | T | 7 | a0001c0001t0001g0149 a0001c0001t0001g0186 a0001c0001t0001g0239 others(4): Show |
7 | HG02056.hp2 HG02132.hp1 HG02523.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.4236+7C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 22/26 | chr6 | 161108866 | |||||||
chr6:161109093 | A | G | 2 | a0002c0010t0002g0022 a0010c0017t0002g0206 |
2 | HG00738.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.4236+234A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 22/26 | chr6 | 161109093 | |||||||
chr6:161109101 | A | G | 5 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0002g0292 others(2): Show |
5 | HG01109.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4236+242A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 22/26 | chr6 | 161109101 | |||||||
chr6:161109156 | G | A | 21 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0208 others(18): Show |
21 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.4236+297G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 22/26 | chr6 | 161109156 | |||||||
chr6:161109272 | T | C | 27 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0208 others(24): Show |
27 | HG00738.hp1 HG01361.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.4236+413T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 22/26 | chr6 | 161109272 | |||||||
chr6:161109280 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4236+421T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 22/26 | chr6 | 161109280 | |||||||
chr6:161109481 | T | G | 6 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | HG01934.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.4237-274T>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 22/26 | chr6 | 161109481 | |||||||
chr6:161109927 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4396+13C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 23/26 | chr6 | 161109927 | |||||||
chr6:161109974 | G | C | 303 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(300): Show |
312 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.4396+60G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 23/26 | chr6 | 161109974 | |||||||
chr6:161109988 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4396+74G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 23/26 | chr6 | 161109988 | |||||||
chr6:161110195 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.4396+281T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 23/26 | chr6 | 161110195 | |||||||
chr6:161110364 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4396+450C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 23/26 | chr6 | 161110364 | |||||||
chr6:161110532 | G | C | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4396+618G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 23/26 | chr6 | 161110532 | |||||||
chr6:161110797 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4396+883C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 23/26 | chr6 | 161110797 | |||||||
chr6:161110806 | G | A | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4396+892G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 23/26 | chr6 | 161110806 | |||||||
chr6:161110940 | G | A | 1 | a0002c0002t0002g0020 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.4397-896G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 23/26 | chr6 | 161110940 | |||||||
chr6:161111316 | A | G | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.4397-520A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 23/26 | chr6 | 161111316 | |||||||
chr6:161111600 | A | T | 1 | a0001c0001t0001g0265 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.4397-236A>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 23/26 | chr6 | 161111600 | |||||||
chr6:161111615 | G | A | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4397-221G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 23/26 | chr6 | 161111615 | |||||||
chr6:161111648 | G | C | 52 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0033 others(49): Show |
52 | HG00609.hp2 HG00621.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.4397-188G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 23/26 | chr6 | 161111648 | |||||||
chr6:161111823 | CT | C | 288 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(285): Show |
295 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.4397-9delT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr6 | 161111823 | ||||||
chr6:161112182 | CTT | C | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.4519+228_4519+229d others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr6 | 161112182 | ||||||
chr6:161112203 | CTT | C | 111 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0033 others(108): Show |
115 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.4519+248_4519+249d others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr6 | 161112203 | ||||||
chr6:161112267 | T | C | 1 | a0001c0001t0002g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4519+309T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 24/26 | chr6 | 161112267 | |||||||
chr6:161112295 | C | T | 254 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(251): Show |
261 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.4519+337C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 24/26 | chr6 | 161112295 | |||||||
chr6:161112851 | ATTAT | A | 17 | a0001c0001t0002g0208 a0002c0002t0002g0013 a0002c0002t0002g0014 others(14): Show |
17 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.4626+83_4626+86del others(4): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr6 | 161112851 | ||||||
chr6:161112889 | C | T | 1 | a0001c0001t0005g0161 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.4626+115C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161112889 | |||||||
chr6:161112984 | T | C | 2 | a0002c0002t0002g0237 a0002c0002t0002g0238 |
2 | NA18956.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.4626+210T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161112984 | |||||||
chr6:161113023 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4626+249A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161113023 | |||||||
chr6:161113301 | T | C | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(268): Show |
278 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.4626+527T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161113301 | |||||||
chr6:161113515 | A | G | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.4626+741A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161113515 | |||||||
chr6:161113555 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4626+781C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161113555 | |||||||
chr6:161113561 | T | TA | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0003g0043 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.4626+793dupA | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr6 | 161113561 | ||||||
chr6:161113583 | C | T | 254 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(251): Show |
261 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.4626+809C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161113583 | |||||||
chr6:161113634 | G | C | 305 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(302): Show |
314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.4626+860G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161113634 | |||||||
chr6:161113761 | AT | A | 11 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0053 others(8): Show |
11 | HG01109.hp2 HG02451.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.4626+998delT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr6 | 161113761 | ||||||
chr6:161113790 | C | CT | 156 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0027 others(153): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.4626+1041dupT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr6 | 161113790 | ||||||
chr6:161113790 | C | CTT | 15 | a0001c0001t0001g0035 a0001c0001t0001g0177 a0001c0001t0001g0186 others(12): Show |
15 | HG01361.hp1 HG01361.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.4626+1040_4626+104 others(6): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr6 | 161113790 | ||||||
chr6:161113790 | CT | C | 9 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0092 others(6): Show |
9 | HG00639.hp1 NA18951.hp2 NA18985.hp2 others(6): Show |
intron_variant | MODIFIER | c.4626+1041delT | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr6 | 161113790 | ||||||
chr6:161113891 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4626+1117G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161113891 | |||||||
chr6:161114055 | G | A | 4 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0006c0009t0002g0286 others(1): Show |
4 | HG02647.hp1 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4627-1068G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161114055 | |||||||
chr6:161114119 | C | G | 4 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0006c0009t0002g0286 others(1): Show |
4 | HG02647.hp1 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4627-1004C>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161114119 | |||||||
chr6:161114159 | C | T | 4 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0006c0009t0002g0286 others(1): Show |
4 | HG02647.hp1 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4627-964C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161114159 | |||||||
chr6:161114160 | G | A | 1 | a0001c0001t0002g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4627-963G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161114160 | |||||||
chr6:161114275 | T | A | 1 | a0001c0001t0001g0265 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.4627-848T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161114275 | |||||||
chr6:161114288 | G | A | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4627-835G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161114288 | |||||||
chr6:161114299 | A | G | 4 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0006c0009t0002g0286 others(1): Show |
4 | HG02647.hp1 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4627-824A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161114299 | |||||||
chr6:161114398 | G | A | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4627-725G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161114398 | |||||||
chr6:161114430 | C | A | 4 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0006c0009t0002g0286 others(1): Show |
4 | HG02647.hp1 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4627-693C>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161114430 | |||||||
chr6:161114585 | C | T | 2 | a0001c0001t0002g0081 a0001c0001t0002g0107 |
2 | NA18950.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.4627-538C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161114585 | |||||||
chr6:161114592 | A | G | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0003g0043 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.4627-531A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161114592 | |||||||
chr6:161114647 | T | A | 1 | a0001c0001t0001g0035 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.4627-476T>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161114647 | |||||||
chr6:161114794 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4627-329G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161114794 | |||||||
chr6:161114795 | C | T | 3 | a0001c0005t0002g0328 a0001c0005t0002g0329 a0001c0018t0002g0320 |
3 | HG01928.hp2 HG01934.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.4627-328C>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161114795 | |||||||
chr6:161115014 | T | C | 5 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(2): Show |
5 | HG02145.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.4627-109T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 25/26 | chr6 | 161115014 | |||||||
chr6:161115451 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4806+149T>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 26/26 | chr6 | 161115451 | |||||||
chr6:161115509 | G | A | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4806+207G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 26/26 | chr6 | 161115509 | |||||||
chr6:161115746 | A | G | 4 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0006c0009t0002g0286 others(1): Show |
4 | HG02647.hp1 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4806+444A>G | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 26/26 | chr6 | 161115746 | |||||||
chr6:161115817 | G | C | 1 | a0001c0001t0001g0225 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4806+515G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 26/26 | chr6 | 161115817 | |||||||
chr6:161115818 | A | C | 1 | a0001c0001t0002g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4806+516A>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 26/26 | chr6 | 161115818 | |||||||
chr6:161115898 | G | C | 6 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0046 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.4806+596G>C | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 26/26 | chr6 | 161115898 | |||||||
chr6:161116290 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4807-560G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 26/26 | chr6 | 161116290 | |||||||
chr6:161116502 | G | A | 1 | a0002c0002t0002g0015 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4807-348G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 26/26 | chr6 | 161116502 | |||||||
chr6:161116613 | G | T | 1 | a0001c0001t0001g0085 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.4807-237G>T | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 26/26 | chr6 | 161116613 | |||||||
chr6:161116691 | TGTTCATT others(34): Show |
T | 1 | a0001c0001t0001g0183 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.4807-158_4807-118d others(43): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 26/26 | chr6 | 161116691 | |||||||
chr6:161116715 | G | A | 2 | a0002c0012t0004g0285 a0012c0011t0004g0284 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4807-135G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 26/26 | chr6 | 161116715 | |||||||
chr6:161116773 | G | A | 3 | a0001c0001t0002g0009 a0006c0009t0002g0286 a0006c0009t0002g0287 |
3 | HG02647.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4807-77G>A | MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 26/26 | chr6 | 161116773 |