Item | Value |
---|---|
geneid | 80122 |
ensemblid | ENSG00000176601.14 |
hgncid | 26249 |
symbol | MAP3K19 |
name | mitogen-activated protein kinase kinase kinase 19 |
refseq_nuc | NM_025052.5 |
refseq_prot | NP_079328.3 |
ensembl_nuc | ENST00000392915.7 |
ensembl_prot | ENSP00000376647.2 |
mane_status | MANE Select |
chr | chr2 |
start | 134964491 |
end | 135047447 |
strand | - |
ver | v1.2 |
region | chr2:134964491-135047447 |
region5000 | chr2:134959491-135052447 |
regionname0 | MAP3K19_chr2_134964491_135047447 |
regionname5000 | MAP3K19_chr2_134959491_135052447 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1328 | 192 | 54 | 39 | 62 | 4 | 31 | 44 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0002 | 0/0 | 1328 | 49 | 3 | 13 | 28 | 2 | 3 | 22 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0003 | 0/0 | 1328 | 46 | 4 | 3 | 39 | 0 | 0 | 29 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0004 | 0/0 | 1328 | 6 | 1 | 0 | 5 | 0 | 0 | 4 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0005 | 0/0 | 1328 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0006 | 0/0 | 1328 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0007 | 0/0 | 1328 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0008 | 0/0 | 1328 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0009 | 0/0 | 1328 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0010 | 0/0 | 1328 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0011 | 0/0 | 1328 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0012 | 0/0 | 1328 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0013 | 0/0 | 1328 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0014 | 0/0 | 1328 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0015 | 0/0 | 1328 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0016 | 0/0 | 1328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0017 | 0/0 | 1328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0018 | 0/0 | 1328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0019 | 0/0 | 1328 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0020 | 0/0 | 1328 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0021 | 0/0 | 1328 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0022 | 0/0 | 1328 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0023 | 0/0 | 379 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(374): Show |
chr2 | 134959491 | 135052447 |
a0024 | 0/0 | 1328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0025 | 0/0 | 1328 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
a0026 | 0/0 | 1328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | MSSMP others(1323): Show |
chr2 | 134959491 | 135052447 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3984 | 114 | 25 | 29 | 45 | 2 | 12 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0001c0002 | 0/1 | 3984 | 58 | 11 | 9 | 17 | 2 | 18 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0001c0005 | 0/0 | 3984 | 14 | 14 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0001c0009 | 0/0 | 3984 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0001c0018 | 0/0 | 3984 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0001c0020 | 0/0 | 3984 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0001c0030 | 0/0 | 3984 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0002c0003 | 0/0 | 3984 | 47 | 3 | 12 | 28 | 2 | 2 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0002c0016 | 0/0 | 3984 | 2 | 0 | 1 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0003c0004 | 0/0 | 3984 | 45 | 4 | 3 | 38 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0003c0021 | 0/0 | 3984 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0004c0006 | 0/0 | 3984 | 6 | 1 | 0 | 5 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0005c0007 | 0/0 | 3984 | 5 | 5 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0006c0008 | 0/0 | 3984 | 5 | 0 | 0 | 5 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0007c0012 | 0/0 | 3984 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0007c0023 | 0/0 | 3984 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0007c0024 | 0/0 | 3984 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0008c0010 | 0/0 | 3984 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0009c0011 | 0/0 | 3984 | 3 | 0 | 0 | 0 | 0 | 3 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0010c0015 | 0/0 | 3984 | 2 | 1 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0011c0013 | 0/0 | 3984 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0012c0017 | 0/0 | 3984 | 2 | 0 | 0 | 1 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0013c0014 | 0/0 | 3984 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0014c0025 | 0/0 | 3984 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0015c0036 | 0/0 | 3984 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0016c0028 | 0/0 | 3984 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0017c0019 | 0/0 | 3984 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0018c0033 | 0/0 | 3984 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0019c0027 | 0/0 | 3984 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0020c0026 | 0/0 | 3984 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0021c0029 | 0/0 | 3984 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0022c0031 | 0/0 | 3984 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0023c0022 | 0/0 | 3984 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0024c0034 | 0/0 | 3984 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0025c0032 | 0/0 | 3984 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 | ||
a0026c0035 | 0/0 | 3984 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | ATGAG others(3979): Show |
chr2 | 134959491 | 135052447 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5032 | 60 | 10 | 11 | 31 | 0 | 8 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0001t0002 | 1/0 | 5032 | 48 | 12 | 18 | 11 | 2 | 4 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0001t0003 | 0/0 | 5032 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0001t0004 | 0/0 | 5032 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0001t0005 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0001t0009 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0002t0001 | 0/1 | 5032 | 54 | 10 | 9 | 16 | 2 | 16 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0002t0002 | 0/0 | 5032 | 2 | 0 | 0 | 0 | 0 | 2 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0002t0003 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0002t0012 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0005t0001 | 0/0 | 5032 | 4 | 4 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0005t0002 | 0/0 | 5032 | 9 | 9 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0005t0005 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0009t0001 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0009t0002 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0009t0004 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0018t0001 | 0/0 | 5032 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0020t0002 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0001c0030t0001 | 0/0 | 5032 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0002c0003t0001 | 0/0 | 5032 | 34 | 3 | 11 | 17 | 1 | 2 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0002c0003t0002 | 0/0 | 5032 | 10 | 0 | 0 | 9 | 1 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0002c0003t0003 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0002c0003t0007 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0002c0003t0013 | 0/0 | 5032 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0002c0016t0001 | 0/0 | 5032 | 2 | 0 | 1 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0003c0004t0001 | 0/0 | 5032 | 13 | 1 | 0 | 12 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0003c0004t0002 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0003c0004t0003 | 0/0 | 5032 | 30 | 3 | 3 | 24 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0003c0004t0010 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0003c0021t0001 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0004c0006t0001 | 0/0 | 5032 | 6 | 1 | 0 | 5 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0005c0007t0001 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0005c0007t0002 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0005c0007t0006 | 0/0 | 5032 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0006c0008t0002 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0006c0008t0003 | 0/0 | 5032 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0007c0012t0001 | 0/0 | 5032 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0007c0023t0004 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0007c0024t0001 | 0/0 | 5032 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0008c0010t0001 | 0/0 | 5032 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0008c0010t0002 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0009c0011t0001 | 0/0 | 5032 | 2 | 0 | 0 | 0 | 0 | 2 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0009c0011t0002 | 0/0 | 5032 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0010c0015t0001 | 0/0 | 5032 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0010c0015t0002 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0011c0013t0004 | 0/0 | 5032 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0012c0017t0001 | 0/0 | 5032 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0012c0017t0003 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0013c0014t0003 | 0/0 | 5032 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0014c0025t0008 | 0/0 | 5032 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0015c0036t0003 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0016c0028t0004 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0017c0019t0005 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0018c0033t0005 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0019c0027t0002 | 0/0 | 5032 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0020c0026t0001 | 0/0 | 5032 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0021c0029t0011 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0022c0031t0002 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0023c0022t0003 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0024c0034t0002 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0025c0032t0001 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
a0026c0035t0002 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | AGTCT others(5027): Show |
chr2 | 134959491 | 135052447 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0307 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0001t0009g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0296 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0002t0012g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0005t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0005t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0005t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0005t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0005t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0005t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0005t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0005t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0005t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0005t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0005t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0005t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0005t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0009t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0009t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0009t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0018t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0020t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0001c0030t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0007g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0003t0013g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0016t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0002c0016t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0004t0010g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0003c0021t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0004c0006t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0004c0006t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0004c0006t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0004c0006t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0004c0006t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0004c0006t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0005c0007t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0005c0007t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0005c0007t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0005c0007t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0005c0007t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0006c0008t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0006c0008t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0006c0008t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0006c0008t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0006c0008t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0007c0012t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0007c0012t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0007c0023t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0007c0024t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0008c0010t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0008c0010t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0008c0010t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0009c0011t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0009c0011t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0009c0011t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0010c0015t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0010c0015t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0011c0013t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0011c0013t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0012c0017t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0012c0017t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0013c0014t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0013c0014t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0014c0025t0008g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0015c0036t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0016c0028t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0017c0019t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0018c0033t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0019c0027t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0020c0026t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0021c0029t0011g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0022c0031t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0023c0022t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0024c0034t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0025c0032t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
a0026c0035t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0002 | c0003 | t0002 | g0138 | EUR | FIN | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0219 | EUR | FIN | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00408 | hp1 | a0003 | c0004 | t0003 | g0162 | EAS | CHS | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | CHS | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00423 | hp1 | a0002 | c0003 | t0001 | g0329 | EAS | CHS | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00423 | hp2 | a0003 | c0004 | t0001 | g0281 | EAS | CHS | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00438 | hp2 | a0003 | c0004 | t0003 | g0286 | EAS | CHS | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0277 | EAS | CHS | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00544 | hp2 | a0003 | c0004 | t0001 | g0183 | EAS | CHS | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00558 | hp2 | a0008 | c0010 | t0002 | g0151 | EAS | CHS | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | CHS | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | CHS | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00639 | hp1 | a0001 | c0018 | t0001 | g0144 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00642 | hp1 | a0002 | c0003 | t0001 | g0323 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00735 | hp2 | a0002 | c0003 | t0001 | g0124 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00738 | hp1 | a0002 | c0003 | t0001 | g0299 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0317 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00741 | hp1 | a0002 | c0003 | t0001 | g0019 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG00741 | hp2 | a0003 | c0004 | t0003 | g0216 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01071 | hp2 | a0002 | c0016 | t0001 | g0279 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01168 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0205 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01169 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01175 | hp1 | a0007 | c0024 | t0001 | g0108 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01243 | hp1 | a0014 | c0025 | t0008 | g0149 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | PUR | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01255 | hp1 | a0003 | c0004 | t0003 | g0167 | AMR | CLM | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0169 | AMR | CLM | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0310 | AMR | CLM | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01256 | hp2 | a0002 | c0003 | t0001 | g0018 | AMR | CLM | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01261 | hp1 | a0010 | c0015 | t0001 | g0103 | AMR | CLM | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0312 | AMR | CLM | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01346 | hp1 | a0003 | c0004 | t0003 | g0166 | AMR | CLM | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01346 | hp2 | a0002 | c0003 | t0001 | g0045 | AMR | CLM | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | CLM | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01496 | hp1 | a0002 | c0003 | t0001 | g0158 | AMR | CLM | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01515 | hp1 | a0002 | c0003 | t0001 | g0266 | EUR | IBS | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0294 | EUR | IBS | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01943 | hp1 | a0002 | c0003 | t0001 | g0304 | AMR | PEL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0121 | AMR | PEL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PEL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01981 | hp2 | a0002 | c0003 | t0013 | g0075 | AMR | PEL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PEL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0141 | AMR | PEL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02015 | hp1 | a0002 | c0003 | t0002 | g0048 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02015 | hp2 | a0008 | c0010 | t0001 | g0150 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02027 | hp1 | a0002 | c0003 | t0001 | g0271 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02027 | hp2 | a0003 | c0004 | t0001 | g0168 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02040 | hp2 | a0003 | c0004 | t0010 | g0188 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02055 | hp1 | a0010 | c0015 | t0002 | g0239 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02055 | hp2 | a0001 | c0020 | t0002 | g0087 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02056 | hp1 | a0002 | c0003 | t0002 | g0227 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02071 | hp1 | a0001 | c0002 | t0012 | g0293 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02071 | hp2 | a0003 | c0004 | t0003 | g0195 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02074 | hp1 | a0002 | c0003 | t0001 | g0267 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02074 | hp2 | a0003 | c0004 | t0003 | g0163 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02080 | hp1 | a0004 | c0006 | t0001 | g0049 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02083 | hp1 | a0002 | c0003 | t0003 | g0264 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02132 | hp2 | a0003 | c0004 | t0002 | g0035 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02135 | hp1 | a0003 | c0004 | t0003 | g0232 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02135 | hp2 | a0015 | c0036 | t0003 | g0252 | EAS | KHV | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02145 | hp2 | a0003 | c0004 | t0003 | g0236 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | CDX | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CDX | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0147 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02258 | hp2 | a0002 | c0003 | t0001 | g0211 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02280 | hp1 | a0005 | c0007 | t0006 | g0014 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02280 | hp2 | a0007 | c0012 | t0001 | g0092 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PEL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02293 | hp2 | a0002 | c0003 | t0001 | g0315 | AMR | PEL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02622 | hp1 | a0001 | c0005 | t0002 | g0096 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02630 | hp2 | a0003 | c0004 | t0001 | g0208 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02647 | hp2 | a0001 | c0005 | t0002 | g0084 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02683 | hp1 | a0009 | c0011 | t0002 | g0243 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0215 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0311 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0242 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02735 | hp2 | a0002 | c0016 | t0001 | g0201 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0224 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0318 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02809 | hp1 | a0003 | c0004 | t0003 | g0082 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02809 | hp2 | a0001 | c0009 | t0001 | g0143 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02818 | hp2 | a0001 | c0005 | t0001 | g0320 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02895 | hp1 | a0001 | c0005 | t0002 | g0089 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02896 | hp1 | a0011 | c0013 | t0004 | g0039 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02896 | hp2 | a0001 | c0005 | t0002 | g0083 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02897 | hp1 | a0011 | c0013 | t0004 | g0040 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0324 | AFR | ESN | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02922 | hp2 | a0001 | c0005 | t0002 | g0097 | AFR | ESN | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02965 | hp1 | a0005 | c0007 | t0001 | g0095 | AFR | ESN | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02965 | hp2 | a0007 | c0012 | t0001 | g0109 | AFR | ESN | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ESN | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03130 | hp2 | a0001 | c0005 | t0001 | g0130 | AFR | ESN | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0111 | AFR | ESN | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03139 | hp2 | a0002 | c0003 | t0001 | g0090 | AFR | ESN | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03195 | hp1 | a0004 | c0006 | t0001 | g0241 | AFR | ESN | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ESN | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03225 | hp1 | a0001 | c0005 | t0002 | g0001 | AFR | MSL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03225 | hp2 | a0001 | c0002 | t0003 | g0102 | AFR | MSL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03239 | hp1 | a0009 | c0011 | t0001 | g0306 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03239 | hp2 | a0002 | c0003 | t0001 | g0127 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03453 | hp1 | a0016 | c0028 | t0004 | g0114 | AFR | MSL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | MSL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03486 | hp1 | a0003 | c0004 | t0003 | g0234 | AFR | MSL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0326 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0155 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0210 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0263 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03516 | hp1 | a0002 | c0003 | t0001 | g0008 | AFR | ESN | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03516 | hp2 | a0017 | c0019 | t0005 | g0146 | AFR | ESN | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03540 | hp1 | a0001 | c0005 | t0002 | g0093 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0225 | AFR | GWD | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03579 | hp1 | a0001 | c0005 | t0001 | g0094 | AFR | MSL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03579 | hp2 | a0018 | c0033 | t0005 | g0148 | AFR | MSL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0072 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03654 | hp2 | a0009 | c0011 | t0001 | g0325 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0231 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | STU | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0319 | SAS | STU | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0070 | SAS | PJL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | BEB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03834 | hp2 | a0001 | c0030 | t0001 | g0078 | SAS | BEB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0247 | SAS | BEB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG04115 | hp1 | a0019 | c0027 | t0002 | g0233 | SAS | STU | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | STU | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG04184 | hp2 | a0012 | c0017 | t0001 | g0043 | SAS | BEB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0202 | SAS | STU | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0327 | SAS | STU | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0217 | SAS | STU | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG04204 | hp2 | a0020 | c0026 | t0001 | g0026 | SAS | STU | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | STU | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0301 | SAS | STU | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18522 | hp2 | a0001 | c0009 | t0004 | g0131 | AFR | YRI | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | YRI | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18939 | hp2 | a0006 | c0008 | t0003 | g0284 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18941 | hp2 | a0006 | c0008 | t0003 | g0156 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18944 | hp2 | a0003 | c0004 | t0003 | g0165 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18947 | hp2 | a0021 | c0029 | t0011 | g0037 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18950 | hp1 | a0002 | c0003 | t0001 | g0328 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18960 | hp2 | a0013 | c0014 | t0003 | g0174 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18962 | hp1 | a0003 | c0004 | t0003 | g0175 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18962 | hp2 | a0003 | c0004 | t0003 | g0005 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18963 | hp1 | a0008 | c0010 | t0001 | g0229 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18963 | hp2 | a0002 | c0003 | t0001 | g0056 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18964 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18965 | hp1 | a0006 | c0008 | t0003 | g0285 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18966 | hp1 | a0002 | c0003 | t0001 | g0164 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18966 | hp2 | a0002 | c0003 | t0002 | g0067 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18967 | hp1 | a0022 | c0031 | t0002 | g0059 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18967 | hp2 | a0003 | c0004 | t0003 | g0228 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18968 | hp1 | a0003 | c0004 | t0003 | g0184 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18968 | hp2 | a0003 | c0004 | t0001 | g0226 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18969 | hp1 | a0003 | c0004 | t0001 | g0015 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18969 | hp2 | a0003 | c0004 | t0001 | g0261 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18971 | hp2 | a0002 | c0003 | t0002 | g0069 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18981 | hp1 | a0003 | c0004 | t0001 | g0172 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18982 | hp1 | a0003 | c0004 | t0003 | g0297 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18983 | hp2 | a0003 | c0004 | t0003 | g0292 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18985 | hp2 | a0006 | c0008 | t0002 | g0280 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18986 | hp1 | a0002 | c0003 | t0001 | g0265 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18987 | hp1 | a0002 | c0003 | t0002 | g0125 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18988 | hp1 | a0002 | c0003 | t0001 | g0278 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18990 | hp1 | a0002 | c0003 | t0002 | g0073 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18990 | hp2 | a0023 | c0022 | t0003 | g0303 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18991 | hp2 | a0002 | c0003 | t0001 | g0275 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18992 | hp1 | a0004 | c0006 | t0001 | g0010 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18993 | hp1 | a0013 | c0014 | t0003 | g0042 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18993 | hp2 | a0003 | c0004 | t0001 | g0288 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18995 | hp1 | a0003 | c0004 | t0003 | g0287 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18995 | hp2 | a0003 | c0021 | t0001 | g0160 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA18999 | hp2 | a0003 | c0004 | t0003 | g0052 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19000 | hp1 | a0003 | c0004 | t0003 | g0154 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19000 | hp2 | a0002 | c0003 | t0001 | g0199 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19002 | hp1 | a0004 | c0006 | t0001 | g0256 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19004 | hp1 | a0003 | c0004 | t0003 | g0198 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19004 | hp2 | a0002 | c0003 | t0007 | g0006 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19006 | hp1 | a0003 | c0004 | t0001 | g0190 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19007 | hp1 | a0002 | c0003 | t0001 | g0203 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19010 | hp2 | a0003 | c0004 | t0003 | g0046 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19030 | hp1 | a0001 | c0005 | t0002 | g0128 | AFR | LWK | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19030 | hp2 | a0007 | c0023 | t0004 | g0064 | AFR | LWK | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19043 | hp1 | a0001 | c0005 | t0005 | g0145 | AFR | LWK | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19043 | hp2 | a0024 | c0034 | t0002 | g0119 | AFR | LWK | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19060 | hp1 | a0002 | c0003 | t0001 | g0196 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19062 | hp1 | a0006 | c0008 | t0003 | g0251 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19062 | hp2 | a0002 | c0003 | t0001 | g0189 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19064 | hp2 | a0012 | c0017 | t0003 | g0055 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19065 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19066 | hp1 | a0002 | c0003 | t0002 | g0161 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19066 | hp2 | a0003 | c0004 | t0003 | g0272 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19070 | hp1 | a0003 | c0004 | t0003 | g0005 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19070 | hp2 | a0002 | c0003 | t0001 | g0034 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19072 | hp1 | a0003 | c0004 | t0003 | g0230 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19074 | hp1 | a0002 | c0003 | t0001 | g0057 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19074 | hp2 | a0002 | c0003 | t0001 | g0197 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19077 | hp1 | a0003 | c0004 | t0003 | g0025 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19078 | hp2 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19079 | hp2 | a0004 | c0006 | t0001 | g0074 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19081 | hp1 | a0001 | c0001 | t0009 | g0177 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19081 | hp2 | a0003 | c0004 | t0003 | g0289 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19082 | hp1 | a0025 | c0032 | t0001 | g0274 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19084 | hp1 | a0003 | c0004 | t0003 | g0302 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19085 | hp1 | a0003 | c0004 | t0001 | g0262 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19085 | hp2 | a0002 | c0003 | t0002 | g0192 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19086 | hp1 | a0004 | c0006 | t0001 | g0250 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19086 | hp2 | a0002 | c0003 | t0002 | g0191 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19091 | hp1 | a0003 | c0004 | t0003 | g0276 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | YRI | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA19240 | hp2 | a0001 | c0005 | t0002 | g0001 | AFR | YRI | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ASW | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA20129 | hp2 | a0001 | c0009 | t0002 | g0134 | AFR | ASW | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0321 | EUR | TSI | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0214 | EUR | TSI | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0051 | SAS | GIH | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA20905 | hp2 | a0002 | c0003 | t0001 | g0212 | SAS | GIH | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0153 | AMR | CLM | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02109 | hp2 | a0001 | c0005 | t0001 | g0088 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02486 | hp2 | a0005 | c0007 | t0006 | g0013 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG02559 | hp2 | a0005 | c0007 | t0002 | g0105 | AFR | ACB | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0209 | AFR | MSL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0085 | AFR | MSL | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA20300 | hp1 | a0005 | c0007 | t0006 | g0011 | AFR | USA | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0204 | AFR | USA | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0322 | AFR | LWK | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
NA21309 | hp2 | a0026 | c0035 | t0002 | g0118 | AFR | LWK | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0296 | REF | REF | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0307 | REF | REF | MAP3K19_chr2_134959491_135052447 | MAP3K19 | chr2 | 134959491 | 135052447 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:134980927 | T | C | 1 | a0014 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.3814A>G | p.Arg1272Gly | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/13 | 4500/5032 | 3814/3987 | 1272/1328 | chr2 | 134980927 | |||
chr2:134981187 | C | T | 1 | a0016 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.3554G>A | p.Arg1185His | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/13 | 4240/5032 | 3554/3987 | 1185/1328 | chr2 | 134981187 | |||
chr2:134981280 | C | T | 2 | a0013 a0015 |
3 | HG02135.hp2 NA18960.hp2 NA18993.hp1 |
missense_variant | MODERATE | c.3461G>A | p.Arg1154His | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/13 | 4147/5032 | 3461/3987 | 1154/1328 | chr2 | 134981280 | |||
chr2:134985828 | C | T | 1 | a0021 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.3044G>A | p.Gly1015Asp | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 3730/5032 | 3044/3987 | 1015/1328 | chr2 | 134985828 | |||
chr2:134985841 | G | A | 1 | a0006 | 5 | NA18939.hp2 NA18941.hp2 NA18965.hp1 others(2): Show |
missense_variant | MODERATE | c.3031C>T | p.Pro1011Ser | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 3717/5032 | 3031/3987 | 1011/1328 | chr2 | 134985841 | |||
chr2:134986023 | T | C | 1 | a0024 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.2849A>G | p.Asn950Ser | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 3535/5032 | 2849/3987 | 950/1328 | chr2 | 134986023 | |||
chr2:134986024 | T | C | 1 | a0011 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.2848A>G | p.Asn950Asp | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 3534/5032 | 2848/3987 | 950/1328 | chr2 | 134986024 | |||
chr2:134986049 | C | T | 1 | a0022 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.2823G>A | p.Met941Ile | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 3509/5032 | 2823/3987 | 941/1328 | chr2 | 134986049 | |||
chr2:134986063 | T | A | 1 | a0017 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.2809A>T | p.Ile937Phe | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 3495/5032 | 2809/3987 | 937/1328 | chr2 | 134986063 | |||
chr2:134986437 | T | C | 5 | a0003 a0006 a0008 others(2): Show |
57 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
missense_variant | MODERATE | c.2435A>G | p.Glu812Gly | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 3121/5032 | 2435/3987 | 812/1328 | chr2 | 134986437 | |||
chr2:134986786 | G | A | 3 | a0004 a0021 a0025 |
8 | HG02080.hp1 HG03195.hp1 NA18947.hp2 others(5): Show |
missense_variant | MODERATE | c.2086C>T | p.Arg696Cys | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 2772/5032 | 2086/3987 | 696/1328 | chr2 | 134986786 | |||
chr2:134986803 | G | A | 1 | a0020 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.2069C>T | p.Ser690Leu | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 2755/5032 | 2069/3987 | 690/1328 | chr2 | 134986803 | |||
chr2:134986846 | C | G | 9 | a0003 a0005 a0006 others(6): Show |
70 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(67): Show |
missense_variant | MODERATE | c.2026G>C | p.Glu676Gln | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 2712/5032 | 2026/3987 | 676/1328 | chr2 | 134986846 | |||
chr2:134986848 | C | T | 1 | a0019 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.2024G>A | p.Arg675Gln | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 2710/5032 | 2024/3987 | 675/1328 | chr2 | 134986848 | |||
chr2:134986899 | T | C | 1 | a0008 | 3 | HG00558.hp2 HG02015.hp2 NA18963.hp1 |
missense_variant | MODERATE | c.1973A>G | p.Asn658Ser | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 2659/5032 | 1973/3987 | 658/1328 | chr2 | 134986899 | |||
chr2:134986993 | A | G | 1 | a0014 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.1879T>C | p.Cys627Arg | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 2565/5032 | 1879/3987 | 627/1328 | chr2 | 134986993 | |||
chr2:134987464 | T | C | 1 | a0011 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.1408A>G | p.Ile470Val | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 2094/5032 | 1408/3987 | 470/1328 | chr2 | 134987464 | |||
chr2:134987559 | G | A | 2 | a0002 a0022 |
50 | HG00280.hp1 HG00423.hp1 HG00642.hp1 others(47): Show |
missense_variant | MODERATE | c.1313C>T | p.Thr438Ile | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 1999/5032 | 1313/3987 | 438/1328 | chr2 | 134987559 | |||
chr2:134987644 | T | C | 1 | a0025 | 1 | NA19082.hp1 | missense_variant | MODERATE | c.1228A>G | p.Met410Val | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 1914/5032 | 1228/3987 | 410/1328 | chr2 | 134987644 | |||
chr2:134987732 | A | T | 1 | a0023 | 1 | NA18990.hp2 | stop_gained | HIGH | c.1140T>A | p.Tyr380* | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 1826/5032 | 1140/3987 | 380/1328 | chr2 | 134987732 | |||
chr2:134987734 | A | G | 1 | a0009 | 3 | HG02683.hp1 HG03239.hp1 HG03654.hp2 |
missense_variant | MODERATE | c.1138T>C | p.Tyr380His | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 1824/5032 | 1138/3987 | 380/1328 | chr2 | 134987734 | |||
chr2:134987821 | A | C | 1 | a0005 | 5 | HG02280.hp1 HG02486.hp2 HG02559.hp2 others(2): Show |
missense_variant | MODERATE | c.1051T>G | p.Cys351Gly | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 1737/5032 | 1051/3987 | 351/1328 | chr2 | 134987821 | |||
chr2:134988078 | G | A | 1 | a0010 | 2 | HG01261.hp1 HG02055.hp1 |
missense_variant | MODERATE | c.794C>T | p.Pro265Leu | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 1480/5032 | 794/3987 | 265/1328 | chr2 | 134988078 | |||
chr2:134998908 | T | C | 1 | a0018 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.404A>G | p.Lys135Arg | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/13 | 1090/5032 | 404/3987 | 135/1328 | chr2 | 134998908 | |||
chr2:134998929 | G | A | 1 | a0012 | 2 | HG04184.hp2 NA19064.hp2 |
missense_variant | MODERATE | c.383C>T | p.Thr128Met | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/13 | 1069/5032 | 383/3987 | 128/1328 | chr2 | 134998929 | |||
chr2:134998936 | T | A | 2 | a0024 a0026 |
2 | NA19043.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.376A>T | p.Ile126Leu | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/13 | 1062/5032 | 376/3987 | 126/1328 | chr2 | 134998936 | |||
chr2:134999951 | G | C | 1 | a0015 | 1 | HG02135.hp2 | missense_variant | MODERATE | c.300C>G | p.Asp100Glu | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 7/13 | 986/5032 | 300/3987 | 100/1328 | chr2 | 134999951 | |||
chr2:135040500 | C | T | 1 | a0005 | 3 | HG02280.hp1 HG02486.hp2 NA20300.hp1 |
splice_region_variant | LOW | c.-421G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/13 | chr2 | 135040500 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:134985827 | G | C | 1 | a0021c0029 | 1 | NA18947.hp2 | synonymous_variant | LOW | c.3045C>G | p.Gly1015Gly | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 3731/5032 | 3045/3987 | 1015/1328 | chr2 | 134985827 | |||
chr2:134985938 | T | C | 1 | a0002c0016 | 2 | HG01071.hp2 HG02735.hp2 |
synonymous_variant | LOW | c.2934A>G | p.Leu978Leu | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 3620/5032 | 2934/3987 | 978/1328 | chr2 | 134985938 | |||
chr2:134986613 | T | C | 1 | a0001c0020 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.2259A>G | p.Leu753Leu | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 2945/5032 | 2259/3987 | 753/1328 | chr2 | 134986613 | |||
chr2:134986799 | A | G | 1 | a0007c0023 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.2073T>C | p.Ala691Ala | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 2759/5032 | 2073/3987 | 691/1328 | chr2 | 134986799 | |||
chr2:134987048 | T | C | 1 | a0001c0030 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.1824A>G | p.Lys608Lys | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 2510/5032 | 1824/3987 | 608/1328 | chr2 | 134987048 | |||
chr2:134987804 | C | T | 1 | a0014c0025 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.1068G>A | p.Thr356Thr | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 1754/5032 | 1068/3987 | 356/1328 | chr2 | 134987804 | |||
chr2:134987822 | G | A | 8 | a0001c0002 a0001c0018 a0009c0011 others(5): Show |
67 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(64): Show |
synonymous_variant | LOW | c.1050C>T | p.Asp350Asp | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 1736/5032 | 1050/3987 | 350/1328 | chr2 | 134987822 | |||
chr2:134987866 | A | G | 1 | a0003c0021 | 1 | NA18995.hp2 | synonymous_variant | LOW | c.1006T>C | p.Leu336Leu | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 1692/5032 | 1006/3987 | 336/1328 | chr2 | 134987866 | |||
chr2:134987975 | C | T | 20 | a0001c0002 a0001c0018 a0003c0004 others(17): Show |
137 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
synonymous_variant | LOW | c.897G>A | p.Arg299Arg | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 1583/5032 | 897/3987 | 299/1328 | chr2 | 134987975 | |||
chr2:134988152 | A | G | 20 | a0001c0002 a0001c0018 a0003c0004 others(17): Show |
137 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
synonymous_variant | LOW | c.720T>C | p.Ser240Ser | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/13 | 1406/5032 | 720/3987 | 240/1328 | chr2 | 134988152 | |||
chr2:134998808 | C | T | 9 | a0001c0005 a0001c0009 a0001c0018 others(6): Show |
26 | HG00639.hp1 HG02055.hp2 HG02109.hp2 others(23): Show |
synonymous_variant | LOW | c.504G>A | p.Leu168Leu | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/13 | 1190/5032 | 504/3987 | 168/1328 | chr2 | 134998808 | |||
chr2:134998874 | C | T | 1 | a0001c0009 | 3 | HG02809.hp2 NA18522.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.438G>A | p.Glu146Glu | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/13 | 1124/5032 | 438/3987 | 146/1328 | chr2 | 134998874 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:134964528 | A | G | 10 | a0001c0001t0003 a0001c0002t0003 a0002c0003t0003 others(7): Show |
44 | HG00408.hp1 HG00438.hp2 HG00741.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*322T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 13/13 | 322 | chr2 | 134964528 | ||||||
chr2:134964573 | A | C | 29 | a0001c0001t0001 a0001c0001t0005 a0001c0002t0001 others(26): Show |
199 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*277T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 13/13 | 277 | chr2 | 134964573 | ||||||
chr2:134964605 | G | C | 1 | a0001c0001t0009 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*245C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 13/13 | 245 | chr2 | 134964605 | ||||||
chr2:134964758 | A | G | 5 | a0001c0001t0004 a0001c0009t0004 a0007c0023t0004 others(2): Show |
7 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*92T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 13/13 | 92 | chr2 | 134964758 | ||||||
chr2:134964778 | T | G | 1 | a0003c0004t0010 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*72A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 13/13 | 72 | chr2 | 134964778 | ||||||
chr2:134964785 | T | C | 1 | a0021c0029t0011 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*65A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 13/13 | 65 | chr2 | 134964785 | ||||||
chr2:134964844 | G | A | 1 | a0001c0002t0012 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 13/13 | 6 | chr2 | 134964844 | ||||||
chr2:135030357 | T | C | 1 | a0014c0025t0008 | 1 | HG01243.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-140A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/13 | chr2 | 135030357 | |||||||
chr2:135030415 | T | C | 4 | a0001c0001t0005 a0001c0005t0005 a0017c0019t0005 others(1): Show |
4 | HG02258.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-198A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/13 | 5768 | chr2 | 135030415 | ||||||
chr2:135040374 | T | A | 1 | a0002c0003t0013 | 1 | HG01981.hp2 | 5_prime_UTR_variant | MODIFIER | c.-295A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/13 | 15727 | chr2 | 135040374 | ||||||
chr2:135040467 | C | T | 1 | a0014c0025t0008 | 1 | HG01243.hp1 | 5_prime_UTR_variant | MODIFIER | c.-388G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/13 | 15820 | chr2 | 135040467 | ||||||
chr2:135047379 | C | T | 1 | a0002c0003t0007 | 1 | NA19004.hp2 | 5_prime_UTR_variant | MODIFIER | c.-618G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/13 | 22732 | chr2 | 135047379 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:134965092 | C | G | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3921-176G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134965092 | |||||||
chr2:134965274 | C | T | 1 | a0001c0001t0004g0085 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3921-358G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134965274 | |||||||
chr2:134965311 | T | C | 38 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0032 others(35): Show |
38 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.3921-395A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134965311 | |||||||
chr2:134965488 | T | C | 1 | a0005c0007t0002g0105 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3921-572A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134965488 | |||||||
chr2:134965598 | T | C | 1 | a0021c0029t0011g0037 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3921-682A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134965598 | |||||||
chr2:134965634 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3921-718A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134965634 | |||||||
chr2:134965665 | C | T | 1 | a0003c0004t0001g0168 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3921-749G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134965665 | |||||||
chr2:134965686 | T | A | 3 | a0001c0002t0001g0024 a0001c0002t0001g0121 a0001c0002t0001g0268 |
3 | HG01978.hp1 NA18960.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.3921-770A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134965686 | |||||||
chr2:134965860 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3921-944G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134965860 | |||||||
chr2:134965880 | C | T | 1 | a0003c0004t0003g0082 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3921-964G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134965880 | |||||||
chr2:134965976 | G | A | 38 | a0001c0001t0003g0193 a0001c0001t0003g0273 a0002c0003t0003g0264 others(35): Show |
39 | HG00408.hp1 HG00438.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.3921-1060C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134965976 | |||||||
chr2:134966005 | TTTTAC | T | 45 | a0001c0001t0003g0193 a0001c0001t0003g0273 a0001c0002t0003g0102 others(42): Show |
46 | HG00408.hp1 HG00438.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.3921-1094_3921-109 others(9): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134966005 | |||||||
chr2:134966072 | A | T | 1 | a0005c0007t0002g0105 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3921-1156T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134966072 | |||||||
chr2:134966130 | T | C | 43 | a0001c0001t0003g0193 a0001c0001t0003g0273 a0001c0002t0003g0102 others(40): Show |
44 | HG00408.hp1 HG00438.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.3921-1214A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134966130 | |||||||
chr2:134966145 | G | A | 30 | a0001c0001t0001g0259 a0001c0002t0001g0024 a0001c0002t0001g0120 others(27): Show |
31 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.3921-1229C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134966145 | |||||||
chr2:134966175 | T | G | 1 | a0011c0013t0004g0039 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3921-1259A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134966175 | |||||||
chr2:134966369 | G | A | 2 | a0003c0004t0003g0292 a0005c0007t0002g0105 |
2 | HG02559.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.3921-1453C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134966369 | |||||||
chr2:134966426 | T | A | 45 | a0001c0001t0003g0193 a0001c0001t0003g0273 a0001c0002t0003g0102 others(42): Show |
46 | HG00408.hp1 HG00438.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.3921-1510A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134966426 | |||||||
chr2:134966566 | A | T | 31 | a0001c0001t0001g0314 a0001c0002t0001g0021 a0001c0002t0001g0023 others(28): Show |
31 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.3921-1650T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134966566 | |||||||
chr2:134966610 | G | A | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3921-1694C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134966610 | |||||||
chr2:134966645 | C | T | 7 | a0001c0001t0002g0081 a0001c0001t0004g0085 a0001c0009t0004g0131 others(4): Show |
7 | HG02559.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.3921-1729G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134966645 | |||||||
chr2:134966698 | T | C | 1 | a0001c0002t0001g0319 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3921-1782A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134966698 | |||||||
chr2:134966717 | G | C | 45 | a0001c0001t0003g0193 a0001c0001t0003g0273 a0001c0002t0003g0102 others(42): Show |
46 | HG00408.hp1 HG00438.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.3921-1801C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134966717 | |||||||
chr2:134966774 | C | T | 1 | a0001c0002t0001g0070 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3921-1858G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134966774 | |||||||
chr2:134966853 | A | G | 45 | a0001c0001t0003g0193 a0001c0001t0003g0273 a0001c0002t0003g0102 others(42): Show |
46 | HG00408.hp1 HG00438.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.3921-1937T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134966853 | |||||||
chr2:134966869 | G | A | 4 | a0001c0001t0002g0081 a0001c0009t0004g0131 a0005c0007t0002g0105 others(1): Show |
4 | HG02559.hp2 HG03130.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.3921-1953C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134966869 | |||||||
chr2:134966956 | G | C | 1 | a0001c0002t0001g0215 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3921-2040C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134966956 | |||||||
chr2:134967175 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3921-2259G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967175 | |||||||
chr2:134967277 | G | T | 31 | a0001c0001t0001g0259 a0001c0002t0001g0024 a0001c0002t0001g0121 others(28): Show |
32 | HG00423.hp1 HG00621.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.3921-2361C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967277 | |||||||
chr2:134967317 | T | C | 1 | a0001c0002t0003g0102 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3921-2401A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967317 | |||||||
chr2:134967375 | G | C | 1 | a0003c0004t0001g0168 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3921-2459C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967375 | |||||||
chr2:134967394 | A | G | 6 | a0001c0001t0001g0058 a0001c0001t0001g0122 a0001c0001t0001g0126 others(3): Show |
6 | HG00558.hp1 HG00609.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.3921-2478T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967394 | |||||||
chr2:134967445 | G | A | 1 | a0001c0009t0002g0134 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3921-2529C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967445 | |||||||
chr2:134967459 | T | C | 1 | a0005c0007t0002g0105 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3921-2543A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967459 | |||||||
chr2:134967573 | A | G | 1 | a0001c0009t0002g0134 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3921-2657T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967573 | |||||||
chr2:134967649 | AT | A | 4 | a0005c0007t0001g0095 a0005c0007t0006g0011 a0005c0007t0006g0013 others(1): Show |
4 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3921-2734delA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967649 | |||||||
chr2:134967809 | A | G | 1 | a0001c0009t0004g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3921-2893T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967809 | |||||||
chr2:134967842 | G | C | 2 | a0003c0004t0001g0004 a0003c0004t0001g0015 |
3 | NA18964.hp2 NA18969.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.3921-2926C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967842 | |||||||
chr2:134967849 | C | A | 112 | a0001c0001t0001g0290 a0001c0001t0001g0314 a0001c0001t0002g0081 others(109): Show |
113 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.3921-2933G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967849 | |||||||
chr2:134967857 | C | CT | 19 | a0001c0001t0001g0290 a0001c0002t0001g0047 a0001c0002t0001g0060 others(16): Show |
19 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.3921-2942dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967857 | |||||||
chr2:134967872 | A | T | 2 | a0001c0001t0001g0123 a0001c0001t0002g0050 |
2 | NA18747.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.3921-2956T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967872 | |||||||
chr2:134967883 | A | G | 2 | a0001c0001t0004g0111 a0016c0028t0004g0114 |
2 | HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3921-2967T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967883 | |||||||
chr2:134967914 | T | G | 1 | a0001c0001t0002g0081 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3921-2998A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967914 | |||||||
chr2:134967934 | A | G | 1 | a0002c0003t0001g0278 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.3921-3018T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967934 | |||||||
chr2:134967958 | A | G | 1 | a0001c0002t0001g0070 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3921-3042T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967958 | |||||||
chr2:134967964 | G | C | 1 | a0001c0001t0002g0081 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3921-3048C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967964 | |||||||
chr2:134967972 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3921-3056T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134967972 | |||||||
chr2:134968005 | G | A | 1 | a0001c0002t0001g0071 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3921-3089C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968005 | |||||||
chr2:134968049 | A | G | 18 | a0001c0001t0001g0305 a0001c0002t0001g0060 a0001c0002t0001g0061 others(15): Show |
18 | HG01496.hp2 HG02080.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.3921-3133T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968049 | |||||||
chr2:134968067 | G | A | 55 | a0001c0001t0001g0290 a0003c0004t0001g0004 a0003c0004t0001g0015 others(52): Show |
57 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.3921-3151C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968067 | |||||||
chr2:134968071 | A | C | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3921-3155T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968071 | |||||||
chr2:134968076 | G | T | 7 | a0004c0006t0001g0010 a0004c0006t0001g0049 a0004c0006t0001g0074 others(4): Show |
7 | HG02080.hp1 HG03195.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.3921-3160C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968076 | |||||||
chr2:134968093 | C | T | 60 | a0001c0001t0001g0112 a0001c0002t0001g0021 a0001c0002t0001g0023 others(57): Show |
60 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.3921-3177G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968093 | |||||||
chr2:134968103 | C | T | 6 | a0001c0001t0001g0112 a0001c0002t0001g0076 a0001c0005t0001g0088 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3921-3187G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968103 | |||||||
chr2:134968114 | G | T | 60 | a0001c0001t0001g0290 a0001c0001t0004g0111 a0003c0004t0001g0004 others(57): Show |
62 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.3921-3198C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968114 | |||||||
chr2:134968118 | C | T | 1 | a0019c0027t0002g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3921-3202G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968118 | |||||||
chr2:134968185 | C | T | 3 | a0001c0001t0002g0050 a0001c0001t0002g0291 a0001c0001t0009g0177 |
3 | HG02132.hp1 NA18941.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.3921-3269G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968185 | |||||||
chr2:134968222 | A | G | 1 | a0001c0002t0001g0060 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3921-3306T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968222 | |||||||
chr2:134968253 | A | C | 2 | a0001c0001t0001g0101 a0016c0028t0004g0114 |
2 | HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3921-3337T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968253 | |||||||
chr2:134968274 | C | T | 1 | a0024c0034t0002g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3921-3358G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968274 | |||||||
chr2:134968275 | G | A | 1 | a0001c0002t0001g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3921-3359C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968275 | |||||||
chr2:134968291 | C | T | 1 | a0001c0009t0001g0143 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3921-3375G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968291 | |||||||
chr2:134968295 | G | A | 132 | a0001c0001t0002g0081 a0001c0001t0004g0111 a0001c0002t0001g0021 others(129): Show |
134 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.3921-3379C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968295 | |||||||
chr2:134968299 | T | A | 1 | a0001c0002t0001g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3921-3383A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968299 | |||||||
chr2:134968317 | G | T | 1 | a0001c0002t0001g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3921-3401C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968317 | |||||||
chr2:134968336 | G | A | 48 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0027 others(45): Show |
49 | HG00558.hp1 HG00609.hp2 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.3921-3420C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968336 | |||||||
chr2:134968375 | T | C | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3921-3459A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968375 | |||||||
chr2:134968401 | G | T | 129 | a0001c0001t0002g0081 a0001c0001t0004g0111 a0001c0002t0001g0021 others(126): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.3921-3485C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968401 | |||||||
chr2:134968420 | A | T | 144 | a0001c0001t0001g0159 a0001c0001t0001g0180 a0001c0001t0001g0181 others(141): Show |
146 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.3921-3504T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968420 | |||||||
chr2:134968427 | T | A | 1 | a0003c0004t0003g0082 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3921-3511A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968427 | |||||||
chr2:134968462 | G | A | 1 | a0002c0003t0001g0328 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3921-3546C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968462 | |||||||
chr2:134968465 | T | C | 142 | a0001c0001t0002g0081 a0001c0001t0002g0244 a0001c0001t0004g0111 others(139): Show |
144 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.3921-3549A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968465 | |||||||
chr2:134968469 | G | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0255 |
2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.3921-3553C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968469 | |||||||
chr2:134968479 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3921-3563C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968479 | |||||||
chr2:134968482 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3921-3566G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968482 | |||||||
chr2:134968488 | G | C | 4 | a0001c0005t0002g0001 a0001c0005t0002g0084 a0001c0005t0002g0096 others(1): Show |
5 | HG02622.hp1 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3921-3572C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968488 | |||||||
chr2:134968510 | GGACGGGG others(33): Show |
G | 8 | a0005c0007t0001g0095 a0005c0007t0002g0105 a0005c0007t0006g0011 others(5): Show |
8 | HG01175.hp1 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3921-3634_3921-359 others(44): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968510 | |||||||
chr2:134968513 | C | T | 1 | a0001c0002t0001g0205 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3921-3597G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968513 | |||||||
chr2:134968530 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3921-3614C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968530 | |||||||
chr2:134968554 | G | A | 9 | a0003c0004t0001g0226 a0004c0006t0001g0010 a0004c0006t0001g0049 others(6): Show |
9 | HG02080.hp1 HG03195.hp1 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.3921-3638C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968554 | |||||||
chr2:134968558 | T | C | 2 | a0001c0001t0002g0081 a0001c0009t0001g0143 |
2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3921-3642A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968558 | |||||||
chr2:134968559 | G | GGCTGCCG others(33): Show |
9 | a0003c0004t0001g0226 a0004c0006t0001g0010 a0004c0006t0001g0049 others(6): Show |
9 | HG02080.hp1 HG03195.hp1 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.3921-3644_3921-364 others(44): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968559 | |||||||
chr2:134968593 | C | T | 1 | a0010c0015t0002g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3921-3677G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968593 | |||||||
chr2:134968598 | C | T | 2 | a0007c0012t0001g0092 a0007c0024t0001g0108 |
2 | HG01175.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.3921-3682G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968598 | |||||||
chr2:134968618 | T | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0044 others(1): Show |
4 | HG01952.hp1 HG01978.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.3921-3702A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968618 | |||||||
chr2:134968639 | G | A | 48 | a0001c0001t0001g0259 a0001c0001t0002g0081 a0001c0002t0001g0016 others(45): Show |
49 | HG00280.hp1 HG00423.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.3921-3723C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968639 | |||||||
chr2:134968693 | G | A | 45 | a0001c0001t0002g0081 a0001c0009t0001g0143 a0003c0004t0001g0004 others(42): Show |
46 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.3921-3777C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968693 | |||||||
chr2:134968693 | G | T | 2 | a0011c0013t0004g0039 a0011c0013t0004g0040 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3921-3777C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968693 | |||||||
chr2:134968719 | A | G | 199 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0027 others(196): Show |
202 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.3921-3803T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968719 | |||||||
chr2:134968730 | G | A | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3921-3814C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968730 | |||||||
chr2:134968731 | G | C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0053 a0001c0001t0001g0178 others(7): Show |
10 | HG01496.hp2 NA18942.hp1 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.3921-3815C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968731 | |||||||
chr2:134968747 | C | T | 1 | a0010c0015t0002g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3921-3831G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968747 | |||||||
chr2:134968755 | G | A | 60 | a0001c0002t0001g0021 a0001c0002t0001g0023 a0001c0002t0001g0024 others(57): Show |
61 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.3921-3839C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968755 | |||||||
chr2:134968788 | T | G | 1 | a0002c0003t0003g0264 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3921-3872A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968788 | |||||||
chr2:134968795 | G | A | 1 | a0004c0006t0001g0256 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3921-3879C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968795 | |||||||
chr2:134968798 | T | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0238 a0001c0005t0001g0130 |
3 | HG00735.hp1 HG02145.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3921-3882A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968798 | |||||||
chr2:134968848 | C | T | 3 | a0001c0002t0001g0104 a0001c0002t0001g0209 a0001c0002t0003g0102 |
3 | HG03041.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3921-3932G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968848 | |||||||
chr2:134968925 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0044 others(1): Show |
4 | HG01952.hp1 HG01978.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.3921-4009C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968925 | |||||||
chr2:134968947 | T | C | 2 | a0011c0013t0004g0039 a0011c0013t0004g0040 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3921-4031A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968947 | |||||||
chr2:134968951 | G | A | 1 | a0018c0033t0005g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3921-4035C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134968951 | |||||||
chr2:134969019 | A | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0194 a0001c0001t0001g0254 others(1): Show |
5 | NA18949.hp2 NA18964.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3921-4103T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134969019 | |||||||
chr2:134969021 | C | T | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3921-4105G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134969021 | |||||||
chr2:134969027 | G | A | 74 | a0001c0001t0001g0112 a0001c0001t0004g0111 a0001c0002t0001g0076 others(71): Show |
76 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.3921-4111C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134969027 | |||||||
chr2:134969068 | C | A | 1 | a0010c0015t0002g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3921-4152G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134969068 | |||||||
chr2:134969097 | C | T | 7 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(4): Show |
7 | HG00735.hp1 HG02145.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3921-4181G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134969097 | |||||||
chr2:134969113 | T | C | 146 | a0001c0001t0001g0112 a0001c0001t0002g0081 a0001c0001t0004g0111 others(143): Show |
148 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.3921-4197A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134969113 | |||||||
chr2:134969134 | G | A | 7 | a0003c0004t0001g0226 a0004c0006t0001g0010 a0004c0006t0001g0074 others(4): Show |
7 | NA18947.hp2 NA18968.hp2 NA18992.hp1 others(4): Show |
intron_variant | MODIFIER | c.3921-4218C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134969134 | |||||||
chr2:134969157 | A | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0027 others(189): Show |
195 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.3921-4241T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134969157 | |||||||
chr2:134969157 | A | T | 2 | a0011c0013t0004g0039 a0011c0013t0004g0040 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3921-4241T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134969157 | |||||||
chr2:134969182 | C | T | 1 | a0003c0004t0003g0195 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3921-4266G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134969182 | |||||||
chr2:134969185 | CA | C | 146 | a0001c0001t0001g0112 a0001c0001t0002g0081 a0001c0001t0004g0111 others(143): Show |
148 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.3921-4270delT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134969185 | |||||||
chr2:134969584 | A | G | 1 | a0010c0015t0001g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3921-4668T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134969584 | |||||||
chr2:134969618 | A | G | 199 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0027 others(196): Show |
202 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.3921-4702T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134969618 | |||||||
chr2:134969961 | T | C | 73 | a0001c0001t0002g0081 a0001c0001t0002g0244 a0001c0002t0001g0021 others(70): Show |
73 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.3921-5045A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134969961 | |||||||
chr2:134969997 | G | GT | 147 | a0001c0001t0001g0112 a0001c0001t0002g0081 a0001c0001t0002g0244 others(144): Show |
149 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.3921-5082dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134969997 | |||||||
chr2:134970073 | C | T | 1 | a0001c0002t0001g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3921-5157G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970073 | |||||||
chr2:134970183 | T | G | 58 | a0001c0001t0001g0246 a0001c0001t0002g0244 a0001c0002t0001g0021 others(55): Show |
58 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.3921-5267A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970183 | |||||||
chr2:134970296 | T | C | 4 | a0001c0002t0001g0106 a0001c0002t0001g0116 a0001c0002t0001g0133 others(1): Show |
4 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3921-5380A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970296 | |||||||
chr2:134970363 | T | C | 1 | a0001c0002t0001g0214 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3921-5447A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970363 | |||||||
chr2:134970439 | A | G | 148 | a0001c0001t0001g0112 a0001c0001t0002g0081 a0001c0001t0002g0244 others(145): Show |
150 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.3921-5523T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970439 | |||||||
chr2:134970489 | A | C | 74 | a0001c0001t0002g0081 a0001c0001t0002g0244 a0001c0002t0001g0021 others(71): Show |
74 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.3921-5573T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970489 | |||||||
chr2:134970527 | T | C | 5 | a0001c0001t0001g0112 a0001c0002t0001g0076 a0001c0005t0001g0088 others(2): Show |
5 | HG02109.hp2 HG02257.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3921-5611A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970527 | |||||||
chr2:134970595 | C | CT | 6 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0159 others(3): Show |
6 | HG03942.hp2 HG04184.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.3921-5680dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970595 | |||||||
chr2:134970598 | T | TTA | 132 | a0001c0001t0001g0112 a0001c0001t0002g0244 a0001c0001t0004g0111 others(129): Show |
134 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.3921-5683_3921-568 others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970598 | |||||||
chr2:134970599 | T | TA | 16 | a0001c0001t0002g0081 a0001c0002t0001g0023 a0001c0005t0002g0128 others(13): Show |
16 | HG01070.hp2 HG01243.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.3921-5684_3921-568 others(5): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970599 | |||||||
chr2:134970601 | T | C | 132 | a0001c0001t0001g0112 a0001c0001t0002g0244 a0001c0001t0004g0111 others(129): Show |
134 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.3921-5685A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970601 | |||||||
chr2:134970602 | T | C | 16 | a0001c0001t0002g0081 a0001c0002t0001g0023 a0001c0005t0002g0128 others(13): Show |
16 | HG01070.hp2 HG01243.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.3921-5686A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970602 | |||||||
chr2:134970690 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3921-5774G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970690 | |||||||
chr2:134970822 | T | C | 1 | a0010c0015t0002g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3921-5906A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970822 | |||||||
chr2:134970824 | T | C | 1 | a0010c0015t0002g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3921-5908A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970824 | |||||||
chr2:134970843 | T | C | 148 | a0001c0001t0001g0112 a0001c0001t0002g0081 a0001c0001t0002g0244 others(145): Show |
150 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.3921-5927A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970843 | |||||||
chr2:134970856 | C | T | 2 | a0003c0004t0003g0166 a0003c0004t0003g0167 |
2 | HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.3921-5940G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970856 | |||||||
chr2:134970877 | A | G | 5 | a0001c0001t0001g0112 a0001c0002t0001g0076 a0001c0005t0001g0088 others(2): Show |
5 | HG02109.hp2 HG02257.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3921-5961T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970877 | |||||||
chr2:134970968 | G | A | 75 | a0001c0001t0001g0032 a0001c0001t0001g0112 a0001c0001t0004g0111 others(72): Show |
77 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.3921-6052C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134970968 | |||||||
chr2:134971114 | T | C | 74 | a0001c0001t0002g0081 a0001c0001t0002g0244 a0001c0002t0001g0021 others(71): Show |
74 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.3921-6198A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134971114 | |||||||
chr2:134971150 | T | C | 148 | a0001c0001t0001g0112 a0001c0001t0002g0081 a0001c0001t0002g0244 others(145): Show |
150 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.3921-6234A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134971150 | |||||||
chr2:134971266 | C | T | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3921-6350G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134971266 | |||||||
chr2:134971307 | G | T | 1 | a0001c0001t0002g0012 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3921-6391C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134971307 | |||||||
chr2:134971388 | G | A | 74 | a0001c0001t0001g0112 a0001c0001t0004g0111 a0001c0002t0001g0076 others(71): Show |
76 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.3921-6472C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134971388 | |||||||
chr2:134971735 | T | A | 1 | a0001c0002t0001g0327 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3921-6819A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134971735 | |||||||
chr2:134971897 | T | C | 1 | a0005c0007t0002g0105 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3921-6981A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134971897 | |||||||
chr2:134972262 | C | T | 2 | a0001c0001t0004g0111 a0016c0028t0004g0114 |
2 | HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3921-7346G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134972262 | |||||||
chr2:134972350 | A | T | 1 | a0024c0034t0002g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3921-7434T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134972350 | |||||||
chr2:134972390 | A | G | 4 | a0005c0007t0001g0095 a0005c0007t0006g0011 a0005c0007t0006g0013 others(1): Show |
4 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3921-7474T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134972390 | |||||||
chr2:134972542 | T | G | 1 | a0004c0006t0001g0250 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3921-7626A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134972542 | |||||||
chr2:134972602 | AT | A | 63 | a0001c0001t0004g0111 a0001c0002t0001g0260 a0003c0004t0001g0004 others(60): Show |
65 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.3921-7687delA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134972602 | |||||||
chr2:134972629 | G | T | 15 | a0001c0001t0001g0112 a0001c0002t0001g0076 a0001c0005t0001g0088 others(12): Show |
15 | HG01261.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.3921-7713C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134972629 | |||||||
chr2:134972666 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0194 a0001c0001t0001g0257 |
4 | NA18949.hp2 NA18964.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.3921-7750C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134972666 | |||||||
chr2:134972729 | G | C | 15 | a0001c0001t0001g0112 a0001c0002t0001g0076 a0001c0005t0001g0088 others(12): Show |
15 | HG01261.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.3921-7813C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134972729 | |||||||
chr2:134973081 | T | C | 1 | a0005c0007t0002g0105 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3920+7740A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134973081 | |||||||
chr2:134973286 | T | C | 1 | a0001c0001t0001g0254 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3920+7535A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134973286 | |||||||
chr2:134973314 | C | T | 147 | a0001c0001t0001g0112 a0001c0001t0002g0081 a0001c0001t0004g0111 others(144): Show |
149 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.3920+7507G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134973314 | |||||||
chr2:134973484 | C | A | 14 | a0001c0001t0002g0081 a0001c0005t0002g0128 a0001c0009t0001g0143 others(11): Show |
14 | HG02080.hp1 HG02809.hp2 HG03130.hp1 others(11): Show |
intron_variant | MODIFIER | c.3920+7337G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134973484 | |||||||
chr2:134973548 | T | G | 1 | a0003c0004t0003g0167 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3920+7273A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134973548 | |||||||
chr2:134973649 | G | T | 147 | a0001c0001t0001g0112 a0001c0001t0002g0081 a0001c0001t0004g0111 others(144): Show |
149 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.3920+7172C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134973649 | |||||||
chr2:134973665 | G | C | 79 | a0001c0001t0001g0009 a0001c0001t0001g0137 a0001c0001t0001g0194 others(76): Show |
81 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.3920+7156C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134973665 | |||||||
chr2:134973669 | C | G | 1 | a0001c0001t0001g0159 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3920+7152G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134973669 | |||||||
chr2:134973723 | T | A | 1 | a0001c0020t0002g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3920+7098A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134973723 | |||||||
chr2:134973818 | C | T | 59 | a0001c0001t0004g0111 a0003c0004t0001g0004 a0003c0004t0001g0015 others(56): Show |
61 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.3920+7003G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134973818 | |||||||
chr2:134973868 | A | T | 1 | a0001c0001t0001g0058 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3920+6953T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134973868 | |||||||
chr2:134973999 | T | G | 4 | a0001c0001t0002g0245 a0001c0001t0003g0273 a0007c0012t0001g0092 others(1): Show |
4 | HG01175.hp1 HG01884.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.3920+6822A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134973999 | |||||||
chr2:134974070 | C | T | 1 | a0003c0004t0003g0167 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3920+6751G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134974070 | |||||||
chr2:134974314 | A | G | 1 | a0001c0002t0001g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3920+6507T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134974314 | |||||||
chr2:134974490 | G | A | 2 | a0011c0013t0004g0039 a0011c0013t0004g0040 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3920+6331C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134974490 | |||||||
chr2:134974927 | G | A | 4 | a0001c0001t0002g0081 a0001c0005t0002g0128 a0001c0009t0001g0143 others(1): Show |
4 | HG02809.hp2 HG03130.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.3920+5894C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134974927 | |||||||
chr2:134975351 | A | G | 1 | a0001c0001t0002g0100 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3920+5470T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134975351 | |||||||
chr2:134975401 | T | C | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3920+5420A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134975401 | |||||||
chr2:134975576 | C | T | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3920+5245G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134975576 | |||||||
chr2:134976010 | C | T | 3 | a0001c0005t0002g0093 a0001c0005t0002g0096 a0001c0005t0002g0097 |
3 | HG02622.hp1 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3920+4811G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134976010 | |||||||
chr2:134976136 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3920+4685C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134976136 | |||||||
chr2:134976278 | T | A | 54 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(51): Show |
56 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.3920+4543A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134976278 | |||||||
chr2:134976439 | A | G | 1 | a0001c0009t0001g0143 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3920+4382T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134976439 | |||||||
chr2:134976456 | T | C | 1 | a0001c0001t0002g0140 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3920+4365A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134976456 | |||||||
chr2:134976747 | T | TA | 8 | a0001c0001t0001g0009 a0001c0001t0001g0137 a0001c0001t0001g0171 others(5): Show |
8 | HG00639.hp2 HG00642.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.3920+4073dupT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134976747 | |||||||
chr2:134976747 | TA | T | 80 | a0001c0001t0002g0081 a0001c0002t0001g0016 a0001c0002t0001g0017 others(77): Show |
80 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.3920+4073delT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134976747 | |||||||
chr2:134976843 | G | A | 1 | a0001c0002t0001g0277 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3920+3978C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134976843 | |||||||
chr2:134977009 | G | A | 3 | a0001c0002t0001g0076 a0001c0002t0001g0209 a0001c0002t0003g0102 |
3 | HG02257.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3920+3812C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977009 | |||||||
chr2:134977047 | G | GA | 23 | a0001c0001t0001g0009 a0001c0001t0001g0246 a0001c0001t0001g0300 others(20): Show |
23 | HG00423.hp1 HG00639.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.3920+3773dupT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977047 | |||||||
chr2:134977047 | G | GAA | 59 | a0001c0001t0001g0159 a0001c0002t0001g0116 a0003c0004t0001g0004 others(56): Show |
61 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.3920+3772_3920+377 others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977047 | |||||||
chr2:134977103 | T | C | 12 | a0001c0001t0002g0081 a0001c0005t0002g0128 a0001c0009t0001g0143 others(9): Show |
12 | HG02080.hp1 HG02809.hp2 HG03130.hp1 others(9): Show |
intron_variant | MODIFIER | c.3920+3718A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977103 | |||||||
chr2:134977142 | T | G | 1 | a0001c0005t0002g0083 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3920+3679A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977142 | |||||||
chr2:134977172 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3920+3649C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977172 | |||||||
chr2:134977174 | T | C | 11 | a0005c0007t0001g0095 a0005c0007t0006g0011 a0005c0007t0006g0013 others(8): Show |
11 | HG01175.hp1 HG01261.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.3920+3647A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977174 | |||||||
chr2:134977185 | C | CT | 68 | a0001c0001t0002g0117 a0001c0002t0001g0016 a0001c0002t0001g0017 others(65): Show |
70 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.3920+3635dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977185 | |||||||
chr2:134977200 | G | A | 1 | a0006c0008t0002g0280 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3920+3621C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977200 | |||||||
chr2:134977296 | C | T | 67 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(64): Show |
69 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.3920+3525G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977296 | |||||||
chr2:134977356 | A | AT | 172 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0022 others(169): Show |
177 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.3920+3464dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977356 | |||||||
chr2:134977356 | A | ATT | 34 | a0001c0001t0001g0032 a0001c0001t0001g0062 a0001c0001t0001g0115 others(31): Show |
34 | HG00438.hp2 HG00544.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.3920+3463_3920+346 others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977356 | |||||||
chr2:134977356 | A | ATTT | 14 | a0001c0001t0001g0041 a0001c0001t0001g0080 a0001c0001t0002g0081 others(11): Show |
14 | HG01981.hp2 HG02080.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.3920+3462_3920+346 others(7): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977356 | |||||||
chr2:134977356 | A | ATTTTT | 51 | a0001c0002t0001g0016 a0001c0002t0001g0021 a0001c0002t0001g0023 others(48): Show |
51 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.3920+3460_3920+346 others(9): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977356 | |||||||
chr2:134977356 | A | ATTTTTT | 16 | a0001c0001t0002g0244 a0001c0002t0001g0017 a0001c0002t0001g0070 others(13): Show |
16 | HG00621.hp1 HG01192.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.3920+3459_3920+346 others(10): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977356 | |||||||
chr2:134977384 | A | G | 2 | a0011c0013t0004g0039 a0011c0013t0004g0040 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3920+3437T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977384 | |||||||
chr2:134977394 | GCT | G | 55 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(52): Show |
57 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.3920+3425_3920+342 others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977394 | |||||||
chr2:134977605 | G | A | 40 | a0002c0003t0001g0003 a0002c0003t0001g0008 a0002c0003t0001g0018 others(37): Show |
41 | HG00280.hp1 HG00423.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.3920+3216C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977605 | |||||||
chr2:134977651 | C | T | 2 | a0007c0012t0001g0092 a0007c0024t0001g0108 |
2 | HG01175.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.3920+3170G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977651 | |||||||
chr2:134977663 | A | G | 68 | a0001c0001t0002g0244 a0001c0002t0001g0016 a0001c0002t0001g0017 others(65): Show |
68 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.3920+3158T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977663 | |||||||
chr2:134977695 | C | T | 4 | a0001c0001t0002g0081 a0001c0005t0002g0128 a0001c0009t0001g0143 others(1): Show |
4 | HG02809.hp2 HG03130.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.3920+3126G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977695 | |||||||
chr2:134977740 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3920+3081A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977740 | |||||||
chr2:134977792 | T | C | 1 | a0024c0034t0002g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3920+3029A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977792 | |||||||
chr2:134977803 | A | G | 55 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(52): Show |
57 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.3920+3018T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977803 | |||||||
chr2:134977812 | G | A | 1 | a0002c0016t0001g0201 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3920+3009C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977812 | |||||||
chr2:134977890 | A | G | 1 | a0003c0004t0003g0154 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.3920+2931T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977890 | |||||||
chr2:134977949 | G | A | 147 | a0001c0001t0002g0081 a0001c0001t0002g0244 a0001c0002t0001g0016 others(144): Show |
149 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.3920+2872C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134977949 | |||||||
chr2:134978067 | T | C | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3920+2754A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134978067 | |||||||
chr2:134978078 | T | C | 68 | a0001c0001t0002g0244 a0001c0002t0001g0016 a0001c0002t0001g0017 others(65): Show |
68 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.3920+2743A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134978078 | |||||||
chr2:134978123 | G | A | 1 | a0003c0004t0003g0025 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.3920+2698C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134978123 | |||||||
chr2:134978188 | GA | G | 53 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(50): Show |
55 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.3920+2632delT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134978188 | |||||||
chr2:134978189 | A | T | 2 | a0003c0004t0003g0228 a0003c0004t0003g0286 |
2 | HG00438.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.3920+2632T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134978189 | |||||||
chr2:134978189 | AT | A | 71 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0021 others(68): Show |
71 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.3920+2631delA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134978189 | |||||||
chr2:134978289 | G | A | 2 | a0007c0012t0001g0092 a0007c0024t0001g0108 |
2 | HG01175.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.3920+2532C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134978289 | |||||||
chr2:134978334 | C | T | 67 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(64): Show |
69 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.3920+2487G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134978334 | |||||||
chr2:134978568 | C | G | 52 | a0001c0001t0001g0259 a0001c0001t0004g0111 a0002c0003t0001g0003 others(49): Show |
53 | HG00280.hp1 HG00423.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.3920+2253G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134978568 | |||||||
chr2:134978668 | C | T | 67 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(64): Show |
69 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.3920+2153G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134978668 | |||||||
chr2:134978868 | A | G | 2 | a0001c0001t0004g0111 a0016c0028t0004g0114 |
2 | HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3920+1953T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134978868 | |||||||
chr2:134978966 | G | A | 5 | a0005c0007t0001g0095 a0005c0007t0002g0105 a0005c0007t0006g0011 others(2): Show |
5 | HG02280.hp1 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.3920+1855C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134978966 | |||||||
chr2:134978976 | G | A | 3 | a0001c0002t0001g0155 a0001c0002t0001g0242 a0001c0002t0001g0263 |
3 | HG02735.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3920+1845C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134978976 | |||||||
chr2:134979016 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3920+1805G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979016 | |||||||
chr2:134979021 | C | G | 1 | a0001c0001t0001g0091 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3920+1800G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979021 | |||||||
chr2:134979088 | C | T | 12 | a0005c0007t0001g0095 a0005c0007t0002g0105 a0005c0007t0006g0011 others(9): Show |
12 | HG01175.hp1 HG01261.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.3920+1733G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979088 | |||||||
chr2:134979209 | G | T | 1 | a0001c0009t0002g0134 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3920+1612C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979209 | |||||||
chr2:134979270 | A | C | 1 | a0001c0002t0001g0214 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3920+1551T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979270 | |||||||
chr2:134979303 | A | G | 1 | a0003c0004t0001g0208 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3920+1518T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979303 | |||||||
chr2:134979443 | C | CGT | 4 | a0001c0001t0002g0031 a0001c0001t0002g0038 a0001c0001t0002g0317 others(1): Show |
4 | HG00738.hp2 HG02040.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.3920+1376_3920+137 others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979443 | |||||||
chr2:134979443 | CGT | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0029 others(77): Show |
82 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.3920+1376_3920+137 others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979443 | |||||||
chr2:134979443 | CGTGT | C | 78 | a0001c0001t0001g0009 a0001c0001t0001g0077 a0001c0001t0001g0099 others(75): Show |
79 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.3920+1374_3920+137 others(8): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979443 | |||||||
chr2:134979443 | CGTGTGT | C | 43 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0101 others(40): Show |
43 | HG00639.hp1 HG00735.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.3920+1372_3920+137 others(10): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979443 | |||||||
chr2:134979443 | CGTGTGTG others(1): Show |
C | 54 | a0001c0001t0001g0115 a0003c0004t0001g0004 a0003c0004t0001g0015 others(51): Show |
56 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.3920+1370_3920+137 others(12): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979443 | |||||||
chr2:134979572 | A | G | 1 | a0001c0001t0002g0291 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3920+1249T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979572 | |||||||
chr2:134979641 | G | GT | 38 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0068 others(35): Show |
38 | HG00423.hp1 HG00558.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.3920+1179dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979641 | |||||||
chr2:134979641 | G | GTT | 61 | a0001c0001t0002g0081 a0001c0002t0001g0016 a0001c0002t0001g0017 others(58): Show |
62 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.3920+1178_3920+117 others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979641 | |||||||
chr2:134979641 | G | GTTT | 46 | a0001c0001t0002g0244 a0001c0002t0001g0121 a0001c0002t0001g0155 others(43): Show |
47 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.3920+1177_3920+117 others(7): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979641 | |||||||
chr2:134979641 | G | GTTTT | 21 | a0003c0004t0001g0168 a0003c0004t0001g0172 a0003c0004t0003g0046 others(18): Show |
21 | HG00438.hp2 HG00558.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.3920+1176_3920+117 others(8): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979641 | |||||||
chr2:134979641 | GTTTTTTT others(5): Show |
G | 1 | a0004c0006t0001g0074 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3920+1168_3920+117 others(16): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979641 | |||||||
chr2:134979690 | G | A | 55 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(52): Show |
57 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.3920+1131C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979690 | |||||||
chr2:134979881 | G | C | 1 | a0020c0026t0001g0026 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3920+940C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134979881 | |||||||
chr2:134980287 | A | C | 1 | a0002c0003t0002g0069 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3920+534T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134980287 | |||||||
chr2:134980338 | G | T | 133 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0021 others(130): Show |
135 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.3920+483C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134980338 | |||||||
chr2:134980427 | A | AATTAGAC | 135 | a0001c0001t0002g0244 a0001c0002t0001g0016 a0001c0002t0001g0017 others(132): Show |
137 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.3920+393_3920+394i others(9): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134980427 | |||||||
chr2:134980436 | C | T | 56 | a0001c0001t0001g0112 a0001c0001t0004g0111 a0001c0005t0001g0088 others(53): Show |
57 | HG00280.hp1 HG00423.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.3920+385G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134980436 | |||||||
chr2:134980461 | C | T | 1 | a0003c0004t0003g0175 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3920+360G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134980461 | |||||||
chr2:134980715 | T | C | 1 | a0002c0003t0001g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3920+106A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134980715 | |||||||
chr2:134980780 | T | A | 3 | a0002c0003t0001g0196 a0002c0003t0001g0197 a0002c0003t0001g0199 |
3 | NA19000.hp2 NA19060.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.3920+41A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 12/12 | chr2 | 134980780 | |||||||
chr2:134981645 | C | T | 1 | a0007c0023t0004g0064 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3223-127G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134981645 | |||||||
chr2:134981880 | C | CT | 6 | a0001c0001t0001g0033 a0001c0001t0001g0159 a0001c0001t0001g0180 others(3): Show |
6 | HG01099.hp2 HG04228.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.3223-363dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134981880 | |||||||
chr2:134981880 | CT | C | 19 | a0001c0001t0002g0050 a0001c0001t0002g0136 a0001c0002t0001g0051 others(16): Show |
19 | HG01168.hp2 HG01358.hp2 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.3223-363delA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134981880 | |||||||
chr2:134981880 | CTT | C | 59 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0021 others(56): Show |
59 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.3223-364_3223-363d others(4): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134981880 | |||||||
chr2:134981880 | CTTT | C | 8 | a0005c0007t0006g0011 a0005c0007t0006g0013 a0005c0007t0006g0014 others(5): Show |
8 | HG01243.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3223-365_3223-363d others(5): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134981880 | |||||||
chr2:134981880 | CTTTT | C | 56 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(53): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.3223-366_3223-363d others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134981880 | |||||||
chr2:134981897 | T | TG | 10 | a0001c0005t0002g0128 a0001c0009t0001g0143 a0004c0006t0001g0010 others(7): Show |
10 | HG02080.hp1 HG02809.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.3223-380_3223-379i others(3): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134981897 | |||||||
chr2:134982039 | C | T | 145 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0021 others(142): Show |
147 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.3223-521G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134982039 | |||||||
chr2:134982113 | C | CT | 77 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0098 others(74): Show |
77 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.3223-596dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134982113 | |||||||
chr2:134982113 | CT | C | 19 | a0001c0001t0002g0050 a0001c0001t0002g0206 a0001c0001t0003g0193 others(16): Show |
19 | HG01175.hp1 HG02055.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.3223-596delA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134982113 | |||||||
chr2:134982113 | CTT | C | 52 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(49): Show |
54 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.3223-597_3223-596d others(4): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134982113 | |||||||
chr2:134982144 | G | A | 1 | a0001c0002t0001g0322 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3223-626C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134982144 | |||||||
chr2:134982154 | G | C | 1 | a0001c0001t0001g0123 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3223-636C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134982154 | |||||||
chr2:134982280 | G | A | 1 | a0001c0002t0001g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3223-762C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134982280 | |||||||
chr2:134982352 | CT | C | 79 | a0001c0001t0001g0009 a0001c0001t0001g0115 a0001c0001t0001g0137 others(76): Show |
81 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.3223-835delA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134982352 | |||||||
chr2:134982393 | C | G | 1 | a0003c0004t0003g0286 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3223-875G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134982393 | |||||||
chr2:134982443 | G | A | 1 | a0002c0003t0001g0323 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3223-925C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134982443 | |||||||
chr2:134982725 | G | A | 146 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0021 others(143): Show |
148 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.3222+951C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134982725 | |||||||
chr2:134982915 | G | T | 53 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(50): Show |
55 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.3222+761C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134982915 | |||||||
chr2:134983156 | A | G | 1 | a0002c0003t0001g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3222+520T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134983156 | |||||||
chr2:134983243 | T | C | 1 | a0001c0001t0004g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3222+433A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134983243 | |||||||
chr2:134983293 | C | A | 55 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(52): Show |
57 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.3222+383G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134983293 | |||||||
chr2:134983306 | A | G | 66 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0021 others(63): Show |
66 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.3222+370T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134983306 | |||||||
chr2:134983379 | T | A | 1 | a0007c0023t0004g0064 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3222+297A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134983379 | |||||||
chr2:134983491 | G | A | 135 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0021 others(132): Show |
137 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.3222+185C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134983491 | |||||||
chr2:134983633 | G | T | 1 | a0001c0002t0001g0202 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3222+43C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 11/12 | chr2 | 134983633 | |||||||
chr2:134983855 | C | A | 55 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(52): Show |
57 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.3073-30G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/12 | chr2 | 134983855 | |||||||
chr2:134983969 | C | T | 4 | a0005c0007t0001g0095 a0005c0007t0006g0011 a0005c0007t0006g0013 others(1): Show |
4 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3073-144G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/12 | chr2 | 134983969 | |||||||
chr2:134984068 | C | T | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3073-243G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/12 | chr2 | 134984068 | |||||||
chr2:134984160 | G | A | 2 | a0001c0002t0001g0311 a0001c0002t0001g0319 |
2 | HG02698.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.3073-335C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/12 | chr2 | 134984160 | |||||||
chr2:134984306 | C | A | 1 | a0001c0002t0001g0153 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3073-481G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/12 | chr2 | 134984306 | |||||||
chr2:134984631 | A | G | 10 | a0001c0001t0002g0066 a0001c0001t0002g0086 a0001c0001t0002g0100 others(7): Show |
10 | HG01884.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.3073-806T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/12 | chr2 | 134984631 | |||||||
chr2:134984719 | G | A | 1 | a0007c0023t0004g0064 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3073-894C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/12 | chr2 | 134984719 | |||||||
chr2:134984755 | C | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0044 others(1): Show |
4 | HG01952.hp1 HG01978.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.3073-930G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/12 | chr2 | 134984755 | |||||||
chr2:134985012 | G | C | 3 | a0001c0001t0001g0068 a0001c0001t0002g0222 a0001c0001t0002g0237 |
3 | HG01106.hp1 HG01175.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.3072+788C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/12 | chr2 | 134985012 | |||||||
chr2:134985029 | T | C | 135 | a0001c0001t0002g0244 a0001c0002t0001g0016 a0001c0002t0001g0017 others(132): Show |
137 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.3072+771A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/12 | chr2 | 134985029 | |||||||
chr2:134985143 | A | G | 1 | a0002c0003t0002g0067 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.3072+657T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/12 | chr2 | 134985143 | |||||||
chr2:134985155 | A | T | 2 | a0007c0012t0001g0109 a0007c0024t0001g0108 |
2 | HG01175.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3072+645T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/12 | chr2 | 134985155 | |||||||
chr2:134985411 | T | A | 1 | a0001c0001t0001g0194 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.3072+389A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/12 | chr2 | 134985411 | |||||||
chr2:134985480 | G | T | 1 | a0001c0002t0001g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3072+320C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/12 | chr2 | 134985480 | |||||||
chr2:134985664 | TCAAA | T | 135 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0021 others(132): Show |
137 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.3072+132_3072+135d others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 10/12 | chr2 | 134985664 | |||||||
chr2:134988317 | T | C | 4 | a0003c0004t0003g0198 a0003c0004t0003g0228 a0003c0004t0003g0276 others(1): Show |
4 | NA18967.hp2 NA19004.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-64A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134988317 | |||||||
chr2:134988395 | T | C | 1 | a0003c0004t0001g0015 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.619-142A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134988395 | |||||||
chr2:134988521 | G | C | 1 | a0002c0003t0001g0003 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.619-268C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134988521 | |||||||
chr2:134988601 | G | A | 5 | a0005c0007t0001g0095 a0005c0007t0002g0105 a0005c0007t0006g0011 others(2): Show |
5 | HG02280.hp1 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.619-348C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134988601 | |||||||
chr2:134988617 | T | C | 1 | a0025c0032t0001g0274 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.619-364A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134988617 | |||||||
chr2:134988805 | T | G | 1 | a0001c0002t0001g0221 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.619-552A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134988805 | |||||||
chr2:134988995 | G | A | 66 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(63): Show |
68 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.619-742C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134988995 | |||||||
chr2:134989186 | C | A | 2 | a0001c0002t0001g0139 a0001c0002t0001g0141 |
2 | HG01358.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.619-933G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134989186 | |||||||
chr2:134989202 | A | C | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.619-949T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134989202 | |||||||
chr2:134989239 | C | A | 4 | a0005c0007t0001g0095 a0005c0007t0006g0011 a0005c0007t0006g0013 others(1): Show |
4 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.619-986G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134989239 | |||||||
chr2:134989383 | C | T | 8 | a0004c0006t0001g0010 a0004c0006t0001g0049 a0004c0006t0001g0074 others(5): Show |
8 | HG02080.hp1 HG03195.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.619-1130G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134989383 | |||||||
chr2:134989431 | G | A | 1 | a0007c0012t0001g0109 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.619-1178C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134989431 | |||||||
chr2:134989756 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0200 |
2 | HG02080.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.619-1503G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134989756 | |||||||
chr2:134989916 | T | C | 1 | a0001c0001t0002g0020 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.618+1621A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134989916 | |||||||
chr2:134990082 | C | CA | 67 | a0001c0001t0001g0129 a0001c0009t0002g0134 a0002c0003t0013g0075 others(64): Show |
69 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.618+1454dupT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990082 | |||||||
chr2:134990216 | T | G | 1 | a0001c0009t0001g0143 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.618+1321A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990216 | |||||||
chr2:134990460 | G | GT | 51 | a0001c0001t0001g0259 a0001c0001t0002g0235 a0001c0005t0002g0128 others(48): Show |
52 | HG00280.hp1 HG00423.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.618+1076dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990460 | |||||||
chr2:134990460 | GT | G | 128 | a0001c0001t0002g0244 a0001c0002t0001g0016 a0001c0002t0001g0021 others(125): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.618+1076delA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990460 | |||||||
chr2:134990468 | T | G | 1 | a0001c0002t0001g0311 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.618+1069A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990468 | |||||||
chr2:134990469 | T | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0027 others(43): Show |
47 | HG00558.hp1 HG00609.hp2 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.618+1068A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990469 | |||||||
chr2:134990531 | C | T | 2 | a0011c0013t0004g0039 a0011c0013t0004g0040 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.618+1006G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990531 | |||||||
chr2:134990546 | G | A | 2 | a0001c0005t0002g0001 a0001c0005t0002g0084 |
3 | HG02647.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.618+991C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990546 | |||||||
chr2:134990626 | G | A | 68 | a0001c0001t0002g0244 a0001c0002t0001g0016 a0001c0002t0001g0017 others(65): Show |
68 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.618+911C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990626 | |||||||
chr2:134990630 | C | T | 9 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(6): Show |
9 | HG00735.hp1 HG02145.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.618+907G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990630 | |||||||
chr2:134990649 | T | C | 1 | a0004c0006t0001g0256 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.618+888A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990649 | |||||||
chr2:134990666 | G | A | 1 | a0007c0023t0004g0064 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.618+871C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990666 | |||||||
chr2:134990705 | A | G | 134 | a0001c0001t0002g0244 a0001c0002t0001g0016 a0001c0002t0001g0017 others(131): Show |
136 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.618+832T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990705 | |||||||
chr2:134990706 | T | A | 134 | a0001c0001t0002g0244 a0001c0002t0001g0016 a0001c0002t0001g0017 others(131): Show |
136 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.618+831A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990706 | |||||||
chr2:134990729 | C | G | 1 | a0001c0001t0002g0030 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.618+808G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990729 | |||||||
chr2:134990816 | T | G | 52 | a0001c0001t0001g0259 a0002c0003t0001g0003 a0002c0003t0001g0007 others(49): Show |
53 | HG00280.hp1 HG00423.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.618+721A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990816 | |||||||
chr2:134990883 | A | G | 1 | a0001c0002t0001g0248 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.618+654T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990883 | |||||||
chr2:134990957 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.618+580C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990957 | |||||||
chr2:134990980 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.618+557C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134990980 | |||||||
chr2:134991000 | C | T | 1 | a0026c0035t0002g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.618+537G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134991000 | |||||||
chr2:134991020 | C | T | 53 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(50): Show |
55 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.618+517G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134991020 | |||||||
chr2:134991031 | AC | A | 3 | a0001c0002t0001g0155 a0001c0002t0001g0242 a0001c0002t0001g0263 |
3 | HG02735.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.618+505delG | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134991031 | |||||||
chr2:134991073 | G | A | 1 | a0022c0031t0002g0059 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.618+464C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134991073 | |||||||
chr2:134991128 | C | T | 10 | a0005c0007t0001g0095 a0005c0007t0002g0105 a0005c0007t0006g0011 others(7): Show |
10 | HG01261.hp1 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.618+409G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134991128 | |||||||
chr2:134991201 | T | C | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.618+336A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134991201 | |||||||
chr2:134991218 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.618+319C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134991218 | |||||||
chr2:134991302 | A | AAAAAC | 49 | a0002c0003t0001g0275 a0003c0004t0001g0004 a0003c0004t0001g0015 others(46): Show |
51 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+230_618+234dup others(5): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134991302 | |||||||
chr2:134991302 | A | AAAAACAA others(3): Show |
4 | a0003c0004t0003g0165 a0003c0004t0003g0216 a0003c0004t0003g0297 others(1): Show |
4 | HG00741.hp2 NA18944.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.618+225_618+234dup others(10): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134991302 | |||||||
chr2:134991302 | AAAAAC | A | 84 | a0001c0001t0001g0122 a0001c0001t0002g0244 a0001c0002t0001g0016 others(81): Show |
84 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.618+230_618+234del others(5): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134991302 | |||||||
chr2:134991527 | C | G | 1 | a0003c0004t0003g0163 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.618+10G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 9/12 | chr2 | 134991527 | |||||||
chr2:134992080 | A | G | 134 | a0001c0001t0002g0244 a0001c0002t0001g0016 a0001c0002t0001g0017 others(131): Show |
136 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.575-500T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134992080 | |||||||
chr2:134992262 | C | A | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.575-682G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134992262 | |||||||
chr2:134992339 | C | T | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.575-759G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134992339 | |||||||
chr2:134992403 | A | C | 1 | a0001c0009t0001g0143 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.575-823T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134992403 | |||||||
chr2:134992453 | T | C | 134 | a0001c0001t0002g0244 a0001c0002t0001g0016 a0001c0002t0001g0017 others(131): Show |
136 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.575-873A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134992453 | |||||||
chr2:134992463 | G | C | 1 | a0001c0002t0001g0221 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.575-883C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134992463 | |||||||
chr2:134992546 | A | G | 1 | a0021c0029t0011g0037 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.575-966T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134992546 | |||||||
chr2:134992675 | A | AT | 70 | a0001c0005t0002g0128 a0001c0009t0002g0134 a0003c0004t0001g0004 others(67): Show |
72 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.575-1096dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134992675 | |||||||
chr2:134992675 | A | ATT | 72 | a0001c0001t0002g0244 a0001c0002t0001g0016 a0001c0002t0001g0017 others(69): Show |
72 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.575-1097_575-1096d others(4): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134992675 | |||||||
chr2:134992724 | T | C | 66 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(63): Show |
68 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.575-1144A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134992724 | |||||||
chr2:134992744 | G | A | 1 | a0008c0010t0001g0229 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.575-1164C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134992744 | |||||||
chr2:134992794 | C | T | 2 | a0003c0004t0003g0198 a0003c0004t0003g0276 |
2 | NA19004.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.575-1214G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134992794 | |||||||
chr2:134992826 | T | A | 3 | a0007c0012t0001g0092 a0007c0012t0001g0109 a0007c0024t0001g0108 |
3 | HG01175.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.575-1246A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134992826 | |||||||
chr2:134993122 | C | T | 134 | a0001c0001t0002g0244 a0001c0002t0001g0016 a0001c0002t0001g0017 others(131): Show |
136 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.575-1542G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134993122 | |||||||
chr2:134993125 | C | T | 68 | a0001c0001t0002g0244 a0001c0002t0001g0016 a0001c0002t0001g0017 others(65): Show |
68 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.575-1545G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134993125 | |||||||
chr2:134993224 | G | A | 65 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(62): Show |
67 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.575-1644C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134993224 | |||||||
chr2:134993279 | T | C | 145 | a0001c0001t0002g0244 a0001c0002t0001g0016 a0001c0002t0001g0017 others(142): Show |
147 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.575-1699A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134993279 | |||||||
chr2:134993347 | A | G | 9 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(6): Show |
9 | HG00735.hp1 HG02145.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.575-1767T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134993347 | |||||||
chr2:134993657 | C | T | 1 | a0003c0004t0003g0052 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.575-2077G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134993657 | |||||||
chr2:134993751 | C | A | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.575-2171G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134993751 | |||||||
chr2:134993831 | C | T | 3 | a0001c0002t0001g0155 a0001c0002t0001g0242 a0001c0002t0001g0263 |
3 | HG02735.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.575-2251G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134993831 | |||||||
chr2:134993862 | G | A | 1 | a0001c0002t0001g0231 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.575-2282C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134993862 | |||||||
chr2:134993922 | A | T | 1 | a0001c0001t0003g0193 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.575-2342T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134993922 | |||||||
chr2:134994271 | T | C | 2 | a0003c0004t0001g0004 a0003c0004t0001g0261 |
3 | NA18964.hp2 NA18969.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.575-2691A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134994271 | |||||||
chr2:134994691 | C | T | 52 | a0001c0001t0002g0244 a0001c0002t0001g0016 a0001c0002t0001g0017 others(49): Show |
52 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.575-3111G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134994691 | |||||||
chr2:134994851 | A | G | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.575-3271T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134994851 | |||||||
chr2:134994985 | G | A | 11 | a0001c0005t0002g0128 a0001c0009t0001g0143 a0001c0009t0002g0134 others(8): Show |
11 | HG02080.hp1 HG02809.hp2 HG03195.hp1 others(8): Show |
intron_variant | MODIFIER | c.575-3405C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134994985 | |||||||
chr2:134995094 | T | G | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.575-3514A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134995094 | |||||||
chr2:134995103 | A | G | 147 | a0001c0001t0002g0079 a0001c0001t0002g0244 a0001c0002t0001g0016 others(144): Show |
149 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.575-3523T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134995103 | |||||||
chr2:134995143 | C | T | 7 | a0001c0002t0001g0051 a0001c0002t0001g0205 a0001c0002t0001g0210 others(4): Show |
7 | HG01168.hp2 HG02698.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.575-3563G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134995143 | |||||||
chr2:134995280 | C | T | 2 | a0008c0010t0001g0150 a0008c0010t0002g0151 |
2 | HG00558.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.574+3458G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134995280 | |||||||
chr2:134995316 | C | CA | 15 | a0001c0001t0001g0300 a0001c0001t0002g0142 a0001c0002t0003g0102 others(12): Show |
15 | HG01261.hp1 HG02080.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.574+3421dupT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134995316 | |||||||
chr2:134995316 | C | CAA | 79 | a0001c0001t0002g0079 a0001c0002t0001g0016 a0001c0002t0001g0017 others(76): Show |
79 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.574+3420_574+3421d others(4): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134995316 | |||||||
chr2:134995316 | C | CAAA | 55 | a0001c0001t0002g0244 a0001c0002t0001g0139 a0001c0002t0002g0224 others(52): Show |
57 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.574+3419_574+3421d others(5): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134995316 | |||||||
chr2:134995492 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.574+3246C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134995492 | |||||||
chr2:134995542 | A | G | 1 | a0018c0033t0005g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.574+3196T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134995542 | |||||||
chr2:134995600 | A | C | 2 | a0011c0013t0004g0039 a0011c0013t0004g0040 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.574+3138T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134995600 | |||||||
chr2:134995688 | G | A | 3 | a0007c0012t0001g0092 a0007c0012t0001g0109 a0007c0024t0001g0108 |
3 | HG01175.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.574+3050C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134995688 | |||||||
chr2:134995695 | T | C | 3 | a0001c0002t0001g0231 a0001c0002t0001g0322 a0001c0018t0001g0144 |
3 | HG00639.hp1 HG03669.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.574+3043A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134995695 | |||||||
chr2:134995757 | A | G | 3 | a0002c0003t0001g0124 a0002c0003t0001g0127 a0002c0003t0001g0211 |
3 | HG00735.hp2 HG02258.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.574+2981T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134995757 | |||||||
chr2:134995758 | T | A | 67 | a0001c0002t0003g0102 a0003c0004t0001g0004 a0003c0004t0001g0015 others(64): Show |
69 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.574+2980A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134995758 | |||||||
chr2:134995898 | G | T | 3 | a0001c0001t0002g0086 a0001c0005t0002g0083 a0001c0005t0002g0089 |
3 | HG02630.hp1 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.574+2840C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134995898 | |||||||
chr2:134995951 | C | CT | 135 | a0001c0001t0002g0079 a0001c0001t0002g0244 a0001c0002t0001g0016 others(132): Show |
137 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.574+2786dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134995951 | |||||||
chr2:134996064 | C | T | 1 | a0004c0006t0001g0250 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.574+2674G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134996064 | |||||||
chr2:134996131 | G | T | 2 | a0011c0013t0004g0039 a0011c0013t0004g0040 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.574+2607C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134996131 | |||||||
chr2:134996192 | C | G | 1 | a0007c0023t0004g0064 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574+2546G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134996192 | |||||||
chr2:134996271 | C | CT | 15 | a0001c0001t0002g0110 a0001c0001t0002g0113 a0002c0003t0001g0008 others(12): Show |
15 | HG00423.hp1 HG00741.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.574+2466dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134996271 | |||||||
chr2:134996271 | CT | C | 15 | a0001c0001t0001g0058 a0001c0001t0001g0091 a0001c0001t0001g0107 others(12): Show |
15 | HG01071.hp2 HG01175.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.574+2466delA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134996271 | |||||||
chr2:134996271 | CTT | C | 120 | a0001c0001t0002g0244 a0001c0002t0001g0017 a0001c0002t0001g0021 others(117): Show |
122 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.574+2465_574+2466d others(4): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134996271 | |||||||
chr2:134996271 | CTTT | C | 7 | a0001c0002t0001g0016 a0001c0002t0001g0176 a0003c0004t0003g0297 others(4): Show |
7 | HG02155.hp1 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.574+2464_574+2466d others(5): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134996271 | |||||||
chr2:134996444 | C | T | 2 | a0003c0004t0003g0234 a0003c0004t0003g0236 |
2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.574+2294G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134996444 | |||||||
chr2:134996460 | G | A | 136 | a0001c0001t0002g0079 a0001c0001t0002g0244 a0001c0002t0001g0016 others(133): Show |
138 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.574+2278C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134996460 | |||||||
chr2:134996495 | T | C | 8 | a0001c0001t0002g0066 a0001c0001t0002g0086 a0001c0001t0002g0100 others(5): Show |
8 | HG01884.hp2 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.574+2243A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134996495 | |||||||
chr2:134996538 | G | T | 1 | a0024c0034t0002g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.574+2200C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134996538 | |||||||
chr2:134996657 | C | T | 7 | a0005c0007t0001g0095 a0005c0007t0002g0105 a0005c0007t0006g0011 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.574+2081G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134996657 | |||||||
chr2:134996689 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.574+2049C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134996689 | |||||||
chr2:134996746 | C | T | 1 | a0002c0003t0001g0124 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.574+1992G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134996746 | |||||||
chr2:134996910 | G | A | 8 | a0004c0006t0001g0010 a0004c0006t0001g0049 a0004c0006t0001g0074 others(5): Show |
8 | HG02080.hp1 HG03195.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.574+1828C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134996910 | |||||||
chr2:134997005 | C | T | 1 | a0007c0023t0004g0064 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574+1733G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997005 | |||||||
chr2:134997061 | A | C | 68 | a0001c0002t0003g0102 a0001c0005t0002g0128 a0002c0003t0013g0075 others(65): Show |
70 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.574+1677T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997061 | |||||||
chr2:134997095 | A | G | 1 | a0001c0009t0002g0134 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.574+1643T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997095 | |||||||
chr2:134997146 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.574+1592G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997146 | |||||||
chr2:134997291 | C | T | 53 | a0003c0004t0001g0004 a0003c0004t0001g0015 a0003c0004t0001g0168 others(50): Show |
55 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.574+1447G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997291 | |||||||
chr2:134997365 | G | T | 137 | a0001c0001t0002g0079 a0001c0001t0002g0244 a0001c0002t0001g0016 others(134): Show |
139 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.574+1373C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997365 | |||||||
chr2:134997447 | T | G | 136 | a0001c0001t0001g0058 a0001c0001t0002g0079 a0001c0001t0002g0244 others(133): Show |
138 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.574+1291A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997447 | |||||||
chr2:134997448 | T | A | 2 | a0003c0004t0003g0234 a0003c0004t0003g0236 |
2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.574+1290A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997448 | |||||||
chr2:134997480 | T | A | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.574+1258A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997480 | |||||||
chr2:134997549 | A | G | 185 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0027 others(182): Show |
188 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.574+1189T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997549 | |||||||
chr2:134997602 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.574+1136G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997602 | |||||||
chr2:134997616 | C | T | 81 | a0001c0001t0002g0079 a0001c0001t0002g0244 a0001c0002t0001g0016 others(78): Show |
81 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.574+1122G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997616 | |||||||
chr2:134997638 | G | A | 1 | a0001c0002t0001g0231 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.574+1100C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997638 | |||||||
chr2:134997679 | C | T | 7 | a0004c0006t0001g0010 a0004c0006t0001g0049 a0004c0006t0001g0074 others(4): Show |
7 | HG02080.hp1 NA18947.hp2 NA18992.hp1 others(4): Show |
intron_variant | MODIFIER | c.574+1059G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997679 | |||||||
chr2:134997726 | T | G | 1 | a0001c0001t0001g0246 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.574+1012A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997726 | |||||||
chr2:134997797 | G | A | 64 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0021 others(61): Show |
64 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.574+941C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997797 | |||||||
chr2:134997804 | C | T | 131 | a0001c0001t0001g0058 a0001c0001t0002g0079 a0001c0001t0002g0244 others(128): Show |
133 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.574+934G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997804 | |||||||
chr2:134997812 | C | T | 5 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0140 others(2): Show |
5 | HG02293.hp1 HG04115.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.574+926G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997812 | |||||||
chr2:134997817 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0002g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.574+910_574+920dup others(11): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997817 | |||||||
chr2:134997817 | C | CAAAAAAA others(5): Show |
10 | a0001c0009t0001g0143 a0001c0009t0002g0134 a0004c0006t0001g0010 others(7): Show |
10 | HG02080.hp1 HG02809.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.574+909_574+920dup others(12): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997817 | |||||||
chr2:134997817 | C | CAAAAAAA others(11): Show |
4 | a0001c0002t0001g0076 a0001c0002t0001g0104 a0001c0002t0001g0209 others(1): Show |
4 | HG02071.hp2 HG02257.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.574+920_574+921ins others(18): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997817 | |||||||
chr2:134997817 | C | CAAAAAAA others(13): Show |
1 | a0001c0002t0001g0214 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.574+920_574+921ins others(20): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997817 | |||||||
chr2:134997817 | C | CAAAAAAA others(18): Show |
1 | a0003c0004t0003g0234 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.574+920_574+921ins others(25): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997817 | |||||||
chr2:134997817 | C | CAAAAAAA others(19): Show |
1 | a0024c0034t0002g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.574+920_574+921ins others(26): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997817 | |||||||
chr2:134997817 | C | CAAAAAAA others(20): Show |
30 | a0001c0002t0001g0016 a0001c0002t0001g0023 a0001c0002t0001g0051 others(27): Show |
30 | HG00544.hp1 HG00639.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.574+920_574+921ins others(27): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997817 | |||||||
chr2:134997817 | C | CAAAAAAA others(21): Show |
18 | a0001c0002t0001g0017 a0001c0002t0001g0021 a0001c0002t0001g0047 others(15): Show |
18 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.574+920_574+921ins others(28): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997817 | |||||||
chr2:134997817 | C | CAAAAAAA others(22): Show |
4 | a0001c0002t0001g0153 a0001c0002t0001g0205 a0001c0002t0001g0217 others(1): Show |
4 | HG01123.hp2 HG01168.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.574+920_574+921ins others(29): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997817 | |||||||
chr2:134997817 | C | CAAAAAAA others(23): Show |
5 | a0001c0002t0001g0024 a0001c0002t0001g0121 a0001c0002t0001g0321 others(2): Show |
5 | HG01978.hp1 HG02071.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.574+920_574+921ins others(30): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997817 | |||||||
chr2:134997817 | C | CAAAAAAA others(24): Show |
1 | a0001c0002t0001g0268 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.574+920_574+921ins others(31): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997817 | |||||||
chr2:134997817 | C | CAAAAAAA others(26): Show |
1 | a0001c0002t0001g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.574+920_574+921ins others(33): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997817 | |||||||
chr2:134997817 | C | CAAAAAAA others(31): Show |
1 | a0001c0002t0001g0169 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.574+920_574+921ins others(38): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997817 | |||||||
chr2:134997817 | C | CAAAAAAA others(32): Show |
2 | a0001c0001t0002g0244 a0001c0002t0001g0225 |
2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.574+920_574+921ins others(39): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997817 | |||||||
chr2:134997820 | A | AAAAAAAA others(10): Show |
5 | a0001c0002t0003g0102 a0003c0004t0003g0154 a0003c0004t0003g0297 others(2): Show |
5 | HG01175.hp1 HG01261.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.574+917_574+918ins others(17): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997820 | |||||||
chr2:134997820 | A | AAAAAAAA others(9): Show |
53 | a0001c0001t0001g0058 a0001c0005t0002g0128 a0003c0004t0001g0004 others(50): Show |
55 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.574+917_574+918ins others(16): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997820 | |||||||
chr2:134997820 | A | AAAAAACA others(9): Show |
2 | a0011c0013t0004g0039 a0011c0013t0004g0040 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.574+917_574+918ins others(16): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997820 | |||||||
chr2:134997928 | C | T | 1 | a0007c0023t0004g0064 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574+810G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134997928 | |||||||
chr2:134998041 | A | G | 9 | a0001c0001t0002g0081 a0001c0005t0002g0128 a0001c0009t0004g0131 others(6): Show |
9 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.574+697T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134998041 | |||||||
chr2:134998046 | T | C | 81 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(78): Show |
81 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.574+692A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134998046 | |||||||
chr2:134998059 | A | G | 273 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0022 others(270): Show |
277 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.574+679T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134998059 | |||||||
chr2:134998065 | G | A | 2 | a0002c0003t0002g0191 a0002c0003t0002g0192 |
2 | NA19085.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.574+673C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134998065 | |||||||
chr2:134998101 | C | T | 1 | a0005c0007t0002g0105 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.574+637G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134998101 | |||||||
chr2:134998329 | A | G | 6 | a0001c0001t0002g0244 a0001c0001t0002g0317 a0001c0002t0001g0169 others(3): Show |
6 | HG00738.hp2 HG01192.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.574+409T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134998329 | |||||||
chr2:134998346 | T | G | 8 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(5): Show |
8 | HG00735.hp1 HG02145.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.574+392A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134998346 | |||||||
chr2:134998578 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.574+160G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134998578 | |||||||
chr2:134998637 | T | C | 1 | a0005c0007t0002g0105 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.574+101A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134998637 | |||||||
chr2:134998695 | G | T | 61 | a0001c0001t0001g0068 a0001c0001t0001g0112 a0001c0001t0001g0123 others(58): Show |
62 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.574+43C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | 134998695 | |||||||
chr2:134999020 | G | T | 1 | a0002c0003t0001g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.315-23C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 7/12 | chr2 | 134999020 | |||||||
chr2:134999291 | T | C | 2 | a0001c0002t0001g0060 a0001c0002t0001g0061 |
2 | NA18939.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.315-294A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 7/12 | chr2 | 134999291 | |||||||
chr2:134999489 | G | A | 2 | a0012c0017t0001g0043 a0012c0017t0003g0055 |
2 | HG04184.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.314+448C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 7/12 | chr2 | 134999489 | |||||||
chr2:134999548 | T | C | 1 | a0001c0001t0002g0063 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.314+389A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 7/12 | chr2 | 134999548 | |||||||
chr2:134999620 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.314+317G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 7/12 | chr2 | 134999620 | |||||||
chr2:134999650 | T | C | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.314+287A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 7/12 | chr2 | 134999650 | |||||||
chr2:134999750 | C | T | 119 | a0001c0001t0001g0091 a0001c0001t0001g0152 a0001c0001t0001g0157 others(116): Show |
123 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.314+187G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 7/12 | chr2 | 134999750 | |||||||
chr2:134999753 | AAC | A | 118 | a0001c0001t0001g0091 a0001c0001t0001g0152 a0001c0001t0001g0157 others(115): Show |
122 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.314+182_314+183del others(2): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 7/12 | chr2 | 134999753 | |||||||
chr2:134999754 | A | T | 1 | a0012c0017t0003g0055 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.314+183T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 7/12 | chr2 | 134999754 | |||||||
chr2:134999897 | A | G | 2 | a0001c0001t0002g0206 a0001c0009t0002g0134 |
2 | HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.314+40T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 7/12 | chr2 | 134999897 | |||||||
chr2:135000016 | C | T | 1 | a0010c0015t0001g0103 | 1 | HG01261.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.236-1G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135000016 | |||||||
chr2:135000082 | A | G | 1 | a0001c0005t0002g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.236-67T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135000082 | |||||||
chr2:135000358 | G | A | 1 | a0001c0002t0001g0311 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.236-343C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135000358 | |||||||
chr2:135000546 | T | C | 4 | a0001c0001t0005g0147 a0001c0005t0005g0145 a0017c0019t0005g0146 others(1): Show |
4 | HG02258.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-531A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135000546 | |||||||
chr2:135000562 | G | A | 1 | a0010c0015t0001g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.236-547C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135000562 | |||||||
chr2:135000593 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.236-578G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135000593 | |||||||
chr2:135000661 | G | T | 129 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(126): Show |
129 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.236-646C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135000661 | |||||||
chr2:135000853 | C | T | 1 | a0007c0012t0001g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.236-838G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135000853 | |||||||
chr2:135000950 | A | T | 129 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(126): Show |
129 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.236-935T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135000950 | |||||||
chr2:135001056 | A | G | 1 | a0001c0001t0002g0235 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.236-1041T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135001056 | |||||||
chr2:135001143 | A | G | 3 | a0001c0005t0001g0130 a0024c0034t0002g0119 a0026c0035t0002g0118 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.236-1128T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135001143 | |||||||
chr2:135001400 | T | C | 1 | a0001c0001t0002g0206 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.236-1385A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135001400 | |||||||
chr2:135001525 | C | T | 88 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(85): Show |
88 | HG00408.hp2 HG00438.hp1 HG00741.hp1 others(85): Show |
intron_variant | MODIFIER | c.236-1510G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135001525 | |||||||
chr2:135001575 | T | C | 13 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(10): Show |
13 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-1560A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135001575 | |||||||
chr2:135001605 | T | G | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.236-1590A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135001605 | |||||||
chr2:135001713 | T | G | 2 | a0001c0001t0002g0244 a0009c0011t0002g0243 |
2 | HG01192.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.236-1698A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135001713 | |||||||
chr2:135001951 | T | C | 1 | a0020c0026t0001g0026 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.236-1936A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135001951 | |||||||
chr2:135002004 | T | C | 1 | a0001c0002t0001g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.236-1989A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135002004 | |||||||
chr2:135002058 | A | C | 1 | a0001c0002t0001g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.236-2043T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135002058 | |||||||
chr2:135002147 | C | T | 3 | a0001c0005t0001g0130 a0024c0034t0002g0119 a0026c0035t0002g0118 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.236-2132G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135002147 | |||||||
chr2:135002227 | G | T | 13 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(10): Show |
13 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-2212C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135002227 | |||||||
chr2:135002253 | G | A | 1 | a0001c0002t0001g0187 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.236-2238C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135002253 | |||||||
chr2:135002415 | C | CTTATT | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0004c0006t0001g0241 others(1): Show |
4 | HG03195.hp1 NA18991.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-2405_236-2401d others(7): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135002415 | |||||||
chr2:135002415 | CTTATT | C | 128 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(125): Show |
128 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.236-2405_236-2401d others(7): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135002415 | |||||||
chr2:135002415 | CTTATTTT others(3): Show |
C | 1 | a0001c0002t0001g0169 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.236-2410_236-2401d others(12): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135002415 | |||||||
chr2:135002610 | CT | C | 62 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0098 others(59): Show |
63 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.236-2596delA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135002610 | |||||||
chr2:135002612 | TTA | T | 100 | a0001c0001t0001g0152 a0001c0001t0001g0157 a0001c0001t0001g0200 others(97): Show |
103 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.236-2599_236-2598d others(4): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135002612 | |||||||
chr2:135002613 | T | A | 11 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(8): Show |
11 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.236-2598A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135002613 | |||||||
chr2:135002674 | C | G | 134 | a0001c0001t0001g0091 a0001c0001t0001g0137 a0001c0001t0001g0152 others(131): Show |
138 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.236-2659G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135002674 | |||||||
chr2:135003508 | A | G | 126 | a0001c0001t0001g0091 a0001c0001t0001g0152 a0001c0001t0001g0157 others(123): Show |
130 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.235+1927T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135003508 | |||||||
chr2:135003542 | G | GTGTT | 121 | a0001c0001t0001g0068 a0001c0001t0001g0091 a0001c0001t0001g0152 others(118): Show |
125 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.235+1889_235+1892d others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135003542 | |||||||
chr2:135003542 | G | GTGTTTGT others(1): Show |
6 | a0001c0001t0001g0207 a0001c0001t0001g0290 a0001c0005t0002g0128 others(3): Show |
6 | HG02630.hp2 NA18944.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+1885_235+1892d others(10): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135003542 | |||||||
chr2:135003542 | GTGTT | G | 13 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(10): Show |
13 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.235+1889_235+1892d others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135003542 | |||||||
chr2:135003542 | GTGTTTGT others(1): Show |
G | 3 | a0001c0005t0001g0130 a0024c0034t0002g0119 a0026c0035t0002g0118 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.235+1885_235+1892d others(10): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135003542 | |||||||
chr2:135003542 | GTGTTTGT others(5): Show |
G | 1 | a0002c0003t0001g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.235+1881_235+1892d others(14): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135003542 | |||||||
chr2:135003595 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.235+1840G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135003595 | |||||||
chr2:135003701 | C | T | 125 | a0001c0001t0001g0091 a0001c0001t0001g0152 a0001c0001t0001g0157 others(122): Show |
129 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.235+1734G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135003701 | |||||||
chr2:135003873 | C | T | 3 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 |
3 | HG00621.hp2 NA18949.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.235+1562G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135003873 | |||||||
chr2:135003900 | A | G | 2 | a0001c0005t0002g0083 a0001c0005t0002g0128 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.235+1535T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135003900 | |||||||
chr2:135004330 | A | T | 1 | a0001c0001t0002g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.235+1105T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135004330 | |||||||
chr2:135004396 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.235+1039G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135004396 | |||||||
chr2:135004445 | A | G | 1 | a0001c0002t0001g0169 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.235+990T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135004445 | |||||||
chr2:135004491 | A | G | 176 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0098 others(173): Show |
180 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.235+944T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135004491 | |||||||
chr2:135004538 | C | G | 5 | a0006c0008t0002g0280 a0006c0008t0003g0156 a0006c0008t0003g0251 others(2): Show |
5 | NA18939.hp2 NA18941.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+897G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135004538 | |||||||
chr2:135004774 | C | T | 123 | a0001c0001t0001g0091 a0001c0001t0001g0152 a0001c0001t0001g0157 others(120): Show |
127 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.235+661G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135004774 | |||||||
chr2:135004830 | C | T | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.235+605G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135004830 | |||||||
chr2:135004859 | C | G | 163 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0107 others(160): Show |
167 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.235+576G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135004859 | |||||||
chr2:135005038 | C | A | 3 | a0001c0005t0001g0130 a0024c0034t0002g0119 a0026c0035t0002g0118 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.235+397G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135005038 | |||||||
chr2:135005086 | G | A | 137 | a0001c0001t0001g0091 a0001c0001t0001g0137 a0001c0001t0001g0152 others(134): Show |
141 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.235+349C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135005086 | |||||||
chr2:135005253 | G | C | 2 | a0001c0002t0001g0322 a0002c0003t0001g0323 |
2 | HG00642.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.235+182C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135005253 | |||||||
chr2:135005410 | C | T | 123 | a0001c0001t0001g0091 a0001c0001t0001g0152 a0001c0001t0001g0157 others(120): Show |
127 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.235+25G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 6/12 | chr2 | 135005410 | |||||||
chr2:135005710 | A | G | 122 | a0001c0001t0001g0091 a0001c0001t0001g0152 a0001c0001t0001g0157 others(119): Show |
126 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.139-179T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135005710 | |||||||
chr2:135005748 | G | A | 137 | a0001c0001t0001g0091 a0001c0001t0001g0137 a0001c0001t0001g0152 others(134): Show |
141 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.139-217C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135005748 | |||||||
chr2:135005813 | C | T | 3 | a0005c0007t0006g0011 a0005c0007t0006g0013 a0005c0007t0006g0014 |
3 | HG02280.hp1 HG02486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.139-282G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135005813 | |||||||
chr2:135005842 | C | T | 1 | a0002c0003t0001g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.139-311G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135005842 | |||||||
chr2:135005979 | T | C | 1 | a0001c0002t0002g0326 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.139-448A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135005979 | |||||||
chr2:135006068 | C | T | 1 | a0005c0007t0002g0105 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.139-537G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135006068 | |||||||
chr2:135006311 | G | A | 1 | a0001c0002t0002g0224 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.139-780C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135006311 | |||||||
chr2:135006614 | A | G | 26 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(23): Show |
26 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.139-1083T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135006614 | |||||||
chr2:135006649 | A | C | 1 | a0003c0004t0001g0004 | 2 | NA18964.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.139-1118T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135006649 | |||||||
chr2:135006671 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.139-1140C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135006671 | |||||||
chr2:135006846 | G | A | 3 | a0001c0005t0001g0130 a0024c0034t0002g0119 a0026c0035t0002g0118 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.139-1315C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135006846 | |||||||
chr2:135006857 | AAAG | A | 3 | a0001c0005t0001g0130 a0024c0034t0002g0119 a0026c0035t0002g0118 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.139-1329_139-1327d others(5): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135006857 | |||||||
chr2:135006863 | G | A | 1 | a0001c0002t0012g0293 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.139-1332C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135006863 | |||||||
chr2:135007164 | C | CA | 8 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(5): Show |
8 | HG02895.hp2 HG02897.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.139-1634dupT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135007164 | |||||||
chr2:135007164 | CA | C | 119 | a0001c0001t0001g0091 a0001c0001t0001g0152 a0001c0001t0001g0157 others(116): Show |
123 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.139-1634delT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135007164 | |||||||
chr2:135007183 | T | G | 26 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(23): Show |
26 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.139-1652A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135007183 | |||||||
chr2:135007302 | T | C | 4 | a0001c0001t0005g0147 a0001c0005t0005g0145 a0017c0019t0005g0146 others(1): Show |
4 | HG02258.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-1771A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135007302 | |||||||
chr2:135007488 | C | T | 1 | a0001c0002t0001g0051 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.139-1957G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135007488 | |||||||
chr2:135007519 | T | A | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-1988A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135007519 | |||||||
chr2:135007932 | G | T | 3 | a0005c0007t0006g0011 a0005c0007t0006g0013 a0005c0007t0006g0014 |
3 | HG02280.hp1 HG02486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.139-2401C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135007932 | |||||||
chr2:135008009 | C | G | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-2478G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135008009 | |||||||
chr2:135008117 | T | C | 1 | a0001c0009t0001g0143 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.139-2586A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135008117 | |||||||
chr2:135008162 | G | A | 1 | a0001c0002t0012g0293 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.139-2631C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135008162 | |||||||
chr2:135008410 | C | A | 1 | a0010c0015t0001g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.139-2879G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135008410 | |||||||
chr2:135008412 | C | T | 2 | a0001c0001t0002g0308 a0001c0001t0002g0309 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.139-2881G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135008412 | |||||||
chr2:135008445 | G | A | 1 | a0015c0036t0003g0252 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.139-2914C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135008445 | |||||||
chr2:135008502 | C | G | 130 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(127): Show |
130 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.139-2971G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135008502 | |||||||
chr2:135008529 | C | T | 2 | a0002c0003t0001g0203 a0003c0004t0003g0228 |
2 | NA18967.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.139-2998G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135008529 | |||||||
chr2:135008590 | A | G | 2 | a0001c0005t0002g0083 a0001c0005t0002g0128 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.139-3059T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135008590 | |||||||
chr2:135009118 | A | AT | 24 | a0001c0001t0001g0254 a0001c0001t0001g0282 a0001c0001t0001g0290 others(21): Show |
25 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.139-3588dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135009118 | |||||||
chr2:135009118 | AT | A | 16 | a0001c0001t0002g0086 a0001c0001t0002g0309 a0001c0005t0001g0088 others(13): Show |
17 | HG01070.hp1 HG01243.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.139-3588delA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135009118 | |||||||
chr2:135009118 | ATT | A | 24 | a0001c0001t0001g0137 a0001c0001t0002g0020 a0001c0001t0002g0036 others(21): Show |
24 | HG00280.hp1 HG00741.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.139-3589_139-3588d others(4): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135009118 | |||||||
chr2:135009118 | ATTT | A | 103 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(100): Show |
103 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.139-3590_139-3588d others(5): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135009118 | |||||||
chr2:135009188 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.139-3657G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135009188 | |||||||
chr2:135009261 | G | A | 1 | a0001c0005t0001g0320 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.139-3730C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135009261 | |||||||
chr2:135009265 | G | A | 1 | a0001c0001t0002g0283 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.139-3734C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135009265 | |||||||
chr2:135009283 | A | G | 2 | a0001c0002t0001g0210 a0001c0002t0001g0221 |
2 | HG01243.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.139-3752T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135009283 | |||||||
chr2:135009320 | G | A | 116 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(113): Show |
116 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.139-3789C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135009320 | |||||||
chr2:135009556 | T | C | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-4025A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135009556 | |||||||
chr2:135009680 | C | A | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-4149G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135009680 | |||||||
chr2:135009768 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.139-4237G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135009768 | |||||||
chr2:135009973 | A | C | 7 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0002g0113 others(4): Show |
7 | HG01884.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-4442T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135009973 | |||||||
chr2:135010002 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.139-4471C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135010002 | |||||||
chr2:135010305 | G | A | 1 | a0010c0015t0001g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.139-4774C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135010305 | |||||||
chr2:135010312 | C | T | 77 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(74): Show |
77 | HG00408.hp2 HG00438.hp1 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.139-4781G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135010312 | |||||||
chr2:135010530 | A | G | 2 | a0001c0001t0002g0253 a0002c0003t0001g0003 |
3 | HG01099.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.139-4999T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135010530 | |||||||
chr2:135010570 | C | T | 1 | a0001c0002t0001g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.139-5039G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135010570 | |||||||
chr2:135010782 | C | A | 165 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0107 others(162): Show |
169 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.139-5251G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135010782 | |||||||
chr2:135010839 | C | G | 1 | a0010c0015t0001g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.139-5308G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135010839 | |||||||
chr2:135010840 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.139-5309T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135010840 | |||||||
chr2:135011245 | A | T | 125 | a0001c0001t0001g0091 a0001c0001t0001g0152 a0001c0001t0001g0157 others(122): Show |
129 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.139-5714T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011245 | |||||||
chr2:135011309 | G | C | 1 | a0003c0004t0003g0234 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.139-5778C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011309 | |||||||
chr2:135011320 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.139-5789C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011320 | |||||||
chr2:135011363 | C | A | 1 | a0001c0002t0001g0051 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.139-5832G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011363 | |||||||
chr2:135011410 | C | G | 53 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0001g0099 others(50): Show |
53 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.139-5879G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011410 | |||||||
chr2:135011415 | C | T | 53 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0001g0099 others(50): Show |
53 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.139-5884G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011415 | |||||||
chr2:135011469 | G | A | 19 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0062 others(16): Show |
20 | HG01952.hp1 HG01978.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.139-5938C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011469 | |||||||
chr2:135011491 | C | A | 13 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(10): Show |
13 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.139-5960G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011491 | |||||||
chr2:135011492 | G | A | 13 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(10): Show |
13 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.139-5961C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011492 | |||||||
chr2:135011498 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.139-5967G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011498 | |||||||
chr2:135011501 | T | C | 1 | a0001c0001t0001g0009 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.139-5970A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011501 | |||||||
chr2:135011523 | C | T | 125 | a0001c0001t0001g0091 a0001c0001t0001g0152 a0001c0001t0001g0157 others(122): Show |
129 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.139-5992G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011523 | |||||||
chr2:135011528 | C | T | 107 | a0001c0001t0001g0152 a0001c0001t0001g0157 a0001c0001t0001g0200 others(104): Show |
110 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.139-5997G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011528 | |||||||
chr2:135011536 | C | CA | 8 | a0001c0001t0001g0122 a0001c0001t0001g0126 a0001c0002t0001g0169 others(5): Show |
8 | HG00558.hp1 HG01255.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-6006dupT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011536 | |||||||
chr2:135011536 | C | CAA | 101 | a0001c0001t0001g0152 a0001c0001t0001g0157 a0001c0001t0001g0200 others(98): Show |
104 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.139-6007_139-6006d others(4): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011536 | |||||||
chr2:135011536 | C | CAAA | 15 | a0001c0001t0001g0091 a0001c0001t0002g0237 a0001c0001t0004g0085 others(12): Show |
16 | HG01175.hp2 HG01243.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.139-6008_139-6006d others(5): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011536 | |||||||
chr2:135011537 | A | C | 1 | a0001c0005t0001g0130 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.139-6006T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011537 | |||||||
chr2:135011557 | C | T | 125 | a0001c0001t0001g0091 a0001c0001t0001g0152 a0001c0001t0001g0157 others(122): Show |
129 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.139-6026G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011557 | |||||||
chr2:135011558 | T | A | 3 | a0001c0002t0001g0321 a0001c0002t0001g0322 a0002c0003t0001g0323 |
3 | HG00642.hp1 NA20805.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.139-6027A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011558 | |||||||
chr2:135011590 | C | T | 1 | a0002c0003t0002g0125 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.139-6059G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011590 | |||||||
chr2:135011665 | T | TGTTG | 4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-6138_139-6135d others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011665 | |||||||
chr2:135011666 | G | GTTGT | 57 | a0001c0001t0001g0009 a0001c0001t0001g0077 a0001c0001t0001g0091 others(54): Show |
58 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.139-6139_139-6136d others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011666 | |||||||
chr2:135011666 | GTTGT | G | 13 | a0001c0001t0001g0029 a0001c0001t0002g0028 a0001c0001t0002g0030 others(10): Show |
13 | HG00438.hp1 HG01255.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.139-6139_139-6136d others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011666 | |||||||
chr2:135011670 | T | G | 1 | a0001c0002t0003g0102 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.139-6139A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135011670 | |||||||
chr2:135012117 | T | C | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.139-6586A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135012117 | |||||||
chr2:135012471 | A | G | 2 | a0001c0001t0002g0100 a0001c0001t0003g0193 |
2 | HG03195.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.139-6940T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135012471 | |||||||
chr2:135012516 | C | T | 5 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(2): Show |
6 | HG00621.hp2 NA18949.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-6985G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135012516 | |||||||
chr2:135012538 | T | G | 1 | a0001c0001t0002g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.139-7007A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135012538 | |||||||
chr2:135012944 | CTTGT | C | 123 | a0001c0001t0001g0091 a0001c0001t0001g0152 a0001c0001t0001g0157 others(120): Show |
127 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.139-7417_139-7414d others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135012944 | |||||||
chr2:135012944 | CTTGTTTG others(1): Show |
C | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-7421_139-7414d others(10): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135012944 | |||||||
chr2:135013041 | C | T | 2 | a0002c0003t0002g0161 a0003c0021t0001g0160 |
2 | NA18995.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.139-7510G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135013041 | |||||||
chr2:135013190 | C | T | 2 | a0002c0003t0001g0124 a0002c0003t0001g0127 |
2 | HG00735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.139-7659G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135013190 | |||||||
chr2:135013314 | A | G | 5 | a0002c0003t0001g0007 a0002c0003t0002g0067 a0002c0003t0002g0069 others(2): Show |
5 | NA18966.hp2 NA18971.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-7783T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135013314 | |||||||
chr2:135013323 | AAAG | A | 104 | a0001c0001t0001g0152 a0001c0001t0001g0157 a0001c0001t0001g0200 others(101): Show |
107 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.139-7795_139-7793d others(5): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135013323 | |||||||
chr2:135013325 | A | AG | 3 | a0001c0001t0001g0065 a0001c0001t0002g0066 a0007c0023t0004g0064 |
3 | HG02257.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.139-7795dupC | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135013325 | |||||||
chr2:135013370 | C | T | 124 | a0001c0001t0001g0091 a0001c0001t0001g0152 a0001c0001t0001g0157 others(121): Show |
128 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.139-7839G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135013370 | |||||||
chr2:135013381 | T | C | 124 | a0001c0001t0001g0091 a0001c0001t0001g0152 a0001c0001t0001g0157 others(121): Show |
128 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.139-7850A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135013381 | |||||||
chr2:135013384 | A | G | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-7853T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135013384 | |||||||
chr2:135013686 | A | G | 1 | a0001c0018t0001g0144 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.138+8029T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135013686 | |||||||
chr2:135013766 | C | T | 1 | a0001c0002t0001g0221 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.138+7949G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135013766 | |||||||
chr2:135013780 | C | T | 23 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(20): Show |
23 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.138+7935G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135013780 | |||||||
chr2:135014002 | T | A | 1 | a0001c0002t0001g0221 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.138+7713A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135014002 | |||||||
chr2:135014182 | A | G | 6 | a0001c0001t0001g0152 a0001c0001t0001g0238 a0001c0001t0001g0246 others(3): Show |
6 | HG00735.hp1 HG01358.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+7533T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135014182 | |||||||
chr2:135014205 | T | G | 1 | a0025c0032t0001g0274 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.138+7510A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135014205 | |||||||
chr2:135014356 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.138+7359C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135014356 | |||||||
chr2:135014358 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.138+7357G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135014358 | |||||||
chr2:135014376 | GA | G | 7 | a0001c0001t0001g0152 a0001c0001t0001g0238 a0001c0001t0001g0246 others(4): Show |
7 | HG00735.hp1 HG01358.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+7338delT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135014376 | |||||||
chr2:135014404 | C | G | 255 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(252): Show |
259 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(256): Show |
intron_variant | MODIFIER | c.138+7311G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135014404 | |||||||
chr2:135014479 | C | T | 82 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(79): Show |
82 | HG00408.hp2 HG00438.hp1 HG00741.hp1 others(79): Show |
intron_variant | MODIFIER | c.138+7236G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135014479 | |||||||
chr2:135014747 | T | C | 4 | a0001c0001t0002g0063 a0001c0002t0001g0060 a0001c0002t0001g0061 others(1): Show |
4 | NA18939.hp1 NA18967.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+6968A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135014747 | |||||||
chr2:135014870 | G | C | 1 | a0001c0009t0001g0143 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.138+6845C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135014870 | |||||||
chr2:135014912 | T | G | 12 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0002g0066 others(9): Show |
12 | HG02257.hp1 HG03017.hp2 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+6803A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135014912 | |||||||
chr2:135015019 | G | A | 2 | a0001c0002t0001g0021 a0001c0002t0001g0023 |
2 | HG01070.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.138+6696C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135015019 | |||||||
chr2:135015306 | A | G | 3 | a0001c0005t0001g0130 a0024c0034t0002g0119 a0026c0035t0002g0118 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.138+6409T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135015306 | |||||||
chr2:135015436 | G | A | 2 | a0001c0001t0002g0081 a0003c0004t0003g0082 |
2 | HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.138+6279C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135015436 | |||||||
chr2:135015585 | T | C | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0002c0003t0001g0271 others(1): Show |
4 | HG02027.hp1 HG03834.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+6130A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135015585 | |||||||
chr2:135015592 | T | C | 1 | a0001c0002t0001g0298 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.138+6123A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135015592 | |||||||
chr2:135015616 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.138+6099G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135015616 | |||||||
chr2:135015661 | G | A | 26 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(23): Show |
26 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.138+6054C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135015661 | |||||||
chr2:135015749 | C | T | 19 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0099 others(16): Show |
20 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.138+5966G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135015749 | |||||||
chr2:135015750 | G | A | 1 | a0003c0004t0003g0228 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.138+5965C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135015750 | |||||||
chr2:135015850 | A | G | 130 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(127): Show |
130 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.138+5865T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135015850 | |||||||
chr2:135015876 | A | C | 130 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(127): Show |
130 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.138+5839T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135015876 | |||||||
chr2:135015879 | G | A | 77 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(74): Show |
77 | HG00408.hp2 HG00438.hp1 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.138+5836C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135015879 | |||||||
chr2:135016032 | T | C | 1 | a0010c0015t0001g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.138+5683A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135016032 | |||||||
chr2:135016047 | T | C | 130 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(127): Show |
130 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.138+5668A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135016047 | |||||||
chr2:135016122 | T | A | 130 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(127): Show |
130 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.138+5593A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135016122 | |||||||
chr2:135016456 | T | G | 3 | a0001c0002t0001g0321 a0001c0002t0001g0322 a0002c0003t0001g0323 |
3 | HG00642.hp1 NA20805.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.138+5259A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135016456 | |||||||
chr2:135016608 | C | A | 1 | a0003c0004t0003g0289 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.138+5107G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135016608 | |||||||
chr2:135016889 | A | G | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+4826T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135016889 | |||||||
chr2:135016949 | A | G | 3 | a0001c0001t0004g0085 a0001c0005t0002g0083 a0003c0004t0003g0234 |
3 | HG02896.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.138+4766T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135016949 | |||||||
chr2:135017111 | A | G | 130 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(127): Show |
130 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.138+4604T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135017111 | |||||||
chr2:135017139 | AT | A | 9 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(6): Show |
9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.138+4575delA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135017139 | |||||||
chr2:135017185 | C | G | 4 | a0001c0001t0005g0147 a0001c0005t0005g0145 a0017c0019t0005g0146 others(1): Show |
4 | HG02258.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+4530G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135017185 | |||||||
chr2:135017194 | T | C | 2 | a0012c0017t0001g0043 a0012c0017t0003g0055 |
2 | HG04184.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.138+4521A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135017194 | |||||||
chr2:135017275 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.138+4440G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135017275 | |||||||
chr2:135017435 | G | T | 1 | a0001c0009t0004g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.138+4280C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135017435 | |||||||
chr2:135017479 | G | C | 130 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(127): Show |
130 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.138+4236C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135017479 | |||||||
chr2:135017554 | G | C | 1 | a0020c0026t0001g0026 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.138+4161C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135017554 | |||||||
chr2:135017560 | C | T | 319 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0022 others(316): Show |
324 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(321): Show |
intron_variant | MODIFIER | c.138+4155G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135017560 | |||||||
chr2:135017614 | C | G | 1 | a0004c0006t0001g0256 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.138+4101G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135017614 | |||||||
chr2:135017633 | A | G | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.138+4082T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135017633 | |||||||
chr2:135017639 | T | G | 1 | a0001c0002t0001g0319 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.138+4076A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135017639 | |||||||
chr2:135017640 | G | A | 1 | a0001c0002t0001g0319 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.138+4075C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135017640 | |||||||
chr2:135017742 | G | GA | 148 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(145): Show |
149 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.138+3972dupT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135017742 | |||||||
chr2:135017904 | A | G | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.138+3811T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135017904 | |||||||
chr2:135017924 | A | T | 4 | a0001c0001t0005g0147 a0001c0005t0005g0145 a0017c0019t0005g0146 others(1): Show |
4 | HG02258.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+3791T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135017924 | |||||||
chr2:135017977 | C | T | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.138+3738G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135017977 | |||||||
chr2:135018081 | C | T | 8 | a0001c0001t0001g0022 a0001c0001t0001g0077 a0001c0002t0001g0021 others(5): Show |
8 | HG01070.hp2 HG01192.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.138+3634G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018081 | |||||||
chr2:135018099 | C | T | 3 | a0002c0003t0001g0164 a0003c0004t0003g0163 a0003c0004t0003g0165 |
3 | HG02074.hp2 NA18944.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.138+3616G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018099 | |||||||
chr2:135018109 | T | C | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+3606A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018109 | |||||||
chr2:135018132 | A | T | 1 | a0002c0003t0001g0056 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.138+3583T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018132 | |||||||
chr2:135018203 | A | G | 3 | a0001c0001t0001g0255 a0003c0004t0001g0288 a0015c0036t0003g0252 |
3 | HG02135.hp2 NA18950.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.138+3512T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018203 | |||||||
chr2:135018216 | G | A | 86 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(83): Show |
86 | HG00408.hp2 HG00438.hp1 HG00741.hp1 others(83): Show |
intron_variant | MODIFIER | c.138+3499C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018216 | |||||||
chr2:135018281 | C | CA | 110 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0029 others(107): Show |
110 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.138+3433dupT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018281 | |||||||
chr2:135018281 | C | CAA | 27 | a0001c0001t0001g0027 a0001c0001t0001g0080 a0001c0001t0001g0101 others(24): Show |
27 | HG00280.hp1 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.138+3432_138+3433d others(4): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018281 | |||||||
chr2:135018281 | CA | C | 90 | a0001c0001t0001g0157 a0001c0001t0001g0200 a0001c0001t0001g0254 others(87): Show |
93 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.138+3433delT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018281 | |||||||
chr2:135018289 | A | G | 14 | a0001c0001t0001g0091 a0001c0001t0002g0086 a0001c0005t0001g0088 others(11): Show |
15 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.138+3426T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018289 | |||||||
chr2:135018290 | A | G | 2 | a0001c0001t0004g0085 a0001c0005t0002g0083 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.138+3425T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018290 | |||||||
chr2:135018349 | T | TA | 3 | a0001c0002t0001g0321 a0001c0002t0001g0322 a0002c0003t0001g0323 |
3 | HG00642.hp1 NA20805.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.138+3365_138+3366i others(3): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018349 | |||||||
chr2:135018700 | C | A | 1 | a0001c0002t0003g0102 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.138+3015G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018700 | |||||||
chr2:135018757 | G | A | 4 | a0001c0001t0005g0147 a0001c0005t0005g0145 a0017c0019t0005g0146 others(1): Show |
4 | HG02258.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+2958C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018757 | |||||||
chr2:135018860 | A | G | 130 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(127): Show |
130 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.138+2855T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018860 | |||||||
chr2:135018946 | G | A | 5 | a0006c0008t0002g0280 a0006c0008t0003g0156 a0006c0008t0003g0251 others(2): Show |
5 | NA18939.hp2 NA18941.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+2769C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018946 | |||||||
chr2:135018966 | T | A | 2 | a0003c0004t0003g0286 a0003c0004t0003g0287 |
2 | HG00438.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.138+2749A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018966 | |||||||
chr2:135018990 | C | T | 6 | a0001c0001t0001g0077 a0001c0001t0001g0173 a0001c0002t0001g0176 others(3): Show |
6 | HG00609.hp2 HG02155.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+2725G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018990 | |||||||
chr2:135018991 | G | C | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+2724C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135018991 | |||||||
chr2:135019014 | G | A | 82 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(79): Show |
82 | HG00408.hp2 HG00438.hp1 HG00741.hp1 others(79): Show |
intron_variant | MODIFIER | c.138+2701C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135019014 | |||||||
chr2:135019084 | A | G | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+2631T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135019084 | |||||||
chr2:135019158 | C | G | 125 | a0001c0001t0001g0091 a0001c0001t0001g0152 a0001c0001t0001g0157 others(122): Show |
129 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.138+2557G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135019158 | |||||||
chr2:135019464 | A | T | 1 | a0001c0002t0001g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.138+2251T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135019464 | |||||||
chr2:135019465 | G | A | 1 | a0001c0002t0001g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.138+2250C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135019465 | |||||||
chr2:135019676 | CT | C | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+2038delA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135019676 | |||||||
chr2:135019692 | A | G | 1 | a0001c0005t0001g0320 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.138+2023T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135019692 | |||||||
chr2:135019934 | A | G | 125 | a0001c0001t0001g0091 a0001c0001t0001g0152 a0001c0001t0001g0157 others(122): Show |
129 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.138+1781T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135019934 | |||||||
chr2:135020024 | C | CT | 17 | a0001c0001t0001g0091 a0001c0001t0002g0086 a0001c0001t0004g0085 others(14): Show |
18 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.138+1690dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135020024 | |||||||
chr2:135020117 | A | T | 1 | a0002c0003t0001g0034 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.138+1598T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135020117 | |||||||
chr2:135020162 | T | G | 8 | a0001c0001t0001g0022 a0001c0001t0001g0077 a0001c0002t0001g0021 others(5): Show |
8 | HG01070.hp2 HG01192.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.138+1553A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135020162 | |||||||
chr2:135020299 | G | A | 3 | a0001c0001t0005g0147 a0001c0005t0005g0145 a0017c0019t0005g0146 |
3 | HG02258.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.138+1416C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135020299 | |||||||
chr2:135020352 | C | T | 103 | a0001c0001t0001g0152 a0001c0001t0001g0157 a0001c0001t0001g0200 others(100): Show |
106 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.138+1363G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135020352 | |||||||
chr2:135020600 | T | C | 1 | a0001c0001t0002g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.138+1115A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135020600 | |||||||
chr2:135020663 | G | A | 3 | a0001c0005t0001g0130 a0024c0034t0002g0119 a0026c0035t0002g0118 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.138+1052C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135020663 | |||||||
chr2:135020669 | T | C | 87 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(84): Show |
87 | HG00408.hp2 HG00438.hp1 HG00741.hp1 others(84): Show |
intron_variant | MODIFIER | c.138+1046A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135020669 | |||||||
chr2:135020696 | C | T | 1 | a0003c0004t0003g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.138+1019G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135020696 | |||||||
chr2:135020697 | G | A | 2 | a0001c0001t0004g0085 a0001c0005t0002g0083 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.138+1018C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135020697 | |||||||
chr2:135020726 | G | T | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0126 others(3): Show |
6 | HG00558.hp1 HG00621.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+989C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135020726 | |||||||
chr2:135020894 | C | A | 14 | a0001c0001t0001g0091 a0001c0001t0002g0086 a0001c0005t0001g0088 others(11): Show |
15 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.138+821G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135020894 | |||||||
chr2:135021057 | A | G | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.138+658T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135021057 | |||||||
chr2:135021086 | G | C | 131 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(128): Show |
131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.138+629C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135021086 | |||||||
chr2:135021138 | C | T | 117 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(114): Show |
117 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.138+577G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135021138 | |||||||
chr2:135021331 | G | C | 1 | a0001c0001t0002g0310 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.138+384C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135021331 | |||||||
chr2:135021407 | G | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | NA18991.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.138+308C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135021407 | |||||||
chr2:135021473 | T | TAC | 94 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(91): Show |
95 | HG00438.hp1 HG00741.hp1 HG01070.hp2 others(92): Show |
intron_variant | MODIFIER | c.138+240_138+241dup others(2): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135021473 | |||||||
chr2:135021473 | T | TACAC | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+238_138+241dup others(4): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135021473 | |||||||
chr2:135021473 | TAC | T | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+240_138+241del others(2): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135021473 | |||||||
chr2:135021549 | G | C | 2 | a0024c0034t0002g0119 a0026c0035t0002g0118 |
2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.138+166C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135021549 | |||||||
chr2:135021575 | T | G | 8 | a0001c0001t0001g0022 a0001c0001t0001g0077 a0001c0002t0001g0021 others(5): Show |
8 | HG01070.hp2 HG01192.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.138+140A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 5/12 | chr2 | 135021575 | |||||||
chr2:135022018 | G | A | 117 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(114): Show |
117 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.23-188C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135022018 | |||||||
chr2:135022035 | A | AT | 82 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(79): Show |
82 | HG00408.hp2 HG00438.hp1 HG00741.hp1 others(79): Show |
intron_variant | MODIFIER | c.23-206dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135022035 | |||||||
chr2:135022267 | G | A | 1 | a0002c0003t0001g0275 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.23-437C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135022267 | |||||||
chr2:135022294 | TG | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-465delC | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135022294 | |||||||
chr2:135022419 | A | C | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-589T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135022419 | |||||||
chr2:135022439 | G | A | 1 | a0001c0002t0001g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.23-609C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135022439 | |||||||
chr2:135022456 | T | C | 2 | a0001c0001t0002g0235 a0003c0004t0003g0234 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.23-626A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135022456 | |||||||
chr2:135022521 | T | C | 23 | a0001c0001t0001g0182 a0001c0001t0001g0185 a0001c0001t0002g0186 others(20): Show |
23 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.23-691A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135022521 | |||||||
chr2:135022598 | A | G | 150 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(147): Show |
151 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.23-768T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135022598 | |||||||
chr2:135022739 | A | C | 1 | a0001c0001t0002g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.23-909T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135022739 | |||||||
chr2:135022880 | C | T | 2 | a0002c0003t0001g0196 a0002c0003t0001g0197 |
2 | NA19060.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.23-1050G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135022880 | |||||||
chr2:135023017 | T | A | 148 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(145): Show |
149 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.23-1187A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135023017 | |||||||
chr2:135023322 | C | A | 3 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0142 |
3 | NA19002.hp2 NA19006.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.22+1304G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135023322 | |||||||
chr2:135023339 | C | T | 4 | a0001c0001t0001g0173 a0001c0002t0001g0176 a0003c0004t0003g0175 others(1): Show |
4 | HG00609.hp2 HG02155.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+1287G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135023339 | |||||||
chr2:135023354 | G | A | 4 | a0001c0005t0001g0130 a0001c0005t0002g0128 a0024c0034t0002g0119 others(1): Show |
4 | HG03130.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+1272C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135023354 | |||||||
chr2:135023465 | C | T | 77 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(74): Show |
77 | HG00408.hp2 HG00438.hp1 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.22+1161G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135023465 | |||||||
chr2:135023531 | T | C | 4 | a0001c0001t0005g0147 a0001c0005t0005g0145 a0017c0019t0005g0146 others(1): Show |
4 | HG02258.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+1095A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135023531 | |||||||
chr2:135023682 | C | T | 4 | a0001c0001t0005g0147 a0001c0005t0005g0145 a0017c0019t0005g0146 others(1): Show |
4 | HG02258.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+944G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135023682 | |||||||
chr2:135023731 | A | T | 131 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(128): Show |
131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.22+895T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135023731 | |||||||
chr2:135023811 | T | C | 1 | a0003c0004t0003g0025 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.22+815A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135023811 | |||||||
chr2:135023821 | G | A | 1 | a0001c0002t0001g0187 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.22+805C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135023821 | |||||||
chr2:135023881 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0002g0301 |
2 | HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.22+745A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135023881 | |||||||
chr2:135023898 | G | GA | 27 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(24): Show |
27 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.22+727dupT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135023898 | |||||||
chr2:135023952 | G | A | 148 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(145): Show |
149 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.22+674C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135023952 | |||||||
chr2:135023989 | T | C | 75 | a0001c0001t0001g0200 a0001c0001t0001g0254 a0001c0001t0001g0255 others(72): Show |
78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.22+637A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135023989 | |||||||
chr2:135024025 | T | A | 1 | a0010c0015t0001g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.22+601A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135024025 | |||||||
chr2:135024065 | C | T | 131 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(128): Show |
131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.22+561G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135024065 | |||||||
chr2:135024343 | A | ACTATAAG others(2): Show |
131 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(128): Show |
131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.22+274_22+282dupGA others(7): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135024343 | |||||||
chr2:135024517 | G | A | 1 | a0002c0016t0001g0201 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.22+109C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 4/12 | chr2 | 135024517 | |||||||
chr2:135024747 | A | C | 1 | a0002c0003t0002g0073 | 1 | NA18990.hp1 | splice_region_variant&intron_variant | LOW | c.-94-6T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135024747 | |||||||
chr2:135024886 | G | A | 131 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(128): Show |
131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.-94-145C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135024886 | |||||||
chr2:135024887 | T | C | 1 | a0001c0001t0002g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-94-146A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135024887 | |||||||
chr2:135025152 | C | T | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-94-411G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025152 | |||||||
chr2:135025189 | T | G | 4 | a0001c0001t0005g0147 a0001c0005t0005g0145 a0017c0019t0005g0146 others(1): Show |
4 | HG02258.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-94-448A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025189 | |||||||
chr2:135025366 | CCTTTT | C | 63 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0041 others(60): Show |
63 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.-94-630_-94-626del others(5): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025366 | |||||||
chr2:135025372 | CTTTTCT | C | 13 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0140 others(10): Show |
13 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.-94-637_-94-632del others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025372 | |||||||
chr2:135025373 | TTTTC | T | 48 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0032 others(45): Show |
48 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-94-636_-94-633del others(4): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025373 | |||||||
chr2:135025375 | T | C | 1 | a0006c0008t0003g0251 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-94-634A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025375 | |||||||
chr2:135025377 | C | CT | 32 | a0001c0001t0001g0159 a0001c0001t0001g0178 a0001c0001t0001g0238 others(29): Show |
32 | HG00423.hp2 HG00621.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.-94-637dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025377 | |||||||
chr2:135025377 | C | T | 1 | a0006c0008t0003g0251 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-94-636G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025377 | |||||||
chr2:135025377 | CT | C | 8 | a0001c0002t0001g0268 a0001c0005t0002g0084 a0002c0003t0001g0189 others(5): Show |
8 | HG01243.hp1 HG01255.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-94-637delA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025377 | |||||||
chr2:135025377 | CTT | C | 10 | a0001c0001t0001g0091 a0001c0001t0004g0085 a0001c0005t0002g0001 others(7): Show |
11 | HG02055.hp2 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-94-638_-94-637del others(2): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025377 | |||||||
chr2:135025379 | T | C | 1 | a0006c0008t0003g0251 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-94-638A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025379 | |||||||
chr2:135025383 | T | C | 1 | a0003c0004t0003g0167 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-94-642A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025383 | |||||||
chr2:135025424 | C | T | 16 | a0001c0001t0001g0091 a0001c0001t0002g0086 a0001c0001t0004g0085 others(13): Show |
17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-94-683G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025424 | |||||||
chr2:135025425 | A | G | 16 | a0001c0001t0001g0091 a0001c0001t0002g0086 a0001c0001t0004g0085 others(13): Show |
17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-94-684T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025425 | |||||||
chr2:135025428 | C | T | 16 | a0001c0001t0001g0091 a0001c0001t0002g0086 a0001c0001t0004g0085 others(13): Show |
17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-94-687G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025428 | |||||||
chr2:135025429 | A | G | 16 | a0001c0001t0001g0091 a0001c0001t0002g0086 a0001c0001t0004g0085 others(13): Show |
17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-94-688T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025429 | |||||||
chr2:135025479 | G | A | 7 | a0001c0002t0001g0248 a0001c0002t0001g0249 a0001c0002t0001g0277 others(4): Show |
8 | HG00544.hp1 HG00609.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.-94-738C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025479 | |||||||
chr2:135025487 | G | A | 27 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(24): Show |
27 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-94-746C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025487 | |||||||
chr2:135025587 | C | T | 131 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(128): Show |
131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.-94-846G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025587 | |||||||
chr2:135025683 | G | A | 2 | a0001c0002t0001g0024 a0002c0003t0001g0057 |
2 | NA18986.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-94-942C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025683 | |||||||
chr2:135025796 | T | C | 131 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(128): Show |
131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.-94-1055A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025796 | |||||||
chr2:135025797 | G | A | 131 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(128): Show |
131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.-94-1056C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025797 | |||||||
chr2:135025850 | T | G | 4 | a0001c0001t0005g0147 a0001c0005t0005g0145 a0017c0019t0005g0146 others(1): Show |
4 | HG02258.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-94-1109A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025850 | |||||||
chr2:135025880 | G | T | 1 | a0002c0003t0001g0328 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-94-1139C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025880 | |||||||
chr2:135025903 | G | T | 1 | a0002c0003t0001g0203 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-94-1162C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025903 | |||||||
chr2:135025925 | T | C | 1 | a0001c0009t0004g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-94-1184A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025925 | |||||||
chr2:135025978 | C | G | 1 | a0002c0003t0002g0073 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-94-1237G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135025978 | |||||||
chr2:135026180 | C | T | 23 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(20): Show |
23 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.-94-1439G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135026180 | |||||||
chr2:135026302 | G | C | 4 | a0001c0005t0001g0130 a0001c0005t0002g0128 a0024c0034t0002g0119 others(1): Show |
4 | HG03130.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-94-1561C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135026302 | |||||||
chr2:135026365 | T | C | 1 | a0005c0007t0006g0011 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-94-1624A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135026365 | |||||||
chr2:135026368 | A | C | 1 | a0001c0001t0001g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-94-1627T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135026368 | |||||||
chr2:135026397 | A | C | 1 | a0001c0002t0001g0133 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-94-1656T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135026397 | |||||||
chr2:135026503 | C | CT | 133 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(130): Show |
133 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.-94-1763dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135026503 | |||||||
chr2:135026604 | T | C | 4 | a0001c0005t0001g0130 a0001c0005t0002g0128 a0024c0034t0002g0119 others(1): Show |
4 | HG03130.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-94-1863A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135026604 | |||||||
chr2:135026635 | C | A | 28 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(25): Show |
28 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-94-1894G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135026635 | |||||||
chr2:135026657 | G | T | 150 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(147): Show |
151 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-94-1916C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135026657 | |||||||
chr2:135026781 | C | T | 50 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(47): Show |
50 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-94-2040G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135026781 | |||||||
chr2:135026798 | G | A | 1 | a0001c0002t0001g0242 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-94-2057C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135026798 | |||||||
chr2:135027082 | C | T | 4 | a0001c0005t0001g0130 a0001c0005t0002g0128 a0024c0034t0002g0119 others(1): Show |
4 | HG03130.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-94-2341G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135027082 | |||||||
chr2:135027101 | C | T | 2 | a0001c0002t0001g0202 a0001c0002t0001g0247 |
2 | HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-94-2360G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135027101 | |||||||
chr2:135027105 | C | T | 4 | a0001c0001t0001g0173 a0001c0002t0001g0176 a0003c0004t0003g0175 others(1): Show |
4 | HG00609.hp2 HG02155.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.-94-2364G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135027105 | |||||||
chr2:135027163 | G | T | 148 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(145): Show |
149 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.-94-2422C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135027163 | |||||||
chr2:135027329 | TAAAG | T | 129 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(126): Show |
129 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.-94-2592_-94-2589d others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135027329 | |||||||
chr2:135027331 | AAGAAAGA others(13): Show |
A | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-94-2610_-94-2591d others(22): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135027331 | |||||||
chr2:135027383 | AAAAAGAA others(6): Show |
A | 27 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(24): Show |
27 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-94-2655_-94-2643d others(15): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135027383 | |||||||
chr2:135027496 | T | A | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-94-2755A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135027496 | |||||||
chr2:135027498 | A | G | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-94-2757T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135027498 | |||||||
chr2:135027579 | A | G | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-95+2733T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135027579 | |||||||
chr2:135028339 | T | G | 1 | a0018c0033t0005g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-95+1973A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135028339 | |||||||
chr2:135028372 | A | G | 1 | a0001c0001t0002g0012 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-95+1940T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135028372 | |||||||
chr2:135028491 | G | A | 2 | a0003c0004t0001g0168 a0003c0004t0010g0188 |
2 | HG02027.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.-95+1821C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135028491 | |||||||
chr2:135028557 | C | CA | 14 | a0001c0001t0001g0152 a0001c0001t0001g0238 a0001c0001t0001g0246 others(11): Show |
14 | HG00735.hp1 HG01358.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-95+1754dupT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135028557 | |||||||
chr2:135028557 | CA | C | 119 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(116): Show |
119 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.-95+1754delT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135028557 | |||||||
chr2:135028557 | CAA | C | 7 | a0001c0001t0005g0147 a0001c0005t0001g0130 a0001c0005t0005g0145 others(4): Show |
7 | HG01243.hp1 HG01256.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-95+1753_-95+1754d others(4): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135028557 | |||||||
chr2:135028578 | A | T | 1 | a0002c0003t0001g0124 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-95+1734T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135028578 | |||||||
chr2:135028715 | A | G | 23 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(20): Show |
23 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.-95+1597T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135028715 | |||||||
chr2:135029071 | G | A | 3 | a0001c0001t0001g0009 a0002c0003t0001g0124 a0002c0003t0001g0127 |
3 | HG00639.hp2 HG00735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-95+1241C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135029071 | |||||||
chr2:135029200 | G | A | 1 | a0002c0003t0001g0003 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-95+1112C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135029200 | |||||||
chr2:135029267 | T | A | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-95+1045A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135029267 | |||||||
chr2:135029325 | G | A | 1 | a0002c0003t0001g0278 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-95+987C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135029325 | |||||||
chr2:135029332 | C | T | 1 | a0003c0004t0001g0172 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-95+980G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135029332 | |||||||
chr2:135029366 | A | ACT | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-95+944_-95+945dup others(2): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135029366 | |||||||
chr2:135029483 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-95+829G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135029483 | |||||||
chr2:135029578 | G | C | 150 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(147): Show |
151 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-95+734C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135029578 | |||||||
chr2:135029687 | G | A | 1 | a0004c0006t0001g0241 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-95+625C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135029687 | |||||||
chr2:135029908 | C | A | 1 | a0006c0008t0003g0156 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-95+404G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135029908 | |||||||
chr2:135030072 | T | C | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-95+240A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135030072 | |||||||
chr2:135030116 | T | C | 4 | a0001c0005t0001g0130 a0001c0005t0002g0128 a0024c0034t0002g0119 others(1): Show |
4 | HG03130.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-95+196A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135030116 | |||||||
chr2:135030147 | C | A | 1 | a0001c0001t0001g0058 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-95+165G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 3/12 | chr2 | 135030147 | |||||||
chr2:135030782 | G | T | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-283-282C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135030782 | |||||||
chr2:135030978 | T | G | 1 | a0018c0033t0005g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-283-478A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135030978 | |||||||
chr2:135031007 | G | A | 2 | a0002c0003t0002g0191 a0002c0003t0002g0192 |
2 | NA19085.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-283-507C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135031007 | |||||||
chr2:135031038 | G | A | 1 | a0005c0007t0006g0011 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-283-538C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135031038 | |||||||
chr2:135031142 | A | G | 4 | a0001c0005t0001g0130 a0001c0005t0002g0128 a0024c0034t0002g0119 others(1): Show |
4 | HG03130.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-283-642T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135031142 | |||||||
chr2:135031158 | TA | T | 126 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(123): Show |
127 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-283-659delT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135031158 | |||||||
chr2:135031159 | A | T | 2 | a0003c0004t0003g0175 a0013c0014t0003g0174 |
2 | NA18960.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-283-659T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135031159 | |||||||
chr2:135031191 | G | T | 3 | a0001c0001t0001g0065 a0001c0001t0002g0066 a0007c0023t0004g0064 |
3 | HG02257.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-283-691C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135031191 | |||||||
chr2:135031271 | T | C | 1 | a0002c0016t0001g0279 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-283-771A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135031271 | |||||||
chr2:135031310 | G | A | 1 | a0015c0036t0003g0252 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-283-810C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135031310 | |||||||
chr2:135031401 | G | A | 1 | a0001c0001t0002g0294 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-283-901C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135031401 | |||||||
chr2:135031429 | G | C | 13 | a0001c0001t0001g0282 a0001c0001t0001g0290 a0001c0001t0002g0283 others(10): Show |
13 | HG00423.hp2 HG00438.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.-283-929C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135031429 | |||||||
chr2:135031517 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-283-1017G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135031517 | |||||||
chr2:135031572 | T | G | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-283-1072A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135031572 | |||||||
chr2:135031711 | C | A | 2 | a0001c0001t0002g0081 a0003c0004t0003g0082 |
2 | HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-283-1211G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135031711 | |||||||
chr2:135031717 | C | G | 27 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(24): Show |
27 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-283-1217G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135031717 | |||||||
chr2:135031800 | A | G | 2 | a0001c0001t0001g0122 a0001c0002t0001g0120 |
2 | HG00621.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-283-1300T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135031800 | |||||||
chr2:135031835 | C | A | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-283-1335G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135031835 | |||||||
chr2:135031902 | G | T | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-283-1402C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135031902 | |||||||
chr2:135032112 | A | G | 148 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(145): Show |
149 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.-283-1612T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032112 | |||||||
chr2:135032121 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-283-1621C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032121 | |||||||
chr2:135032194 | T | C | 12 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0044 others(9): Show |
12 | HG01346.hp2 HG01952.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.-283-1694A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032194 | |||||||
chr2:135032214 | A | G | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-283-1714T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032214 | |||||||
chr2:135032281 | C | T | 1 | a0015c0036t0003g0252 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-283-1781G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032281 | |||||||
chr2:135032284 | G | A | 1 | a0001c0001t0003g0193 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-283-1784C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032284 | |||||||
chr2:135032370 | A | AAG | 26 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(23): Show |
26 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.-283-1871_-283-187 others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032370 | |||||||
chr2:135032372 | A | AAAAGAG | 6 | a0001c0001t0002g0012 a0001c0001t0005g0147 a0001c0002t0001g0076 others(3): Show |
6 | HG01243.hp1 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-283-1873_-283-187 others(10): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032372 | |||||||
chr2:135032372 | A | AAAGAG | 99 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(96): Show |
99 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-283-1873_-283-187 others(9): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032372 | |||||||
chr2:135032372 | A | G | 27 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(24): Show |
27 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-283-1872T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032372 | |||||||
chr2:135032374 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-283-1874C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032374 | |||||||
chr2:135032379 | G | C | 1 | a0001c0002t0001g0247 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-283-1879C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032379 | |||||||
chr2:135032500 | G | C | 4 | a0001c0001t0005g0147 a0001c0005t0005g0145 a0017c0019t0005g0146 others(1): Show |
4 | HG02258.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-283-2000C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032500 | |||||||
chr2:135032543 | C | G | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-283-2043G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032543 | |||||||
chr2:135032583 | G | GT | 22 | a0001c0001t0001g0091 a0001c0001t0002g0081 a0001c0001t0002g0086 others(19): Show |
23 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.-283-2084dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032583 | |||||||
chr2:135032586 | T | TG | 131 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(128): Show |
131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.-283-2087_-283-208 others(5): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032586 | |||||||
chr2:135032604 | A | T | 18 | a0001c0001t0001g0091 a0001c0001t0002g0086 a0001c0001t0004g0085 others(15): Show |
19 | HG00639.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-283-2104T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032604 | |||||||
chr2:135032609 | T | A | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(2): Show |
5 | HG02258.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-283-2109A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032609 | |||||||
chr2:135032623 | A | T | 2 | a0001c0005t0002g0096 a0001c0005t0002g0097 |
2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-283-2123T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032623 | |||||||
chr2:135032631 | T | A | 4 | a0001c0005t0001g0130 a0001c0005t0002g0128 a0024c0034t0002g0119 others(1): Show |
4 | HG03130.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-283-2131A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032631 | |||||||
chr2:135032759 | A | G | 9 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(6): Show |
9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.-283-2259T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032759 | |||||||
chr2:135032803 | G | A | 9 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(6): Show |
9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.-283-2303C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032803 | |||||||
chr2:135032811 | GATTCTTA others(6): Show |
G | 1 | a0001c0001t0002g0028 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-283-2324_-283-231 others(17): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032811 | |||||||
chr2:135032813 | T | C | 9 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(6): Show |
9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.-283-2313A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032813 | |||||||
chr2:135032816 | T | C | 9 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(6): Show |
9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.-283-2316A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032816 | |||||||
chr2:135032817 | T | C | 9 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(6): Show |
9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.-283-2317A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032817 | |||||||
chr2:135032858 | A | G | 2 | a0002c0003t0001g0164 a0003c0004t0003g0163 |
2 | HG02074.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-283-2358T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032858 | |||||||
chr2:135032927 | G | C | 1 | a0003c0004t0003g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-283-2427C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032927 | |||||||
chr2:135032939 | C | T | 1 | a0002c0003t0013g0075 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-283-2439G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135032939 | |||||||
chr2:135033057 | C | T | 2 | a0001c0001t0001g0171 a0001c0002t0001g0170 |
2 | NA18999.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-283-2557G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033057 | |||||||
chr2:135033163 | G | C | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-283-2663C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033163 | |||||||
chr2:135033191 | C | T | 1 | a0018c0033t0005g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-283-2691G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033191 | |||||||
chr2:135033197 | G | A | 1 | a0003c0004t0001g0288 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-283-2697C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033197 | |||||||
chr2:135033214 | C | T | 1 | a0001c0005t0002g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-283-2714G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033214 | |||||||
chr2:135033232 | C | A | 2 | a0001c0001t0002g0081 a0003c0004t0003g0082 |
2 | HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-283-2732G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033232 | |||||||
chr2:135033240 | G | T | 76 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(73): Show |
76 | HG00408.hp2 HG00438.hp1 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.-283-2740C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033240 | |||||||
chr2:135033302 | T | A | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-283-2802A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033302 | |||||||
chr2:135033352 | A | G | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-283-2852T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033352 | |||||||
chr2:135033363 | T | C | 150 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(147): Show |
151 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-283-2863A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033363 | |||||||
chr2:135033364 | G | A | 27 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(24): Show |
27 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-283-2864C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033364 | |||||||
chr2:135033402 | G | A | 1 | a0002c0003t0001g0034 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-283-2902C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033402 | |||||||
chr2:135033442 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-283-2942G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033442 | |||||||
chr2:135033445 | T | C | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-283-2945A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033445 | |||||||
chr2:135033450 | C | A | 2 | a0001c0001t0002g0081 a0003c0004t0003g0082 |
2 | HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-283-2950G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033450 | |||||||
chr2:135033464 | A | ACACCCCG others(141): Show |
4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-283-2965_-283-296 others(152): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033464 | |||||||
chr2:135033464 | A | ACACCCCG others(762): Show |
1 | a0001c0002t0003g0102 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-283-2965_-283-296 others(773): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033464 | |||||||
chr2:135033467 | C | CCCCGGAC others(1138): Show |
1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1149): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(2032): Show |
1 | a0007c0024t0001g0108 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(2043): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(2030): Show |
1 | a0001c0001t0002g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(2041): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(2032): Show |
1 | a0001c0001t0001g0107 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(2043): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1189): Show |
3 | a0001c0001t0005g0147 a0001c0005t0005g0145 a0017c0019t0005g0146 |
3 | HG02258.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-283-2968_-283-296 others(1200): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1713): Show |
1 | a0018c0033t0005g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1724): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(141): Show |
3 | a0001c0005t0001g0130 a0024c0034t0002g0119 a0026c0035t0002g0118 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-283-2968_-283-296 others(152): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(665): Show |
1 | a0001c0002t0001g0104 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(676): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(665): Show |
1 | a0002c0003t0001g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(676): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1568): Show |
1 | a0005c0007t0002g0105 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1579): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1875): Show |
1 | a0001c0002t0001g0324 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1886): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(2609): Show |
1 | a0001c0002t0001g0121 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(2620): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1875): Show |
1 | a0001c0001t0001g0009 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1886): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1875): Show |
12 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0123 others(9): Show |
12 | HG00735.hp2 HG01884.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-283-2968_-283-296 others(1886): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1876): Show |
1 | a0001c0001t0001g0122 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1887): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1142): Show |
1 | a0001c0001t0001g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1153): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1286): Show |
1 | a0003c0004t0001g0015 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1297): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1189): Show |
1 | a0001c0009t0002g0134 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1200): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1878): Show |
1 | a0001c0002t0001g0120 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1889): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(142): Show |
1 | a0001c0018t0001g0144 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(153): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(238): Show |
3 | a0001c0002t0001g0133 a0001c0009t0001g0143 a0001c0009t0004g0131 |
3 | HG02451.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-283-2968_-283-296 others(249): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1094): Show |
1 | a0007c0012t0001g0109 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1105): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(764): Show |
1 | a0001c0001t0001g0041 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(775): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(763): Show |
27 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0032 others(24): Show |
27 | HG00438.hp1 HG01952.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.-283-2968_-283-296 others(774): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(764): Show |
1 | a0013c0014t0003g0042 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(775): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1876): Show |
1 | a0001c0001t0004g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1887): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1287): Show |
3 | a0001c0002t0001g0327 a0001c0002t0002g0326 a0009c0011t0001g0325 |
3 | HG03491.hp1 HG03654.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-283-2968_-283-296 others(1298): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1287): Show |
18 | a0001c0001t0001g0022 a0001c0001t0001g0077 a0001c0001t0002g0020 others(15): Show |
18 | HG00741.hp1 HG01070.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.-283-2968_-283-296 others(1298): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1238): Show |
2 | a0011c0013t0004g0039 a0011c0013t0004g0040 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-283-2968_-283-296 others(1249): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1287): Show |
1 | a0001c0002t0001g0076 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1298): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1287): Show |
1 | a0003c0004t0002g0035 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1298): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1288): Show |
3 | a0001c0001t0001g0065 a0001c0001t0002g0066 a0007c0023t0004g0064 |
3 | HG02257.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-283-2968_-283-296 others(1299): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1292): Show |
1 | a0002c0003t0002g0067 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1303): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1385): Show |
1 | a0002c0003t0001g0007 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1396): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1198): Show |
1 | a0010c0015t0001g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1209): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(812): Show |
1 | a0002c0003t0002g0073 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(823): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(764): Show |
1 | a0001c0001t0002g0012 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(775): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(766): Show |
1 | a0001c0001t0001g0080 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(777): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(764): Show |
5 | a0001c0001t0002g0028 a0001c0002t0001g0047 a0002c0003t0002g0048 others(2): Show |
5 | HG00408.hp2 HG02015.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.-283-2968_-283-296 others(775): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1288): Show |
2 | a0002c0003t0001g0018 a0020c0026t0001g0026 |
2 | HG01256.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-283-2968_-283-296 others(1299): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1290): Show |
1 | a0021c0029t0011g0037 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1301): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1289): Show |
1 | a0001c0002t0001g0021 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1300): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(1293): Show |
1 | a0001c0001t0001g0068 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(1304): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(765): Show |
1 | a0002c0003t0001g0045 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(776): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(766): Show |
1 | a0001c0001t0002g0038 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(777): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(767): Show |
1 | a0012c0017t0001g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(778): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(90): Show |
9 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(6): Show |
9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.-283-2968_-283-296 others(101): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | CCCCGGAC others(766): Show |
1 | a0001c0001t0001g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-283-2968_-283-296 others(777): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033467 | C | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-283-2967G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033467 | |||||||
chr2:135033474 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-283-2974G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033474 | |||||||
chr2:135033475 | G | A | 2 | a0001c0002t0012g0293 a0003c0004t0003g0289 |
2 | HG02071.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-283-2975C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033475 | |||||||
chr2:135033479 | C | T | 1 | a0003c0004t0003g0195 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-283-2979G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033479 | |||||||
chr2:135033488 | G | A | 1 | a0001c0005t0002g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-283-2988C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033488 | |||||||
chr2:135033494 | A | G | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-283-2994T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033494 | |||||||
chr2:135033500 | T | TAACCCCC others(5): Show |
1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-283-3001_-283-300 others(16): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033500 | |||||||
chr2:135033507 | T | C | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-283-3007A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033507 | |||||||
chr2:135033510 | C | T | 12 | a0001c0001t0002g0020 a0001c0001t0002g0036 a0001c0002t0001g0016 others(9): Show |
12 | HG00741.hp1 HG01256.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.-283-3010G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033510 | |||||||
chr2:135033512 | A | G | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-283-3012T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033512 | |||||||
chr2:135033514 | T | A | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-283-3014A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033514 | |||||||
chr2:135033515 | A | C | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-283-3015T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033515 | |||||||
chr2:135033521 | A | G | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-283-3021T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033521 | |||||||
chr2:135033524 | C | T | 131 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(128): Show |
131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.-283-3024G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033524 | |||||||
chr2:135033528 | C | G | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-283-3028G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033528 | |||||||
chr2:135033529 | A | G | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-283-3029T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033529 | |||||||
chr2:135033532 | G | T | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-283-3032C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033532 | |||||||
chr2:135033534 | C | A | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-283-3034G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033534 | |||||||
chr2:135033535 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-283-3035C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033535 | |||||||
chr2:135033535 | G | C | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-283-3035C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033535 | |||||||
chr2:135033540 | T | C | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-283-3040A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033540 | |||||||
chr2:135033552 | C | A | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-283-3052G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033552 | |||||||
chr2:135033552 | C | T | 133 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(130): Show |
133 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.-283-3052G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033552 | |||||||
chr2:135033557 | C | T | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-283-3057G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033557 | |||||||
chr2:135033563 | G | GC | 324 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0022 others(321): Show |
329 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(326): Show |
intron_variant | MODIFIER | c.-283-3064dupG | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033563 | |||||||
chr2:135033565 | G | C | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-283-3065C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033565 | |||||||
chr2:135033566 | G | A | 1 | a0001c0001t0001g0300 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-283-3066C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033566 | |||||||
chr2:135033567 | G | T | 1 | a0001c0018t0001g0144 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-283-3067C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033567 | |||||||
chr2:135033568 | C | G | 2 | a0001c0005t0002g0128 a0001c0018t0001g0144 |
2 | HG00639.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-283-3068G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033568 | |||||||
chr2:135033569 | G | C | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-283-3069C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033569 | |||||||
chr2:135033584 | C | A | 121 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(118): Show |
121 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.-283-3084G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033584 | |||||||
chr2:135033588 | C | T | 1 | a0002c0003t0001g0034 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-283-3088G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033588 | |||||||
chr2:135033589 | G | T | 1 | a0001c0005t0002g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-283-3089C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033589 | |||||||
chr2:135033597 | A | G | 11 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(8): Show |
11 | HG00639.hp1 HG02559.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-283-3097T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033597 | |||||||
chr2:135033605 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-283-3105G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033605 | |||||||
chr2:135033646 | T | C | 2 | a0001c0002t0001g0104 a0005c0007t0002g0105 |
2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-283-3146A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033646 | |||||||
chr2:135033667 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-283-3167G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033667 | |||||||
chr2:135033669 | C | T | 1 | a0018c0033t0005g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-283-3169G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033669 | |||||||
chr2:135033678 | C | G | 1 | a0001c0001t0001g0159 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-283-3178G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033678 | |||||||
chr2:135033686 | C | T | 120 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(117): Show |
120 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.-283-3186G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033686 | |||||||
chr2:135033710 | A | C | 4 | a0001c0001t0001g0029 a0001c0001t0002g0028 a0001c0001t0002g0030 others(1): Show |
4 | HG00438.hp1 HG02040.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.-283-3210T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033710 | |||||||
chr2:135033724 | C | T | 41 | a0001c0001t0001g0002 a0001c0001t0001g0159 a0001c0001t0001g0171 others(38): Show |
42 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.-283-3224G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033724 | |||||||
chr2:135033729 | T | C | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-283-3229A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033729 | |||||||
chr2:135033770 | T | C | 11 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(8): Show |
11 | HG00639.hp1 HG02559.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-283-3270A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033770 | |||||||
chr2:135033772 | G | A | 121 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(118): Show |
121 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.-283-3272C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033772 | |||||||
chr2:135033773 | C | A | 121 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(118): Show |
121 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.-283-3273G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033773 | |||||||
chr2:135033799 | G | A | 1 | a0001c0018t0001g0144 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-283-3299C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033799 | |||||||
chr2:135033802 | C | A | 2 | a0001c0002t0001g0104 a0005c0007t0002g0105 |
2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-283-3302G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033802 | |||||||
chr2:135033819 | CG | C | 316 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0022 others(313): Show |
321 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.-283-3320delC | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033819 | |||||||
chr2:135033820 | G | GGGGGGCT others(390): Show |
4 | a0001c0005t0001g0130 a0001c0005t0002g0128 a0024c0034t0002g0119 others(1): Show |
4 | HG03130.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-283-3321_-283-332 others(401): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033820 | |||||||
chr2:135033820 | G | GGGGGGCT others(614): Show |
4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-283-3321_-283-332 others(625): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033820 | |||||||
chr2:135033820 | G | GGGGGGCT others(264): Show |
1 | a0001c0018t0001g0144 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-283-3321_-283-332 others(275): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033820 | |||||||
chr2:135033857 | T | C | 3 | a0001c0002t0001g0104 a0001c0018t0001g0144 a0005c0007t0002g0105 |
3 | HG00639.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-283-3357A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033857 | |||||||
chr2:135033869 | C | T | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-283-3369G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033869 | |||||||
chr2:135033895 | G | A | 2 | a0001c0001t0002g0081 a0003c0004t0003g0082 |
2 | HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-283-3395C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033895 | |||||||
chr2:135033920 | C | T | 1 | a0007c0012t0001g0109 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-283-3420G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033920 | |||||||
chr2:135033951 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-283-3451C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033951 | |||||||
chr2:135033955 | G | A | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-283-3455C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033955 | |||||||
chr2:135033978 | C | G | 1 | a0001c0002t0001g0242 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-283-3478G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033978 | |||||||
chr2:135033978 | C | T | 4 | a0001c0005t0001g0130 a0001c0005t0002g0128 a0024c0034t0002g0119 others(1): Show |
4 | HG03130.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-283-3478G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033978 | |||||||
chr2:135033990 | C | T | 1 | a0005c0007t0002g0105 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-283-3490G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033990 | |||||||
chr2:135033994 | C | T | 1 | a0005c0007t0002g0105 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-283-3494G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135033994 | |||||||
chr2:135034035 | G | A | 1 | a0003c0004t0001g0168 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-283-3535C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034035 | |||||||
chr2:135034096 | G | A | 1 | a0005c0007t0002g0105 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-283-3596C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034096 | |||||||
chr2:135034097 | G | T | 1 | a0018c0033t0005g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-283-3597C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034097 | |||||||
chr2:135034108 | G | A | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-283-3608C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034108 | |||||||
chr2:135034142 | A | T | 1 | a0009c0011t0002g0243 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-283-3642T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034142 | |||||||
chr2:135034173 | G | T | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-283-3673C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034173 | |||||||
chr2:135034269 | C | T | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-283-3769G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034269 | |||||||
chr2:135034293 | G | T | 1 | a0001c0002t0001g0169 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-283-3793C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034293 | |||||||
chr2:135034344 | G | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-283-3844C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034344 | |||||||
chr2:135034411 | C | G | 1 | a0001c0001t0001g0300 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-283-3911G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034411 | |||||||
chr2:135034413 | G | C | 1 | a0001c0001t0001g0300 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-283-3913C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034413 | |||||||
chr2:135034480 | G | A | 11 | a0001c0001t0001g0068 a0001c0002t0001g0070 a0001c0002t0001g0071 others(8): Show |
11 | HG00423.hp1 HG03017.hp2 HG03654.hp1 others(8): Show |
intron_variant | MODIFIER | c.-283-3980C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034480 | |||||||
chr2:135034488 | A | G | 133 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(130): Show |
133 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.-283-3988T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034488 | |||||||
chr2:135034523 | G | A | 1 | a0002c0003t0001g0127 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-283-4023C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034523 | |||||||
chr2:135034559 | A | G | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-283-4059T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034559 | |||||||
chr2:135034561 | C | T | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-283-4061G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034561 | |||||||
chr2:135034563 | CG | C | 9 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(6): Show |
9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.-283-4064delC | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034563 | |||||||
chr2:135034668 | C | T | 4 | a0001c0005t0001g0130 a0001c0005t0002g0128 a0024c0034t0002g0119 others(1): Show |
4 | HG03130.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-283-4168G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034668 | |||||||
chr2:135034768 | G | C | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-283-4268C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034768 | |||||||
chr2:135034824 | A | AGAGGGGG others(5): Show |
2 | a0001c0001t0002g0244 a0009c0011t0002g0243 |
2 | HG01192.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.-283-4336_-283-432 others(16): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034824 | |||||||
chr2:135034824 | AGAGGGG | A | 6 | a0001c0001t0001g0152 a0001c0001t0001g0238 a0001c0001t0002g0240 others(3): Show |
6 | HG00735.hp1 HG02055.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.-283-4330_-283-432 others(10): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034824 | |||||||
chr2:135034824 | AGAGGGGG others(5): Show |
A | 133 | a0001c0001t0001g0022 a0001c0001t0001g0029 a0001c0001t0001g0032 others(130): Show |
134 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.-283-4336_-283-432 others(16): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034824 | |||||||
chr2:135034824 | AGAGGGGG others(11): Show |
A | 9 | a0001c0001t0005g0147 a0001c0005t0001g0130 a0001c0005t0002g0128 others(6): Show |
9 | HG02258.hp1 HG03130.hp2 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-283-4342_-283-432 others(22): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034824 | |||||||
chr2:135034827 | GGGGGAGG others(4): Show |
G | 3 | a0001c0002t0001g0021 a0001c0005t0002g0084 a0020c0026t0001g0026 |
3 | HG01192.hp1 HG02647.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-283-4338_-283-432 others(15): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034827 | |||||||
chr2:135034832 | A | AG | 6 | a0001c0001t0001g0002 a0001c0001t0001g0305 a0001c0001t0002g0245 others(3): Show |
6 | HG01496.hp2 HG01884.hp1 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.-283-4333dupC | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034832 | |||||||
chr2:135034832 | A | G | 1 | a0001c0001t0002g0218 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-283-4332T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034832 | |||||||
chr2:135034833 | GGGGGAGG others(4): Show |
G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0010c0015t0001g0103 |
3 | HG00639.hp2 HG01261.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-283-4344_-283-433 others(15): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034833 | |||||||
chr2:135034838 | A | AG | 6 | a0001c0001t0001g0300 a0002c0003t0001g0323 a0003c0004t0001g0168 others(3): Show |
6 | HG00642.hp1 HG02027.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.-283-4339dupC | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034838 | |||||||
chr2:135034839 | GGGGGAGG others(4): Show |
G | 2 | a0001c0005t0002g0083 a0002c0003t0001g0007 |
2 | HG02896.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-283-4350_-283-434 others(15): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034839 | |||||||
chr2:135034844 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-283-4344T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034844 | |||||||
chr2:135034850 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-283-4350T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034850 | |||||||
chr2:135034855 | G | T | 1 | a0004c0006t0001g0250 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-283-4355C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034855 | |||||||
chr2:135034870 | A | G | 1 | a0001c0002t0001g0249 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-283-4370T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034870 | |||||||
chr2:135034958 | A | G | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-283-4458T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135034958 | |||||||
chr2:135035067 | CTATATGA others(52): Show |
C | 1 | a0001c0002t0001g0242 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-283-4626_-283-456 others(63): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135035067 | |||||||
chr2:135035127 | T | A | 1 | a0001c0002t0001g0242 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-283-4627A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135035127 | |||||||
chr2:135035351 | C | T | 1 | a0003c0004t0003g0025 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-283-4851G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135035351 | |||||||
chr2:135035518 | T | C | 12 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0002g0066 others(9): Show |
12 | HG02257.hp1 HG03017.hp2 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.-284+4845A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135035518 | |||||||
chr2:135035540 | T | C | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-284+4823A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135035540 | |||||||
chr2:135035688 | CAAT | C | 16 | a0001c0001t0001g0091 a0001c0001t0002g0086 a0001c0001t0004g0085 others(13): Show |
17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-284+4672_-284+467 others(7): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135035688 | |||||||
chr2:135035757 | T | C | 27 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(24): Show |
27 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-284+4606A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135035757 | |||||||
chr2:135035920 | C | T | 1 | a0001c0002t0001g0248 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-284+4443G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135035920 | |||||||
chr2:135035937 | C | T | 3 | a0001c0002t0001g0321 a0001c0002t0001g0322 a0002c0003t0001g0323 |
3 | HG00642.hp1 NA20805.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-284+4426G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135035937 | |||||||
chr2:135035942 | T | C | 2 | a0001c0001t0002g0244 a0009c0011t0002g0243 |
2 | HG01192.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.-284+4421A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135035942 | |||||||
chr2:135035995 | C | T | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-284+4368G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135035995 | |||||||
chr2:135036114 | T | G | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-284+4249A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036114 | |||||||
chr2:135036128 | G | T | 1 | a0002c0003t0001g0299 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-284+4235C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036128 | |||||||
chr2:135036190 | A | G | 4 | a0001c0001t0005g0147 a0001c0005t0005g0145 a0017c0019t0005g0146 others(1): Show |
4 | HG02258.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-284+4173T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036190 | |||||||
chr2:135036275 | T | C | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-284+4088A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036275 | |||||||
chr2:135036557 | T | A | 1 | a0004c0006t0001g0074 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-284+3806A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036557 | |||||||
chr2:135036635 | TTATGTG | T | 3 | a0001c0001t0005g0147 a0001c0005t0005g0145 a0017c0019t0005g0146 |
3 | HG02258.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-284+3722_-284+372 others(10): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036635 | |||||||
chr2:135036635 | TTATGTGT others(3): Show |
T | 1 | a0018c0033t0005g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-284+3718_-284+372 others(14): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036635 | |||||||
chr2:135036637 | A | ATG | 10 | a0001c0001t0001g0181 a0001c0002t0001g0076 a0001c0002t0001g0104 others(7): Show |
10 | HG02109.hp2 HG02257.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-284+3724_-284+372 others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036637 | |||||||
chr2:135036637 | A | ATGTG | 4 | a0001c0001t0001g0091 a0001c0005t0002g0001 a0001c0005t0002g0084 others(1): Show |
4 | HG02647.hp2 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-284+3722_-284+372 others(8): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036637 | |||||||
chr2:135036637 | ATG | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0123 a0001c0001t0001g0157 others(57): Show |
61 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.-284+3724_-284+372 others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036637 | |||||||
chr2:135036637 | ATGTG | A | 110 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(107): Show |
113 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.-284+3722_-284+372 others(8): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036637 | |||||||
chr2:135036637 | ATGTGTG | A | 20 | a0001c0001t0001g0173 a0001c0001t0002g0050 a0001c0001t0002g0081 others(17): Show |
20 | HG00280.hp1 HG00609.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.-284+3720_-284+372 others(10): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036637 | |||||||
chr2:135036637 | ATGTGTGT others(1): Show |
A | 74 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(71): Show |
74 | HG00408.hp2 HG00438.hp1 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.-284+3718_-284+372 others(12): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036637 | |||||||
chr2:135036637 | ATGTGTGT others(3): Show |
A | 5 | a0001c0002t0001g0072 a0001c0005t0001g0130 a0013c0014t0003g0042 others(2): Show |
5 | HG03130.hp2 HG03654.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-284+3716_-284+372 others(14): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036637 | |||||||
chr2:135036637 | ATGTGTGT others(5): Show |
A | 1 | a0001c0001t0001g0032 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-284+3714_-284+372 others(16): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036637 | |||||||
chr2:135036637 | ATGTGTGT others(9): Show |
A | 6 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(3): Show |
6 | HG00639.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-284+3710_-284+372 others(20): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036637 | |||||||
chr2:135036643 | G | A | 1 | a0003c0004t0003g0292 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-284+3720C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036643 | |||||||
chr2:135036771 | G | A | 9 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(6): Show |
9 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.-284+3592C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036771 | |||||||
chr2:135036797 | A | G | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-284+3566T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036797 | |||||||
chr2:135036893 | A | T | 5 | a0002c0003t0001g0164 a0003c0004t0003g0163 a0003c0004t0003g0165 others(2): Show |
5 | HG01255.hp1 HG01346.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-284+3470T>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036893 | |||||||
chr2:135036999 | C | CT | 16 | a0001c0001t0001g0091 a0001c0001t0002g0086 a0001c0001t0004g0085 others(13): Show |
17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-284+3363dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036999 | |||||||
chr2:135036999 | CTTT | C | 130 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(127): Show |
130 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.-284+3361_-284+336 others(7): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135036999 | |||||||
chr2:135037107 | C | T | 27 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(24): Show |
27 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-284+3256G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037107 | |||||||
chr2:135037116 | C | A | 4 | a0001c0005t0001g0130 a0001c0005t0002g0128 a0024c0034t0002g0119 others(1): Show |
4 | HG03130.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-284+3247G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037116 | |||||||
chr2:135037158 | G | A | 1 | a0001c0002t0012g0293 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-284+3205C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037158 | |||||||
chr2:135037273 | C | T | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-284+3090G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037273 | |||||||
chr2:135037325 | A | G | 1 | a0008c0010t0001g0150 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-284+3038T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037325 | |||||||
chr2:135037356 | C | T | 27 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(24): Show |
27 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-284+3007G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037356 | |||||||
chr2:135037413 | G | A | 2 | a0001c0002t0001g0104 a0005c0007t0002g0105 |
2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-284+2950C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037413 | |||||||
chr2:135037416 | G | A | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-284+2947C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037416 | |||||||
chr2:135037430 | T | C | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-284+2933A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037430 | |||||||
chr2:135037436 | G | A | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-284+2927C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037436 | |||||||
chr2:135037470 | A | C | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-284+2893T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037470 | |||||||
chr2:135037525 | G | A | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-284+2838C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037525 | |||||||
chr2:135037576 | G | A | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-284+2787C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037576 | |||||||
chr2:135037580 | T | G | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-284+2783A>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037580 | |||||||
chr2:135037652 | C | T | 32 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0112 others(29): Show |
32 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.-284+2711G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037652 | |||||||
chr2:135037715 | C | A | 1 | a0001c0001t0002g0245 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-284+2648G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037715 | |||||||
chr2:135037815 | C | T | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-284+2548G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037815 | |||||||
chr2:135037826 | C | T | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-284+2537G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037826 | |||||||
chr2:135037873 | C | T | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-284+2490G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037873 | |||||||
chr2:135037937 | T | A | 1 | a0001c0001t0001g0246 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-284+2426A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037937 | |||||||
chr2:135037991 | G | A | 2 | a0001c0001t0002g0081 a0003c0004t0003g0082 |
2 | HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-284+2372C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135037991 | |||||||
chr2:135038025 | T | C | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-284+2338A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135038025 | |||||||
chr2:135038165 | A | G | 1 | a0001c0002t0001g0024 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-284+2198T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135038165 | |||||||
chr2:135038302 | T | C | 1 | a0001c0002t0001g0247 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-284+2061A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135038302 | |||||||
chr2:135038307 | GTATGTAT others(5): Show |
G | 1 | a0001c0009t0004g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-284+2044_-284+205 others(16): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135038307 | |||||||
chr2:135038345 | A | G | 1 | a0003c0004t0003g0162 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-284+2018T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135038345 | |||||||
chr2:135038430 | A | C | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-284+1933T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135038430 | |||||||
chr2:135038585 | G | T | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-284+1778C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135038585 | |||||||
chr2:135038678 | G | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0122 a0001c0001t0001g0123 others(7): Show |
10 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.-284+1685C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135038678 | |||||||
chr2:135038732 | C | T | 77 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(74): Show |
77 | HG00408.hp2 HG00438.hp1 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.-284+1631G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135038732 | |||||||
chr2:135038840 | C | A | 124 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0029 others(121): Show |
124 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.-284+1523G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135038840 | |||||||
chr2:135039058 | T | C | 59 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0257 others(56): Show |
62 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.-284+1305A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135039058 | |||||||
chr2:135039123 | CT | C | 7 | a0001c0001t0002g0081 a0001c0001t0002g0294 a0001c0001t0002g0295 others(4): Show |
7 | HG01169.hp1 HG01515.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-284+1239delA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135039123 | |||||||
chr2:135039123 | CTTT | C | 16 | a0001c0001t0001g0137 a0001c0001t0002g0020 a0001c0001t0002g0132 others(13): Show |
16 | HG00280.hp1 HG00741.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.-284+1237_-284+123 others(7): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135039123 | |||||||
chr2:135039123 | CTTTT | C | 116 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(113): Show |
116 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.-284+1236_-284+123 others(8): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135039123 | |||||||
chr2:135039349 | G | A | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-284+1014C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135039349 | |||||||
chr2:135039395 | A | C | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-284+968T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135039395 | |||||||
chr2:135039419 | C | CAA | 121 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(118): Show |
121 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.-284+942_-284+943d others(4): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135039419 | |||||||
chr2:135039419 | C | CAAA | 7 | a0001c0001t0002g0012 a0001c0001t0002g0142 a0001c0001t0005g0147 others(4): Show |
7 | HG02258.hp1 HG03516.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.-284+941_-284+943d others(5): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135039419 | |||||||
chr2:135039470 | C | T | 3 | a0001c0001t0001g0159 a0002c0003t0002g0161 a0003c0021t0001g0160 |
3 | NA18985.hp1 NA18995.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-284+893G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135039470 | |||||||
chr2:135039653 | A | G | 134 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(131): Show |
134 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.-284+710T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135039653 | |||||||
chr2:135039817 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-284+546A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135039817 | |||||||
chr2:135039985 | T | C | 3 | a0001c0001t0001g0305 a0002c0003t0001g0299 a0002c0003t0001g0304 |
3 | HG00738.hp1 HG01496.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.-284+378A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135039985 | |||||||
chr2:135040177 | C | T | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-284+186G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135040177 | |||||||
chr2:135040303 | C | T | 4 | a0001c0002t0001g0104 a0001c0018t0001g0144 a0005c0007t0002g0105 others(1): Show |
4 | HG00639.hp1 HG01261.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-284+60G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 2/12 | chr2 | 135040303 | |||||||
chr2:135040512 | A | C | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-423-10T>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135040512 | |||||||
chr2:135040561 | T | TGAAAA | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-423-64_-423-60dup others(5): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135040561 | |||||||
chr2:135040619 | A | G | 1 | a0002c0003t0001g0158 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-423-117T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135040619 | |||||||
chr2:135041065 | G | A | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-423-563C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135041065 | |||||||
chr2:135041082 | T | C | 1 | a0001c0005t0001g0130 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-423-580A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135041082 | |||||||
chr2:135041151 | C | T | 1 | a0001c0001t0002g0012 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-423-649G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135041151 | |||||||
chr2:135041188 | C | T | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-423-686G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135041188 | |||||||
chr2:135041338 | C | CT | 6 | a0001c0001t0001g0300 a0001c0001t0005g0147 a0001c0005t0005g0145 others(3): Show |
6 | HG02258.hp1 HG03516.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.-423-837dupA | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135041338 | |||||||
chr2:135041444 | G | A | 4 | a0001c0001t0005g0147 a0001c0005t0005g0145 a0017c0019t0005g0146 others(1): Show |
4 | HG02258.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-423-942C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135041444 | |||||||
chr2:135041469 | T | C | 1 | a0001c0009t0001g0143 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-423-967A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135041469 | |||||||
chr2:135041496 | G | A | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-423-994C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135041496 | |||||||
chr2:135041512 | T | C | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-423-1010A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135041512 | |||||||
chr2:135041637 | C | A | 1 | a0001c0002t0001g0076 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-423-1135G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135041637 | |||||||
chr2:135041840 | C | T | 4 | a0001c0002t0001g0104 a0001c0018t0001g0144 a0005c0007t0002g0105 others(1): Show |
4 | HG00639.hp1 HG01261.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-423-1338G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135041840 | |||||||
chr2:135041840 | CAAG | C | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-423-1341_-423-133 others(7): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135041840 | |||||||
chr2:135042467 | A | ACTCCAGC others(574): Show |
1 | a0001c0001t0001g0157 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-423-2546_-423-196 others(585): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135042467 | |||||||
chr2:135042501 | C | CA | 7 | a0001c0001t0001g0300 a0001c0001t0001g0305 a0001c0001t0002g0301 others(4): Show |
7 | HG00642.hp1 HG01496.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.-423-2000dupT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135042501 | |||||||
chr2:135042501 | CA | C | 15 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(12): Show |
15 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.-423-2000delT | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135042501 | |||||||
chr2:135042515 | A | AAG | 16 | a0001c0001t0001g0091 a0001c0001t0002g0086 a0001c0001t0004g0085 others(13): Show |
17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-423-2014_-423-201 others(6): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135042515 | |||||||
chr2:135042515 | A | G | 131 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(128): Show |
131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.-423-2013T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135042515 | |||||||
chr2:135042754 | A | G | 2 | a0001c0002t0001g0104 a0005c0007t0002g0105 |
2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-423-2252T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135042754 | |||||||
chr2:135042954 | G | A | 14 | a0001c0001t0001g0137 a0001c0001t0002g0132 a0001c0001t0002g0135 others(11): Show |
14 | HG00280.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-423-2452C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135042954 | |||||||
chr2:135043031 | C | T | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-423-2529G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135043031 | |||||||
chr2:135043048 | G | A | 1 | a0001c0001t0005g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-423-2546C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135043048 | |||||||
chr2:135043167 | G | A | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-423-2665C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135043167 | |||||||
chr2:135043187 | A | G | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-423-2685T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135043187 | |||||||
chr2:135043225 | A | G | 3 | a0001c0001t0005g0147 a0001c0005t0005g0145 a0017c0019t0005g0146 |
3 | HG02258.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-423-2723T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135043225 | |||||||
chr2:135043409 | C | T | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-423-2907G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135043409 | |||||||
chr2:135043526 | C | A | 16 | a0001c0001t0001g0091 a0001c0001t0002g0086 a0001c0001t0004g0085 others(13): Show |
17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-423-3024G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135043526 | |||||||
chr2:135043658 | C | T | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-423-3156G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135043658 | |||||||
chr2:135043681 | T | C | 2 | a0001c0001t0001g0077 a0001c0030t0001g0078 |
2 | HG02683.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-423-3179A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135043681 | |||||||
chr2:135043818 | T | A | 1 | a0010c0015t0001g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-423-3316A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135043818 | |||||||
chr2:135043819 | C | T | 1 | a0010c0015t0001g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-423-3317G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135043819 | |||||||
chr2:135044210 | T | A | 1 | a0001c0001t0002g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-424+2975A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135044210 | |||||||
chr2:135044310 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-424+2875C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135044310 | |||||||
chr2:135044356 | C | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-424+2829G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135044356 | |||||||
chr2:135044385 | G | A | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-424+2800C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135044385 | |||||||
chr2:135044386 | T | A | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-424+2799A>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135044386 | |||||||
chr2:135044450 | C | T | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-424+2735G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135044450 | |||||||
chr2:135044458 | T | C | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-424+2727A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135044458 | |||||||
chr2:135044474 | A | G | 1 | a0003c0004t0003g0154 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-424+2711T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135044474 | |||||||
chr2:135044480 | C | A | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-424+2705G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135044480 | |||||||
chr2:135044578 | G | A | 132 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(129): Show |
132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-424+2607C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135044578 | |||||||
chr2:135044588 | C | G | 1 | a0001c0002t0001g0153 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-424+2597G>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135044588 | |||||||
chr2:135044656 | T | C | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-424+2529A>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135044656 | |||||||
chr2:135045097 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-424+2088G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135045097 | |||||||
chr2:135045124 | G | A | 1 | a0001c0018t0001g0144 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-424+2061C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135045124 | |||||||
chr2:135045320 | C | T | 1 | a0004c0006t0001g0010 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-424+1865G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135045320 | |||||||
chr2:135045473 | G | T | 1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-424+1712C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135045473 | |||||||
chr2:135045855 | G | T | 315 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0022 others(312): Show |
320 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.-424+1330C>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135045855 | |||||||
chr2:135045924 | T | TTAAAAAT others(320): Show |
1 | a0018c0033t0005g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-424+1260_-424+126 others(331): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135045924 | |||||||
chr2:135045924 | T | TTAAAAAT others(322): Show |
1 | a0014c0025t0008g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-424+1260_-424+126 others(333): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135045924 | |||||||
chr2:135045924 | T | TTAAAAAT others(320): Show |
3 | a0001c0001t0005g0147 a0001c0005t0005g0145 a0017c0019t0005g0146 |
3 | HG02258.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-424+1260_-424+126 others(331): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135045924 | |||||||
chr2:135045957 | C | T | 2 | a0008c0010t0001g0150 a0008c0010t0002g0151 |
2 | HG00558.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.-424+1228G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135045957 | |||||||
chr2:135046045 | C | A | 1 | a0001c0002t0001g0319 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-424+1140G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135046045 | |||||||
chr2:135046196 | A | G | 150 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0027 others(147): Show |
151 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-424+989T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135046196 | |||||||
chr2:135046236 | A | G | 77 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(74): Show |
77 | HG00408.hp2 HG00438.hp1 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.-424+949T>C | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135046236 | |||||||
chr2:135046346 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-424+839G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135046346 | |||||||
chr2:135046363 | C | T | 1 | a0002c0003t0001g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-424+822G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135046363 | |||||||
chr2:135046438 | G | A | 1 | a0001c0005t0001g0320 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-424+747C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135046438 | |||||||
chr2:135046496 | G | A | 3 | a0001c0002t0001g0321 a0001c0002t0001g0322 a0002c0003t0001g0323 |
3 | HG00642.hp1 NA20805.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-424+689C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135046496 | |||||||
chr2:135046575 | C | A | 1 | a0001c0002t0001g0324 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-424+610G>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135046575 | |||||||
chr2:135046645 | C | T | 1 | a0002c0003t0001g0007 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-424+540G>A | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135046645 | |||||||
chr2:135046873 | G | C | 3 | a0001c0002t0001g0327 a0001c0002t0002g0326 a0009c0011t0001g0325 |
3 | HG03491.hp1 HG03654.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-424+312C>G | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135046873 | |||||||
chr2:135046985 | G | A | 2 | a0002c0003t0001g0328 a0002c0003t0001g0329 |
2 | HG00423.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-424+200C>T | MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 1/12 | chr2 | 135046985 |