Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5606 |
| ensemblid | ENSG00000034152.20 |
| hgncid | 6843 |
| symbol | MAP2K3 |
| name | mitogen-activated protein kinase kinase 3 |
| refseq_nuc | NM_145109.3 |
| refseq_prot | NP_659731.1 |
| ensembl_nuc | ENST00000342679.9 |
| ensembl_prot | ENSP00000345083.4 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 21284711 |
| end | 21315232 |
| strand | + |
| ver | v1.2 |
| region | chr17:21284711-21315232 |
| region5000 | chr17:21279711-21320232 |
| regionname0 | MAP2K3_chr17_21284711_21315232 |
| regionname5000 | MAP2K3_chr17_21279711_21320232 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 347 | 362 | 87 | 68 | 145 | 10 | 50 | 107 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | MESPA others(342): Show |
chr17 | 21279711 | 21320232 |
| a0002 | 0/0 | 347 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | MESPA others(342): Show |
chr17 | 21279711 | 21320232 |
| a0003 | 0/0 | 347 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | MESPA others(342): Show |
chr17 | 21279711 | 21320232 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1041 | 246 | 49 | 46 | 108 | 9 | 33 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | ATGGA others(1036): Show |
chr17 | 21279711 | 21320232 | ||
| a0001c0002 | 0/1 | 1041 | 98 | 24 | 22 | 34 | 1 | 16 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | ATGGA others(1036): Show |
chr17 | 21279711 | 21320232 | ||
| a0001c0003 | 0/0 | 1041 | 6 | 6 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | ATGGA others(1036): Show |
chr17 | 21279711 | 21320232 | ||
| a0001c0004 | 0/0 | 1041 | 6 | 6 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | ATGGA others(1036): Show |
chr17 | 21279711 | 21320232 | ||
| a0001c0005 | 0/0 | 1041 | 3 | 0 | 0 | 3 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | ATGGA others(1036): Show |
chr17 | 21279711 | 21320232 | ||
| a0001c0006 | 0/0 | 1041 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | ATGGA others(1036): Show |
chr17 | 21279711 | 21320232 | ||
| a0001c0010 | 0/0 | 1041 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | ATGGA others(1036): Show |
chr17 | 21279711 | 21320232 | ||
| a0002c0007 | 0/0 | 1041 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | ATGGA others(1036): Show |
chr17 | 21279711 | 21320232 | ||
| a0002c0008 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | ATGGA others(1036): Show |
chr17 | 21279711 | 21320232 | ||
| a0003c0009 | 0/0 | 1041 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | ATGGA others(1036): Show |
chr17 | 21279711 | 21320232 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2255 | 114 | 28 | 14 | 50 | 2 | 20 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2250): Show |
chr17 | 21279711 | 21320232 |
| a0001c0001t0002 | 1/0 | 2256 | 112 | 14 | 31 | 50 | 5 | 11 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2251): Show |
chr17 | 21279711 | 21320232 |
| a0001c0001t0003 | 0/0 | 2254 | 11 | 4 | 1 | 4 | 1 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2249): Show |
chr17 | 21279711 | 21320232 |
| a0001c0001t0007 | 0/0 | 2261 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2256): Show |
chr17 | 21279711 | 21320232 |
| a0001c0001t0010 | 0/0 | 2256 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2251): Show |
chr17 | 21279711 | 21320232 |
| a0001c0001t0011 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2251): Show |
chr17 | 21279711 | 21320232 |
| a0001c0001t0013 | 0/0 | 2255 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2250): Show |
chr17 | 21279711 | 21320232 |
| a0001c0001t0014 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2251): Show |
chr17 | 21279711 | 21320232 |
| a0001c0001t0016 | 0/0 | 2255 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2250): Show |
chr17 | 21279711 | 21320232 |
| a0001c0001t0018 | 0/0 | 2255 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2250): Show |
chr17 | 21279711 | 21320232 |
| a0001c0001t0021 | 0/0 | 2243 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2238): Show |
chr17 | 21279711 | 21320232 |
| a0001c0002t0001 | 0/1 | 2255 | 68 | 10 | 16 | 28 | 0 | 13 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2250): Show |
chr17 | 21279711 | 21320232 |
| a0001c0002t0002 | 0/0 | 2256 | 9 | 3 | 4 | 1 | 1 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2251): Show |
chr17 | 21279711 | 21320232 |
| a0001c0002t0003 | 0/0 | 2254 | 3 | 1 | 0 | 1 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2249): Show |
chr17 | 21279711 | 21320232 |
| a0001c0002t0004 | 0/0 | 2255 | 6 | 6 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2250): Show |
chr17 | 21279711 | 21320232 |
| a0001c0002t0006 | 0/0 | 2255 | 4 | 1 | 1 | 0 | 0 | 2 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2250): Show |
chr17 | 21279711 | 21320232 |
| a0001c0002t0007 | 0/0 | 2261 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2256): Show |
chr17 | 21279711 | 21320232 |
| a0001c0002t0008 | 0/0 | 2256 | 3 | 3 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2251): Show |
chr17 | 21279711 | 21320232 |
| a0001c0002t0015 | 0/0 | 2255 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2250): Show |
chr17 | 21279711 | 21320232 |
| a0001c0002t0019 | 0/0 | 2255 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2250): Show |
chr17 | 21279711 | 21320232 |
| a0001c0002t0020 | 0/0 | 2255 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2250): Show |
chr17 | 21279711 | 21320232 |
| a0001c0003t0005 | 0/0 | 2253 | 5 | 5 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2248): Show |
chr17 | 21279711 | 21320232 |
| a0001c0003t0017 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2248): Show |
chr17 | 21279711 | 21320232 |
| a0001c0004t0001 | 0/0 | 2255 | 6 | 6 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2250): Show |
chr17 | 21279711 | 21320232 |
| a0001c0005t0001 | 0/0 | 2255 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2250): Show |
chr17 | 21279711 | 21320232 |
| a0001c0005t0002 | 0/0 | 2256 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2251): Show |
chr17 | 21279711 | 21320232 |
| a0001c0006t0003 | 0/0 | 2254 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2249): Show |
chr17 | 21279711 | 21320232 |
| a0001c0006t0012 | 0/0 | 2257 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2252): Show |
chr17 | 21279711 | 21320232 |
| a0001c0010t0002 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2251): Show |
chr17 | 21279711 | 21320232 |
| a0002c0007t0009 | 0/0 | 2256 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2251): Show |
chr17 | 21279711 | 21320232 |
| a0002c0008t0001 | 0/0 | 2255 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2250): Show |
chr17 | 21279711 | 21320232 |
| a0003c0009t0001 | 0/0 | 2255 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | AGTCT others(2250): Show |
chr17 | 21279711 | 21320232 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0002 | 0/0 | 17 | 0 | 3 | 9 | 1 | 4 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0004 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0001 | 1/0 | 21 | 1 | 4 | 13 | 1 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0008 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0007g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0010g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0011g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0013g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0014g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0016g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0018g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0001t0021g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0003 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0009 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0227 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0002g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0004g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0006g0021 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0007g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0008g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0008g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0008g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0015g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0019g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0002t0020g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0003t0005g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0003t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0003t0017g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0004t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0004t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0004t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0004t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0004t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0005t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0005t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0005t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0006t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0006t0012g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0001c0010t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0002c0007t0009g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0002c0007t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0002c0008t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| a0003c0009t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0219 | EUR | GBR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0020 | EUR | GBR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | FIN | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0122 | EUR | FIN | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00408 | hp1 | a0001 | c0002 | t0019 | g0199 | EAS | CHS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | CHS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | CHS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | CHS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | CHS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | CHS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0187 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0190 | AMR | PUR | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01255 | hp2 | a0001 | c0002 | t0006 | g0021 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0220 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01433 | hp2 | a0001 | c0002 | t0015 | g0222 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0175 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0218 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0188 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | KHV | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0193 | EAS | KHV | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02074 | hp2 | a0001 | c0001 | t0021 | g0055 | EAS | KHV | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | KHV | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | KHV | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02145 | hp1 | a0001 | c0001 | t0014 | g0063 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CDX | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02257 | hp1 | a0001 | c0002 | t0004 | g0006 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0174 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02451 | hp1 | a0001 | c0001 | t0013 | g0085 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0210 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0213 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02615 | hp1 | a0001 | c0006 | t0012 | g0057 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0172 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02647 | hp2 | a0001 | c0004 | t0001 | g0235 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02683 | hp2 | a0001 | c0002 | t0006 | g0021 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0236 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02723 | hp2 | a0002 | c0007 | t0009 | g0239 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0197 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02738 | hp2 | a0001 | c0002 | t0006 | g0021 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02809 | hp2 | a0001 | c0002 | t0008 | g0230 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02818 | hp1 | a0001 | c0003 | t0005 | g0012 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02886 | hp1 | a0001 | c0002 | t0008 | g0232 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0221 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02895 | hp1 | a0001 | c0003 | t0017 | g0042 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02895 | hp2 | a0001 | c0003 | t0005 | g0012 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02896 | hp1 | a0001 | c0003 | t0005 | g0012 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02896 | hp2 | a0001 | c0004 | t0001 | g0237 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | ESN | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | ESN | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0171 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03041 | hp2 | a0001 | c0002 | t0004 | g0006 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03098 | hp2 | a0001 | c0001 | t0011 | g0233 | AFR | MSL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | ESN | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | MSL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03225 | hp1 | a0001 | c0004 | t0001 | g0044 | AFR | MSL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0108 | AFR | MSL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03453 | hp1 | a0001 | c0002 | t0004 | g0006 | AFR | MSL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03453 | hp2 | a0002 | c0007 | t0009 | g0238 | AFR | MSL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03486 | hp1 | a0001 | c0002 | t0008 | g0231 | AFR | MSL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | MSL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0040 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0217 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0040 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0176 | AFR | ESN | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03579 | hp1 | a0001 | c0003 | t0005 | g0042 | AFR | MSL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0006 | AFR | MSL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03654 | hp1 | a0001 | c0001 | t0007 | g0086 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0203 | SAS | STU | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0072 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0212 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0224 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | BEB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0211 | SAS | BEB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03927 | hp2 | a0001 | c0002 | t0003 | g0181 | SAS | BEB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | BEB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0216 | SAS | BEB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | STU | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0054 | SAS | STU | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | STU | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | STU | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG04228 | hp2 | a0001 | c0010 | t0002 | g0056 | SAS | STU | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18522 | hp1 | a0001 | c0006 | t0003 | g0173 | AFR | YRI | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | CHB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | CHB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | CHB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | CHB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0209 | AFR | YRI | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18906 | hp2 | a0001 | c0004 | t0001 | g0234 | AFR | YRI | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18945 | hp2 | a0001 | c0002 | t0007 | g0003 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18946 | hp1 | a0001 | c0005 | t0001 | g0030 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18956 | hp1 | a0001 | c0001 | t0016 | g0014 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18956 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18957 | hp2 | a0001 | c0001 | t0010 | g0155 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18997 | hp2 | a0003 | c0009 | t0001 | g0098 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18998 | hp1 | a0001 | c0005 | t0002 | g0166 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18999 | hp2 | a0001 | c0005 | t0002 | g0030 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19030 | hp1 | a0001 | c0003 | t0005 | g0012 | AFR | LWK | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | LWK | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0036 | AFR | LWK | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19062 | hp1 | a0001 | c0002 | t0007 | g0003 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19067 | hp1 | a0001 | c0002 | t0020 | g0194 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19240 | hp1 | a0002 | c0008 | t0001 | g0073 | AFR | YRI | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | YRI | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ASW | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA20129 | hp2 | a0001 | c0004 | t0001 | g0044 | AFR | ASW | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0082 | EUR | TSI | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA20805 | hp1 | a0001 | c0001 | t0018 | g0070 | EUR | TSI | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0229 | EUR | TSI | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | GIH | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | GIH | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03471 | hp1 | a0001 | c0002 | t0004 | g0006 | AFR | MSL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| HG06807 | hp2 | a0001 | c0002 | t0006 | g0118 | AFR | USA | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0119 | AFR | LWK | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0227 | REF | REF | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0001 | REF | REF | MAP2K3_chr17_21279711_21320232 | MAP2K3 | chr17 | 21279711 | 21320232 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:21298923 | C | A | 1 | a0002 | 3 | HG02723.hp2 HG03453.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.162C>A | p.Asp54Glu | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/12 | 372/2256 | 162/1044 | 54/347 | chr17 | 21298923 | |||
| chr17:21302144 | G | A | 1 | a0003 | 1 | NA18997.hp2 | missense_variant&splice_region_variant | MODERATE | c.401G>A | p.Gly134Glu | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/12 | 611/2256 | 401/1044 | 134/347 | chr17 | 21302144 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:21298438 | A | C | 1 | a0002c0007 | 2 | HG02723.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.75A>C | p.Leu25Leu | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 2/12 | 285/2256 | 75/1044 | 25/347 | chr17 | 21298438 | |||
| chr17:21300954 | T | C | 4 | a0001c0002 a0001c0003 a0001c0004 others(1): Show |
111 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(108): Show |
synonymous_variant | LOW | c.360T>C | p.Cys120Cys | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/12 | 570/2256 | 360/1044 | 120/347 | chr17 | 21300954 | |||
| chr17:21302145 | A | G | 1 | a0003c0009 | 1 | NA18997.hp2 | splice_region_variant&synonymous_variant | LOW | c.402A>G | p.Gly134Gly | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/12 | 612/2256 | 402/1044 | 134/347 | chr17 | 21302145 | |||
| chr17:21302241 | T | C | 1 | a0001c0010 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.498T>C | p.Leu166Leu | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/12 | 708/2256 | 498/1044 | 166/347 | chr17 | 21302241 | |||
| chr17:21304517 | C | T | 1 | a0001c0004 | 6 | HG02647.hp2 HG02717.hp2 HG02896.hp2 others(3): Show |
synonymous_variant | LOW | c.660C>T | p.Ala220Ala | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 8/12 | 870/2256 | 660/1044 | 220/347 | chr17 | 21304517 | |||
| chr17:21304532 | C | T | 1 | a0001c0003 | 6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
synonymous_variant | LOW | c.675C>T | p.Ala225Ala | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 8/12 | 885/2256 | 675/1044 | 225/347 | chr17 | 21304532 | |||
| chr17:21312171 | C | T | 1 | a0001c0005 | 3 | NA18946.hp1 NA18998.hp1 NA18999.hp2 |
synonymous_variant | LOW | c.804C>T | p.Tyr268Tyr | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 10/12 | 1014/2256 | 804/1044 | 268/347 | chr17 | 21312171 | |||
| chr17:21314164 | C | A | 1 | a0001c0006 | 2 | HG02615.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.978C>A | p.Thr326Thr | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 12/12 | 1188/2256 | 978/1044 | 326/347 | chr17 | 21314164 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:21284769 | C | A | 1 | a0002c0007t0009 | 2 | HG02723.hp2 HG03453.hp2 |
5_prime_UTR_variant | MODIFIER | c.-152C>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/12 | 152 | chr17 | 21284769 | ||||||
| chr17:21284780 | T | TCGC | 3 | a0001c0001t0011 a0001c0002t0008 a0001c0006t0012 |
5 | HG02615.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-116_-114dupCGC | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/12 | 113 | INFO_REALIGN_3_PRIME | chr17 | 21284780 | |||||
| chr17:21284780 | T | TCGCCGC | 2 | a0001c0001t0007 a0001c0002t0007 |
3 | HG03654.hp1 NA18945.hp2 NA19062.hp1 |
5_prime_UTR_variant | MODIFIER | c.-119_-114dupCGCCGC | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/12 | 113 | INFO_REALIGN_3_PRIME | chr17 | 21284780 | |||||
| chr17:21284780 | TCGCCGCC others(5): Show |
T | 1 | a0001c0001t0021 | 1 | HG02074.hp2 | 5_prime_UTR_variant | MODIFIER | c.-125_-114delCGCCGC others(6): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/12 | 114 | INFO_REALIGN_3_PRIME | chr17 | 21284780 | |||||
| chr17:21284787 | C | T | 1 | a0001c0002t0006 | 4 | HG01255.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-134C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/12 | chr17 | 21284787 | |||||||
| chr17:21284805 | CGCT | C | 2 | a0001c0001t0011 a0001c0002t0008 |
4 | HG02809.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-112_-110delGCT | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/12 | 110 | INFO_REALIGN_3_PRIME | chr17 | 21284805 | |||||
| chr17:21284823 | C | T | 1 | a0001c0002t0020 | 1 | NA19067.hp1 | 5_prime_UTR_variant | MODIFIER | c.-98C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/12 | 98 | chr17 | 21284823 | ||||||
| chr17:21284838 | C | T | 1 | a0001c0002t0019 | 1 | HG00408.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-83C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/12 | chr17 | 21284838 | |||||||
| chr17:21284872 | C | T | 1 | a0001c0002t0004 | 6 | HG02257.hp1 HG03041.hp2 HG03225.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-49C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/12 | chr17 | 21284872 | |||||||
| chr17:21314414 | T | C | 1 | a0001c0001t0013 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*184T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 12/12 | 184 | chr17 | 21314414 | ||||||
| chr17:21314537 | G | T | 1 | a0001c0002t0008 | 3 | HG02809.hp2 HG02886.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*307G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 12/12 | 307 | chr17 | 21314537 | ||||||
| chr17:21314673 | C | T | 1 | a0001c0001t0018 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*443C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 12/12 | 443 | chr17 | 21314673 | ||||||
| chr17:21314768 | C | T | 1 | a0001c0003t0017 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*538C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 12/12 | 538 | chr17 | 21314768 | ||||||
| chr17:21315054 | C | T | 1 | a0001c0001t0016 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*824C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 12/12 | 824 | chr17 | 21315054 | ||||||
| chr17:21315151 | G | A | 1 | a0001c0001t0010 | 2 | NA18956.hp2 NA18957.hp2 |
3_prime_UTR_variant | MODIFIER | c.*921G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 12/12 | 921 | chr17 | 21315151 | ||||||
| chr17:21315199 | G | C | 1 | a0001c0001t0014 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*969G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 12/12 | 969 | chr17 | 21315199 | ||||||
| chr17:21315213 | TA | T | 17 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0013 others(14): Show |
210 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*980delA | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 12/12 | 980 | INFO_REALIGN_3_PRIME | chr17 | 21315213 | |||||
| chr17:21315213 | TAA | T | 4 | a0001c0001t0003 a0001c0002t0003 a0001c0006t0003 others(1): Show |
16 | HG00323.hp1 HG01943.hp2 HG02055.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*979_*980delAA | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 12/12 | 979 | INFO_REALIGN_3_PRIME | chr17 | 21315213 | |||||
| chr17:21315213 | TAAA | T | 2 | a0001c0003t0005 a0001c0003t0017 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*978_*980delAAA | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 12/12 | 978 | INFO_REALIGN_3_PRIME | chr17 | 21315213 | |||||
| chr17:21315215 | A | T | 1 | a0001c0002t0015 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*985A>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 12/12 | 985 | chr17 | 21315215 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:21285079 | C | T | 1 | a0001c0002t0006g0021 | 3 | HG01255.hp2 HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.49+110C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21285079 | |||||||
| chr17:21285087 | G | T | 1 | a0001c0001t0002g0240 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.49+118G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21285087 | |||||||
| chr17:21285143 | A | G | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.49+174A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21285143 | |||||||
| chr17:21285176 | C | T | 6 | a0001c0001t0001g0043 a0001c0004t0001g0044 a0001c0004t0001g0234 others(3): Show |
8 | HG01433.hp1 HG02055.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+207C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21285176 | |||||||
| chr17:21285390 | G | T | 9 | a0001c0001t0011g0233 a0001c0002t0008g0230 a0001c0002t0008g0231 others(6): Show |
12 | HG02723.hp2 HG02809.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+421G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21285390 | |||||||
| chr17:21285759 | G | A | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.49+790G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21285759 | |||||||
| chr17:21285899 | A | AT | 75 | a0001c0001t0001g0043 a0001c0001t0001g0177 a0001c0001t0001g0178 others(72): Show |
103 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.49+942dupT | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21285899 | ||||||
| chr17:21285899 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.49+930A>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21285899 | |||||||
| chr17:21285934 | T | C | 1 | a0001c0001t0002g0045 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.49+965T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21285934 | |||||||
| chr17:21286286 | T | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
259 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.49+1317T>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21286286 | |||||||
| chr17:21286889 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.49+1920G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21286889 | |||||||
| chr17:21286921 | C | T | 1 | a0001c0002t0001g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.49+1952C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21286921 | |||||||
| chr17:21287105 | C | T | 2 | a0001c0002t0006g0021 a0001c0002t0006g0118 |
4 | HG01255.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+2136C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21287105 | |||||||
| chr17:21287215 | C | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(88): Show |
135 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.49+2246C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21287215 | |||||||
| chr17:21287256 | T | G | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | HG00323.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.49+2287T>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21287256 | |||||||
| chr17:21287646 | G | T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 |
3 | HG02109.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.49+2677G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21287646 | |||||||
| chr17:21287655 | G | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0111 others(6): Show |
15 | HG00741.hp1 HG02109.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.49+2686G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21287655 | |||||||
| chr17:21287783 | C | T | 1 | a0001c0002t0001g0228 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.49+2814C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21287783 | |||||||
| chr17:21288013 | A | G | 1 | a0001c0001t0002g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.49+3044A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21288013 | |||||||
| chr17:21288523 | C | T | 1 | a0001c0002t0001g0171 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.49+3554C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21288523 | |||||||
| chr17:21288758 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.49+3789G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21288758 | |||||||
| chr17:21288761 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0002g0035 a0001c0001t0002g0170 |
3 | HG01070.hp2 HG01071.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.49+3792C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21288761 | |||||||
| chr17:21288837 | T | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.49+3868T>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21288837 | |||||||
| chr17:21288954 | C | T | 1 | a0001c0002t0001g0171 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.49+3985C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21288954 | |||||||
| chr17:21288989 | A | T | 2 | a0001c0001t0002g0034 a0001c0001t0002g0169 |
3 | HG01256.hp1 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.49+4020A>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21288989 | |||||||
| chr17:21289242 | G | A | 1 | a0001c0002t0004g0006 | 5 | HG02257.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+4273G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21289242 | |||||||
| chr17:21289283 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.49+4314C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21289283 | |||||||
| chr17:21289593 | C | T | 60 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0195 others(57): Show |
86 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.49+4624C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21289593 | |||||||
| chr17:21289863 | A | G | 1 | a0001c0001t0002g0167 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.49+4894A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21289863 | |||||||
| chr17:21289891 | T | C | 2 | a0001c0002t0001g0037 a0001c0002t0001g0180 |
3 | HG01192.hp1 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.49+4922T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21289891 | |||||||
| chr17:21289991 | G | T | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.49+5022G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21289991 | |||||||
| chr17:21290079 | G | C | 1 | a0001c0001t0001g0023 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.49+5110G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21290079 | |||||||
| chr17:21290082 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.49+5113C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21290082 | |||||||
| chr17:21290097 | A | G | 6 | a0001c0001t0011g0233 a0001c0002t0004g0006 a0001c0002t0004g0108 others(3): Show |
10 | HG02257.hp1 HG02809.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+5128A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21290097 | |||||||
| chr17:21290098 | T | C | 1 | a0001c0001t0002g0130 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.49+5129T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21290098 | |||||||
| chr17:21290120 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
129 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.49+5151C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21290120 | |||||||
| chr17:21290160 | C | T | 1 | a0001c0002t0001g0041 | 2 | HG01081.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.49+5191C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21290160 | |||||||
| chr17:21290306 | G | A | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
255 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.49+5337G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21290306 | |||||||
| chr17:21290405 | G | A | 3 | a0001c0002t0001g0171 a0001c0002t0006g0021 a0001c0002t0006g0118 |
5 | HG01255.hp2 HG02683.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+5436G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21290405 | |||||||
| chr17:21290429 | C | T | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.49+5460C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21290429 | |||||||
| chr17:21290699 | C | T | 1 | a0001c0005t0002g0166 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.49+5730C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21290699 | |||||||
| chr17:21290824 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.49+5855G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21290824 | |||||||
| chr17:21290879 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.49+5910A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21290879 | |||||||
| chr17:21290880 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.49+5911G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21290880 | |||||||
| chr17:21290933 | C | A | 1 | a0001c0001t0001g0058 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.49+5964C>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21290933 | |||||||
| chr17:21290958 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.49+5989G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21290958 | |||||||
| chr17:21291008 | C | T | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+6039C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291008 | |||||||
| chr17:21291070 | G | A | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.49+6101G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291070 | |||||||
| chr17:21291100 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.49+6131C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291100 | |||||||
| chr17:21291101 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.49+6132G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291101 | |||||||
| chr17:21291169 | G | A | 4 | a0001c0001t0002g0016 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
6 | HG02132.hp1 NA18965.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+6200G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291169 | |||||||
| chr17:21291192 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
132 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.49+6223C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291192 | |||||||
| chr17:21291219 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.49+6250G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291219 | |||||||
| chr17:21291225 | T | C | 1 | a0001c0002t0003g0181 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.49+6256T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291225 | |||||||
| chr17:21291243 | A | AAAAATAA others(4): Show |
1 | a0001c0001t0001g0168 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.49+6277_49+6287dup others(11): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291243 | ||||||
| chr17:21291262 | T | TCAATACA others(8): Show |
4 | a0001c0001t0001g0027 a0001c0003t0005g0012 a0001c0003t0005g0042 others(1): Show |
8 | HG01070.hp1 HG01099.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+6344_49+6358dup others(15): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291262 | ||||||
| chr17:21291262 | T | TCAATACA others(23): Show |
1 | a0001c0001t0001g0105 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.49+6329_49+6358dup others(30): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291262 | ||||||
| chr17:21291278 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.49+6309C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291278 | |||||||
| chr17:21291313 | C | G | 3 | a0001c0001t0002g0020 a0001c0001t0002g0225 a0001c0001t0002g0226 |
5 | HG00140.hp2 HG01123.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+6344C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291313 | |||||||
| chr17:21291318 | G | C | 3 | a0001c0001t0002g0020 a0001c0001t0002g0225 a0001c0001t0002g0226 |
5 | HG00140.hp2 HG01123.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+6349G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291318 | |||||||
| chr17:21291320 | A | G | 3 | a0001c0001t0002g0020 a0001c0001t0002g0225 a0001c0001t0002g0226 |
5 | HG00140.hp2 HG01123.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+6351A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291320 | |||||||
| chr17:21291325 | A | G | 2 | a0001c0002t0001g0180 a0001c0006t0012g0057 |
2 | HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.49+6356A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291325 | |||||||
| chr17:21291328 | G | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
137 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.49+6359G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291328 | |||||||
| chr17:21291333 | C | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
130 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.49+6364C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291333 | |||||||
| chr17:21291335 | G | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
137 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.49+6366G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291335 | |||||||
| chr17:21291336 | T | C | 3 | a0001c0001t0002g0020 a0001c0001t0002g0225 a0001c0001t0002g0226 |
5 | HG00140.hp2 HG01123.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+6367T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291336 | |||||||
| chr17:21291341 | T | C | 5 | a0001c0001t0002g0020 a0001c0001t0002g0225 a0001c0001t0002g0226 others(2): Show |
7 | HG00140.hp2 HG01123.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+6372T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291341 | |||||||
| chr17:21291341 | T | TACAACAC others(3): Show |
1 | a0001c0004t0001g0044 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.49+6376_49+6377ins others(10): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291341 | ||||||
| chr17:21291341 | T | TACAACAC others(13): Show |
3 | a0001c0001t0001g0043 a0001c0004t0001g0236 a0001c0004t0001g0237 |
4 | HG01433.hp1 HG02055.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+6376_49+6377ins others(20): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291341 | ||||||
| chr17:21291341 | T | TACAACAC others(18): Show |
1 | a0002c0007t0009g0238 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.49+6376_49+6377ins others(25): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291341 | ||||||
| chr17:21291341 | T | TACAACAC others(23): Show |
2 | a0001c0004t0001g0234 a0001c0004t0001g0235 |
2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.49+6376_49+6377ins others(30): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291341 | ||||||
| chr17:21291341 | T | TAGAATAC others(28): Show |
1 | a0001c0001t0003g0106 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.49+6373_49+6374ins others(35): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291341 | ||||||
| chr17:21291346 | T | C | 16 | a0001c0001t0001g0043 a0001c0001t0002g0020 a0001c0001t0002g0225 others(13): Show |
20 | HG00140.hp2 HG01123.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.49+6377T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291346 | |||||||
| chr17:21291346 | T | TACAAC | 1 | a0001c0002t0004g0006 | 5 | HG02257.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+6405_49+6409dup others(5): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291346 | ||||||
| chr17:21291346 | T | TACAACAC others(3): Show |
7 | a0001c0001t0011g0233 a0001c0002t0001g0054 a0001c0002t0001g0223 others(4): Show |
7 | HG02886.hp1 HG03098.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+6400_49+6409dup others(10): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291346 | ||||||
| chr17:21291346 | T | TACAACAC others(8): Show |
46 | a0001c0001t0001g0027 a0001c0001t0002g0019 a0001c0001t0002g0195 others(43): Show |
68 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.49+6395_49+6409dup others(15): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291346 | ||||||
| chr17:21291346 | T | TACAACAC others(13): Show |
19 | a0001c0001t0001g0060 a0001c0001t0003g0182 a0001c0002t0001g0009 others(16): Show |
24 | HG00642.hp1 HG00738.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.49+6390_49+6409dup others(20): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291346 | ||||||
| chr17:21291346 | T | TACAACAC others(18): Show |
2 | a0001c0002t0001g0171 a0001c0002t0006g0021 |
4 | HG01255.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+6385_49+6409dup others(25): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291346 | ||||||
| chr17:21291346 | T | TACAACAC others(23): Show |
1 | a0002c0007t0009g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49+6380_49+6409dup others(30): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291346 | ||||||
| chr17:21291346 | T | TAGAATAC others(33): Show |
6 | a0001c0001t0001g0005 a0001c0001t0001g0177 a0001c0001t0001g0178 others(3): Show |
9 | NA18950.hp2 NA18960.hp2 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+6378_49+6379ins others(40): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291346 | ||||||
| chr17:21291346 | T | TAGAATAC others(38): Show |
41 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(38): Show |
64 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.49+6378_49+6379ins others(45): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291346 | ||||||
| chr17:21291346 | T | TAGAATAC others(43): Show |
37 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(34): Show |
50 | HG00408.hp2 HG00741.hp1 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.49+6378_49+6379ins others(50): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291346 | ||||||
| chr17:21291346 | T | TAGAATAC others(48): Show |
6 | a0001c0001t0001g0062 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG01361.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+6378_49+6379ins others(55): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291346 | ||||||
| chr17:21291346 | TACAACAC others(3): Show |
T | 2 | a0001c0001t0001g0165 a0001c0001t0002g0033 |
3 | HG00558.hp1 HG02027.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.49+6400_49+6409del others(10): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291346 | ||||||
| chr17:21291360 | A | ACACAACA others(3): Show |
1 | a0001c0001t0001g0105 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.49+6400_49+6401ins others(10): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291360 | ||||||
| chr17:21291373 | C | CAACACAA others(3): Show |
1 | a0001c0002t0001g0037 | 2 | HG01192.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.49+6409_49+6410ins others(10): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21291373 | ||||||
| chr17:21291373 | C | T | 1 | a0001c0002t0001g0180 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49+6404C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291373 | |||||||
| chr17:21291378 | C | CAACACAA others(8): Show |
1 | a0001c0002t0015g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.49+6409_49+6410ins others(15): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291378 | |||||||
| chr17:21291689 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.49+6720C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291689 | |||||||
| chr17:21291748 | A | C | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-6665A>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291748 | |||||||
| chr17:21291768 | A | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
259 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.50-6645A>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291768 | |||||||
| chr17:21291780 | G | A | 1 | a0001c0001t0013g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.50-6633G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291780 | |||||||
| chr17:21291782 | G | A | 1 | a0001c0001t0013g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.50-6631G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291782 | |||||||
| chr17:21291868 | C | T | 4 | a0001c0002t0004g0006 a0001c0002t0004g0108 a0002c0007t0009g0238 others(1): Show |
8 | HG02257.hp1 HG02723.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-6545C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291868 | |||||||
| chr17:21291869 | G | A | 1 | a0001c0001t0007g0086 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.50-6544G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291869 | |||||||
| chr17:21291968 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.50-6445C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291968 | |||||||
| chr17:21291984 | C | T | 3 | a0001c0001t0001g0052 a0001c0002t0001g0190 a0001c0002t0001g0221 |
3 | HG00597.hp2 HG01243.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.50-6429C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21291984 | |||||||
| chr17:21292012 | T | A | 80 | a0001c0001t0001g0043 a0001c0001t0002g0019 a0001c0001t0002g0020 others(77): Show |
110 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.50-6401T>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292012 | |||||||
| chr17:21292077 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.50-6336C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292077 | |||||||
| chr17:21292111 | C | T | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.50-6302C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292111 | |||||||
| chr17:21292160 | T | G | 1 | a0001c0001t0001g0061 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.50-6253T>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292160 | |||||||
| chr17:21292166 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.50-6247G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292166 | |||||||
| chr17:21292213 | G | C | 5 | a0001c0001t0001g0062 a0001c0001t0001g0087 a0001c0005t0002g0166 others(2): Show |
5 | HG02723.hp2 HG03453.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-6200G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292213 | |||||||
| chr17:21292359 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
133 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.50-6054A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292359 | |||||||
| chr17:21292390 | T | A | 1 | a0001c0001t0001g0177 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.50-6023T>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292390 | |||||||
| chr17:21292513 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.50-5900C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292513 | |||||||
| chr17:21292631 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.50-5782C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292631 | |||||||
| chr17:21292679 | G | T | 1 | a0001c0002t0004g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.50-5734G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292679 | |||||||
| chr17:21292689 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0088 a0001c0001t0001g0089 |
3 | HG03688.hp2 HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.50-5724G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292689 | |||||||
| chr17:21292717 | C | T | 2 | a0001c0003t0005g0042 a0001c0003t0017g0042 |
2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.50-5696C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292717 | |||||||
| chr17:21292720 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0088 a0001c0001t0001g0089 |
3 | HG03688.hp2 HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.50-5693C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292720 | |||||||
| chr17:21292725 | A | G | 8 | a0001c0001t0001g0059 a0001c0001t0001g0088 a0001c0001t0001g0089 others(5): Show |
10 | HG01346.hp2 HG01358.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.50-5688A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292725 | |||||||
| chr17:21292766 | C | T | 6 | a0001c0001t0001g0043 a0001c0004t0001g0044 a0001c0004t0001g0234 others(3): Show |
8 | HG01433.hp1 HG02055.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-5647C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292766 | |||||||
| chr17:21292767 | G | A | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-5646G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292767 | |||||||
| chr17:21292783 | G | GGTCCCTC others(4): Show |
1 | a0001c0001t0002g0136 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.50-5627_50-5626ins others(11): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21292783 | ||||||
| chr17:21292862 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.50-5551C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292862 | |||||||
| chr17:21292913 | T | A | 1 | a0001c0001t0001g0065 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.50-5500T>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21292913 | |||||||
| chr17:21293044 | A | G | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.50-5369A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293044 | |||||||
| chr17:21293064 | C | G | 1 | a0001c0001t0001g0023 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.50-5349C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293064 | |||||||
| chr17:21293128 | C | G | 1 | a0001c0001t0002g0158 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.50-5285C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293128 | |||||||
| chr17:21293129 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0090 |
2 | HG01069.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.50-5284G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293129 | |||||||
| chr17:21293178 | T | C | 1 | a0001c0001t0002g0137 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.50-5235T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293178 | |||||||
| chr17:21293192 | C | T | 2 | a0001c0001t0002g0129 a0001c0002t0002g0176 |
2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.50-5221C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293192 | |||||||
| chr17:21293208 | T | C | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.50-5205T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293208 | |||||||
| chr17:21293236 | G | A | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.50-5177G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293236 | |||||||
| chr17:21293282 | C | T | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.50-5131C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293282 | |||||||
| chr17:21293283 | A | G | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.50-5130A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293283 | |||||||
| chr17:21293284 | G | A | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.50-5129G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293284 | |||||||
| chr17:21293296 | G | A | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.50-5117G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293296 | |||||||
| chr17:21293296 | G | C | 1 | a0001c0002t0001g0191 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.50-5117G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293296 | |||||||
| chr17:21293308 | TG | T | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-5104delG | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293308 | |||||||
| chr17:21293331 | G | A | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.50-5082G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293331 | |||||||
| chr17:21293457 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.50-4956A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293457 | |||||||
| chr17:21293482 | T | C | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.50-4931T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293482 | |||||||
| chr17:21293529 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.50-4884C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293529 | |||||||
| chr17:21293581 | C | T | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-4832C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293581 | |||||||
| chr17:21293586 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.50-4827C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293586 | |||||||
| chr17:21293608 | G | T | 1 | a0001c0001t0011g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.50-4805G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293608 | |||||||
| chr17:21293667 | C | G | 1 | a0001c0001t0002g0240 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.50-4746C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293667 | |||||||
| chr17:21293677 | C | T | 1 | a0001c0002t0001g0175 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.50-4736C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293677 | |||||||
| chr17:21293721 | C | T | 1 | a0001c0001t0013g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.50-4692C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21293721 | |||||||
| chr17:21294127 | G | A | 1 | a0001c0001t0002g0138 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.50-4286G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21294127 | |||||||
| chr17:21294211 | T | C | 1 | a0001c0002t0001g0191 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.50-4202T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21294211 | |||||||
| chr17:21294234 | T | C | 1 | a0001c0001t0002g0139 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.50-4179T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21294234 | |||||||
| chr17:21294256 | C | G | 1 | a0001c0001t0002g0157 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.50-4157C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21294256 | |||||||
| chr17:21294508 | C | G | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.50-3905C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21294508 | |||||||
| chr17:21294514 | G | A | 1 | a0001c0001t0011g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.50-3899G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21294514 | |||||||
| chr17:21294548 | G | A | 4 | a0001c0001t0002g0028 a0001c0001t0002g0123 a0001c0001t0002g0124 others(1): Show |
5 | HG01891.hp2 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-3865G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21294548 | |||||||
| chr17:21294551 | G | A | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-3862G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21294551 | |||||||
| chr17:21294609 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0090 |
2 | HG01069.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.50-3804C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21294609 | |||||||
| chr17:21294672 | T | C | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.50-3741T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21294672 | |||||||
| chr17:21294748 | G | C | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.50-3665G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21294748 | |||||||
| chr17:21294769 | C | T | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-3644C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21294769 | |||||||
| chr17:21294806 | G | T | 67 | a0001c0001t0001g0081 a0001c0001t0002g0019 a0001c0001t0002g0020 others(64): Show |
93 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.50-3607G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21294806 | |||||||
| chr17:21295010 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.50-3403C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21295010 | |||||||
| chr17:21295031 | G | T | 2 | a0001c0001t0001g0061 a0001c0002t0002g0176 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.50-3382G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21295031 | |||||||
| chr17:21295093 | T | C | 67 | a0001c0001t0001g0081 a0001c0001t0002g0019 a0001c0001t0002g0020 others(64): Show |
93 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.50-3320T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21295093 | |||||||
| chr17:21295237 | A | G | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.50-3176A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21295237 | |||||||
| chr17:21295292 | T | C | 3 | a0001c0002t0008g0230 a0001c0002t0008g0231 a0001c0002t0008g0232 |
3 | HG02809.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.50-3121T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21295292 | |||||||
| chr17:21295364 | G | A | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-3049G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21295364 | |||||||
| chr17:21295381 | G | A | 4 | a0001c0002t0001g0036 a0001c0002t0001g0192 a0001c0002t0002g0036 others(1): Show |
4 | HG02056.hp1 HG02976.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-3032G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21295381 | |||||||
| chr17:21295386 | T | C | 1 | a0001c0001t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.50-3027T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21295386 | |||||||
| chr17:21295483 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.50-2930T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21295483 | |||||||
| chr17:21295487 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.50-2926T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21295487 | |||||||
| chr17:21295660 | T | C | 92 | a0001c0001t0001g0081 a0001c0001t0002g0019 a0001c0001t0002g0020 others(89): Show |
128 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.50-2753T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21295660 | |||||||
| chr17:21295717 | C | T | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.50-2696C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21295717 | |||||||
| chr17:21295739 | T | C | 84 | a0001c0001t0001g0081 a0001c0001t0002g0019 a0001c0001t0002g0020 others(81): Show |
111 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.50-2674T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21295739 | |||||||
| chr17:21295799 | G | A | 80 | a0001c0001t0001g0081 a0001c0001t0002g0019 a0001c0001t0002g0020 others(77): Show |
107 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.50-2614G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21295799 | |||||||
| chr17:21295800 | GC | G | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-2611delC | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21295800 | ||||||
| chr17:21295932 | GCTGGGGG others(43): Show |
G | 1 | a0001c0001t0001g0091 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.50-2480_50-2431del others(50): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21295932 | |||||||
| chr17:21295963 | G | T | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.50-2450G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21295963 | |||||||
| chr17:21295965 | G | A | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.50-2448G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21295965 | |||||||
| chr17:21296297 | A | G | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.50-2116A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21296297 | |||||||
| chr17:21296342 | CAG | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0067 a0001c0001t0001g0111 |
3 | HG02622.hp1 HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.50-2067_50-2066del others(2): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21296342 | ||||||
| chr17:21296557 | C | T | 22 | a0001c0001t0002g0020 a0001c0001t0002g0225 a0001c0001t0002g0226 others(19): Show |
33 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.50-1856C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21296557 | |||||||
| chr17:21296568 | A | C | 3 | a0001c0002t0001g0036 a0001c0002t0002g0036 a0001c0002t0002g0174 |
3 | HG02258.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.50-1845A>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21296568 | |||||||
| chr17:21296732 | C | T | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.50-1681C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21296732 | |||||||
| chr17:21296756 | G | T | 1 | a0001c0002t0003g0210 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.50-1657G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21296756 | |||||||
| chr17:21296794 | G | T | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.50-1619G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21296794 | |||||||
| chr17:21296812 | A | G | 3 | a0001c0002t0001g0036 a0001c0002t0002g0036 a0001c0002t0002g0174 |
3 | HG02258.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.50-1601A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21296812 | |||||||
| chr17:21296825 | G | A | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.50-1588G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21296825 | |||||||
| chr17:21296826 | C | T | 5 | a0001c0004t0001g0044 a0001c0004t0001g0234 a0001c0004t0001g0235 others(2): Show |
6 | HG02647.hp2 HG02717.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-1587C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21296826 | |||||||
| chr17:21296900 | A | AGCT | 151 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
216 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.50-1488_50-1486dup others(3): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21296900 | ||||||
| chr17:21296900 | A | AGCTGCT | 4 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0018g0070 others(1): Show |
4 | HG01243.hp1 HG01261.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-1491_50-1486dup others(6): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21296900 | ||||||
| chr17:21297166 | C | T | 8 | a0001c0002t0001g0040 a0001c0002t0001g0215 a0001c0002t0001g0216 others(5): Show |
12 | HG00140.hp1 HG00735.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-1247C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21297166 | |||||||
| chr17:21297177 | C | T | 1 | a0001c0002t0015g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.50-1236C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21297177 | |||||||
| chr17:21297191 | G | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
258 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.50-1222G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21297191 | |||||||
| chr17:21297197 | G | A | 1 | a0001c0002t0006g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.50-1216G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21297197 | |||||||
| chr17:21297513 | C | G | 1 | a0001c0001t0002g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.50-900C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21297513 | |||||||
| chr17:21297601 | G | C | 5 | a0001c0002t0001g0171 a0001c0002t0004g0006 a0001c0002t0004g0108 others(2): Show |
11 | HG01255.hp2 HG02257.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.50-812G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21297601 | |||||||
| chr17:21297634 | G | A | 1 | a0001c0002t0001g0172 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.50-779G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21297634 | |||||||
| chr17:21297748 | G | A | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.50-665G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21297748 | |||||||
| chr17:21297773 | C | T | 1 | a0001c0002t0001g0209 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.50-640C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21297773 | |||||||
| chr17:21298004 | TA | T | 94 | a0001c0001t0001g0081 a0001c0001t0002g0019 a0001c0001t0002g0020 others(91): Show |
130 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.50-407delA | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 21298004 | ||||||
| chr17:21298077 | C | T | 1 | a0001c0002t0001g0214 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.50-336C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21298077 | |||||||
| chr17:21298130 | G | A | 83 | a0001c0001t0001g0081 a0001c0001t0002g0019 a0001c0001t0002g0020 others(80): Show |
110 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.50-283G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21298130 | |||||||
| chr17:21298274 | G | T | 3 | a0001c0002t0001g0172 a0001c0002t0001g0175 a0001c0006t0003g0173 |
3 | HG01934.hp2 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.50-139G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | chr17 | 21298274 | |||||||
| chr17:21298524 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.116+45C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 2/11 | chr17 | 21298524 | |||||||
| chr17:21298622 | T | C | 8 | a0001c0002t0001g0040 a0001c0002t0001g0171 a0001c0002t0004g0006 others(5): Show |
15 | HG01255.hp2 HG02257.hp1 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+143T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 2/11 | chr17 | 21298622 | |||||||
| chr17:21298790 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0102 |
2 | HG00544.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.117-88C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 2/11 | chr17 | 21298790 | |||||||
| chr17:21298840 | G | T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0060 a0001c0001t0001g0065 others(8): Show |
14 | HG01069.hp1 HG01261.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.117-38G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 2/11 | chr17 | 21298840 | |||||||
| chr17:21299005 | TG | T | 4 | a0001c0002t0001g0040 a0001c0002t0001g0171 a0001c0002t0006g0021 others(1): Show |
7 | HG01255.hp2 HG02683.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+85delG | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 21299005 | ||||||
| chr17:21299057 | C | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0058 others(5): Show |
11 | HG00408.hp2 HG00438.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.165+131C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21299057 | |||||||
| chr17:21299117 | A | G | 1 | a0001c0002t0001g0208 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.165+191A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21299117 | |||||||
| chr17:21299128 | C | T | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.165+202C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21299128 | |||||||
| chr17:21299144 | G | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0060 a0001c0001t0001g0065 others(1): Show |
6 | HG02970.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+218G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21299144 | |||||||
| chr17:21299396 | C | CTGCCTCA others(43): Show |
1 | a0001c0001t0001g0091 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.165+470_165+471ins others(50): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21299396 | |||||||
| chr17:21299472 | C | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
251 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.165+546C>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21299472 | |||||||
| chr17:21299542 | C | T | 2 | a0001c0002t0001g0037 a0001c0002t0001g0180 |
3 | HG01192.hp1 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.165+616C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21299542 | |||||||
| chr17:21299553 | G | A | 1 | a0001c0001t0002g0140 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.165+627G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21299553 | |||||||
| chr17:21299681 | C | CA | 15 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0078 others(12): Show |
19 | HG00438.hp1 HG00558.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.165+773dupA | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 21299681 | ||||||
| chr17:21299681 | CA | C | 15 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0099 others(12): Show |
22 | HG01168.hp1 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.165+773delA | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 21299681 | ||||||
| chr17:21299710 | C | T | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.165+784C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21299710 | |||||||
| chr17:21299754 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.166-791G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21299754 | |||||||
| chr17:21299839 | C | T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 |
3 | HG02109.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.166-706C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21299839 | |||||||
| chr17:21299889 | G | A | 1 | a0001c0001t0021g0055 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.166-656G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21299889 | |||||||
| chr17:21300011 | G | C | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.166-534G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21300011 | |||||||
| chr17:21300019 | C | T | 7 | a0001c0002t0001g0036 a0001c0002t0001g0172 a0001c0002t0001g0175 others(4): Show |
7 | HG01934.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-526C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21300019 | |||||||
| chr17:21300026 | C | G | 69 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0036 others(66): Show |
91 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.166-519C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21300026 | |||||||
| chr17:21300103 | C | T | 1 | a0001c0001t0010g0155 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.166-442C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21300103 | |||||||
| chr17:21300155 | T | TG | 3 | a0001c0002t0008g0230 a0001c0002t0008g0231 a0001c0002t0008g0232 |
3 | HG02809.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.166-389dupG | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 21300155 | ||||||
| chr17:21300254 | C | T | 5 | a0001c0004t0001g0044 a0001c0004t0001g0234 a0001c0004t0001g0235 others(2): Show |
6 | HG02647.hp2 HG02717.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-291C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21300254 | |||||||
| chr17:21300255 | A | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
241 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.166-290A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21300255 | |||||||
| chr17:21300363 | G | A | 3 | a0001c0004t0001g0234 a0001c0004t0001g0235 a0001c0004t0001g0236 |
3 | HG02647.hp2 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.166-182G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21300363 | |||||||
| chr17:21300406 | C | T | 1 | a0001c0002t0001g0206 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.166-139C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 3/11 | chr17 | 21300406 | |||||||
| chr17:21300735 | C | T | 1 | a0001c0002t0001g0172 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.279+77C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 4/11 | chr17 | 21300735 | |||||||
| chr17:21301079 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.399+86C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21301079 | |||||||
| chr17:21301121 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.399+128C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21301121 | |||||||
| chr17:21301250 | A | G | 166 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
239 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.399+257A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21301250 | |||||||
| chr17:21301256 | AC | A | 1 | a0001c0002t0004g0006 | 5 | HG02257.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.399+264delC | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21301256 | |||||||
| chr17:21301323 | C | T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 |
3 | HG02109.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.399+330C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21301323 | |||||||
| chr17:21301492 | A | G | 1 | a0002c0008t0001g0073 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.399+499A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21301492 | |||||||
| chr17:21301565 | C | A | 79 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0036 others(76): Show |
111 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(108): Show |
intron_variant | MODIFIER | c.399+572C>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21301565 | |||||||
| chr17:21301670 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
129 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.400-473G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21301670 | |||||||
| chr17:21301676 | C | G | 1 | a0001c0002t0001g0054 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.400-467C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21301676 | |||||||
| chr17:21301681 | C | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0087 a0001c0001t0001g0090 |
3 | HG01069.hp1 HG01261.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.400-462C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21301681 | |||||||
| chr17:21301745 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.400-398C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21301745 | |||||||
| chr17:21301783 | T | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
142 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.400-360T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21301783 | |||||||
| chr17:21301799 | T | C | 1 | a0001c0001t0002g0240 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.400-344T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21301799 | |||||||
| chr17:21301810 | G | A | 3 | a0001c0001t0002g0064 a0001c0001t0002g0080 a0001c0001t0011g0233 |
3 | HG01099.hp2 HG01361.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.400-333G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21301810 | |||||||
| chr17:21301848 | C | A | 6 | a0001c0002t0001g0040 a0001c0002t0001g0171 a0001c0002t0004g0006 others(3): Show |
13 | HG01255.hp2 HG02257.hp1 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.400-295C>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21301848 | |||||||
| chr17:21301888 | T | C | 45 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0038 others(42): Show |
64 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.400-255T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21301888 | |||||||
| chr17:21302040 | C | T | 8 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0002g0031 others(5): Show |
10 | HG00609.hp1 HG00609.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.400-103C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21302040 | |||||||
| chr17:21302086 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.400-57G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 5/11 | chr17 | 21302086 | |||||||
| chr17:21302294 | G | C | 69 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0036 others(66): Show |
91 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.516+35G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/11 | chr17 | 21302294 | |||||||
| chr17:21302425 | C | T | 1 | a0001c0001t0011g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.516+166C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/11 | chr17 | 21302425 | |||||||
| chr17:21302458 | C | T | 6 | a0001c0001t0001g0089 a0001c0004t0001g0044 a0001c0004t0001g0234 others(3): Show |
7 | HG02647.hp2 HG02717.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.516+199C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/11 | chr17 | 21302458 | |||||||
| chr17:21302459 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.516+200G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/11 | chr17 | 21302459 | |||||||
| chr17:21302574 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.516+315C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/11 | chr17 | 21302574 | |||||||
| chr17:21302697 | G | A | 1 | a0001c0001t0002g0151 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.516+438G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/11 | chr17 | 21302697 | |||||||
| chr17:21302713 | A | G | 1 | a0001c0001t0002g0151 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.516+454A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/11 | chr17 | 21302713 | |||||||
| chr17:21302886 | C | T | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.517-297C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/11 | chr17 | 21302886 | |||||||
| chr17:21302916 | G | A | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.517-267G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/11 | chr17 | 21302916 | |||||||
| chr17:21302956 | C | T | 4 | a0001c0001t0002g0150 a0001c0005t0001g0030 a0001c0005t0002g0030 others(1): Show |
4 | HG02735.hp1 NA18946.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-227C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/11 | chr17 | 21302956 | |||||||
| chr17:21303035 | G | A | 1 | a0001c0002t0001g0197 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.517-148G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/11 | chr17 | 21303035 | |||||||
| chr17:21303073 | C | T | 4 | a0001c0002t0001g0036 a0001c0002t0002g0036 a0001c0002t0002g0174 others(1): Show |
4 | HG02258.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-110C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/11 | chr17 | 21303073 | |||||||
| chr17:21303128 | C | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
128 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.517-55C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/11 | chr17 | 21303128 | |||||||
| chr17:21303132 | A | G | 3 | a0001c0001t0002g0170 a0001c0002t0001g0220 a0001c0002t0002g0176 |
3 | HG01256.hp2 HG01981.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.517-51A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/11 | chr17 | 21303132 | |||||||
| chr17:21303152 | G | A | 1 | a0001c0002t0001g0215 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.517-31G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 6/11 | chr17 | 21303152 | |||||||
| chr17:21303244 | C | T | 52 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0037 others(49): Show |
70 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.568+10C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 7/11 | chr17 | 21303244 | |||||||
| chr17:21303277 | A | G | 3 | a0001c0002t0001g0172 a0001c0002t0001g0175 a0001c0006t0003g0173 |
3 | HG01934.hp2 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.568+43A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 7/11 | chr17 | 21303277 | |||||||
| chr17:21303330 | G | A | 1 | a0001c0001t0002g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.568+96G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 7/11 | chr17 | 21303330 | |||||||
| chr17:21303349 | C | T | 1 | a0001c0002t0001g0213 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.568+115C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 7/11 | chr17 | 21303349 | |||||||
| chr17:21303442 | T | C | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.568+208T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 7/11 | chr17 | 21303442 | |||||||
| chr17:21303453 | G | A | 1 | a0003c0009t0001g0098 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.568+219G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 7/11 | chr17 | 21303453 | |||||||
| chr17:21303581 | C | A | 1 | a0001c0002t0002g0198 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.568+347C>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 7/11 | chr17 | 21303581 | |||||||
| chr17:21303659 | A | G | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.568+425A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 7/11 | chr17 | 21303659 | |||||||
| chr17:21303672 | C | T | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.568+438C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 7/11 | chr17 | 21303672 | |||||||
| chr17:21303848 | C | T | 1 | a0001c0002t0001g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.569-578C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 7/11 | chr17 | 21303848 | |||||||
| chr17:21303935 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.569-491C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 7/11 | chr17 | 21303935 | |||||||
| chr17:21303964 | T | C | 7 | a0001c0001t0001g0035 a0001c0001t0002g0020 a0001c0001t0002g0034 others(4): Show |
13 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.569-462T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 7/11 | chr17 | 21303964 | |||||||
| chr17:21303965 | A | G | 7 | a0001c0001t0001g0035 a0001c0001t0002g0020 a0001c0001t0002g0034 others(4): Show |
13 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.569-461A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 7/11 | chr17 | 21303965 | |||||||
| chr17:21304005 | T | C | 1 | a0002c0008t0001g0073 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.569-421T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 7/11 | chr17 | 21304005 | |||||||
| chr17:21304015 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.569-411A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 7/11 | chr17 | 21304015 | |||||||
| chr17:21304131 | C | T | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.569-295C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 7/11 | chr17 | 21304131 | |||||||
| chr17:21304597 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.696+44G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 8/11 | chr17 | 21304597 | |||||||
| chr17:21304604 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.696+51A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 8/11 | chr17 | 21304604 | |||||||
| chr17:21304625 | C | T | 3 | a0001c0002t0001g0036 a0001c0002t0002g0036 a0001c0002t0002g0174 |
3 | HG02258.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.696+72C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 8/11 | chr17 | 21304625 | |||||||
| chr17:21304626 | C | T | 1 | a0001c0002t0002g0176 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.696+73C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 8/11 | chr17 | 21304626 | |||||||
| chr17:21304627 | G | A | 1 | a0001c0001t0003g0072 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.696+74G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 8/11 | chr17 | 21304627 | |||||||
| chr17:21304633 | A | G | 1 | a0001c0002t0002g0176 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.696+80A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 8/11 | chr17 | 21304633 | |||||||
| chr17:21304670 | G | A | 4 | a0001c0001t0002g0029 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
5 | HG00642.hp2 HG02818.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.696+117G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 8/11 | chr17 | 21304670 | |||||||
| chr17:21304677 | G | A | 5 | a0001c0001t0002g0029 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
7 | HG00642.hp2 HG02055.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.696+124G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 8/11 | chr17 | 21304677 | |||||||
| chr17:21304680 | G | A | 1 | a0001c0001t0003g0025 | 2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.696+127G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 8/11 | chr17 | 21304680 | |||||||
| chr17:21304909 | G | A | 52 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0037 others(49): Show |
70 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.697-142G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 8/11 | chr17 | 21304909 | |||||||
| chr17:21304936 | C | T | 1 | a0001c0004t0001g0044 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.697-115C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 8/11 | chr17 | 21304936 | |||||||
| chr17:21305035 | C | A | 1 | a0001c0002t0001g0186 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.697-16C>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 8/11 | chr17 | 21305035 | |||||||
| chr17:21305037 | C | G | 1 | a0001c0001t0002g0164 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.697-14C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 8/11 | chr17 | 21305037 | |||||||
| chr17:21305596 | G | A | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.774+468G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21305596 | |||||||
| chr17:21305716 | G | A | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.774+588G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21305716 | |||||||
| chr17:21305731 | G | A | 1 | a0001c0001t0002g0152 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.774+603G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21305731 | |||||||
| chr17:21305771 | A | C | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.774+643A>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21305771 | |||||||
| chr17:21305834 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.774+706G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21305834 | |||||||
| chr17:21305835 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.774+707A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21305835 | |||||||
| chr17:21306034 | G | A | 1 | a0001c0001t0002g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.774+906G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21306034 | |||||||
| chr17:21306057 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.774+929C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21306057 | |||||||
| chr17:21306111 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.774+983C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21306111 | |||||||
| chr17:21306188 | C | G | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.774+1060C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21306188 | |||||||
| chr17:21306265 | G | A | 1 | a0001c0002t0001g0211 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.774+1137G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21306265 | |||||||
| chr17:21306296 | C | G | 1 | a0001c0002t0001g0215 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.774+1168C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21306296 | |||||||
| chr17:21306380 | C | T | 9 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0123 others(6): Show |
11 | HG00642.hp2 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.774+1252C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21306380 | |||||||
| chr17:21306411 | C | G | 2 | a0002c0007t0009g0238 a0002c0007t0009g0239 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.774+1283C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21306411 | |||||||
| chr17:21306462 | C | T | 1 | a0001c0002t0008g0232 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.774+1334C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21306462 | |||||||
| chr17:21306538 | A | G | 1 | a0001c0001t0002g0095 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.774+1410A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21306538 | |||||||
| chr17:21306554 | T | C | 1 | a0001c0001t0002g0095 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.774+1426T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21306554 | |||||||
| chr17:21306555 | T | C | 1 | a0001c0001t0002g0095 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.774+1427T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21306555 | |||||||
| chr17:21306637 | C | A | 1 | a0002c0007t0009g0238 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.774+1509C>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21306637 | |||||||
| chr17:21306742 | C | A | 1 | a0001c0002t0006g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.774+1614C>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21306742 | |||||||
| chr17:21306808 | G | C | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.774+1680G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21306808 | |||||||
| chr17:21306937 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.774+1809C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21306937 | |||||||
| chr17:21307037 | C | T | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.774+1909C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307037 | |||||||
| chr17:21307286 | T | G | 1 | a0001c0001t0002g0145 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.774+2158T>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307286 | |||||||
| chr17:21307356 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.774+2228C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307356 | |||||||
| chr17:21307370 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.774+2242A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307370 | |||||||
| chr17:21307371 | C | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.774+2243C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307371 | |||||||
| chr17:21307382 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.774+2254A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307382 | |||||||
| chr17:21307405 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.774+2277G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307405 | |||||||
| chr17:21307425 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.774+2297C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307425 | |||||||
| chr17:21307447 | A | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
234 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.774+2319A>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307447 | |||||||
| chr17:21307535 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.774+2407T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307535 | |||||||
| chr17:21307571 | C | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
221 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.774+2443C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307571 | |||||||
| chr17:21307576 | A | G | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.774+2448A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307576 | |||||||
| chr17:21307606 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
139 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.774+2478A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307606 | |||||||
| chr17:21307642 | T | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
229 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.774+2514T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307642 | |||||||
| chr17:21307693 | T | G | 1 | a0001c0002t0001g0214 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.774+2565T>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307693 | |||||||
| chr17:21307718 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0002g0017 |
3 | HG01993.hp1 HG02293.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.774+2590C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307718 | |||||||
| chr17:21307734 | A | G | 68 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0036 others(65): Show |
87 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.774+2606A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307734 | |||||||
| chr17:21307740 | C | T | 68 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0036 others(65): Show |
87 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.774+2612C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307740 | |||||||
| chr17:21307748 | G | A | 1 | a0001c0002t0002g0176 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.774+2620G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307748 | |||||||
| chr17:21307751 | T | C | 68 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0036 others(65): Show |
87 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.774+2623T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307751 | |||||||
| chr17:21307763 | C | T | 68 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0036 others(65): Show |
87 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.774+2635C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307763 | |||||||
| chr17:21307788 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
141 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.774+2660C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307788 | |||||||
| chr17:21307824 | C | T | 1 | a0001c0002t0001g0214 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.774+2696C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307824 | |||||||
| chr17:21307838 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.774+2710C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307838 | |||||||
| chr17:21307845 | C | CT | 93 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(90): Show |
123 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.774+2745dupT | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 21307845 | ||||||
| chr17:21307845 | C | CTT | 30 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0052 others(27): Show |
31 | HG00140.hp1 HG00597.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.774+2744_774+2745d others(4): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 21307845 | ||||||
| chr17:21307845 | CT | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0046 others(11): Show |
18 | HG01070.hp1 HG01099.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.774+2745delT | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 21307845 | ||||||
| chr17:21307845 | CTTTTTTT others(5): Show |
C | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.774+2734_774+2745d others(14): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 21307845 | ||||||
| chr17:21307900 | G | T | 1 | a0001c0001t0002g0162 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.774+2772G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307900 | |||||||
| chr17:21307949 | G | A | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.774+2821G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307949 | |||||||
| chr17:21307986 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.774+2858G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21307986 | |||||||
| chr17:21308000 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.774+2872C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21308000 | |||||||
| chr17:21308044 | C | T | 1 | a0001c0001t0002g0045 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.774+2916C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21308044 | |||||||
| chr17:21308155 | C | CT | 19 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0074 others(16): Show |
20 | HG00597.hp2 HG01433.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.774+3039dupT | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 21308155 | ||||||
| chr17:21308219 | T | G | 58 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0037 others(55): Show |
77 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.774+3091T>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21308219 | |||||||
| chr17:21308235 | C | G | 2 | a0001c0002t0001g0038 a0001c0002t0001g0189 |
3 | NA18943.hp2 NA19058.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.774+3107C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21308235 | |||||||
| chr17:21308337 | G | A | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.774+3209G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21308337 | |||||||
| chr17:21308411 | G | C | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.774+3283G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21308411 | |||||||
| chr17:21308418 | G | A | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.774+3290G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21308418 | |||||||
| chr17:21308439 | C | G | 3 | a0001c0002t0001g0172 a0001c0002t0001g0175 a0001c0006t0003g0173 |
3 | HG01934.hp2 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.774+3311C>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21308439 | |||||||
| chr17:21308439 | C | T | 1 | a0001c0002t0020g0194 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.774+3311C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21308439 | |||||||
| chr17:21308511 | G | A | 2 | a0001c0002t0001g0183 a0001c0002t0001g0184 |
2 | HG02027.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.774+3383G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21308511 | |||||||
| chr17:21308528 | G | T | 3 | a0001c0002t0008g0230 a0001c0002t0008g0231 a0001c0002t0008g0232 |
3 | HG02809.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.774+3400G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21308528 | |||||||
| chr17:21308608 | A | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
9 | HG00621.hp1 NA18947.hp1 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.774+3480A>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21308608 | |||||||
| chr17:21308608 | AT | A | 8 | a0001c0001t0002g0033 a0001c0001t0002g0141 a0001c0001t0002g0142 others(5): Show |
10 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.774+3492delT | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 21308608 | ||||||
| chr17:21308838 | G | C | 1 | a0001c0002t0001g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.775-3304G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21308838 | |||||||
| chr17:21308860 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.775-3282A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21308860 | |||||||
| chr17:21309291 | C | T | 1 | a0001c0002t0015g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.775-2851C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21309291 | |||||||
| chr17:21309409 | T | C | 71 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0036 others(68): Show |
93 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.775-2733T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21309409 | |||||||
| chr17:21309508 | G | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(54): Show |
87 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.775-2634G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21309508 | |||||||
| chr17:21309598 | A | T | 1 | a0001c0001t0018g0070 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.775-2544A>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21309598 | |||||||
| chr17:21309668 | C | T | 2 | a0001c0001t0002g0127 a0001c0001t0002g0128 |
2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.775-2474C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21309668 | |||||||
| chr17:21309676 | C | T | 2 | a0001c0002t0001g0175 a0001c0006t0003g0173 |
2 | HG01934.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.775-2466C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21309676 | |||||||
| chr17:21309712 | C | T | 67 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0036 others(64): Show |
86 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.775-2430C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21309712 | |||||||
| chr17:21309738 | C | T | 67 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0036 others(64): Show |
86 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.775-2404C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21309738 | |||||||
| chr17:21309763 | G | A | 3 | a0001c0002t0001g0040 a0001c0002t0001g0171 a0001c0002t0006g0021 |
6 | HG01255.hp2 HG02683.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-2379G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21309763 | |||||||
| chr17:21309905 | C | T | 4 | a0001c0002t0001g0036 a0001c0002t0001g0213 a0001c0002t0002g0036 others(1): Show |
4 | HG02258.hp2 HG02602.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-2237C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21309905 | |||||||
| chr17:21309910 | T | G | 1 | a0001c0002t0019g0199 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.775-2232T>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21309910 | |||||||
| chr17:21309933 | A | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
9 | HG00621.hp1 NA18947.hp1 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.775-2209A>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21309933 | |||||||
| chr17:21309940 | A | T | 6 | a0001c0002t0001g0040 a0001c0002t0001g0171 a0001c0002t0004g0006 others(3): Show |
13 | HG01255.hp2 HG02257.hp1 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.775-2202A>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21309940 | |||||||
| chr17:21309941 | T | A | 1 | a0001c0001t0002g0140 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.775-2201T>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21309941 | |||||||
| chr17:21309945 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.775-2197G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21309945 | |||||||
| chr17:21310009 | G | T | 3 | a0001c0002t0008g0230 a0001c0002t0008g0231 a0001c0002t0008g0232 |
3 | HG02809.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.775-2133G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21310009 | |||||||
| chr17:21310268 | C | A | 1 | a0001c0002t0001g0211 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.775-1874C>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21310268 | |||||||
| chr17:21310277 | T | G | 1 | a0001c0002t0001g0202 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.775-1865T>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21310277 | |||||||
| chr17:21310284 | T | C | 1 | a0001c0001t0001g0043 | 2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.775-1858T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21310284 | |||||||
| chr17:21310308 | C | T | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-1834C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21310308 | |||||||
| chr17:21310317 | T | C | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-1825T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21310317 | |||||||
| chr17:21310470 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.775-1672A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21310470 | |||||||
| chr17:21310489 | G | T | 4 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 others(1): Show |
7 | HG02615.hp1 HG02818.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.775-1653G>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21310489 | |||||||
| chr17:21310641 | C | T | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.775-1501C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21310641 | |||||||
| chr17:21310710 | G | A | 52 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0037 others(49): Show |
70 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.775-1432G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21310710 | |||||||
| chr17:21310715 | C | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0024 others(12): Show |
23 | HG00741.hp1 HG01433.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.775-1427C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21310715 | |||||||
| chr17:21310936 | C | T | 3 | a0001c0003t0005g0012 a0001c0003t0005g0042 a0001c0003t0017g0042 |
6 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-1206C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21310936 | |||||||
| chr17:21310941 | G | A | 58 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0037 others(55): Show |
77 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.775-1201G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21310941 | |||||||
| chr17:21310958 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.775-1184C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21310958 | |||||||
| chr17:21311063 | A | G | 1 | a0001c0001t0002g0134 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.775-1079A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311063 | |||||||
| chr17:21311120 | T | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
128 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.775-1022T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311120 | |||||||
| chr17:21311167 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0096 |
2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.775-975C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311167 | |||||||
| chr17:21311180 | C | A | 1 | a0001c0002t0001g0214 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.775-962C>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311180 | |||||||
| chr17:21311234 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.775-908C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311234 | |||||||
| chr17:21311243 | G | C | 1 | a0001c0004t0001g0234 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.775-899G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311243 | |||||||
| chr17:21311253 | G | A | 1 | a0001c0001t0003g0092 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.775-889G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311253 | |||||||
| chr17:21311255 | T | A | 1 | a0001c0002t0008g0230 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.775-887T>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311255 | |||||||
| chr17:21311304 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.775-838A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311304 | |||||||
| chr17:21311561 | C | T | 1 | a0001c0004t0001g0235 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.775-581C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311561 | |||||||
| chr17:21311562 | G | A | 3 | a0001c0002t0001g0172 a0001c0002t0001g0175 a0001c0006t0003g0173 |
3 | HG01934.hp2 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.775-580G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311562 | |||||||
| chr17:21311594 | G | A | 68 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0036 others(65): Show |
87 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.775-548G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311594 | |||||||
| chr17:21311607 | G | GCT | 8 | a0001c0002t0001g0209 a0001c0002t0003g0193 a0001c0002t0008g0231 others(5): Show |
9 | HG02056.hp1 HG02647.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.775-534_775-533dup others(2): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 21311607 | ||||||
| chr17:21311608 | C | CTCTG | 5 | a0001c0002t0001g0040 a0001c0002t0006g0021 a0001c0002t0008g0230 others(2): Show |
8 | HG01255.hp2 HG02683.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.775-533_775-532ins others(4): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 21311608 | ||||||
| chr17:21311608 | C | CTG | 20 | a0001c0001t0001g0153 a0001c0001t0001g0168 a0001c0001t0002g0008 others(17): Show |
28 | HG00438.hp1 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.775-490_775-489dup others(2): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 21311608 | ||||||
| chr17:21311608 | C | CTGTG | 5 | a0001c0001t0001g0161 a0001c0001t0002g0122 a0001c0001t0002g0124 others(2): Show |
5 | HG00323.hp2 HG01943.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-492_775-489dup others(4): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 21311608 | ||||||
| chr17:21311608 | C | CTGTGTGT others(3): Show |
1 | a0001c0001t0002g0160 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.775-498_775-489dup others(10): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 21311608 | ||||||
| chr17:21311608 | CTG | C | 41 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0127 others(38): Show |
55 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.775-490_775-489del others(2): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 21311608 | ||||||
| chr17:21311608 | CTGTG | C | 11 | a0001c0001t0001g0154 a0001c0001t0002g0019 a0001c0001t0002g0034 others(8): Show |
14 | HG01256.hp1 HG01358.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.775-492_775-489del others(4): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 21311608 | ||||||
| chr17:21311608 | CTGTGTG | C | 7 | a0001c0002t0001g0009 a0001c0002t0001g0038 a0001c0002t0001g0119 others(4): Show |
12 | HG00642.hp1 HG00738.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.775-494_775-489del others(6): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 21311608 | ||||||
| chr17:21311608 | CTGTGTGT others(1): Show |
C | 9 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0049 others(6): Show |
9 | HG00741.hp2 HG01943.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.775-496_775-489del others(8): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 21311608 | ||||||
| chr17:21311608 | CTGTGTGT others(3): Show |
C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(65): Show |
106 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.775-498_775-489del others(10): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 21311608 | ||||||
| chr17:21311608 | CTGTGTGT others(5): Show |
C | 16 | a0001c0001t0001g0015 a0001c0001t0001g0060 a0001c0001t0001g0065 others(13): Show |
22 | HG01069.hp1 HG01261.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.775-500_775-489del others(12): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 21311608 | ||||||
| chr17:21311610 | G | C | 14 | a0001c0002t0001g0184 a0001c0002t0001g0191 a0001c0002t0001g0192 others(11): Show |
18 | HG00140.hp1 HG01256.hp2 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.775-532G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311610 | |||||||
| chr17:21311612 | G | C | 34 | a0001c0002t0001g0003 a0001c0002t0001g0036 a0001c0002t0001g0037 others(31): Show |
47 | HG00408.hp1 HG00621.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.775-530G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311612 | |||||||
| chr17:21311614 | G | C | 5 | a0001c0002t0001g0172 a0001c0002t0001g0188 a0001c0002t0001g0197 others(2): Show |
5 | HG02004.hp2 HG02615.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-528G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311614 | |||||||
| chr17:21311616 | G | C | 7 | a0001c0002t0001g0009 a0001c0002t0001g0038 a0001c0002t0001g0119 others(4): Show |
12 | HG00642.hp1 HG00738.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.775-526G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311616 | |||||||
| chr17:21311618 | G | C | 8 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | HG00741.hp2 HG01943.hp2 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.775-524G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311618 | |||||||
| chr17:21311620 | G | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(63): Show |
104 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.775-522G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311620 | |||||||
| chr17:21311622 | G | C | 13 | a0001c0001t0001g0015 a0001c0001t0001g0060 a0001c0001t0001g0065 others(10): Show |
16 | HG01069.hp1 HG01261.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.775-520G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311622 | |||||||
| chr17:21311652 | G | C | 1 | a0002c0008t0001g0073 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.775-490G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311652 | |||||||
| chr17:21311883 | T | A | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.775-259T>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311883 | |||||||
| chr17:21311884 | A | G | 1 | a0001c0006t0012g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.775-258A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311884 | |||||||
| chr17:21311892 | C | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
228 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.775-250C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311892 | |||||||
| chr17:21311984 | C | T | 3 | a0001c0002t0008g0230 a0001c0002t0008g0231 a0001c0002t0008g0232 |
3 | HG02809.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.775-158C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21311984 | |||||||
| chr17:21312076 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.775-66C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 9/11 | chr17 | 21312076 | |||||||
| chr17:21312427 | G | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0067 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.914+146G>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 10/11 | chr17 | 21312427 | |||||||
| chr17:21312646 | G | A | 2 | a0001c0006t0003g0173 a0001c0006t0012g0057 |
2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.914+365G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 10/11 | chr17 | 21312646 | |||||||
| chr17:21312743 | C | T | 2 | a0001c0002t0004g0006 a0001c0002t0004g0108 |
6 | HG02257.hp1 HG03041.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.914+462C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 10/11 | chr17 | 21312743 | |||||||
| chr17:21312776 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.914+495G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 10/11 | chr17 | 21312776 | |||||||
| chr17:21312783 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.914+502C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 10/11 | chr17 | 21312783 | |||||||
| chr17:21312847 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
129 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.914+566G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 10/11 | chr17 | 21312847 | |||||||
| chr17:21312918 | C | CA | 19 | a0001c0001t0001g0068 a0001c0001t0001g0101 a0001c0001t0002g0053 others(16): Show |
27 | HG00438.hp2 HG01243.hp1 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.915-559dupA | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 21312918 | ||||||
| chr17:21312918 | C | CAA | 15 | a0001c0002t0001g0037 a0001c0002t0001g0039 a0001c0002t0001g0119 others(12): Show |
17 | HG01192.hp1 HG01192.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.915-560_915-559dup others(2): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 21312918 | ||||||
| chr17:21312918 | C | CAAA | 36 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0038 others(33): Show |
52 | HG00140.hp1 HG00408.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.915-561_915-559dup others(3): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 21312918 | ||||||
| chr17:21312982 | A | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.915-510A>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 10/11 | chr17 | 21312982 | |||||||
| chr17:21313031 | G | A | 1 | a0001c0003t0005g0012 | 4 | HG02818.hp1 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.915-461G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 10/11 | chr17 | 21313031 | |||||||
| chr17:21313290 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
128 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.915-202G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 10/11 | chr17 | 21313290 | |||||||
| chr17:21313397 | C | T | 1 | a0001c0002t0001g0175 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.915-95C>T | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 10/11 | chr17 | 21313397 | |||||||
| chr17:21313550 | G | A | 1 | a0001c0002t0015g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.960+13G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 11/11 | chr17 | 21313550 | |||||||
| chr17:21313652 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.960+115T>C | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 11/11 | chr17 | 21313652 | |||||||
| chr17:21313798 | G | GAAGGCTT others(12): Show |
1 | a0001c0002t0001g0201 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.960+263_960+281dup others(19): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 21313798 | ||||||
| chr17:21314085 | A | G | 1 | a0001c0002t0001g0054 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.961-62A>G | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 11/11 | chr17 | 21314085 | |||||||
| chr17:21314088 | G | A | 1 | a0001c0002t0001g0054 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.961-59G>A | MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 11/11 | chr17 | 21314088 |