Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5608 |
| ensemblid | ENSG00000108984.16 |
| hgncid | 6846 |
| symbol | MAP2K6 |
| name | mitogen-activated protein kinase kinase 6 |
| refseq_nuc | NM_002758.4 |
| refseq_prot | NP_002749.2 |
| ensembl_nuc | ENST00000590474.7 |
| ensembl_prot | ENSP00000468348.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 69414697 |
| end | 69553865 |
| strand | + |
| ver | v1.2 |
| region | chr17:69414697-69553865 |
| region5000 | chr17:69409697-69558865 |
| regionname0 | MAP2K6_chr17_69414697_69553865 |
| regionname5000 | MAP2K6_chr17_69409697_69558865 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1002 | 159 | 51 | 27 | 57 | 8 | 14 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | ATGTC others(997): Show |
chr17 | 69409697 | 69558865 | ||
| a0001c0002 | 0/0 | 1002 | 101 | 27 | 17 | 35 | 4 | 18 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | ATGTC others(997): Show |
chr17 | 69409697 | 69558865 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 13404 | 44 | 5 | 8 | 26 | 1 | 4 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13399): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0002 | 0/0 | 13405 | 14 | 5 | 3 | 2 | 1 | 3 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0003 | 0/0 | 13400 | 10 | 1 | 1 | 8 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13395): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0004 | 0/0 | 13406 | 6 | 1 | 1 | 4 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13401): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0005 | 1/0 | 13405 | 7 | 2 | 3 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0006 | 0/0 | 13401 | 7 | 4 | 3 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13396): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0007 | 0/0 | 13405 | 8 | 1 | 0 | 6 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0008 | 0/0 | 13400 | 5 | 3 | 2 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13395): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0009 | 0/0 | 13405 | 2 | 1 | 0 | 0 | 1 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0010 | 0/0 | 13400 | 4 | 3 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13395): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0011 | 0/0 | 13405 | 3 | 0 | 1 | 0 | 2 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0012 | 0/0 | 13405 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0013 | 0/0 | 13400 | 2 | 1 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13395): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0014 | 0/0 | 13401 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13396): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0015 | 0/0 | 13400 | 3 | 0 | 0 | 3 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13395): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0016 | 0/0 | 13406 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13401): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0017 | 0/0 | 13405 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0018 | 0/0 | 13404 | 2 | 1 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13399): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0020 | 0/0 | 13405 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0021 | 0/0 | 13404 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13399): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0022 | 0/0 | 13404 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13399): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0023 | 0/0 | 13403 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13398): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0024 | 0/0 | 13402 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13397): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0025 | 0/0 | 13400 | 2 | 1 | 0 | 0 | 1 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13395): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0026 | 0/0 | 13400 | 2 | 0 | 0 | 0 | 2 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13395): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0027 | 0/0 | 13400 | 2 | 0 | 2 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13395): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0028 | 0/0 | 13399 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13394): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0030 | 0/0 | 13406 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13401): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0031 | 0/0 | 13405 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0034 | 0/0 | 13406 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13401): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0035 | 0/0 | 13405 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0036 | 0/0 | 13405 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0037 | 0/1 | 13405 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0038 | 0/0 | 13405 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0039 | 0/0 | 13405 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0040 | 0/0 | 13405 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0042 | 0/0 | 13404 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13399): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0043 | 0/0 | 13404 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13399): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0047 | 0/0 | 13404 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13399): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0048 | 0/0 | 13404 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13399): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0051 | 0/0 | 13403 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13398): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0054 | 0/0 | 13400 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13395): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0055 | 0/0 | 13404 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13399): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0056 | 0/0 | 13402 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13397): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0058 | 0/0 | 13401 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13396): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0059 | 0/0 | 13400 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13395): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0060 | 0/0 | 13400 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13395): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0061 | 0/0 | 13399 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13394): Show |
chr17 | 69409697 | 69558865 |
| a0001c0001t0065 | 0/0 | 13400 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13395): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0001 | 0/0 | 13404 | 27 | 1 | 8 | 11 | 1 | 6 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13399): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0002 | 0/0 | 13405 | 10 | 3 | 1 | 0 | 2 | 4 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0003 | 0/0 | 13400 | 14 | 1 | 0 | 12 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13395): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0004 | 0/0 | 13406 | 9 | 5 | 1 | 3 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13401): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0005 | 0/0 | 13405 | 5 | 2 | 0 | 1 | 0 | 2 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0006 | 0/0 | 13401 | 4 | 3 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13396): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0007 | 0/0 | 13405 | 2 | 1 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0008 | 0/0 | 13400 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13395): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0009 | 0/0 | 13405 | 2 | 0 | 2 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0012 | 0/0 | 13405 | 2 | 0 | 0 | 0 | 0 | 2 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0013 | 0/0 | 13400 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13395): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0014 | 0/0 | 13401 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13396): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0017 | 0/0 | 13405 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0019 | 0/0 | 13403 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13398): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0021 | 0/0 | 13404 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13399): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0023 | 0/0 | 13403 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13398): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0024 | 0/0 | 13402 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13397): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0029 | 0/0 | 13405 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0032 | 0/0 | 13405 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0033 | 0/0 | 13406 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13401): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0041 | 0/0 | 13405 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0044 | 0/0 | 13404 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13399): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0045 | 0/0 | 13404 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13399): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0046 | 0/0 | 13404 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13399): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0049 | 0/0 | 13404 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13399): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0050 | 0/0 | 13404 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13399): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0052 | 0/0 | 13404 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13399): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0053 | 0/0 | 13405 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13400): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0057 | 0/0 | 13400 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13395): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0062 | 0/0 | 13399 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13394): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0063 | 0/0 | 13400 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13395): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0064 | 0/0 | 13401 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13396): Show |
chr17 | 69409697 | 69558865 |
| a0001c0002t0066 | 0/0 | 13399 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | AGTTC others(13394): Show |
chr17 | 69409697 | 69558865 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0005g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0005g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0006g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0006g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0006g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0007g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0007g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0007g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0007g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0008g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0008g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0009g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0010g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0010g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0010g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0011g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0011g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0011g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0012g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0013g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0013g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0014g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0015g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0015g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0015g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0016g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0016g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0017g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0018g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0018g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0020g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0020g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0021g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0022g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0022g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0023g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0024g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0025g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0025g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0026g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0026g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0027g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0027g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0028g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0028g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0030g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0031g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0034g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0035g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0036g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0037g0083 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0038g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0039g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0040g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0042g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0043g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0047g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0048g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0051g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0054g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0055g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0056g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0058g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0059g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0060g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0061g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0001t0065g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0005g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0005g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0006g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0007g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0009g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0009g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0012g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0012g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0013g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0014g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0014g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0017g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0019g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0019g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0021g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0023g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0024g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0029g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0032g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0033g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0041g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0044g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0045g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0046g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0049g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0050g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0052g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0053g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0057g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0062g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0063g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0064g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| a0001c0002t0066g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0194 | EUR | GBR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00099 | hp2 | a0001 | c0001 | t0025 | g0055 | EUR | GBR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | GBR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00140 | hp2 | a0001 | c0001 | t0011 | g0019 | EUR | GBR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00323 | hp1 | a0001 | c0001 | t0009 | g0056 | EUR | FIN | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0141 | EUR | FIN | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00408 | hp1 | a0001 | c0002 | t0003 | g0154 | EAS | CHS | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | CHS | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | CHS | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0205 | EAS | CHS | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00558 | hp2 | a0001 | c0002 | t0004 | g0188 | EAS | CHS | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0237 | EAS | CHS | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00609 | hp2 | a0001 | c0002 | t0003 | g0142 | EAS | CHS | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | CHS | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00639 | hp1 | a0001 | c0002 | t0004 | g0053 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00639 | hp2 | a0001 | c0002 | t0009 | g0121 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00733 | hp1 | a0001 | c0001 | t0008 | g0103 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0086 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0130 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0110 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0195 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01074 | hp2 | a0001 | c0002 | t0009 | g0120 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01099 | hp1 | a0001 | c0001 | t0008 | g0075 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0182 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01106 | hp1 | a0001 | c0001 | t0011 | g0013 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0129 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01109 | hp1 | a0001 | c0001 | t0010 | g0095 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01109 | hp2 | a0001 | c0002 | t0050 | g0087 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01168 | hp2 | a0001 | c0001 | t0027 | g0021 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01169 | hp2 | a0001 | c0001 | t0027 | g0020 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01192 | hp1 | a0001 | c0001 | t0059 | g0218 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01243 | hp1 | a0001 | c0002 | t0023 | g0088 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0050 | AMR | PUR | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0206 | AMR | CLM | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0036 | AMR | CLM | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0207 | AMR | CLM | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01346 | hp2 | a0001 | c0002 | t0006 | g0045 | AMR | CLM | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01516 | hp1 | a0001 | c0001 | t0026 | g0191 | EUR | IBS | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0035 | EUR | IBS | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01517 | hp1 | a0001 | c0002 | t0013 | g0085 | EUR | IBS | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01517 | hp2 | a0001 | c0001 | t0026 | g0192 | EUR | IBS | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01884 | hp1 | a0001 | c0001 | t0020 | g0071 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01884 | hp2 | a0001 | c0001 | t0058 | g0067 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01891 | hp1 | a0001 | c0001 | t0039 | g0012 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | PEL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0163 | AMR | PEL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01975 | hp2 | a0001 | c0001 | t0017 | g0140 | AMR | PEL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02015 | hp1 | a0001 | c0002 | t0005 | g0240 | EAS | KHV | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02015 | hp2 | a0001 | c0001 | t0038 | g0040 | EAS | KHV | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | KHV | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0166 | EAS | KHV | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | KHV | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02071 | hp2 | a0001 | c0001 | t0013 | g0091 | EAS | KHV | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02135 | hp1 | a0001 | c0002 | t0049 | g0230 | EAS | KHV | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02145 | hp1 | a0001 | c0001 | t0013 | g0137 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02145 | hp2 | a0001 | c0002 | t0006 | g0100 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02155 | hp1 | a0001 | c0002 | t0004 | g0174 | EAS | CDX | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0093 | EAS | CDX | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0080 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02257 | hp2 | a0001 | c0001 | t0055 | g0169 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02258 | hp1 | a0001 | c0001 | t0010 | g0200 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02258 | hp2 | a0001 | c0001 | t0028 | g0096 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02273 | hp2 | a0001 | c0002 | t0017 | g0232 | AMR | PEL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02280 | hp1 | a0001 | c0002 | t0063 | g0078 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0057 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | PEL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02523 | hp1 | a0001 | c0002 | t0019 | g0215 | EAS | KHV | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02523 | hp2 | a0001 | c0002 | t0019 | g0167 | EAS | KHV | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02572 | hp1 | a0001 | c0001 | t0025 | g0094 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02572 | hp2 | a0001 | c0001 | t0020 | g0128 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02602 | hp1 | a0001 | c0002 | t0005 | g0164 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0173 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02615 | hp2 | a0001 | c0002 | t0006 | g0051 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02622 | hp1 | a0001 | c0002 | t0057 | g0214 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02622 | hp2 | a0001 | c0002 | t0005 | g0030 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02630 | hp1 | a0001 | c0001 | t0034 | g0027 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02630 | hp2 | a0001 | c0001 | t0030 | g0046 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0114 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02647 | hp2 | a0001 | c0002 | t0064 | g0199 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02698 | hp1 | a0001 | c0002 | t0021 | g0196 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02698 | hp2 | a0001 | c0001 | t0007 | g0028 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0133 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0061 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0259 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0116 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0241 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0066 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02809 | hp2 | a0001 | c0001 | t0016 | g0074 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0033 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0104 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02896 | hp1 | a0001 | c0002 | t0014 | g0131 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0203 | AFR | ESN | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02922 | hp2 | a0001 | c0001 | t0024 | g0097 | AFR | ESN | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02965 | hp1 | a0001 | c0001 | t0061 | g0073 | AFR | ESN | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02965 | hp2 | a0001 | c0002 | t0004 | g0014 | AFR | ESN | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02970 | hp1 | a0001 | c0001 | t0022 | g0101 | AFR | ESN | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0017 | AFR | ESN | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02976 | hp1 | a0001 | c0001 | t0056 | g0059 | AFR | ESN | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02976 | hp2 | a0001 | c0002 | t0024 | g0105 | AFR | ESN | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03017 | hp1 | a0001 | c0002 | t0005 | g0175 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03041 | hp2 | a0001 | c0001 | t0022 | g0102 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03098 | hp1 | a0001 | c0001 | t0040 | g0009 | AFR | MSL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | MSL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0016 | AFR | ESN | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | ESN | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03195 | hp1 | a0001 | c0002 | t0003 | g0070 | AFR | ESN | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0026 | AFR | ESN | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | MSL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0038 | AFR | MSL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03453 | hp1 | a0001 | c0002 | t0062 | g0060 | AFR | MSL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03453 | hp2 | a0001 | c0002 | t0007 | g0202 | AFR | MSL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03486 | hp2 | a0001 | c0001 | t0054 | g0150 | AFR | MSL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0176 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03491 | hp1 | a0001 | c0002 | t0012 | g0208 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03491 | hp2 | a0001 | c0001 | t0021 | g0025 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03492 | hp1 | a0001 | c0002 | t0012 | g0024 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0077 | AFR | ESN | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0049 | AFR | ESN | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03540 | hp1 | a0001 | c0001 | t0065 | g0149 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03540 | hp2 | a0001 | c0001 | t0018 | g0132 | AFR | GWD | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03688 | hp1 | a0001 | c0001 | t0035 | g0217 | SAS | STU | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03688 | hp2 | a0001 | c0002 | t0041 | g0125 | SAS | STU | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03704 | hp1 | a0001 | c0002 | t0007 | g0037 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03704 | hp2 | a0001 | c0001 | t0042 | g0090 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0018 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03710 | hp2 | a0001 | c0001 | t0051 | g0172 | SAS | PJL | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0209 | SAS | STU | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0113 | SAS | STU | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG04184 | hp1 | a0001 | c0001 | t0023 | g0064 | SAS | BEB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG04184 | hp2 | a0001 | c0001 | t0018 | g0216 | SAS | BEB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0223 | SAS | STU | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | CHB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | CHB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0052 | AFR | YRI | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18906 | hp2 | a0001 | c0002 | t0014 | g0062 | AFR | YRI | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18941 | hp1 | a0001 | c0002 | t0053 | g0146 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18956 | hp1 | a0001 | c0002 | t0003 | g0239 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18964 | hp1 | a0001 | c0001 | t0015 | g0219 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18970 | hp1 | a0001 | c0001 | t0031 | g0252 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18970 | hp2 | a0001 | c0001 | t0007 | g0111 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18971 | hp1 | a0001 | c0002 | t0044 | g0003 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18975 | hp1 | a0001 | c0002 | t0003 | g0189 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18975 | hp2 | a0001 | c0001 | t0060 | g0224 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18977 | hp1 | a0001 | c0002 | t0046 | g0242 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18978 | hp1 | a0001 | c0002 | t0003 | g0124 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18981 | hp2 | a0001 | c0001 | t0007 | g0157 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18983 | hp2 | a0001 | c0002 | t0045 | g0152 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18997 | hp1 | a0001 | c0001 | t0015 | g0118 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18997 | hp2 | a0001 | c0002 | t0003 | g0248 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0139 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19010 | hp1 | a0001 | c0001 | t0047 | g0177 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0213 | AFR | LWK | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19030 | hp2 | a0001 | c0001 | t0043 | g0117 | AFR | LWK | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19043 | hp1 | a0001 | c0001 | t0014 | g0002 | AFR | LWK | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19043 | hp2 | a0001 | c0002 | t0005 | g0015 | AFR | LWK | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19054 | hp1 | a0001 | c0001 | t0007 | g0155 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19054 | hp2 | a0001 | c0002 | t0003 | g0250 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19062 | hp1 | a0001 | c0001 | t0007 | g0044 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19062 | hp2 | a0001 | c0002 | t0003 | g0123 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19068 | hp2 | a0001 | c0001 | t0015 | g0136 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19081 | hp2 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19082 | hp1 | a0001 | c0001 | t0048 | g0231 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19083 | hp1 | a0001 | c0002 | t0029 | g0227 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19084 | hp1 | a0001 | c0002 | t0003 | g0249 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19084 | hp2 | a0001 | c0002 | t0004 | g0198 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19085 | hp1 | a0001 | c0001 | t0012 | g0143 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19086 | hp1 | a0001 | c0001 | t0007 | g0256 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA20129 | hp1 | a0001 | c0002 | t0033 | g0109 | AFR | ASW | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ASW | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA20805 | hp1 | a0001 | c0001 | t0011 | g0107 | EUR | TSI | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0260 | EUR | TSI | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA20905 | hp1 | a0001 | c0002 | t0003 | g0233 | SAS | GIH | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | GIH | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01123 | hp1 | a0001 | c0002 | t0032 | g0054 | AMR | CLM | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0108 | AMR | CLM | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02109 | hp2 | a0001 | c0002 | t0008 | g0081 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02486 | hp1 | a0001 | c0002 | t0066 | g0225 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02559 | hp1 | a0001 | c0001 | t0028 | g0072 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG02559 | hp2 | a0001 | c0002 | t0006 | g0076 | AFR | ACB | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG06807 | hp1 | a0001 | c0002 | t0052 | g0115 | AFR | USA | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0099 | AFR | USA | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18955 | hp1 | a0001 | c0001 | t0007 | g0246 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | USA | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| NA20300 | hp2 | a0001 | c0001 | t0036 | g0126 | AFR | USA | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0037 | g0083 | REF | REF | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0153 | REF | REF | MAP2K6_chr17_69409697_69558865 | MAP2K6 | chr17 | 69409697 | 69558865 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:69516862 | C | A | 1 | a0001c0002 | 101 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(98): Show |
synonymous_variant | LOW | c.91C>A | p.Arg31Arg | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 3/12 | 379/13405 | 91/1005 | 31/334 | chr17 | 69516862 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:69542199 | CA | C | 30 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(27): Show |
73 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*456delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 456 | INFO_REALIGN_3_PRIME | chr17 | 69542199 | |||||
| chr17:69542399 | T | C | 1 | a0001c0001t0054 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*646T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 646 | chr17 | 69542399 | ||||||
| chr17:69542418 | T | C | 1 | a0001c0002t0029 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*665T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 665 | chr17 | 69542418 | ||||||
| chr17:69542492 | C | G | 1 | a0001c0001t0015 | 3 | NA18964.hp1 NA18997.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*739C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 739 | chr17 | 69542492 | ||||||
| chr17:69542829 | C | G | 29 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(26): Show |
72 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1076C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 1076 | chr17 | 69542829 | ||||||
| chr17:69542835 | T | G | 3 | a0001c0001t0024 a0001c0001t0056 a0001c0002t0024 |
3 | HG02922.hp2 HG02976.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1082T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 1082 | chr17 | 69542835 | ||||||
| chr17:69543052 | C | T | 1 | a0001c0002t0066 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1299C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 1299 | chr17 | 69543052 | ||||||
| chr17:69543087 | G | C | 29 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(26): Show |
72 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1334G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 1334 | chr17 | 69543087 | ||||||
| chr17:69543122 | T | G | 1 | a0001c0002t0066 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1369T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 1369 | chr17 | 69543122 | ||||||
| chr17:69543310 | C | T | 8 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0014 others(5): Show |
22 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1557C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 1557 | chr17 | 69543310 | ||||||
| chr17:69543321 | C | T | 1 | a0001c0002t0063 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1568C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 1568 | chr17 | 69543321 | ||||||
| chr17:69543430 | C | T | 30 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(27): Show |
76 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1677C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 1677 | chr17 | 69543430 | ||||||
| chr17:69543565 | C | T | 4 | a0001c0001t0006 a0001c0001t0014 a0001c0002t0006 others(1): Show |
14 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1812C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 1812 | chr17 | 69543565 | ||||||
| chr17:69543710 | G | T | 2 | a0001c0001t0013 a0001c0002t0013 |
3 | HG01517.hp1 HG02071.hp2 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1957G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 1957 | chr17 | 69543710 | ||||||
| chr17:69543776 | T | C | 1 | a0001c0001t0030 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2023T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 2023 | chr17 | 69543776 | ||||||
| chr17:69544000 | A | G | 4 | a0001c0001t0010 a0001c0001t0028 a0001c0002t0062 others(1): Show |
8 | HG01109.hp1 HG02258.hp1 HG02258.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2247A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 2247 | chr17 | 69544000 | ||||||
| chr17:69544122 | G | A | 1 | a0001c0001t0031 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2369G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 2369 | chr17 | 69544122 | ||||||
| chr17:69544222 | A | G | 54 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(51): Show |
172 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*2469A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 2469 | chr17 | 69544222 | ||||||
| chr17:69544298 | T | C | 1 | a0001c0001t0011 | 3 | HG00140.hp2 HG01106.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2545T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 2545 | chr17 | 69544298 | ||||||
| chr17:69544497 | C | T | 1 | a0001c0002t0053 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2744C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 2744 | chr17 | 69544497 | ||||||
| chr17:69544564 | C | T | 1 | a0001c0001t0039 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2811C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 2811 | chr17 | 69544564 | ||||||
| chr17:69544855 | G | A | 1 | a0001c0002t0032 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3102G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 3102 | chr17 | 69544855 | ||||||
| chr17:69545062 | C | T | 4 | a0001c0001t0006 a0001c0001t0014 a0001c0002t0006 others(1): Show |
14 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3309C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 3309 | chr17 | 69545062 | ||||||
| chr17:69545103 | C | T | 4 | a0001c0001t0006 a0001c0001t0014 a0001c0002t0006 others(1): Show |
14 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3350C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 3350 | chr17 | 69545103 | ||||||
| chr17:69545151 | C | A | 2 | a0001c0002t0057 a0001c0002t0063 |
2 | HG02280.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3398C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 3398 | chr17 | 69545151 | ||||||
| chr17:69545154 | G | T | 1 | a0001c0002t0052 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3401G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 3401 | chr17 | 69545154 | ||||||
| chr17:69545194 | C | G | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(28): Show |
78 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*3441C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 3441 | chr17 | 69545194 | ||||||
| chr17:69545545 | G | T | 1 | a0001c0001t0027 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3792G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 3792 | chr17 | 69545545 | ||||||
| chr17:69546020 | C | CA | 6 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0030 others(3): Show |
20 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4285dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 4286 | INFO_REALIGN_3_PRIME | chr17 | 69546020 | |||||
| chr17:69546020 | CA | C | 19 | a0001c0001t0001 a0001c0001t0018 a0001c0001t0021 others(16): Show |
90 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*4285delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 4285 | INFO_REALIGN_3_PRIME | chr17 | 69546020 | |||||
| chr17:69546020 | CAA | C | 24 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0010 others(21): Show |
66 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*4284_*4285delAA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 4284 | INFO_REALIGN_3_PRIME | chr17 | 69546020 | |||||
| chr17:69546020 | CAAA | C | 6 | a0001c0001t0008 a0001c0001t0061 a0001c0001t0065 others(3): Show |
10 | HG00733.hp1 HG01099.hp1 HG02109.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4283_*4285delAAA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 4283 | INFO_REALIGN_3_PRIME | chr17 | 69546020 | |||||
| chr17:69546204 | CTT | C | 4 | a0001c0001t0010 a0001c0001t0028 a0001c0002t0062 others(1): Show |
8 | HG01109.hp1 HG02258.hp1 HG02258.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4453_*4454delTT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 4453 | INFO_REALIGN_3_PRIME | chr17 | 69546204 | |||||
| chr17:69546352 | T | C | 61 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(58): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*4599T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 4599 | chr17 | 69546352 | ||||||
| chr17:69546367 | C | G | 1 | a0001c0002t0050 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4614C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 4614 | chr17 | 69546367 | ||||||
| chr17:69546447 | A | G | 1 | a0001c0001t0022 | 2 | HG02970.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4694A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 4694 | chr17 | 69546447 | ||||||
| chr17:69546606 | C | T | 11 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0014 others(8): Show |
25 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4853C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 4853 | chr17 | 69546606 | ||||||
| chr17:69546648 | G | A | 8 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0014 others(5): Show |
22 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4895G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 4895 | chr17 | 69546648 | ||||||
| chr17:69546821 | A | T | 1 | a0001c0002t0049 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5068A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 5068 | chr17 | 69546821 | ||||||
| chr17:69546848 | CT | C | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(28): Show |
78 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*5108delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 5108 | INFO_REALIGN_3_PRIME | chr17 | 69546848 | |||||
| chr17:69546972 | G | C | 32 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(29): Show |
79 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*5219G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 5219 | chr17 | 69546972 | ||||||
| chr17:69546998 | C | T | 1 | a0001c0002t0041 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5245C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 5245 | chr17 | 69546998 | ||||||
| chr17:69547035 | G | T | 2 | a0001c0001t0009 a0001c0002t0009 |
4 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5282G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 5282 | chr17 | 69547035 | ||||||
| chr17:69547075 | T | G | 30 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(27): Show |
77 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*5322T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 5322 | chr17 | 69547075 | ||||||
| chr17:69547171 | G | A | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(28): Show |
78 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*5418G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 5418 | chr17 | 69547171 | ||||||
| chr17:69547208 | G | A | 1 | a0001c0001t0043 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5455G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 5455 | chr17 | 69547208 | ||||||
| chr17:69547226 | A | G | 2 | a0001c0001t0014 a0001c0002t0014 |
3 | HG02896.hp1 NA18906.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5473A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 5473 | chr17 | 69547226 | ||||||
| chr17:69547293 | A | C | 2 | a0001c0001t0024 a0001c0002t0024 |
2 | HG02922.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5540A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 5540 | chr17 | 69547293 | ||||||
| chr17:69547365 | C | T | 1 | a0001c0001t0040 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5612C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 5612 | chr17 | 69547365 | ||||||
| chr17:69547394 | T | A | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(28): Show |
78 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*5641T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 5641 | chr17 | 69547394 | ||||||
| chr17:69547473 | A | T | 8 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0054 others(5): Show |
33 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*5720A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 5720 | chr17 | 69547473 | ||||||
| chr17:69547728 | A | C | 1 | a0001c0001t0022 | 2 | HG02970.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5975A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 5975 | chr17 | 69547728 | ||||||
| chr17:69547734 | C | T | 3 | a0001c0001t0024 a0001c0001t0056 a0001c0002t0024 |
3 | HG02922.hp2 HG02976.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5981C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 5981 | chr17 | 69547734 | ||||||
| chr17:69548013 | T | C | 72 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(69): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
3_prime_UTR_variant | MODIFIER | c.*6260T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 6260 | chr17 | 69548013 | ||||||
| chr17:69548117 | C | T | 2 | a0001c0001t0048 a0001c0001t0060 |
2 | NA18975.hp2 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6364C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 6364 | chr17 | 69548117 | ||||||
| chr17:69548123 | G | A | 7 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0054 others(4): Show |
31 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*6370G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 6370 | chr17 | 69548123 | ||||||
| chr17:69548205 | T | G | 1 | a0001c0001t0054 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6452T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 6452 | chr17 | 69548205 | ||||||
| chr17:69548402 | G | T | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(28): Show |
78 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*6649G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 6649 | chr17 | 69548402 | ||||||
| chr17:69548432 | AT | A | 13 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0015 others(10): Show |
42 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*6688delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 6688 | INFO_REALIGN_3_PRIME | chr17 | 69548432 | |||||
| chr17:69548684 | G | T | 2 | a0001c0001t0020 a0001c0001t0040 |
3 | HG01884.hp1 HG02572.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6931G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 6931 | chr17 | 69548684 | ||||||
| chr17:69548688 | C | G | 4 | a0001c0001t0010 a0001c0001t0028 a0001c0002t0062 others(1): Show |
8 | HG01109.hp1 HG02258.hp1 HG02258.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6935C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 6935 | chr17 | 69548688 | ||||||
| chr17:69548838 | G | A | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(28): Show |
78 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*7085G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 7085 | chr17 | 69548838 | ||||||
| chr17:69548863 | G | A | 1 | a0001c0001t0065 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7110G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 7110 | chr17 | 69548863 | ||||||
| chr17:69548952 | A | C | 1 | a0001c0001t0015 | 3 | NA18964.hp1 NA18997.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7199A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 7199 | chr17 | 69548952 | ||||||
| chr17:69548969 | T | C | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(28): Show |
78 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*7216T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 7216 | chr17 | 69548969 | ||||||
| chr17:69549039 | C | T | 3 | a0001c0001t0021 a0001c0001t0051 a0001c0002t0021 |
3 | HG02698.hp1 HG03491.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7286C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 7286 | chr17 | 69549039 | ||||||
| chr17:69549210 | G | A | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(28): Show |
78 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*7457G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 7457 | chr17 | 69549210 | ||||||
| chr17:69549309 | A | C | 1 | a0001c0002t0057 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7556A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 7556 | chr17 | 69549309 | ||||||
| chr17:69549321 | T | G | 1 | a0001c0002t0044 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7568T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 7568 | chr17 | 69549321 | ||||||
| chr17:69549393 | T | C | 3 | a0001c0001t0010 a0001c0002t0057 a0001c0002t0063 |
6 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7640T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 7640 | chr17 | 69549393 | ||||||
| chr17:69549454 | A | G | 32 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(29): Show |
79 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*7701A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 7701 | chr17 | 69549454 | ||||||
| chr17:69549503 | G | T | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(28): Show |
78 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*7750G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 7750 | chr17 | 69549503 | ||||||
| chr17:69549547 | C | T | 1 | a0001c0001t0034 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7794C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 7794 | chr17 | 69549547 | ||||||
| chr17:69549929 | G | C | 1 | a0001c0002t0045 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8176G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 8176 | chr17 | 69549929 | ||||||
| chr17:69549955 | G | T | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(28): Show |
78 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*8202G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 8202 | chr17 | 69549955 | ||||||
| chr17:69550026 | A | G | 3 | a0001c0001t0010 a0001c0002t0057 a0001c0002t0063 |
6 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8273A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 8273 | chr17 | 69550026 | ||||||
| chr17:69550136 | C | T | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(28): Show |
78 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*8383C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 8383 | chr17 | 69550136 | ||||||
| chr17:69550227 | G | A | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(28): Show |
78 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*8474G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 8474 | chr17 | 69550227 | ||||||
| chr17:69550536 | G | A | 2 | a0001c0001t0010 a0001c0002t0057 |
5 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8783G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 8783 | chr17 | 69550536 | ||||||
| chr17:69550555 | G | A | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(28): Show |
78 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*8802G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 8802 | chr17 | 69550555 | ||||||
| chr17:69550596 | G | T | 1 | a0001c0001t0047 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8843G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 8843 | chr17 | 69550596 | ||||||
| chr17:69550661 | C | A | 1 | a0001c0001t0065 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8908C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 8908 | chr17 | 69550661 | ||||||
| chr17:69550737 | C | T | 1 | a0001c0001t0026 | 2 | HG01516.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8984C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 8984 | chr17 | 69550737 | ||||||
| chr17:69550786 | C | T | 1 | a0001c0001t0065 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9033C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 9033 | chr17 | 69550786 | ||||||
| chr17:69550895 | C | T | 57 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(54): Show |
176 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*9142C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 9142 | chr17 | 69550895 | ||||||
| chr17:69550945 | G | C | 17 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0015 others(14): Show |
47 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*9192G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 9192 | chr17 | 69550945 | ||||||
| chr17:69551574 | G | T | 1 | a0001c0001t0035 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9821G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 9821 | chr17 | 69551574 | ||||||
| chr17:69551695 | G | T | 1 | a0001c0001t0026 | 2 | HG01516.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9942G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 9942 | chr17 | 69551695 | ||||||
| chr17:69551867 | C | G | 5 | a0001c0001t0013 a0001c0001t0025 a0001c0001t0026 others(2): Show |
9 | HG00099.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*10114C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 10114 | chr17 | 69551867 | ||||||
| chr17:69552029 | G | A | 1 | a0001c0001t0026 | 2 | HG01516.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10276G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 10276 | chr17 | 69552029 | ||||||
| chr17:69552067 | C | A | 1 | a0001c0001t0038 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10314C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 10314 | chr17 | 69552067 | ||||||
| chr17:69552301 | T | C | 1 | a0001c0001t0036 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10548T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 10548 | chr17 | 69552301 | ||||||
| chr17:69552339 | A | G | 32 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(29): Show |
79 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*10586A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 10586 | chr17 | 69552339 | ||||||
| chr17:69552387 | T | C | 1 | a0001c0002t0033 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10634T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 10634 | chr17 | 69552387 | ||||||
| chr17:69552708 | T | G | 2 | a0001c0001t0020 a0001c0001t0040 |
3 | HG01884.hp1 HG02572.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10955T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 10955 | chr17 | 69552708 | ||||||
| chr17:69552742 | T | C | 1 | a0001c0002t0046 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10989T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 10989 | chr17 | 69552742 | ||||||
| chr17:69552981 | T | A | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(28): Show |
78 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*11228T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 11228 | chr17 | 69552981 | ||||||
| chr17:69553320 | G | A | 13 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0015 others(10): Show |
42 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*11567G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 11567 | chr17 | 69553320 | ||||||
| chr17:69553602 | C | T | 1 | a0001c0001t0056 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11849C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 12/12 | 11849 | chr17 | 69553602 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:69415160 | CAGAG | C | 3 | a0001c0002t0001g0258 a0001c0002t0001g0259 a0001c0002t0001g0260 |
3 | HG02735.hp1 HG03139.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.16+163_16+166delAG others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69415160 | ||||||
| chr17:69415241 | C | CT | 53 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0220 others(50): Show |
53 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.16+246dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69415241 | ||||||
| chr17:69415718 | A | G | 2 | a0001c0001t0005g0206 a0001c0001t0005g0207 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.16+718A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69415718 | |||||||
| chr17:69416022 | G | A | 65 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.16+1022G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69416022 | |||||||
| chr17:69416049 | T | C | 2 | a0001c0001t0058g0067 a0001c0002t0002g0066 |
2 | HG01884.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.16+1049T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69416049 | |||||||
| chr17:69416056 | A | G | 65 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.16+1056A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69416056 | |||||||
| chr17:69416221 | C | T | 65 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.16+1221C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69416221 | |||||||
| chr17:69416421 | C | G | 1 | a0001c0001t0004g0205 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.16+1421C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69416421 | |||||||
| chr17:69416466 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.16+1466G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69416466 | |||||||
| chr17:69416490 | A | C | 65 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.16+1490A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69416490 | |||||||
| chr17:69416596 | A | G | 2 | a0001c0001t0002g0204 a0001c0002t0004g0203 |
2 | HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.16+1596A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69416596 | |||||||
| chr17:69416660 | A | G | 2 | a0001c0001t0001g0201 a0001c0002t0007g0202 |
2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.16+1660A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69416660 | |||||||
| chr17:69416674 | GT | G | 65 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.16+1679delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69416674 | ||||||
| chr17:69416719 | A | G | 2 | a0001c0001t0010g0200 a0001c0002t0064g0199 |
2 | HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.16+1719A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69416719 | |||||||
| chr17:69416731 | A | G | 65 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.16+1731A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69416731 | |||||||
| chr17:69416825 | G | A | 65 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.16+1825G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69416825 | |||||||
| chr17:69416869 | A | G | 1 | a0001c0002t0001g0065 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.16+1869A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69416869 | |||||||
| chr17:69416916 | G | A | 65 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.16+1916G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69416916 | |||||||
| chr17:69416975 | C | T | 65 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.16+1975C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69416975 | |||||||
| chr17:69417262 | T | C | 119 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.16+2262T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69417262 | |||||||
| chr17:69417343 | T | C | 137 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(134): Show |
137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.16+2343T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69417343 | |||||||
| chr17:69417390 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.16+2390C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69417390 | |||||||
| chr17:69418117 | G | A | 2 | a0001c0002t0001g0209 a0001c0002t0012g0208 |
2 | HG03491.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.16+3117G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69418117 | |||||||
| chr17:69418166 | G | A | 19 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0220 others(16): Show |
19 | HG00438.hp2 HG00621.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.16+3166G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69418166 | |||||||
| chr17:69418280 | AG | A | 3 | a0001c0001t0001g0201 a0001c0002t0007g0202 a0001c0002t0063g0078 |
3 | HG02280.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.16+3284delG | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69418280 | ||||||
| chr17:69418419 | A | G | 2 | a0001c0002t0001g0197 a0001c0002t0004g0198 |
2 | NA18612.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.16+3419A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69418419 | |||||||
| chr17:69418529 | CT | C | 140 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(137): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.16+3538delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69418529 | ||||||
| chr17:69418647 | C | G | 6 | a0001c0001t0001g0193 a0001c0001t0026g0191 a0001c0001t0026g0192 others(3): Show |
6 | HG00099.hp1 HG01071.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.16+3647C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69418647 | |||||||
| chr17:69418865 | T | C | 1 | a0001c0002t0001g0082 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.16+3865T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69418865 | |||||||
| chr17:69418876 | C | CA | 136 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(133): Show |
136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.16+3886dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69418876 | ||||||
| chr17:69418894 | T | C | 54 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0220 others(51): Show |
54 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.16+3894T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69418894 | |||||||
| chr17:69418906 | A | C | 65 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.16+3906A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69418906 | |||||||
| chr17:69419132 | C | T | 2 | a0001c0001t0001g0190 a0001c0002t0003g0189 |
2 | NA18971.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.16+4132C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69419132 | |||||||
| chr17:69419136 | A | G | 140 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(137): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.16+4136A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69419136 | |||||||
| chr17:69419284 | G | A | 1 | a0001c0001t0002g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.16+4284G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69419284 | |||||||
| chr17:69419288 | C | T | 1 | a0001c0002t0004g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16+4288C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69419288 | |||||||
| chr17:69419314 | G | A | 1 | a0001c0002t0004g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16+4314G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69419314 | |||||||
| chr17:69419392 | G | T | 1 | a0001c0002t0004g0188 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.16+4392G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69419392 | |||||||
| chr17:69419437 | A | G | 1 | a0001c0002t0004g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16+4437A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69419437 | |||||||
| chr17:69419732 | G | C | 1 | a0001c0001t0003g0226 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.16+4732G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69419732 | |||||||
| chr17:69419778 | T | A | 58 | a0001c0001t0001g0201 a0001c0001t0001g0211 a0001c0001t0001g0212 others(55): Show |
58 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.16+4778T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69419778 | |||||||
| chr17:69419913 | C | CA | 75 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0211 others(72): Show |
75 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.16+4928dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69419913 | ||||||
| chr17:69419913 | C | CAA | 68 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(65): Show |
68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.16+4927_16+4928dup others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69419913 | ||||||
| chr17:69419977 | C | T | 3 | a0001c0001t0008g0075 a0001c0002t0002g0077 a0001c0002t0006g0076 |
3 | HG01099.hp1 HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.16+4977C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69419977 | |||||||
| chr17:69420012 | G | T | 6 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0003g0185 others(3): Show |
6 | HG01099.hp2 HG01192.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.16+5012G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69420012 | |||||||
| chr17:69420120 | T | C | 65 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.16+5120T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69420120 | |||||||
| chr17:69420166 | G | A | 1 | a0001c0001t0005g0001 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.16+5166G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69420166 | |||||||
| chr17:69420683 | C | T | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+5683C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69420683 | |||||||
| chr17:69420737 | A | AT | 140 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(137): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.16+5746dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69420737 | ||||||
| chr17:69420872 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.16+5872T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69420872 | |||||||
| chr17:69421045 | C | A | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+6045C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69421045 | |||||||
| chr17:69421045 | C | T | 65 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.16+6045C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69421045 | |||||||
| chr17:69421138 | C | T | 7 | a0001c0001t0016g0074 a0001c0001t0020g0071 a0001c0001t0028g0072 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.16+6138C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69421138 | |||||||
| chr17:69421432 | A | G | 1 | a0001c0002t0001g0065 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.16+6432A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69421432 | |||||||
| chr17:69421497 | C | T | 3 | a0001c0001t0008g0075 a0001c0002t0002g0077 a0001c0002t0006g0076 |
3 | HG01099.hp1 HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.16+6497C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69421497 | |||||||
| chr17:69421544 | G | GT | 8 | a0001c0001t0001g0181 a0001c0001t0016g0074 a0001c0001t0020g0071 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.16+6556dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69421544 | ||||||
| chr17:69421626 | C | T | 2 | a0001c0001t0008g0075 a0001c0002t0006g0076 |
2 | HG01099.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.16+6626C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69421626 | |||||||
| chr17:69421716 | T | C | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+6716T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69421716 | |||||||
| chr17:69421768 | C | T | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.16+6768C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69421768 | |||||||
| chr17:69421790 | GCCTCGGC others(1333): Show |
G | 1 | a0001c0001t0001g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.16+6822_16+8161del | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69421790 | ||||||
| chr17:69421914 | G | A | 3 | a0001c0001t0008g0061 a0001c0001t0056g0059 a0001c0002t0014g0062 |
3 | HG02717.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.16+6914G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69421914 | |||||||
| chr17:69422090 | C | G | 1 | a0001c0001t0003g0179 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.16+7090C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69422090 | |||||||
| chr17:69422124 | A | AT | 74 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(71): Show |
74 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.16+7149dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69422124 | ||||||
| chr17:69422124 | A | ATT | 6 | a0001c0001t0004g0050 a0001c0001t0005g0032 a0001c0001t0008g0049 others(3): Show |
6 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+7148_16+7149dup others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69422124 | ||||||
| chr17:69422124 | AT | A | 45 | a0001c0001t0001g0119 a0001c0001t0001g0135 a0001c0001t0001g0211 others(42): Show |
45 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.16+7149delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69422124 | ||||||
| chr17:69422124 | ATT | A | 14 | a0001c0001t0001g0190 a0001c0001t0001g0212 a0001c0001t0001g0220 others(11): Show |
14 | HG00621.hp2 HG01074.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.16+7148_16+7149del others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69422124 | ||||||
| chr17:69422229 | T | A | 15 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0220 others(12): Show |
15 | HG00438.hp2 HG00621.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.16+7229T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69422229 | |||||||
| chr17:69422383 | C | T | 2 | a0001c0001t0008g0075 a0001c0002t0006g0076 |
2 | HG01099.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.16+7383C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69422383 | |||||||
| chr17:69422392 | G | A | 1 | a0001c0002t0001g0161 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.16+7392G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69422392 | |||||||
| chr17:69422423 | C | T | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+7423C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69422423 | |||||||
| chr17:69422522 | G | A | 2 | a0001c0001t0010g0200 a0001c0002t0064g0199 |
2 | HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.16+7522G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69422522 | |||||||
| chr17:69422847 | G | A | 65 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.16+7847G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69422847 | |||||||
| chr17:69422859 | G | T | 65 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.16+7859G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69422859 | |||||||
| chr17:69422873 | TTTTGTTT others(1): Show |
T | 3 | a0001c0001t0010g0200 a0001c0002t0004g0203 a0001c0002t0064g0199 |
3 | HG02258.hp1 HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.16+7894_16+7901del others(8): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69422873 | ||||||
| chr17:69422895 | T | C | 1 | a0001c0002t0004g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16+7895T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69422895 | |||||||
| chr17:69422946 | C | T | 5 | a0001c0001t0001g0201 a0001c0001t0002g0068 a0001c0001t0002g0204 others(2): Show |
5 | HG02109.hp1 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+7946C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69422946 | |||||||
| chr17:69422947 | G | A | 2 | a0001c0001t0010g0200 a0001c0002t0064g0199 |
2 | HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.16+7947G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69422947 | |||||||
| chr17:69422989 | T | C | 66 | a0001c0001t0001g0201 a0001c0001t0001g0211 a0001c0001t0001g0212 others(63): Show |
66 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.16+7989T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69422989 | |||||||
| chr17:69423104 | C | T | 1 | a0001c0001t0003g0004 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.16+8104C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69423104 | |||||||
| chr17:69423126 | G | A | 65 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.16+8126G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69423126 | |||||||
| chr17:69423204 | A | G | 3 | a0001c0001t0001g0079 a0001c0001t0006g0080 a0001c0002t0008g0081 |
3 | HG02109.hp2 HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.16+8204A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69423204 | |||||||
| chr17:69423476 | C | T | 1 | a0001c0002t0004g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16+8476C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69423476 | |||||||
| chr17:69423559 | T | C | 1 | a0001c0001t0014g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.16+8559T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69423559 | |||||||
| chr17:69423681 | A | G | 1 | a0001c0001t0003g0058 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.16+8681A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69423681 | |||||||
| chr17:69423704 | G | A | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+8704G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69423704 | |||||||
| chr17:69423790 | C | T | 1 | a0001c0002t0001g0082 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.16+8790C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69423790 | |||||||
| chr17:69423912 | A | G | 3 | a0001c0001t0009g0056 a0001c0001t0009g0057 a0001c0001t0025g0055 |
3 | HG00099.hp2 HG00323.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.16+8912A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69423912 | |||||||
| chr17:69424136 | G | T | 1 | a0001c0002t0004g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16+9136G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69424136 | |||||||
| chr17:69424292 | T | C | 59 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0220 others(56): Show |
59 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.16+9292T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69424292 | |||||||
| chr17:69424442 | T | C | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0003g0004 others(2): Show |
5 | HG03490.hp1 HG03492.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+9442T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69424442 | |||||||
| chr17:69424621 | C | T | 5 | a0001c0001t0016g0074 a0001c0001t0020g0071 a0001c0001t0028g0072 others(2): Show |
5 | HG01884.hp1 HG02559.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+9621C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69424621 | |||||||
| chr17:69425006 | A | G | 2 | a0001c0001t0002g0006 a0001c0001t0002g0007 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.16+10006A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69425006 | |||||||
| chr17:69425335 | T | C | 161 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(158): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.16+10335T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69425335 | |||||||
| chr17:69425345 | C | G | 1 | a0001c0001t0002g0180 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.16+10345C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69425345 | |||||||
| chr17:69425457 | C | T | 2 | a0001c0001t0010g0200 a0001c0002t0064g0199 |
2 | HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.16+10457C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69425457 | |||||||
| chr17:69425462 | A | G | 4 | a0001c0001t0001g0201 a0001c0001t0002g0068 a0001c0001t0002g0204 others(1): Show |
4 | HG02451.hp1 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+10462A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69425462 | |||||||
| chr17:69425548 | T | C | 2 | a0001c0001t0008g0075 a0001c0002t0006g0076 |
2 | HG01099.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.16+10548T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69425548 | |||||||
| chr17:69425563 | G | A | 2 | a0001c0001t0002g0008 a0001c0002t0004g0203 |
2 | HG00738.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.16+10563G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69425563 | |||||||
| chr17:69425723 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0040g0009 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.16+10723G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69425723 | |||||||
| chr17:69425807 | G | A | 1 | a0001c0002t0003g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.16+10807G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69425807 | |||||||
| chr17:69425838 | C | T | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+10838C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69425838 | |||||||
| chr17:69426124 | C | G | 1 | a0001c0001t0003g0179 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.16+11124C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69426124 | |||||||
| chr17:69426130 | T | A | 4 | a0001c0001t0001g0201 a0001c0001t0002g0068 a0001c0001t0002g0204 others(1): Show |
4 | HG02451.hp1 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+11130T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69426130 | |||||||
| chr17:69426226 | A | G | 161 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(158): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.16+11226A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69426226 | |||||||
| chr17:69426350 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.16+11350C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69426350 | |||||||
| chr17:69426630 | A | G | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.16+11630A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69426630 | |||||||
| chr17:69426723 | C | T | 1 | a0001c0001t0010g0200 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.16+11723C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69426723 | |||||||
| chr17:69426756 | C | T | 1 | a0001c0002t0066g0225 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.16+11756C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69426756 | |||||||
| chr17:69426797 | TA | T | 70 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.16+11810delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69426797 | ||||||
| chr17:69426869 | A | G | 1 | a0001c0001t0047g0177 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.16+11869A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69426869 | |||||||
| chr17:69427003 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.16+12003G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69427003 | |||||||
| chr17:69427011 | T | C | 4 | a0001c0001t0001g0229 a0001c0001t0004g0228 a0001c0002t0029g0227 others(1): Show |
4 | HG02135.hp1 NA18960.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+12011T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69427011 | |||||||
| chr17:69427087 | A | G | 66 | a0001c0001t0001g0201 a0001c0001t0001g0211 a0001c0001t0001g0212 others(63): Show |
66 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.16+12087A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69427087 | |||||||
| chr17:69427128 | C | T | 1 | a0001c0002t0032g0054 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.16+12128C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69427128 | |||||||
| chr17:69427133 | G | A | 67 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(64): Show |
67 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.16+12133G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69427133 | |||||||
| chr17:69427275 | T | A | 1 | a0001c0001t0039g0012 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.16+12275T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69427275 | |||||||
| chr17:69427586 | C | T | 1 | a0001c0001t0009g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.16+12586C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69427586 | |||||||
| chr17:69428009 | G | T | 2 | a0001c0002t0002g0176 a0001c0002t0005g0175 |
2 | HG03017.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.16+13009G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69428009 | |||||||
| chr17:69428125 | C | T | 4 | a0001c0001t0001g0201 a0001c0001t0002g0068 a0001c0001t0002g0204 others(1): Show |
4 | HG02451.hp1 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+13125C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69428125 | |||||||
| chr17:69428267 | G | C | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+13267G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69428267 | |||||||
| chr17:69428647 | C | T | 157 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(154): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.16+13647C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69428647 | |||||||
| chr17:69428856 | TTG | T | 7 | a0001c0001t0002g0106 a0001c0001t0016g0074 a0001c0001t0020g0071 others(4): Show |
7 | HG01884.hp1 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.16+13858_16+13859d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69428856 | ||||||
| chr17:69428857 | TG | T | 16 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0008g0103 others(13): Show |
16 | HG00733.hp1 HG01109.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.16+13858delG | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69428857 | |||||||
| chr17:69428858 | G | T | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+13858G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69428858 | |||||||
| chr17:69428863 | TG | T | 128 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(125): Show |
128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.16+13864delG | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69428863 | |||||||
| chr17:69428864 | G | T | 31 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0098 others(28): Show |
31 | HG00733.hp1 HG01109.hp1 HG01516.hp2 others(28): Show |
intron_variant | MODIFIER | c.16+13864G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69428864 | |||||||
| chr17:69428867 | T | G | 4 | a0001c0001t0001g0201 a0001c0001t0002g0068 a0001c0001t0002g0204 others(1): Show |
4 | HG02451.hp1 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+13867T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69428867 | |||||||
| chr17:69428931 | A | AAC | 10 | a0001c0001t0001g0079 a0001c0001t0001g0201 a0001c0001t0002g0068 others(7): Show |
10 | HG01516.hp1 HG01517.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.16+13958_16+13959d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69428931 | ||||||
| chr17:69428931 | A | AACAC | 24 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0002g0106 others(21): Show |
24 | HG00733.hp1 HG01099.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.16+13956_16+13959d others(6): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69428931 | ||||||
| chr17:69428931 | A | AACACAC | 4 | a0001c0001t0016g0052 a0001c0002t0002g0066 a0001c0002t0004g0053 others(1): Show |
4 | HG00639.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+13954_16+13959d others(8): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69428931 | ||||||
| chr17:69428931 | A | AACACACA others(1): Show |
59 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(56): Show |
59 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.16+13952_16+13959d others(10): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69428931 | ||||||
| chr17:69428931 | A | AACACACA others(3): Show |
6 | a0001c0001t0005g0001 a0001c0001t0010g0016 a0001c0001t0011g0013 others(3): Show |
6 | HG01106.hp1 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+13950_16+13959d others(12): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69428931 | ||||||
| chr17:69428931 | A | AACACACA others(7): Show |
1 | a0001c0002t0001g0258 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.16+13946_16+13959d others(16): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69428931 | ||||||
| chr17:69428931 | AAC | A | 2 | a0001c0002t0001g0255 a0001c0002t0004g0174 |
2 | HG02056.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.16+13958_16+13959d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69428931 | ||||||
| chr17:69429037 | A | G | 1 | a0001c0002t0063g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16+14037A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69429037 | |||||||
| chr17:69429059 | C | T | 1 | a0001c0002t0002g0173 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.16+14059C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69429059 | |||||||
| chr17:69429172 | C | T | 58 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0220 others(55): Show |
58 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.16+14172C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69429172 | |||||||
| chr17:69429283 | GA | G | 155 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(152): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.16+14300delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69429283 | ||||||
| chr17:69429478 | G | A | 3 | a0001c0001t0048g0231 a0001c0002t0003g0233 a0001c0002t0017g0232 |
3 | HG02273.hp2 NA19082.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.16+14478G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69429478 | |||||||
| chr17:69429518 | T | TA | 6 | a0001c0001t0001g0193 a0001c0001t0006g0110 a0001c0001t0026g0191 others(3): Show |
6 | HG00099.hp1 HG01071.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+14528dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69429518 | ||||||
| chr17:69429651 | T | C | 1 | a0001c0001t0011g0013 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.16+14651T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69429651 | |||||||
| chr17:69430006 | T | C | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+15006T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69430006 | |||||||
| chr17:69430087 | G | T | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+15087G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69430087 | |||||||
| chr17:69430176 | A | G | 1 | a0001c0001t0002g0254 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.16+15176A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69430176 | |||||||
| chr17:69430228 | C | T | 59 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0220 others(56): Show |
59 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.16+15228C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69430228 | |||||||
| chr17:69430251 | G | A | 1 | a0001c0001t0007g0111 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.16+15251G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69430251 | |||||||
| chr17:69430375 | T | A | 59 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0220 others(56): Show |
59 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.16+15375T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69430375 | |||||||
| chr17:69430409 | A | G | 20 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0002g0106 others(17): Show |
20 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.16+15409A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69430409 | |||||||
| chr17:69430471 | A | T | 160 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(157): Show |
160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.16+15471A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69430471 | |||||||
| chr17:69430501 | C | T | 1 | a0001c0002t0003g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.16+15501C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69430501 | |||||||
| chr17:69430526 | T | C | 4 | a0001c0001t0001g0201 a0001c0001t0002g0068 a0001c0001t0002g0204 others(1): Show |
4 | HG02451.hp1 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+15526T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69430526 | |||||||
| chr17:69430674 | C | G | 1 | a0001c0002t0033g0109 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.16+15674C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69430674 | |||||||
| chr17:69430697 | A | G | 2 | a0001c0001t0058g0067 a0001c0002t0002g0066 |
2 | HG01884.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.16+15697A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69430697 | |||||||
| chr17:69430758 | C | G | 2 | a0001c0001t0008g0075 a0001c0002t0006g0076 |
2 | HG01099.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.16+15758C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69430758 | |||||||
| chr17:69430876 | A | G | 1 | a0001c0002t0004g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16+15876A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69430876 | |||||||
| chr17:69430902 | T | G | 1 | a0001c0001t0001g0112 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.16+15902T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69430902 | |||||||
| chr17:69430989 | G | A | 4 | a0001c0001t0008g0061 a0001c0001t0056g0059 a0001c0002t0014g0062 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+15989G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69430989 | |||||||
| chr17:69431355 | CTT | C | 20 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0002g0106 others(17): Show |
20 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.16+16356_16+16357d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69431355 | |||||||
| chr17:69431519 | G | A | 1 | a0001c0001t0010g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.16+16519G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69431519 | |||||||
| chr17:69431628 | G | C | 1 | a0001c0001t0048g0231 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.16+16628G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69431628 | |||||||
| chr17:69431683 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.16+16683C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69431683 | |||||||
| chr17:69431706 | C | T | 1 | a0001c0001t0010g0200 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.16+16706C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69431706 | |||||||
| chr17:69431720 | G | A | 1 | a0001c0002t0004g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16+16720G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69431720 | |||||||
| chr17:69431752 | C | T | 1 | a0001c0002t0004g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16+16752C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69431752 | |||||||
| chr17:69431775 | A | G | 20 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0002g0106 others(17): Show |
20 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.16+16775A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69431775 | |||||||
| chr17:69431949 | G | A | 2 | a0001c0001t0008g0075 a0001c0002t0006g0076 |
2 | HG01099.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.16+16949G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69431949 | |||||||
| chr17:69432092 | C | G | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+17092C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69432092 | |||||||
| chr17:69432207 | T | A | 2 | a0001c0002t0002g0113 a0001c0002t0002g0173 |
2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.16+17207T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69432207 | |||||||
| chr17:69432492 | T | C | 1 | a0001c0001t0007g0114 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.16+17492T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69432492 | |||||||
| chr17:69432535 | C | T | 1 | a0001c0002t0003g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.16+17535C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69432535 | |||||||
| chr17:69432590 | G | A | 1 | a0001c0002t0004g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16+17590G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69432590 | |||||||
| chr17:69432680 | G | C | 2 | a0001c0001t0023g0064 a0001c0002t0001g0018 |
2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.16+17680G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69432680 | |||||||
| chr17:69432708 | A | T | 6 | a0001c0001t0002g0106 a0001c0001t0004g0050 a0001c0001t0008g0049 others(3): Show |
6 | HG00639.hp1 HG01243.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+17708A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69432708 | |||||||
| chr17:69432810 | TA | T | 158 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(155): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.16+17827delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69432810 | ||||||
| chr17:69432906 | C | A | 2 | a0001c0001t0001g0201 a0001c0002t0007g0202 |
2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.16+17906C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69432906 | |||||||
| chr17:69432937 | T | C | 1 | a0001c0001t0025g0094 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.16+17937T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69432937 | |||||||
| chr17:69432997 | A | T | 1 | a0001c0001t0005g0170 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.16+17997A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69432997 | |||||||
| chr17:69433262 | T | C | 1 | a0001c0001t0011g0019 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.16+18262T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69433262 | |||||||
| chr17:69433415 | A | G | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+18415A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69433415 | |||||||
| chr17:69434003 | C | G | 2 | a0001c0001t0002g0048 a0001c0001t0055g0169 |
2 | HG00735.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.16+19003C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69434003 | |||||||
| chr17:69434837 | C | T | 1 | a0001c0001t0023g0064 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.16+19837C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69434837 | |||||||
| chr17:69435042 | T | A | 1 | a0001c0001t0001g0112 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.16+20042T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69435042 | |||||||
| chr17:69435130 | A | G | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+20130A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69435130 | |||||||
| chr17:69435263 | C | T | 1 | a0001c0002t0001g0168 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.16+20263C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69435263 | |||||||
| chr17:69435418 | C | G | 2 | a0001c0002t0001g0209 a0001c0002t0012g0208 |
2 | HG03491.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.16+20418C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69435418 | |||||||
| chr17:69435546 | A | G | 63 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0220 others(60): Show |
63 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.16+20546A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69435546 | |||||||
| chr17:69435560 | G | A | 3 | a0001c0001t0058g0067 a0001c0002t0002g0066 a0001c0002t0004g0203 |
3 | HG01884.hp2 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.16+20560G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69435560 | |||||||
| chr17:69435631 | G | C | 1 | a0001c0002t0004g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16+20631G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69435631 | |||||||
| chr17:69435674 | A | T | 1 | a0001c0001t0002g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.16+20674A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69435674 | |||||||
| chr17:69435865 | G | A | 1 | a0001c0002t0021g0196 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.16+20865G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69435865 | |||||||
| chr17:69435865 | G | T | 1 | a0001c0001t0001g0178 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.16+20865G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69435865 | |||||||
| chr17:69435991 | G | A | 1 | a0001c0001t0010g0200 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.16+20991G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69435991 | |||||||
| chr17:69436019 | TA | T | 6 | a0001c0001t0001g0079 a0001c0001t0001g0201 a0001c0001t0006g0080 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.16+21033delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69436019 | ||||||
| chr17:69436019 | TAA | T | 158 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(155): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.16+21032_16+21033d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69436019 | ||||||
| chr17:69436030 | A | C | 1 | a0001c0002t0001g0005 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.16+21030A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69436030 | |||||||
| chr17:69436188 | T | C | 162 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(159): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.16+21188T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69436188 | |||||||
| chr17:69436244 | T | G | 162 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(159): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.16+21244T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69436244 | |||||||
| chr17:69436314 | T | G | 3 | a0001c0001t0058g0067 a0001c0002t0001g0259 a0001c0002t0002g0066 |
3 | HG01884.hp2 HG02735.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.16+21314T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69436314 | |||||||
| chr17:69436628 | C | T | 69 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.16+21628C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69436628 | |||||||
| chr17:69436658 | T | G | 1 | a0001c0001t0003g0179 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.16+21658T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69436658 | |||||||
| chr17:69436694 | C | T | 18 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0002g0106 others(15): Show |
18 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.16+21694C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69436694 | |||||||
| chr17:69436740 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.16+21740G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69436740 | |||||||
| chr17:69436754 | C | G | 6 | a0001c0001t0001g0201 a0001c0001t0002g0068 a0001c0001t0002g0204 others(3): Show |
6 | HG01099.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+21754C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69436754 | |||||||
| chr17:69436787 | C | T | 69 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.16+21787C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69436787 | |||||||
| chr17:69436833 | A | T | 159 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(156): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.16+21833A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69436833 | |||||||
| chr17:69437074 | G | A | 69 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.16+22074G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69437074 | |||||||
| chr17:69437329 | G | A | 5 | a0001c0001t0004g0050 a0001c0001t0008g0049 a0001c0001t0016g0052 others(2): Show |
5 | HG00639.hp1 HG01243.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+22329G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69437329 | |||||||
| chr17:69437364 | G | A | 1 | a0001c0001t0058g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.16+22364G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69437364 | |||||||
| chr17:69437434 | G | A | 4 | a0001c0001t0002g0068 a0001c0001t0002g0204 a0001c0001t0008g0075 others(1): Show |
4 | HG01099.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+22434G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69437434 | |||||||
| chr17:69437821 | G | A | 1 | a0001c0002t0001g0258 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.16+22821G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69437821 | |||||||
| chr17:69438007 | G | A | 1 | a0001c0002t0001g0022 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.16+23007G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69438007 | |||||||
| chr17:69438071 | C | T | 2 | a0001c0001t0058g0067 a0001c0002t0002g0066 |
2 | HG01884.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.16+23071C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69438071 | |||||||
| chr17:69438084 | T | C | 70 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0112 others(67): Show |
70 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.16+23084T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69438084 | |||||||
| chr17:69438313 | T | G | 1 | a0001c0002t0004g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16+23313T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69438313 | |||||||
| chr17:69438562 | C | G | 1 | a0001c0001t0004g0166 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.16+23562C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69438562 | |||||||
| chr17:69438838 | G | A | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+23838G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69438838 | |||||||
| chr17:69438909 | G | A | 67 | a0001c0001t0001g0011 a0001c0001t0001g0112 a0001c0001t0001g0119 others(64): Show |
67 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.16+23909G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69438909 | |||||||
| chr17:69439162 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.16+24162G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69439162 | |||||||
| chr17:69439637 | G | C | 1 | a0001c0001t0002g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.16+24637G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69439637 | |||||||
| chr17:69439717 | C | T | 1 | a0001c0001t0030g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.16+24717C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69439717 | |||||||
| chr17:69439847 | G | A | 1 | a0001c0002t0044g0003 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.16+24847G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69439847 | |||||||
| chr17:69439874 | A | G | 1 | a0001c0001t0003g0179 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.16+24874A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69439874 | |||||||
| chr17:69439923 | A | G | 1 | a0001c0001t0060g0224 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.16+24923A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69439923 | |||||||
| chr17:69439935 | C | T | 8 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0220 others(5): Show |
8 | HG00438.hp2 HG00621.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.16+24935C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69439935 | |||||||
| chr17:69440160 | G | A | 3 | a0001c0001t0002g0204 a0001c0001t0008g0075 a0001c0002t0006g0076 |
3 | HG01099.hp1 HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.16+25160G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69440160 | |||||||
| chr17:69440173 | G | A | 2 | a0001c0001t0023g0064 a0001c0002t0001g0018 |
2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.16+25173G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69440173 | |||||||
| chr17:69440253 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.16+25253A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69440253 | |||||||
| chr17:69440278 | C | T | 1 | a0001c0002t0063g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16+25278C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69440278 | |||||||
| chr17:69440534 | A | G | 1 | a0001c0002t0021g0196 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.16+25534A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69440534 | |||||||
| chr17:69440680 | C | G | 1 | a0001c0002t0004g0053 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.16+25680C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69440680 | |||||||
| chr17:69440752 | T | C | 4 | a0001c0001t0001g0229 a0001c0001t0004g0228 a0001c0002t0029g0227 others(1): Show |
4 | HG02135.hp1 NA18960.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+25752T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69440752 | |||||||
| chr17:69440874 | T | C | 2 | a0001c0002t0004g0213 a0001c0002t0066g0225 |
2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.16+25874T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69440874 | |||||||
| chr17:69440975 | C | T | 3 | a0001c0001t0002g0204 a0001c0001t0008g0075 a0001c0002t0006g0076 |
3 | HG01099.hp1 HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.16+25975C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69440975 | |||||||
| chr17:69441006 | A | G | 1 | a0001c0001t0002g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.16+26006A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69441006 | |||||||
| chr17:69441058 | G | A | 156 | a0001c0001t0001g0011 a0001c0001t0001g0084 a0001c0001t0001g0098 others(153): Show |
156 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.16+26058G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69441058 | |||||||
| chr17:69441076 | G | C | 1 | a0001c0002t0053g0146 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.16+26076G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69441076 | |||||||
| chr17:69441599 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0060g0224 |
2 | NA18956.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.16+26599C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69441599 | |||||||
| chr17:69441821 | A | C | 1 | a0001c0001t0016g0074 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.16+26821A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69441821 | |||||||
| chr17:69441845 | G | A | 67 | a0001c0001t0001g0011 a0001c0001t0001g0112 a0001c0001t0001g0119 others(64): Show |
67 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.16+26845G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69441845 | |||||||
| chr17:69442006 | C | A | 1 | a0001c0002t0002g0066 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.16+27006C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69442006 | |||||||
| chr17:69442364 | C | T | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+27364C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69442364 | |||||||
| chr17:69442687 | T | C | 1 | a0001c0002t0063g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16+27687T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69442687 | |||||||
| chr17:69443012 | T | G | 1 | a0001c0002t0052g0115 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.16+28012T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69443012 | |||||||
| chr17:69443034 | T | G | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+28034T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69443034 | |||||||
| chr17:69443097 | C | T | 3 | a0001c0001t0001g0079 a0001c0001t0006g0080 a0001c0002t0008g0081 |
3 | HG02109.hp2 HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.16+28097C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69443097 | |||||||
| chr17:69443246 | G | A | 1 | a0001c0002t0004g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16+28246G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69443246 | |||||||
| chr17:69443298 | C | G | 61 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0220 others(58): Show |
61 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.16+28298C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69443298 | |||||||
| chr17:69443312 | G | C | 70 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0112 others(67): Show |
70 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.16+28312G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69443312 | |||||||
| chr17:69443443 | C | T | 3 | a0001c0001t0001g0079 a0001c0001t0006g0080 a0001c0002t0008g0081 |
3 | HG02109.hp2 HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.16+28443C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69443443 | |||||||
| chr17:69443747 | T | C | 3 | a0001c0001t0001g0079 a0001c0001t0006g0080 a0001c0002t0008g0081 |
3 | HG02109.hp2 HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.16+28747T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69443747 | |||||||
| chr17:69443782 | G | T | 3 | a0001c0001t0002g0204 a0001c0001t0008g0075 a0001c0002t0006g0076 |
3 | HG01099.hp1 HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.16+28782G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69443782 | |||||||
| chr17:69444056 | C | G | 1 | a0001c0002t0005g0164 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.16+29056C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69444056 | |||||||
| chr17:69444285 | G | A | 2 | a0001c0002t0002g0176 a0001c0002t0005g0175 |
2 | HG03017.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.16+29285G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69444285 | |||||||
| chr17:69444524 | A | G | 1 | a0001c0001t0031g0252 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.16+29524A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69444524 | |||||||
| chr17:69444670 | T | G | 159 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0084 others(156): Show |
159 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.16+29670T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69444670 | |||||||
| chr17:69444789 | A | C | 1 | a0001c0002t0001g0144 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.16+29789A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69444789 | |||||||
| chr17:69444797 | G | T | 2 | a0001c0001t0001g0201 a0001c0002t0007g0202 |
2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.16+29797G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69444797 | |||||||
| chr17:69445044 | C | T | 67 | a0001c0001t0001g0011 a0001c0001t0001g0112 a0001c0001t0001g0119 others(64): Show |
67 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.16+30044C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69445044 | |||||||
| chr17:69445185 | T | C | 74 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0112 others(71): Show |
74 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.16+30185T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69445185 | |||||||
| chr17:69445254 | A | G | 5 | a0001c0001t0002g0210 a0001c0002t0001g0092 a0001c0002t0001g0197 others(2): Show |
5 | HG00558.hp2 HG02071.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+30254A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69445254 | |||||||
| chr17:69445340 | C | T | 1 | a0001c0002t0008g0081 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.16+30340C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69445340 | |||||||
| chr17:69445351 | G | A | 2 | a0001c0001t0058g0067 a0001c0002t0002g0066 |
2 | HG01884.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.16+30351G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69445351 | |||||||
| chr17:69445808 | T | C | 74 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0112 others(71): Show |
74 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.16+30808T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69445808 | |||||||
| chr17:69446032 | G | C | 1 | a0001c0002t0029g0227 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.16+31032G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69446032 | |||||||
| chr17:69446133 | C | T | 62 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0220 others(59): Show |
62 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.16+31133C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69446133 | |||||||
| chr17:69446189 | G | A | 2 | a0001c0001t0001g0201 a0001c0002t0007g0202 |
2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.16+31189G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69446189 | |||||||
| chr17:69446395 | G | T | 3 | a0001c0001t0002g0204 a0001c0001t0008g0075 a0001c0002t0006g0076 |
3 | HG01099.hp1 HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.16+31395G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69446395 | |||||||
| chr17:69446545 | A | G | 1 | a0001c0002t0004g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16+31545A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69446545 | |||||||
| chr17:69446575 | CT | C | 62 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0220 others(59): Show |
62 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.16+31578delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69446575 | ||||||
| chr17:69446718 | G | T | 1 | a0001c0002t0052g0115 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.16+31718G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69446718 | |||||||
| chr17:69446727 | G | A | 159 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0084 others(156): Show |
159 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.16+31727G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69446727 | |||||||
| chr17:69446769 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.16+31769G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69446769 | |||||||
| chr17:69446860 | GTT | G | 159 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0084 others(156): Show |
159 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.16+31873_16+31874d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69446860 | ||||||
| chr17:69446970 | C | T | 159 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0084 others(156): Show |
159 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.16+31970C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69446970 | |||||||
| chr17:69446976 | CT | C | 158 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0084 others(155): Show |
158 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.16+31994delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69446976 | ||||||
| chr17:69446996 | A | C | 62 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0220 others(59): Show |
62 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.16+31996A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69446996 | |||||||
| chr17:69446999 | C | T | 1 | a0001c0001t0013g0091 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.16+31999C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69446999 | |||||||
| chr17:69447127 | G | A | 1 | a0001c0002t0004g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16+32127G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69447127 | |||||||
| chr17:69447131 | C | G | 1 | a0001c0001t0002g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.16+32131C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69447131 | |||||||
| chr17:69447271 | G | A | 74 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0112 others(71): Show |
74 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.16+32271G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69447271 | |||||||
| chr17:69447304 | C | T | 74 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0112 others(71): Show |
74 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.16+32304C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69447304 | |||||||
| chr17:69447636 | A | G | 67 | a0001c0001t0001g0011 a0001c0001t0001g0112 a0001c0001t0001g0119 others(64): Show |
67 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.16+32636A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69447636 | |||||||
| chr17:69447695 | T | C | 20 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0002g0106 others(17): Show |
20 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.16+32695T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69447695 | |||||||
| chr17:69447737 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.16+32737G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69447737 | |||||||
| chr17:69448244 | GT | G | 152 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0084 others(149): Show |
152 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.16+33258delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69448244 | ||||||
| chr17:69448251 | T | G | 19 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0002g0106 others(16): Show |
19 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.16+33251T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69448251 | |||||||
| chr17:69448289 | G | C | 1 | a0001c0002t0001g0223 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.16+33289G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69448289 | |||||||
| chr17:69448339 | C | CT | 19 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0002g0106 others(16): Show |
19 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.16+33347dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69448339 | ||||||
| chr17:69448402 | T | G | 186 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0079 others(183): Show |
186 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.16+33402T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69448402 | |||||||
| chr17:69448425 | G | A | 137 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0112 others(134): Show |
137 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.16+33425G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69448425 | |||||||
| chr17:69448514 | G | A | 1 | a0001c0001t0002g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.16+33514G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69448514 | |||||||
| chr17:69448623 | A | T | 1 | a0001c0002t0063g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16+33623A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69448623 | |||||||
| chr17:69448652 | T | A | 1 | a0001c0001t0039g0012 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.16+33652T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69448652 | |||||||
| chr17:69448721 | C | T | 4 | a0001c0001t0002g0210 a0001c0002t0001g0197 a0001c0002t0004g0188 others(1): Show |
4 | HG00558.hp2 NA18612.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+33721C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69448721 | |||||||
| chr17:69448849 | A | G | 1 | a0001c0002t0063g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16+33849A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69448849 | |||||||
| chr17:69448956 | T | C | 18 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0002g0106 others(15): Show |
18 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.16+33956T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69448956 | |||||||
| chr17:69449034 | G | A | 3 | a0001c0002t0004g0213 a0001c0002t0057g0214 a0001c0002t0066g0225 |
3 | HG02486.hp1 HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.16+34034G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449034 | |||||||
| chr17:69449182 | T | C | 1 | a0001c0002t0001g0116 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.16+34182T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449182 | |||||||
| chr17:69449214 | C | G | 22 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0002g0106 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.16+34214C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449214 | |||||||
| chr17:69449489 | C | CCTTTCTT others(1): Show |
71 | a0001c0001t0001g0079 a0001c0001t0001g0112 a0001c0001t0001g0119 others(68): Show |
71 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.16+34494_16+34501d others(10): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449489 | ||||||
| chr17:69449489 | C | CCTTTCTT others(5): Show |
1 | a0001c0001t0002g0180 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.16+34490_16+34501d others(14): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449489 | ||||||
| chr17:69449498 | CTTT | C | 75 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0001g0201 others(72): Show |
75 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.16+34502_16+34504d others(5): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449498 | ||||||
| chr17:69449499 | T | TTTCTTTC others(19): Show |
1 | a0001c0002t0003g0142 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.16+34501_16+34502i others(28): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449499 | ||||||
| chr17:69449499 | T | TTTCTTTC others(15): Show |
10 | a0001c0001t0001g0011 a0001c0001t0001g0171 a0001c0001t0002g0141 others(7): Show |
10 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.16+34501_16+34502i others(24): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449499 | ||||||
| chr17:69449499 | T | TTTCTTTC others(29): Show |
1 | a0001c0001t0001g0187 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.16+34501_16+34502i others(38): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449499 | ||||||
| chr17:69449503 | T | G | 12 | a0001c0001t0001g0011 a0001c0001t0001g0171 a0001c0001t0001g0187 others(9): Show |
12 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.16+34503T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449503 | |||||||
| chr17:69449510 | TTTC | T | 53 | a0001c0001t0001g0201 a0001c0001t0001g0229 a0001c0001t0001g0236 others(50): Show |
53 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.16+34513_16+34515d others(5): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449510 | ||||||
| chr17:69449511 | TTC | T | 22 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0002g0106 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.16+34513_16+34514d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449511 | ||||||
| chr17:69449517 | G | T | 75 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0001g0201 others(72): Show |
75 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.16+34517G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449517 | |||||||
| chr17:69449517 | GTCTTTCT others(11): Show |
G | 2 | a0001c0001t0002g0010 a0001c0001t0040g0009 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.16+34531_16+34548d others(20): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449517 | ||||||
| chr17:69449529 | TTGTCTTT others(1): Show |
T | 6 | a0001c0001t0001g0211 a0001c0001t0001g0222 a0001c0001t0018g0216 others(3): Show |
6 | HG00438.hp2 HG00621.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.16+34531_16+34538d others(10): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449529 | ||||||
| chr17:69449531 | G | GTCTT | 3 | a0001c0001t0010g0200 a0001c0002t0001g0151 a0001c0002t0053g0146 |
3 | HG02258.hp1 NA18941.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.16+34557_16+34560d others(6): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449531 | ||||||
| chr17:69449531 | G | GTCTTTCT others(9): Show |
1 | a0001c0001t0007g0044 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.16+34545_16+34560d others(18): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449531 | ||||||
| chr17:69449531 | G | GTCTTTCT others(11): Show |
2 | a0001c0002t0001g0127 a0001c0002t0001g0168 |
2 | NA18612.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.16+34544_16+34545i others(20): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449531 | ||||||
| chr17:69449531 | G | GTCTTTCT others(15): Show |
2 | a0001c0001t0001g0112 a0001c0001t0001g0181 |
2 | HG02135.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.16+34544_16+34545i others(24): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449531 | ||||||
| chr17:69449531 | G | T | 4 | a0001c0001t0001g0212 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
4 | HG01074.hp1 HG01169.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+34531G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449531 | |||||||
| chr17:69449531 | GTCTT | G | 7 | a0001c0001t0002g0063 a0001c0001t0007g0028 a0001c0001t0009g0056 others(4): Show |
7 | HG00323.hp1 HG01069.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.16+34557_16+34560d others(6): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449531 | ||||||
| chr17:69449535 | T | TTCTTTCT others(3): Show |
18 | a0001c0001t0001g0119 a0001c0001t0002g0180 a0001c0001t0013g0091 others(15): Show |
18 | HG00639.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.16+34544_16+34545i others(12): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449535 | ||||||
| chr17:69449535 | T | TTCTTTCT others(17): Show |
3 | a0001c0001t0001g0122 a0001c0001t0036g0126 a0001c0002t0001g0184 |
3 | HG02293.hp1 HG02293.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.16+34544_16+34545i others(26): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449535 | ||||||
| chr17:69449537 | CTTTCTTT others(17): Show |
C | 1 | a0001c0002t0066g0225 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.16+34561_16+34584d others(26): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449537 | ||||||
| chr17:69449539 | T | TTCTTTG | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0138 others(12): Show |
15 | HG01346.hp1 HG02145.hp1 HG02273.hp1 others(12): Show |
intron_variant | MODIFIER | c.16+34544_16+34545i others(8): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449539 | ||||||
| chr17:69449541 | CTTTCTTT others(13): Show |
C | 1 | a0001c0002t0004g0213 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.16+34561_16+34580d others(22): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449541 | ||||||
| chr17:69449543 | T | TTG | 11 | a0001c0001t0001g0190 a0001c0001t0003g0185 a0001c0001t0005g0206 others(8): Show |
11 | HG01257.hp1 HG01258.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.16+34544_16+34545i others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449543 | ||||||
| chr17:69449543 | TTC | T | 10 | a0001c0001t0002g0210 a0001c0001t0002g0254 a0001c0001t0006g0110 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.16+34545_16+34546d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449543 | ||||||
| chr17:69449543 | TTCTTTC | T | 9 | a0001c0001t0001g0079 a0001c0001t0001g0201 a0001c0001t0001g0245 others(6): Show |
9 | HG00558.hp2 HG02135.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.16+34545_16+34550d others(8): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449543 | ||||||
| chr17:69449543 | TTCTTTCT others(3): Show |
T | 26 | a0001c0001t0001g0229 a0001c0001t0001g0236 a0001c0001t0001g0238 others(23): Show |
26 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.16+34545_16+34554d others(12): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449543 | ||||||
| chr17:69449543 | TTCTTTCT others(7): Show |
T | 3 | a0001c0001t0001g0253 a0001c0001t0003g0226 a0001c0001t0003g0234 |
3 | NA18979.hp2 NA19058.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.16+34545_16+34558d others(16): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449543 | ||||||
| chr17:69449543 | TTCTTTCT others(11): Show |
T | 4 | a0001c0001t0001g0247 a0001c0001t0007g0246 a0001c0002t0001g0255 others(1): Show |
4 | HG02056.hp1 NA18955.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+34545_16+34562d others(20): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449543 | ||||||
| chr17:69449543 | TTCTTTCT others(15): Show |
T | 2 | a0001c0002t0003g0248 a0001c0002t0003g0249 |
2 | NA18997.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.16+34545_16+34566d others(24): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449543 | ||||||
| chr17:69449545 | CTTTCTTT others(15): Show |
C | 21 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0002g0106 others(18): Show |
21 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.16+34547_16+34568d others(24): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449545 | ||||||
| chr17:69449545 | CTTTCTTT others(19): Show |
C | 1 | a0001c0001t0028g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.16+34547_16+34572d others(28): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449545 | ||||||
| chr17:69449547 | T | G | 6 | a0001c0001t0006g0110 a0001c0001t0006g0129 a0001c0001t0006g0130 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+34547T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449547 | |||||||
| chr17:69449549 | C | A | 1 | a0001c0001t0011g0019 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.16+34549C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449549 | |||||||
| chr17:69449549 | CTTTCTTT others(5): Show |
C | 1 | a0001c0001t0001g0043 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.16+34561_16+34572d others(14): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449549 | ||||||
| chr17:69449551 | T | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0201 a0001c0002t0007g0202 |
3 | HG02723.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.16+34551T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449551 | |||||||
| chr17:69449553 | C | A | 11 | a0001c0001t0001g0031 a0001c0001t0002g0008 a0001c0001t0005g0032 others(8): Show |
11 | HG00733.hp2 HG00738.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.16+34553C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449553 | |||||||
| chr17:69449553 | CTTTCTTT others(1): Show |
C | 8 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0003g0042 others(5): Show |
8 | HG00099.hp2 HG02523.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.16+34561_16+34568d others(10): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449553 | ||||||
| chr17:69449557 | C | A | 26 | a0001c0001t0001g0039 a0001c0001t0001g0089 a0001c0001t0002g0047 others(23): Show |
26 | HG00408.hp2 HG00423.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.16+34557C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449557 | |||||||
| chr17:69449557 | CTTTA | C | 17 | a0001c0001t0001g0031 a0001c0001t0002g0008 a0001c0001t0002g0204 others(14): Show |
17 | HG00733.hp2 HG00738.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.16+34561_16+34564d others(6): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449557 | ||||||
| chr17:69449561 | A | C | 160 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0079 others(157): Show |
160 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.16+34561A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449561 | |||||||
| chr17:69449561 | ATTTC | A | 3 | a0001c0001t0010g0200 a0001c0002t0001g0065 a0001c0002t0003g0154 |
3 | HG00408.hp1 HG01168.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.16+34589_16+34592d others(6): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449561 | ||||||
| chr17:69449563 | T | G | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+34563T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449563 | |||||||
| chr17:69449565 | C | A | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0003g0042 others(3): Show |
6 | HG00099.hp2 HG02523.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+34565C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449565 | |||||||
| chr17:69449569 | C | A | 1 | a0001c0001t0001g0043 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.16+34569C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449569 | |||||||
| chr17:69449569 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.16+34569C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449569 | |||||||
| chr17:69449593 | T | C | 2 | a0001c0001t0008g0075 a0001c0002t0002g0113 |
2 | HG01099.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.16+34593T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449593 | |||||||
| chr17:69449595 | C | T | 2 | a0001c0001t0008g0075 a0001c0002t0002g0113 |
2 | HG01099.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.16+34595C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449595 | |||||||
| chr17:69449601 | T | C | 4 | a0001c0001t0002g0210 a0001c0002t0001g0197 a0001c0002t0004g0188 others(1): Show |
4 | HG00558.hp2 NA18612.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+34601T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449601 | |||||||
| chr17:69449605 | C | T | 2 | a0001c0001t0008g0075 a0001c0002t0002g0113 |
2 | HG01099.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.16+34605C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449605 | |||||||
| chr17:69449609 | C | CT | 15 | a0001c0001t0001g0178 a0001c0001t0002g0010 a0001c0001t0002g0063 others(12): Show |
15 | HG00323.hp1 HG00733.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.16+34632dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449609 | ||||||
| chr17:69449609 | CT | C | 57 | a0001c0001t0001g0158 a0001c0001t0001g0211 a0001c0001t0001g0212 others(54): Show |
57 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.16+34632delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449609 | ||||||
| chr17:69449609 | CTTT | C | 20 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0008g0103 others(17): Show |
20 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.16+34630_16+34632d others(5): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69449609 | ||||||
| chr17:69449611 | T | C | 2 | a0001c0001t0008g0075 a0001c0002t0002g0113 |
2 | HG01099.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.16+34611T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449611 | |||||||
| chr17:69449613 | T | C | 2 | a0001c0001t0008g0075 a0001c0002t0002g0113 |
2 | HG01099.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.16+34613T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449613 | |||||||
| chr17:69449754 | C | G | 1 | a0001c0001t0014g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.16+34754C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449754 | |||||||
| chr17:69449775 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.16+34775G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449775 | |||||||
| chr17:69449795 | A | T | 22 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0002g0106 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.16+34795A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449795 | |||||||
| chr17:69449815 | A | G | 22 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0002g0106 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.16+34815A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449815 | |||||||
| chr17:69449815 | A | T | 69 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0112 others(66): Show |
69 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.16+34815A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449815 | |||||||
| chr17:69449902 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.16+34902C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449902 | |||||||
| chr17:69449996 | G | A | 1 | a0001c0002t0001g0255 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.16+34996G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69449996 | |||||||
| chr17:69450020 | C | T | 69 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0112 others(66): Show |
69 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.16+35020C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69450020 | |||||||
| chr17:69450101 | AT | A | 67 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(64): Show |
67 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.16+35123delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69450101 | ||||||
| chr17:69450101 | ATT | A | 8 | a0001c0001t0003g0042 a0001c0001t0003g0244 a0001c0001t0006g0023 others(5): Show |
8 | HG00738.hp1 HG01975.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.16+35122_16+35123d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69450101 | ||||||
| chr17:69450101 | ATTT | A | 133 | a0001c0001t0001g0079 a0001c0001t0001g0112 a0001c0001t0001g0119 others(130): Show |
133 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.16+35121_16+35123d others(5): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69450101 | ||||||
| chr17:69450101 | ATTTT | A | 20 | a0001c0001t0001g0011 a0001c0001t0001g0084 a0001c0001t0001g0098 others(17): Show |
20 | HG00733.hp1 HG01109.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.16+35120_16+35123d others(6): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69450101 | ||||||
| chr17:69450141 | C | T | 1 | a0001c0001t0016g0052 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.16+35141C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69450141 | |||||||
| chr17:69450472 | T | G | 1 | a0001c0002t0004g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16+35472T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69450472 | |||||||
| chr17:69450629 | C | T | 22 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0002g0106 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.16+35629C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69450629 | |||||||
| chr17:69450701 | AT | A | 6 | a0001c0001t0002g0063 a0001c0001t0002g0180 a0001c0001t0005g0001 others(3): Show |
6 | HG01069.hp2 HG01891.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.16+35716delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69450701 | ||||||
| chr17:69450702 | T | G | 22 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0002g0106 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.16+35702T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69450702 | |||||||
| chr17:69450740 | A | T | 1 | a0001c0002t0063g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16+35740A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69450740 | |||||||
| chr17:69451220 | G | T | 22 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0002g0106 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.16+36220G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69451220 | |||||||
| chr17:69451344 | C | T | 1 | a0001c0002t0029g0227 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.16+36344C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69451344 | |||||||
| chr17:69451569 | G | A | 2 | a0001c0001t0015g0219 a0001c0002t0001g0223 |
2 | HG04228.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.16+36569G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69451569 | |||||||
| chr17:69451756 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.16+36756A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69451756 | |||||||
| chr17:69451904 | G | C | 37 | a0001c0001t0001g0098 a0001c0001t0001g0134 a0001c0001t0001g0193 others(34): Show |
37 | HG00099.hp1 HG01071.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.16+36904G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69451904 | |||||||
| chr17:69451904 | G | T | 3 | a0001c0001t0006g0080 a0001c0001t0016g0052 a0001c0002t0004g0053 |
3 | HG00639.hp1 HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.16+36904G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69451904 | |||||||
| chr17:69451961 | A | G | 156 | a0001c0001t0001g0011 a0001c0001t0001g0043 a0001c0001t0001g0084 others(153): Show |
156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.16+36961A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69451961 | |||||||
| chr17:69452137 | A | G | 1 | a0001c0001t0018g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.16+37137A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69452137 | |||||||
| chr17:69452246 | A | G | 3 | a0001c0001t0002g0204 a0001c0001t0008g0075 a0001c0002t0006g0076 |
3 | HG01099.hp1 HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.16+37246A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69452246 | |||||||
| chr17:69452730 | G | A | 11 | a0001c0001t0002g0204 a0001c0001t0008g0049 a0001c0001t0010g0016 others(8): Show |
11 | HG01346.hp2 HG02109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.16+37730G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69452730 | |||||||
| chr17:69452912 | T | C | 1 | a0001c0001t0004g0050 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+37912T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69452912 | |||||||
| chr17:69453245 | A | G | 36 | a0001c0001t0001g0043 a0001c0001t0001g0079 a0001c0001t0001g0089 others(33): Show |
36 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(33): Show |
intron_variant | MODIFIER | c.16+38245A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69453245 | |||||||
| chr17:69453475 | G | C | 3 | a0001c0002t0001g0086 a0001c0002t0023g0088 a0001c0002t0050g0087 |
3 | HG00738.hp1 HG01109.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.16+38475G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69453475 | |||||||
| chr17:69453487 | C | T | 1 | a0001c0001t0003g0244 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.16+38487C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69453487 | |||||||
| chr17:69453777 | G | C | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+38777G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69453777 | |||||||
| chr17:69453989 | A | G | 3 | a0001c0001t0004g0050 a0001c0001t0006g0080 a0001c0001t0014g0002 |
3 | HG01243.hp2 HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.16+38989A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69453989 | |||||||
| chr17:69453999 | T | C | 4 | a0001c0001t0004g0050 a0001c0001t0006g0080 a0001c0001t0014g0002 others(1): Show |
4 | HG01243.hp2 HG02257.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+38999T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69453999 | |||||||
| chr17:69454463 | C | T | 2 | a0001c0001t0001g0181 a0001c0002t0001g0127 |
2 | HG02135.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.16+39463C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69454463 | |||||||
| chr17:69454766 | C | G | 1 | a0001c0002t0001g0005 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.16+39766C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69454766 | |||||||
| chr17:69455008 | A | G | 1 | a0001c0001t0002g0063 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.16+40008A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455008 | |||||||
| chr17:69455034 | TA | T | 46 | a0001c0001t0001g0043 a0001c0001t0001g0079 a0001c0001t0001g0089 others(43): Show |
46 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.16+40035delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455034 | |||||||
| chr17:69455035 | A | T | 3 | a0001c0001t0002g0010 a0001c0001t0002g0204 a0001c0001t0040g0009 |
3 | HG02451.hp1 HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.16+40035A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455035 | |||||||
| chr17:69455035 | AT | A | 146 | a0001c0001t0001g0031 a0001c0001t0001g0084 a0001c0001t0001g0098 others(143): Show |
146 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.16+40050delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69455035 | ||||||
| chr17:69455037 | T | A | 1 | a0001c0001t0011g0013 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.16+40037T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455037 | |||||||
| chr17:69455039 | T | A | 4 | a0001c0001t0004g0050 a0001c0001t0006g0080 a0001c0001t0014g0002 others(1): Show |
4 | HG01243.hp2 HG02257.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+40039T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455039 | |||||||
| chr17:69455039 | T | G | 44 | a0001c0001t0001g0031 a0001c0001t0001g0178 a0001c0001t0002g0006 others(41): Show |
44 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.16+40039T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455039 | |||||||
| chr17:69455131 | C | T | 2 | a0001c0001t0027g0020 a0001c0001t0027g0021 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.16+40131C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455131 | |||||||
| chr17:69455326 | A | G | 2 | a0001c0002t0001g0022 a0001c0002t0032g0054 |
2 | HG01123.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.16+40326A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455326 | |||||||
| chr17:69455420 | T | G | 5 | a0001c0001t0004g0050 a0001c0001t0006g0080 a0001c0001t0010g0095 others(2): Show |
5 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+40420T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455420 | |||||||
| chr17:69455437 | G | A | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+40437G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455437 | |||||||
| chr17:69455614 | T | C | 209 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(206): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.16+40614T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455614 | |||||||
| chr17:69455643 | A | G | 170 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0084 others(167): Show |
170 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.16+40643A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455643 | |||||||
| chr17:69455722 | T | C | 150 | a0001c0001t0001g0031 a0001c0001t0001g0084 a0001c0001t0001g0098 others(147): Show |
150 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.16+40722T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455722 | |||||||
| chr17:69455764 | G | A | 170 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0084 others(167): Show |
170 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.16+40764G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455764 | |||||||
| chr17:69455812 | G | A | 169 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0084 others(166): Show |
169 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.16+40812G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455812 | |||||||
| chr17:69455851 | G | GT | 7 | a0001c0001t0001g0162 a0001c0001t0004g0166 a0001c0001t0005g0032 others(4): Show |
7 | HG00621.hp1 HG02056.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.16+40877dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69455851 | ||||||
| chr17:69455851 | GT | G | 117 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0043 others(114): Show |
117 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.16+40877delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69455851 | ||||||
| chr17:69455851 | GTT | G | 6 | a0001c0001t0004g0228 a0001c0001t0025g0055 a0001c0002t0001g0082 others(3): Show |
6 | HG00099.hp2 HG01099.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.16+40876_16+40877d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69455851 | ||||||
| chr17:69455851 | GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0001g0134 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.16+40864_16+40877d others(16): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69455851 | ||||||
| chr17:69455865 | T | G | 19 | a0001c0001t0001g0039 a0001c0001t0001g0193 a0001c0001t0002g0141 others(16): Show |
19 | HG00323.hp2 HG00735.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.16+40865T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455865 | |||||||
| chr17:69455896 | C | T | 88 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0001g0079 others(85): Show |
88 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.16+40896C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455896 | |||||||
| chr17:69455964 | A | G | 209 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(206): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.16+40964A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455964 | |||||||
| chr17:69455984 | T | C | 40 | a0001c0001t0001g0043 a0001c0001t0001g0079 a0001c0001t0001g0089 others(37): Show |
40 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.16+40984T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69455984 | |||||||
| chr17:69456033 | G | A | 1 | a0001c0002t0005g0015 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.16+41033G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69456033 | |||||||
| chr17:69456295 | C | T | 2 | a0001c0002t0002g0026 a0001c0002t0004g0038 |
2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.16+41295C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69456295 | |||||||
| chr17:69456387 | T | C | 94 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0089 others(91): Show |
94 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.16+41387T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69456387 | |||||||
| chr17:69456469 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.16+41469A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69456469 | |||||||
| chr17:69456470 | T | C | 3 | a0001c0002t0001g0022 a0001c0002t0001g0086 a0001c0002t0032g0054 |
3 | HG00738.hp1 HG01123.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.16+41470T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69456470 | |||||||
| chr17:69456708 | C | T | 1 | a0001c0002t0064g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16+41708C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69456708 | |||||||
| chr17:69456838 | C | A | 1 | a0001c0001t0005g0170 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.16+41838C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69456838 | |||||||
| chr17:69456877 | G | A | 117 | a0001c0001t0001g0031 a0001c0001t0001g0084 a0001c0001t0001g0098 others(114): Show |
117 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.16+41877G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69456877 | |||||||
| chr17:69456993 | G | A | 1 | a0001c0001t0040g0009 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.16+41993G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69456993 | |||||||
| chr17:69457012 | C | G | 37 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0001g0229 others(34): Show |
37 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.16+42012C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69457012 | |||||||
| chr17:69457103 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.16+42103C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69457103 | |||||||
| chr17:69457136 | T | C | 37 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0001g0229 others(34): Show |
37 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.16+42136T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69457136 | |||||||
| chr17:69457154 | T | C | 63 | a0001c0001t0001g0031 a0001c0001t0001g0178 a0001c0001t0001g0211 others(60): Show |
63 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.16+42154T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69457154 | |||||||
| chr17:69457333 | T | C | 38 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0001g0229 others(35): Show |
38 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.16+42333T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69457333 | |||||||
| chr17:69457410 | T | A | 38 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0001g0229 others(35): Show |
38 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.16+42410T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69457410 | |||||||
| chr17:69457562 | G | T | 1 | a0001c0001t0001g0084 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16+42562G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69457562 | |||||||
| chr17:69457564 | G | T | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+42564G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69457564 | |||||||
| chr17:69457700 | G | A | 38 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0001g0229 others(35): Show |
38 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.16+42700G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69457700 | |||||||
| chr17:69457795 | G | A | 38 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0001g0229 others(35): Show |
38 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.16+42795G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69457795 | |||||||
| chr17:69457820 | A | C | 38 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0001g0229 others(35): Show |
38 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.16+42820A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69457820 | |||||||
| chr17:69457825 | A | C | 58 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0001g0112 others(55): Show |
58 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.16+42825A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69457825 | |||||||
| chr17:69457831 | G | A | 38 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0001g0229 others(35): Show |
38 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.16+42831G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69457831 | |||||||
| chr17:69457851 | A | T | 3 | a0001c0001t0009g0056 a0001c0001t0009g0057 a0001c0001t0025g0055 |
3 | HG00099.hp2 HG00323.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.16+42851A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69457851 | |||||||
| chr17:69457916 | A | G | 1 | a0001c0001t0023g0064 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.16+42916A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69457916 | |||||||
| chr17:69457922 | C | T | 2 | a0001c0001t0002g0010 a0001c0001t0040g0009 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.16+42922C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69457922 | |||||||
| chr17:69457992 | A | C | 39 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0001g0229 others(36): Show |
39 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.16+42992A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69457992 | |||||||
| chr17:69458049 | T | C | 21 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0001g0134 others(18): Show |
21 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.16+43049T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69458049 | |||||||
| chr17:69458081 | T | G | 2 | a0001c0001t0002g0010 a0001c0001t0040g0009 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.16+43081T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69458081 | |||||||
| chr17:69458142 | C | T | 2 | a0001c0001t0002g0010 a0001c0001t0040g0009 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.16+43142C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69458142 | |||||||
| chr17:69458163 | C | T | 12 | a0001c0001t0001g0229 a0001c0001t0011g0107 a0001c0001t0012g0143 others(9): Show |
12 | HG01168.hp2 HG01169.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.16+43163C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69458163 | |||||||
| chr17:69458188 | G | A | 2 | a0001c0001t0001g0236 a0001c0002t0003g0237 |
2 | HG00609.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.16+43188G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69458188 | |||||||
| chr17:69458316 | G | A | 40 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0001g0229 others(37): Show |
40 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.16+43316G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69458316 | |||||||
| chr17:69458333 | G | A | 5 | a0001c0002t0004g0213 a0001c0002t0008g0081 a0001c0002t0057g0214 others(2): Show |
5 | HG02109.hp2 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+43333G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69458333 | |||||||
| chr17:69458352 | C | T | 23 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0001c0001t0001g0243 others(20): Show |
23 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.16+43352C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69458352 | |||||||
| chr17:69458468 | C | G | 1 | a0001c0002t0003g0123 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.16+43468C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69458468 | |||||||
| chr17:69458483 | C | T | 1 | a0001c0001t0038g0040 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.16+43483C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69458483 | |||||||
| chr17:69458517 | C | T | 4 | a0001c0001t0008g0061 a0001c0001t0010g0016 a0001c0002t0006g0045 others(1): Show |
4 | HG01346.hp2 HG02717.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+43517C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69458517 | |||||||
| chr17:69458633 | A | G | 5 | a0001c0002t0004g0213 a0001c0002t0008g0081 a0001c0002t0057g0214 others(2): Show |
5 | HG02109.hp2 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+43633A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69458633 | |||||||
| chr17:69458699 | T | C | 38 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0001g0229 others(35): Show |
38 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.16+43699T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69458699 | |||||||
| chr17:69458714 | C | T | 21 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0001g0134 others(18): Show |
21 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.16+43714C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69458714 | |||||||
| chr17:69458891 | A | G | 1 | a0001c0001t0003g0160 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.16+43891A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69458891 | |||||||
| chr17:69459040 | T | C | 21 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0001g0134 others(18): Show |
21 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.16+44040T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69459040 | |||||||
| chr17:69459155 | T | G | 2 | a0001c0001t0002g0010 a0001c0001t0040g0009 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.16+44155T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69459155 | |||||||
| chr17:69459254 | G | T | 40 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0001g0229 others(37): Show |
40 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.16+44254G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69459254 | |||||||
| chr17:69459279 | T | G | 5 | a0001c0001t0001g0084 a0001c0001t0058g0067 a0001c0002t0003g0070 others(2): Show |
5 | HG01884.hp2 HG03195.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+44279T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69459279 | |||||||
| chr17:69459438 | A | G | 2 | a0001c0001t0002g0010 a0001c0001t0040g0009 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.16+44438A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69459438 | |||||||
| chr17:69459627 | G | T | 1 | a0001c0001t0051g0172 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.16+44627G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69459627 | |||||||
| chr17:69459687 | G | A | 2 | a0001c0002t0002g0026 a0001c0002t0004g0038 |
2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.16+44687G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69459687 | |||||||
| chr17:69459709 | C | CA | 34 | a0001c0001t0001g0079 a0001c0001t0001g0148 a0001c0001t0001g0229 others(31): Show |
34 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.16+44735dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69459709 | ||||||
| chr17:69459709 | C | CAA | 9 | a0001c0001t0001g0089 a0001c0001t0002g0063 a0001c0001t0007g0028 others(6): Show |
9 | HG00733.hp1 HG01069.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.16+44734_16+44735d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69459709 | ||||||
| chr17:69459709 | CA | C | 133 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.16+44735delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69459709 | ||||||
| chr17:69459709 | CAA | C | 22 | a0001c0001t0001g0122 a0001c0001t0001g0236 a0001c0001t0001g0243 others(19): Show |
22 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.16+44734_16+44735d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69459709 | ||||||
| chr17:69459813 | C | T | 23 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0001c0001t0001g0243 others(20): Show |
23 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.16+44813C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69459813 | |||||||
| chr17:69460400 | G | A | 200 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.17-45380G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69460400 | |||||||
| chr17:69460440 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.17-45340G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69460440 | |||||||
| chr17:69460532 | C | G | 6 | a0001c0001t0002g0010 a0001c0001t0008g0061 a0001c0001t0010g0016 others(3): Show |
6 | HG01346.hp2 HG02451.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.17-45248C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69460532 | |||||||
| chr17:69460532 | C | T | 1 | a0001c0001t0047g0177 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.17-45248C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69460532 | |||||||
| chr17:69460697 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.17-45083C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69460697 | |||||||
| chr17:69460830 | G | A | 33 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0001g0229 others(30): Show |
33 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.17-44950G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69460830 | |||||||
| chr17:69460875 | C | G | 1 | a0001c0001t0001g0138 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.17-44905C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69460875 | |||||||
| chr17:69461192 | C | A | 1 | a0001c0001t0010g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.17-44588C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69461192 | |||||||
| chr17:69461350 | C | T | 2 | a0001c0002t0002g0077 a0001c0002t0004g0038 |
2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.17-44430C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69461350 | |||||||
| chr17:69461991 | C | T | 1 | a0001c0001t0008g0049 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.17-43789C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69461991 | |||||||
| chr17:69462109 | C | A | 1 | a0001c0001t0011g0107 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.17-43671C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69462109 | |||||||
| chr17:69462420 | C | T | 1 | a0001c0001t0006g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.17-43360C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69462420 | |||||||
| chr17:69462511 | C | T | 1 | a0001c0001t0008g0075 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.17-43269C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69462511 | |||||||
| chr17:69462526 | C | T | 1 | a0001c0001t0008g0075 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.17-43254C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69462526 | |||||||
| chr17:69462605 | C | T | 2 | a0001c0001t0006g0133 a0001c0001t0018g0132 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.17-43175C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69462605 | |||||||
| chr17:69462664 | A | G | 204 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0043 others(201): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.17-43116A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69462664 | |||||||
| chr17:69462927 | A | C | 95 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0089 others(92): Show |
95 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.17-42853A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69462927 | |||||||
| chr17:69462950 | CT | C | 23 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0001g0134 others(20): Show |
23 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.17-42810delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69462950 | ||||||
| chr17:69462950 | CTT | C | 12 | a0001c0001t0001g0112 a0001c0001t0001g0181 a0001c0001t0002g0007 others(9): Show |
12 | HG01346.hp2 HG02135.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.17-42811_17-42810d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69462950 | ||||||
| chr17:69462950 | CTTT | C | 171 | a0001c0001t0001g0031 a0001c0001t0001g0079 a0001c0001t0001g0084 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.17-42812_17-42810d others(5): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69462950 | ||||||
| chr17:69463192 | C | T | 2 | a0001c0002t0002g0077 a0001c0002t0004g0038 |
2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.17-42588C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69463192 | |||||||
| chr17:69463257 | C | A | 1 | a0001c0001t0002g0180 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.17-42523C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69463257 | |||||||
| chr17:69463306 | GTA | G | 3 | a0001c0001t0014g0002 a0001c0002t0002g0077 a0001c0002t0004g0038 |
3 | HG03209.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.17-42464_17-42463d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69463306 | ||||||
| chr17:69463386 | T | A | 23 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0001g0134 others(20): Show |
23 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.17-42394T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69463386 | |||||||
| chr17:69463503 | CAT | C | 4 | a0001c0001t0008g0061 a0001c0001t0010g0016 a0001c0002t0006g0045 others(1): Show |
4 | HG01346.hp2 HG02717.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-42274_17-42273d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69463503 | ||||||
| chr17:69463510 | A | G | 2 | a0001c0002t0002g0077 a0001c0002t0004g0038 |
2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.17-42270A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69463510 | |||||||
| chr17:69463526 | G | A | 80 | a0001c0001t0001g0031 a0001c0001t0001g0138 a0001c0001t0001g0178 others(77): Show |
80 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.17-42254G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69463526 | |||||||
| chr17:69463606 | C | T | 2 | a0001c0001t0001g0190 a0001c0002t0003g0189 |
2 | NA18971.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.17-42174C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69463606 | |||||||
| chr17:69463614 | C | A | 4 | a0001c0001t0004g0034 a0001c0001t0010g0017 a0001c0001t0027g0020 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-42166C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69463614 | |||||||
| chr17:69463616 | C | A | 173 | a0001c0001t0001g0031 a0001c0001t0001g0079 a0001c0001t0001g0084 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.17-42164C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69463616 | |||||||
| chr17:69463618 | A | G | 1 | a0001c0001t0008g0049 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.17-42162A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69463618 | |||||||
| chr17:69463621 | T | G | 26 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0001g0134 others(23): Show |
26 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.17-42159T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69463621 | |||||||
| chr17:69463677 | C | T | 187 | a0001c0001t0001g0031 a0001c0001t0001g0079 a0001c0001t0001g0084 others(184): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.17-42103C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69463677 | |||||||
| chr17:69463691 | T | C | 1 | a0001c0002t0012g0208 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.17-42089T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69463691 | |||||||
| chr17:69463698 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.17-42082A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69463698 | |||||||
| chr17:69463710 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.17-42070A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69463710 | |||||||
| chr17:69463718 | A | G | 1 | a0001c0001t0002g0048 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.17-42062A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69463718 | |||||||
| chr17:69463751 | G | T | 2 | a0001c0001t0002g0010 a0001c0001t0040g0009 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.17-42029G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69463751 | |||||||
| chr17:69463845 | C | T | 1 | a0001c0001t0014g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.17-41935C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69463845 | |||||||
| chr17:69464011 | C | G | 1 | a0001c0002t0005g0015 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.17-41769C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69464011 | |||||||
| chr17:69464282 | A | G | 1 | a0001c0001t0006g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.17-41498A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69464282 | |||||||
| chr17:69464444 | C | T | 1 | a0001c0002t0001g0127 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.17-41336C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69464444 | |||||||
| chr17:69464456 | A | T | 1 | a0001c0001t0001g0220 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.17-41324A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69464456 | |||||||
| chr17:69464458 | T | G | 1 | a0001c0001t0010g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.17-41322T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69464458 | |||||||
| chr17:69464530 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.17-41250C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69464530 | |||||||
| chr17:69464531 | G | A | 82 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0138 others(79): Show |
82 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.17-41249G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69464531 | |||||||
| chr17:69464668 | C | T | 1 | a0001c0001t0002g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.17-41112C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69464668 | |||||||
| chr17:69464672 | G | A | 82 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0138 others(79): Show |
82 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.17-41108G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69464672 | |||||||
| chr17:69464814 | C | T | 1 | a0001c0002t0063g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.17-40966C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69464814 | |||||||
| chr17:69464876 | C | T | 20 | a0001c0001t0001g0134 a0001c0001t0001g0193 a0001c0001t0002g0141 others(17): Show |
20 | HG00323.hp2 HG01071.hp2 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.17-40904C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69464876 | |||||||
| chr17:69464961 | G | A | 1 | a0001c0002t0005g0240 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.17-40819G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69464961 | |||||||
| chr17:69465028 | T | C | 2 | a0001c0002t0002g0077 a0001c0002t0004g0038 |
2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.17-40752T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69465028 | |||||||
| chr17:69465441 | A | G | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.17-40339A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69465441 | |||||||
| chr17:69465623 | C | CT | 152 | a0001c0001t0001g0011 a0001c0001t0001g0043 a0001c0001t0001g0079 others(149): Show |
152 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.17-40144dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69465623 | ||||||
| chr17:69465623 | C | CTT | 5 | a0001c0001t0001g0084 a0001c0001t0058g0067 a0001c0002t0003g0070 others(2): Show |
5 | HG01884.hp2 HG03195.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-40145_17-40144d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69465623 | ||||||
| chr17:69465650 | G | A | 4 | a0001c0001t0001g0084 a0001c0002t0003g0070 a0001c0002t0007g0202 others(1): Show |
4 | HG03195.hp1 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-40130G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69465650 | |||||||
| chr17:69465747 | A | G | 1 | a0001c0002t0001g0195 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.17-40033A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69465747 | |||||||
| chr17:69465764 | C | T | 1 | a0001c0001t0014g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.17-40016C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69465764 | |||||||
| chr17:69466063 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.17-39717A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69466063 | |||||||
| chr17:69466111 | TA | T | 12 | a0001c0001t0001g0119 a0001c0001t0001g0253 a0001c0001t0003g0069 others(9): Show |
12 | HG02109.hp1 HG02615.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.17-39652delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69466111 | ||||||
| chr17:69466111 | TAA | T | 206 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(203): Show |
206 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.17-39653_17-39652d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69466111 | ||||||
| chr17:69466170 | C | T | 1 | a0001c0002t0049g0230 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.17-39610C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69466170 | |||||||
| chr17:69466258 | C | T | 4 | a0001c0001t0001g0245 a0001c0001t0003g0058 a0001c0002t0001g0082 others(1): Show |
4 | HG00423.hp1 NA18956.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-39522C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69466258 | |||||||
| chr17:69466271 | C | T | 2 | a0001c0001t0016g0052 a0001c0002t0006g0051 |
2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.17-39509C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69466271 | |||||||
| chr17:69466386 | G | C | 3 | a0001c0001t0002g0047 a0001c0001t0054g0150 a0001c0001t0065g0149 |
3 | HG01891.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.17-39394G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69466386 | |||||||
| chr17:69466551 | G | T | 1 | a0001c0002t0003g0239 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.17-39229G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69466551 | |||||||
| chr17:69466586 | A | G | 2 | a0001c0001t0007g0114 a0001c0002t0002g0026 |
2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.17-39194A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69466586 | |||||||
| chr17:69466647 | C | T | 1 | a0001c0001t0007g0028 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.17-39133C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69466647 | |||||||
| chr17:69466658 | G | A | 17 | a0001c0001t0001g0043 a0001c0001t0001g0138 a0001c0001t0001g0221 others(14): Show |
17 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.17-39122G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69466658 | |||||||
| chr17:69466708 | A | G | 16 | a0001c0001t0001g0098 a0001c0001t0002g0010 a0001c0001t0002g0106 others(13): Show |
16 | HG00639.hp1 HG00733.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.17-39072A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69466708 | |||||||
| chr17:69466840 | A | G | 37 | a0001c0001t0001g0043 a0001c0001t0001g0098 a0001c0001t0001g0193 others(34): Show |
37 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.17-38940A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69466840 | |||||||
| chr17:69466848 | A | C | 3 | a0001c0001t0010g0200 a0001c0001t0028g0072 a0001c0002t0063g0078 |
3 | HG02258.hp1 HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.17-38932A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69466848 | |||||||
| chr17:69466868 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.17-38912A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69466868 | |||||||
| chr17:69466937 | C | T | 1 | a0001c0002t0032g0054 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.17-38843C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69466937 | |||||||
| chr17:69467104 | CCTT | C | 25 | a0001c0001t0001g0031 a0001c0001t0001g0084 a0001c0001t0002g0006 others(22): Show |
25 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.17-38673_17-38671d others(5): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69467104 | ||||||
| chr17:69467225 | C | T | 2 | a0001c0001t0002g0047 a0001c0002t0003g0070 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.17-38555C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69467225 | |||||||
| chr17:69467779 | G | GT | 14 | a0001c0001t0001g0112 a0001c0001t0001g0148 a0001c0001t0003g0069 others(11): Show |
14 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.17-37991dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69467779 | ||||||
| chr17:69467848 | T | A | 4 | a0001c0001t0010g0200 a0001c0001t0028g0072 a0001c0001t0028g0096 others(1): Show |
4 | HG02258.hp1 HG02258.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-37932T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69467848 | |||||||
| chr17:69467919 | C | A | 12 | a0001c0001t0003g0069 a0001c0001t0006g0110 a0001c0001t0006g0129 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.17-37861C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69467919 | |||||||
| chr17:69467938 | G | A | 3 | a0001c0001t0001g0079 a0001c0001t0004g0034 a0001c0002t0004g0014 |
3 | HG02965.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.17-37842G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69467938 | |||||||
| chr17:69467961 | T | C | 1 | a0001c0002t0001g0151 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.17-37819T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69467961 | |||||||
| chr17:69467962 | C | A | 1 | a0001c0002t0001g0151 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.17-37818C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69467962 | |||||||
| chr17:69467963 | A | C | 1 | a0001c0002t0001g0151 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.17-37817A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69467963 | |||||||
| chr17:69467978 | C | T | 1 | a0001c0002t0004g0188 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.17-37802C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69467978 | |||||||
| chr17:69467986 | G | A | 159 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0043 others(156): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.17-37794G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69467986 | |||||||
| chr17:69467988 | A | C | 1 | a0001c0002t0001g0151 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.17-37792A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69467988 | |||||||
| chr17:69468024 | C | A | 1 | a0001c0002t0001g0151 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.17-37756C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69468024 | |||||||
| chr17:69468201 | A | G | 1 | a0001c0001t0003g0234 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.17-37579A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69468201 | |||||||
| chr17:69468289 | T | A | 1 | a0001c0002t0001g0151 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.17-37491T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69468289 | |||||||
| chr17:69468398 | C | T | 1 | a0001c0001t0035g0217 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.17-37382C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69468398 | |||||||
| chr17:69468428 | G | A | 159 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0043 others(156): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.17-37352G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69468428 | |||||||
| chr17:69468461 | T | A | 1 | a0001c0002t0001g0151 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.17-37319T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69468461 | |||||||
| chr17:69468568 | G | A | 1 | a0001c0002t0001g0259 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.17-37212G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69468568 | |||||||
| chr17:69468733 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.17-37047T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69468733 | |||||||
| chr17:69468873 | A | G | 3 | a0001c0001t0007g0246 a0001c0001t0060g0224 a0001c0002t0003g0250 |
3 | NA18955.hp1 NA18975.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.17-36907A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69468873 | |||||||
| chr17:69468931 | A | G | 6 | a0001c0001t0002g0047 a0001c0001t0005g0001 a0001c0001t0008g0104 others(3): Show |
6 | HG01891.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.17-36849A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69468931 | |||||||
| chr17:69468970 | T | C | 1 | a0001c0002t0029g0227 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.17-36810T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69468970 | |||||||
| chr17:69469034 | G | T | 1 | a0001c0001t0002g0106 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.17-36746G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69469034 | |||||||
| chr17:69469148 | T | G | 184 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0043 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.17-36632T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69469148 | |||||||
| chr17:69469217 | G | C | 8 | a0001c0001t0001g0147 a0001c0001t0001g0257 a0001c0001t0059g0218 others(5): Show |
8 | HG01192.hp1 HG02056.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-36563G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69469217 | |||||||
| chr17:69469504 | C | T | 1 | a0001c0001t0008g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.17-36276C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69469504 | |||||||
| chr17:69469530 | G | A | 1 | a0001c0001t0003g0226 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.17-36250G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69469530 | |||||||
| chr17:69469545 | C | T | 2 | a0001c0001t0002g0048 a0001c0001t0011g0107 |
2 | HG00735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.17-36235C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69469545 | |||||||
| chr17:69469718 | G | A | 1 | a0001c0002t0001g0255 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.17-36062G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69469718 | |||||||
| chr17:69470122 | T | C | 4 | a0001c0001t0001g0145 a0001c0001t0001g0193 a0001c0001t0026g0191 others(1): Show |
4 | HG01346.hp1 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-35658T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69470122 | |||||||
| chr17:69470176 | C | T | 12 | a0001c0001t0001g0112 a0001c0001t0002g0008 a0001c0001t0022g0101 others(9): Show |
12 | HG00621.hp1 HG00733.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.17-35604C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69470176 | |||||||
| chr17:69470240 | T | G | 1 | a0001c0002t0001g0151 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.17-35540T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69470240 | |||||||
| chr17:69470252 | T | C | 1 | a0001c0001t0007g0114 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.17-35528T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69470252 | |||||||
| chr17:69470436 | A | T | 1 | a0001c0002t0001g0151 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.17-35344A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69470436 | |||||||
| chr17:69470447 | G | C | 3 | a0001c0001t0008g0049 a0001c0001t0016g0052 a0001c0002t0006g0051 |
3 | HG02615.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.17-35333G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69470447 | |||||||
| chr17:69470460 | G | A | 1 | a0001c0001t0008g0075 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.17-35320G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69470460 | |||||||
| chr17:69470753 | C | G | 1 | a0001c0001t0042g0090 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.17-35027C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69470753 | |||||||
| chr17:69471092 | A | C | 1 | a0001c0001t0028g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.17-34688A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69471092 | |||||||
| chr17:69471143 | C | T | 1 | a0001c0002t0004g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.17-34637C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69471143 | |||||||
| chr17:69471387 | T | A | 1 | a0001c0002t0001g0151 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.17-34393T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69471387 | |||||||
| chr17:69471435 | A | G | 4 | a0001c0001t0010g0016 a0001c0001t0058g0067 a0001c0001t0061g0073 others(1): Show |
4 | HG01884.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-34345A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69471435 | |||||||
| chr17:69471735 | A | T | 1 | a0001c0001t0015g0136 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.17-34045A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69471735 | |||||||
| chr17:69471795 | G | C | 1 | a0001c0001t0005g0170 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.17-33985G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69471795 | |||||||
| chr17:69471816 | A | G | 166 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0043 others(163): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.17-33964A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69471816 | |||||||
| chr17:69471924 | A | C | 1 | a0001c0001t0002g0008 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.17-33856A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69471924 | |||||||
| chr17:69472430 | C | T | 70 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0098 others(67): Show |
70 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.17-33350C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69472430 | |||||||
| chr17:69472485 | G | A | 49 | a0001c0001t0001g0043 a0001c0001t0001g0119 a0001c0001t0001g0147 others(46): Show |
49 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.17-33295G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69472485 | |||||||
| chr17:69472535 | C | T | 158 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0043 others(155): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.17-33245C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69472535 | |||||||
| chr17:69472570 | T | A | 5 | a0001c0001t0006g0133 a0001c0001t0007g0114 a0001c0001t0018g0132 others(2): Show |
5 | HG01346.hp2 HG02647.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-33210T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69472570 | |||||||
| chr17:69472690 | A | G | 27 | a0001c0001t0001g0112 a0001c0001t0002g0008 a0001c0001t0002g0180 others(24): Show |
27 | HG00621.hp1 HG00733.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.17-33090A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69472690 | |||||||
| chr17:69472741 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.17-33039C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69472741 | |||||||
| chr17:69472859 | C | T | 1 | a0001c0001t0007g0114 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.17-32921C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69472859 | |||||||
| chr17:69472987 | G | A | 4 | a0001c0001t0001g0138 a0001c0001t0001g0148 a0001c0002t0003g0248 others(1): Show |
4 | NA18997.hp2 NA18998.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-32793G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69472987 | |||||||
| chr17:69473307 | A | G | 22 | a0001c0001t0001g0089 a0001c0001t0001g0138 a0001c0001t0001g0145 others(19): Show |
22 | HG00639.hp2 HG01074.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.17-32473A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69473307 | |||||||
| chr17:69473332 | T | C | 1 | a0001c0002t0007g0037 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.17-32448T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69473332 | |||||||
| chr17:69473408 | A | G | 1 | a0001c0002t0003g0093 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.17-32372A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69473408 | |||||||
| chr17:69473699 | A | T | 158 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0043 others(155): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.17-32081A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69473699 | |||||||
| chr17:69473737 | T | C | 20 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0047 others(17): Show |
20 | HG00323.hp2 HG01257.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.17-32043T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69473737 | |||||||
| chr17:69473750 | C | T | 1 | a0001c0001t0006g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.17-32030C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69473750 | |||||||
| chr17:69473772 | G | C | 1 | a0001c0001t0018g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.17-32008G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69473772 | |||||||
| chr17:69473905 | G | A | 2 | a0001c0001t0010g0200 a0001c0002t0063g0078 |
2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.17-31875G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69473905 | |||||||
| chr17:69474098 | A | G | 6 | a0001c0001t0008g0075 a0001c0001t0010g0016 a0001c0001t0058g0067 others(3): Show |
6 | HG01099.hp1 HG01884.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.17-31682A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69474098 | |||||||
| chr17:69474125 | C | T | 1 | a0001c0001t0028g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.17-31655C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69474125 | |||||||
| chr17:69474198 | T | C | 158 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0043 others(155): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.17-31582T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69474198 | |||||||
| chr17:69474315 | G | A | 4 | a0001c0001t0010g0016 a0001c0001t0058g0067 a0001c0001t0061g0073 others(1): Show |
4 | HG01884.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-31465G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69474315 | |||||||
| chr17:69474526 | A | C | 9 | a0001c0001t0006g0033 a0001c0001t0006g0133 a0001c0001t0010g0016 others(6): Show |
9 | HG01346.hp2 HG01884.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.17-31254A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69474526 | |||||||
| chr17:69474747 | G | C | 157 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0043 others(154): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.17-31033G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69474747 | |||||||
| chr17:69474787 | T | C | 4 | a0001c0001t0010g0016 a0001c0001t0058g0067 a0001c0001t0061g0073 others(1): Show |
4 | HG01884.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-30993T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69474787 | |||||||
| chr17:69474881 | T | G | 23 | a0001c0001t0001g0089 a0001c0001t0001g0138 a0001c0001t0001g0145 others(20): Show |
23 | HG00639.hp2 HG01074.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.17-30899T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69474881 | |||||||
| chr17:69475164 | G | GT | 42 | a0001c0001t0001g0039 a0001c0001t0001g0098 a0001c0001t0001g0119 others(39): Show |
42 | HG00733.hp1 HG00735.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.17-30594dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69475164 | ||||||
| chr17:69475164 | GT | G | 14 | a0001c0001t0002g0008 a0001c0001t0002g0180 a0001c0001t0003g0234 others(11): Show |
14 | HG00621.hp1 HG00733.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.17-30594delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69475164 | ||||||
| chr17:69475174 | T | TG | 4 | a0001c0001t0006g0033 a0001c0001t0006g0133 a0001c0001t0018g0132 others(1): Show |
4 | HG01346.hp2 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-30606_17-30605i others(3): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69475174 | |||||||
| chr17:69475286 | A | T | 19 | a0001c0001t0001g0112 a0001c0001t0002g0008 a0001c0001t0002g0180 others(16): Show |
19 | HG00621.hp1 HG00733.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.17-30494A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69475286 | |||||||
| chr17:69475314 | G | A | 1 | a0001c0001t0007g0114 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.17-30466G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69475314 | |||||||
| chr17:69475335 | A | AT | 57 | a0001c0001t0001g0089 a0001c0001t0001g0112 a0001c0001t0001g0138 others(54): Show |
57 | HG00621.hp1 HG00639.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.17-30439dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69475335 | ||||||
| chr17:69475610 | G | T | 7 | a0001c0001t0001g0079 a0001c0001t0004g0034 a0001c0001t0024g0097 others(4): Show |
7 | HG00639.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.17-30170G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69475610 | |||||||
| chr17:69475637 | A | G | 1 | a0001c0001t0005g0207 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.17-30143A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69475637 | |||||||
| chr17:69475896 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.17-29884G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69475896 | |||||||
| chr17:69476089 | A | G | 1 | a0001c0001t0007g0114 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.17-29691A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69476089 | |||||||
| chr17:69476124 | G | A | 1 | a0001c0001t0065g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.17-29656G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69476124 | |||||||
| chr17:69476143 | T | A | 1 | a0001c0002t0064g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.17-29637T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69476143 | |||||||
| chr17:69476496 | T | G | 1 | a0001c0001t0011g0019 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.17-29284T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69476496 | |||||||
| chr17:69476544 | C | T | 1 | a0001c0001t0013g0137 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.17-29236C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69476544 | |||||||
| chr17:69476752 | C | G | 1 | a0001c0001t0008g0075 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.17-29028C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69476752 | |||||||
| chr17:69476771 | T | C | 242 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0043 others(239): Show |
242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.17-29009T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69476771 | |||||||
| chr17:69476772 | G | A | 3 | a0001c0001t0001g0201 a0001c0001t0004g0050 a0001c0001t0006g0080 |
3 | HG01243.hp2 HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.17-29008G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69476772 | |||||||
| chr17:69476872 | A | G | 203 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0043 others(200): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.17-28908A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69476872 | |||||||
| chr17:69476942 | G | T | 1 | a0001c0002t0062g0060 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.17-28838G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69476942 | |||||||
| chr17:69477141 | A | G | 92 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0112 others(89): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.17-28639A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69477141 | |||||||
| chr17:69477229 | G | A | 4 | a0001c0001t0010g0200 a0001c0001t0028g0072 a0001c0001t0028g0096 others(1): Show |
4 | HG02258.hp1 HG02258.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-28551G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69477229 | |||||||
| chr17:69477395 | G | C | 4 | a0001c0001t0010g0016 a0001c0001t0058g0067 a0001c0001t0061g0073 others(1): Show |
4 | HG01884.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-28385G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69477395 | |||||||
| chr17:69477621 | C | G | 1 | a0001c0001t0065g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.17-28159C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69477621 | |||||||
| chr17:69477870 | A | G | 102 | a0001c0001t0001g0043 a0001c0001t0001g0079 a0001c0001t0001g0098 others(99): Show |
102 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.17-27910A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69477870 | |||||||
| chr17:69478042 | G | A | 2 | a0001c0001t0010g0200 a0001c0002t0063g0078 |
2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.17-27738G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69478042 | |||||||
| chr17:69478057 | T | C | 72 | a0001c0001t0001g0031 a0001c0001t0001g0084 a0001c0001t0001g0089 others(69): Show |
72 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.17-27723T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69478057 | |||||||
| chr17:69478265 | A | G | 1 | a0001c0001t0028g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.17-27515A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69478265 | |||||||
| chr17:69478395 | G | T | 41 | a0001c0001t0001g0089 a0001c0001t0001g0138 a0001c0001t0001g0145 others(38): Show |
41 | HG00323.hp2 HG00639.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.17-27385G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69478395 | |||||||
| chr17:69478644 | C | T | 1 | a0001c0002t0004g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.17-27136C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69478644 | |||||||
| chr17:69478854 | C | A | 1 | a0001c0001t0010g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.17-26926C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69478854 | |||||||
| chr17:69479040 | T | C | 1 | a0001c0001t0004g0166 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.17-26740T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69479040 | |||||||
| chr17:69479226 | A | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0141 |
3 | HG00323.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.17-26554A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69479226 | |||||||
| chr17:69479287 | T | C | 2 | a0001c0002t0002g0173 a0001c0002t0002g0176 |
2 | HG02602.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.17-26493T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69479287 | |||||||
| chr17:69479719 | CT | C | 21 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0141 others(18): Show |
21 | HG00323.hp2 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.17-26045delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69479719 | ||||||
| chr17:69479719 | CTT | C | 18 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(15): Show |
18 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-26046_17-26045d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69479719 | ||||||
| chr17:69480146 | C | A | 1 | a0001c0002t0004g0053 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.17-25634C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69480146 | |||||||
| chr17:69480209 | G | A | 1 | a0001c0001t0002g0008 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.17-25571G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69480209 | |||||||
| chr17:69480228 | T | C | 2 | a0001c0001t0010g0200 a0001c0002t0063g0078 |
2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.17-25552T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69480228 | |||||||
| chr17:69480276 | C | T | 1 | a0001c0002t0003g0239 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.17-25504C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69480276 | |||||||
| chr17:69480328 | C | T | 1 | a0001c0001t0035g0217 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.17-25452C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69480328 | |||||||
| chr17:69480329 | G | A | 31 | a0001c0001t0001g0084 a0001c0001t0002g0006 a0001c0001t0002g0007 others(28): Show |
31 | HG00323.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.17-25451G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69480329 | |||||||
| chr17:69480433 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0002g0106 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.17-25347G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69480433 | |||||||
| chr17:69480458 | A | G | 1 | a0001c0002t0064g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.17-25322A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69480458 | |||||||
| chr17:69480514 | G | C | 2 | a0001c0001t0028g0072 a0001c0001t0028g0096 |
2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.17-25266G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69480514 | |||||||
| chr17:69480672 | A | C | 28 | a0001c0001t0001g0089 a0001c0001t0001g0138 a0001c0001t0001g0145 others(25): Show |
28 | HG00639.hp2 HG01074.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.17-25108A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69480672 | |||||||
| chr17:69480788 | A | T | 152 | a0001c0001t0001g0043 a0001c0001t0001g0079 a0001c0001t0001g0089 others(149): Show |
152 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.17-24992A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69480788 | |||||||
| chr17:69480818 | A | G | 4 | a0001c0001t0007g0114 a0001c0001t0008g0061 a0001c0001t0065g0149 others(1): Show |
4 | HG02647.hp1 HG02717.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-24962A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69480818 | |||||||
| chr17:69480870 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.17-24910A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69480870 | |||||||
| chr17:69480927 | TAG | T | 154 | a0001c0001t0001g0043 a0001c0001t0001g0079 a0001c0001t0001g0089 others(151): Show |
154 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.17-24851_17-24850d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69480927 | ||||||
| chr17:69480930 | A | C | 154 | a0001c0001t0001g0043 a0001c0001t0001g0079 a0001c0001t0001g0089 others(151): Show |
154 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.17-24850A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69480930 | |||||||
| chr17:69480934 | A | AC | 154 | a0001c0001t0001g0043 a0001c0001t0001g0079 a0001c0001t0001g0089 others(151): Show |
154 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.17-24846_17-24845i others(3): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69480934 | |||||||
| chr17:69480935 | A | C | 154 | a0001c0001t0001g0043 a0001c0001t0001g0079 a0001c0001t0001g0089 others(151): Show |
154 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.17-24845A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69480935 | |||||||
| chr17:69480966 | G | T | 148 | a0001c0001t0001g0043 a0001c0001t0001g0079 a0001c0001t0001g0089 others(145): Show |
148 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.17-24814G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69480966 | |||||||
| chr17:69481144 | G | A | 2 | a0001c0001t0007g0114 a0001c0002t0064g0199 |
2 | HG02647.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.17-24636G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69481144 | |||||||
| chr17:69481207 | C | T | 3 | a0001c0002t0004g0213 a0001c0002t0057g0214 a0001c0002t0066g0225 |
3 | HG02486.hp1 HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.17-24573C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69481207 | |||||||
| chr17:69481424 | C | A | 1 | a0001c0001t0035g0217 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.17-24356C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69481424 | |||||||
| chr17:69481475 | G | A | 23 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0141 others(20): Show |
23 | HG00323.hp2 HG01257.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.17-24305G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69481475 | |||||||
| chr17:69481493 | G | A | 2 | a0001c0001t0002g0006 a0001c0001t0002g0007 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.17-24287G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69481493 | |||||||
| chr17:69481599 | G | C | 1 | a0001c0001t0055g0169 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.17-24181G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69481599 | |||||||
| chr17:69481742 | A | G | 18 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(15): Show |
18 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-24038A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69481742 | |||||||
| chr17:69481884 | C | T | 18 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(15): Show |
18 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-23896C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69481884 | |||||||
| chr17:69481895 | A | G | 10 | a0001c0001t0005g0001 a0001c0001t0007g0114 a0001c0001t0008g0104 others(7): Show |
10 | HG01884.hp2 HG02559.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.17-23885A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69481895 | |||||||
| chr17:69482010 | C | T | 1 | a0001c0002t0066g0225 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.17-23770C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69482010 | |||||||
| chr17:69482315 | A | G | 2 | a0001c0001t0010g0200 a0001c0002t0063g0078 |
2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.17-23465A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69482315 | |||||||
| chr17:69482431 | C | T | 1 | a0001c0002t0006g0045 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.17-23349C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69482431 | |||||||
| chr17:69482695 | TA | T | 148 | a0001c0001t0001g0043 a0001c0001t0001g0079 a0001c0001t0001g0089 others(145): Show |
148 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.17-23083delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69482695 | ||||||
| chr17:69483142 | G | A | 3 | a0001c0001t0010g0016 a0001c0001t0061g0073 a0001c0002t0007g0202 |
3 | HG02965.hp1 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.17-22638G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69483142 | |||||||
| chr17:69483151 | T | TGATCTCT others(20): Show |
1 | a0001c0002t0001g0018 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.17-22610_17-22584d others(29): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69483151 | ||||||
| chr17:69483254 | G | A | 4 | a0001c0001t0001g0178 a0001c0001t0001g0247 a0001c0001t0001g0253 others(1): Show |
4 | NA18945.hp2 NA18960.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-22526G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69483254 | |||||||
| chr17:69483256 | G | T | 4 | a0001c0001t0001g0178 a0001c0001t0001g0247 a0001c0001t0001g0253 others(1): Show |
4 | NA18945.hp2 NA18960.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-22524G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69483256 | |||||||
| chr17:69483473 | C | T | 2 | a0001c0002t0005g0164 a0001c0002t0005g0175 |
2 | HG02602.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.17-22307C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69483473 | |||||||
| chr17:69483612 | A | G | 1 | a0001c0001t0040g0009 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.17-22168A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69483612 | |||||||
| chr17:69483671 | A | G | 1 | a0001c0001t0002g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.17-22109A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69483671 | |||||||
| chr17:69483736 | G | C | 1 | a0001c0001t0065g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.17-22044G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69483736 | |||||||
| chr17:69483998 | A | G | 2 | a0001c0001t0010g0200 a0001c0002t0063g0078 |
2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.17-21782A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69483998 | |||||||
| chr17:69484066 | G | A | 2 | a0001c0001t0002g0204 a0001c0001t0020g0071 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.17-21714G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69484066 | |||||||
| chr17:69484460 | C | G | 2 | a0001c0001t0010g0200 a0001c0002t0063g0078 |
2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.17-21320C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69484460 | |||||||
| chr17:69484554 | A | T | 18 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(15): Show |
18 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-21226A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69484554 | |||||||
| chr17:69484684 | A | G | 1 | a0001c0001t0007g0114 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.17-21096A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69484684 | |||||||
| chr17:69484712 | G | A | 23 | a0001c0001t0001g0135 a0001c0001t0001g0158 a0001c0001t0001g0162 others(20): Show |
23 | HG01074.hp1 HG01169.hp1 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.17-21068G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69484712 | |||||||
| chr17:69484748 | G | A | 2 | a0001c0001t0008g0061 a0001c0002t0002g0026 |
2 | HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.17-21032G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69484748 | |||||||
| chr17:69484850 | A | G | 28 | a0001c0001t0001g0089 a0001c0001t0001g0138 a0001c0001t0001g0145 others(25): Show |
28 | HG00639.hp2 HG01074.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.17-20930A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69484850 | |||||||
| chr17:69485060 | T | A | 6 | a0001c0001t0003g0069 a0001c0002t0002g0077 a0001c0002t0004g0213 others(3): Show |
6 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.17-20720T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69485060 | |||||||
| chr17:69485091 | G | A | 98 | a0001c0001t0001g0043 a0001c0001t0001g0079 a0001c0001t0001g0098 others(95): Show |
98 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.17-20689G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69485091 | |||||||
| chr17:69485100 | A | G | 6 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.17-20680A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69485100 | |||||||
| chr17:69485153 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.17-20627C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69485153 | |||||||
| chr17:69485342 | G | A | 1 | a0001c0001t0035g0217 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.17-20438G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69485342 | |||||||
| chr17:69485414 | G | T | 2 | a0001c0001t0006g0133 a0001c0001t0018g0132 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.17-20366G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69485414 | |||||||
| chr17:69485432 | C | G | 3 | a0001c0001t0028g0072 a0001c0001t0028g0096 a0001c0002t0064g0199 |
3 | HG02258.hp2 HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.17-20348C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69485432 | |||||||
| chr17:69485772 | C | G | 12 | a0001c0001t0002g0010 a0001c0001t0006g0023 a0001c0001t0006g0033 others(9): Show |
12 | HG00639.hp1 HG01346.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.17-20008C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69485772 | |||||||
| chr17:69485813 | C | A | 49 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(46): Show |
49 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.17-19967C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69485813 | |||||||
| chr17:69485843 | T | C | 46 | a0001c0001t0001g0089 a0001c0001t0001g0145 a0001c0001t0001g0193 others(43): Show |
46 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.17-19937T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69485843 | |||||||
| chr17:69485979 | C | CT | 28 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0010 others(25): Show |
28 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.17-19793dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69485979 | ||||||
| chr17:69486124 | A | C | 3 | a0001c0001t0058g0067 a0001c0001t0061g0073 a0001c0002t0007g0202 |
3 | HG01884.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.17-19656A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69486124 | |||||||
| chr17:69486145 | A | AG | 8 | a0001c0001t0006g0110 a0001c0001t0006g0129 a0001c0001t0006g0130 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.17-19634dupG | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69486145 | ||||||
| chr17:69486173 | C | A | 172 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0098 others(169): Show |
172 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.17-19607C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69486173 | |||||||
| chr17:69486212 | G | A | 175 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0098 others(172): Show |
175 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.17-19568G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69486212 | |||||||
| chr17:69486424 | T | C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0171 a0001c0002t0001g0255 |
3 | HG02056.hp1 NA18956.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.17-19356T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69486424 | |||||||
| chr17:69486609 | C | T | 157 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0112 others(154): Show |
157 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.17-19171C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69486609 | |||||||
| chr17:69486774 | AG | A | 24 | a0001c0001t0001g0084 a0001c0001t0002g0006 a0001c0001t0002g0007 others(21): Show |
24 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.17-19002delG | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69486774 | ||||||
| chr17:69486902 | C | T | 5 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.17-18878C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69486902 | |||||||
| chr17:69487030 | T | A | 7 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.17-18750T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69487030 | |||||||
| chr17:69487083 | G | A | 2 | a0001c0001t0030g0046 a0001c0002t0002g0077 |
2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.17-18697G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69487083 | |||||||
| chr17:69487135 | C | T | 1 | a0001c0001t0028g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.17-18645C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69487135 | |||||||
| chr17:69487501 | T | C | 28 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(25): Show |
28 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.17-18279T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69487501 | |||||||
| chr17:69487514 | G | A | 3 | a0001c0001t0008g0075 a0001c0002t0002g0026 a0001c0002t0062g0060 |
3 | HG01099.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.17-18266G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69487514 | |||||||
| chr17:69487515 | C | T | 3 | a0001c0001t0028g0072 a0001c0001t0028g0096 a0001c0002t0064g0199 |
3 | HG02258.hp2 HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.17-18265C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69487515 | |||||||
| chr17:69487657 | C | T | 2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.17-18123C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69487657 | |||||||
| chr17:69487755 | T | C | 3 | a0001c0001t0005g0108 a0001c0001t0027g0020 a0001c0001t0027g0021 |
3 | HG01123.hp2 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.17-18025T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69487755 | |||||||
| chr17:69487878 | A | C | 4 | a0001c0002t0001g0086 a0001c0002t0001g0260 a0001c0002t0023g0088 others(1): Show |
4 | HG00738.hp1 HG01109.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-17902A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69487878 | |||||||
| chr17:69488116 | C | A | 1 | a0001c0001t0018g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.17-17664C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69488116 | |||||||
| chr17:69488127 | A | T | 3 | a0001c0001t0001g0145 a0001c0001t0002g0063 a0001c0001t0013g0137 |
3 | HG01069.hp2 HG01346.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.17-17653A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69488127 | |||||||
| chr17:69488179 | A | G | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.17-17601A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69488179 | |||||||
| chr17:69488416 | G | A | 3 | a0001c0001t0008g0075 a0001c0002t0002g0026 a0001c0002t0062g0060 |
3 | HG01099.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.17-17364G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69488416 | |||||||
| chr17:69488487 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.17-17293A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69488487 | |||||||
| chr17:69488571 | C | T | 5 | a0001c0001t0008g0061 a0001c0002t0004g0203 a0001c0002t0006g0045 others(2): Show |
5 | HG01346.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-17209C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69488571 | |||||||
| chr17:69488592 | A | G | 149 | a0001c0001t0001g0089 a0001c0001t0001g0119 a0001c0001t0001g0148 others(146): Show |
149 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.17-17188A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69488592 | |||||||
| chr17:69488788 | G | A | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-16992G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69488788 | |||||||
| chr17:69488883 | C | G | 2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.17-16897C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69488883 | |||||||
| chr17:69489119 | C | G | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-16661C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69489119 | |||||||
| chr17:69489220 | C | CA | 11 | a0001c0001t0001g0031 a0001c0001t0001g0084 a0001c0001t0011g0013 others(8): Show |
11 | HG01106.hp1 HG01258.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.17-16541dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69489220 | ||||||
| chr17:69489220 | CA | C | 9 | a0001c0001t0006g0133 a0001c0001t0007g0044 a0001c0001t0018g0132 others(6): Show |
9 | HG02280.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.17-16541delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69489220 | ||||||
| chr17:69489239 | A | AG | 5 | a0001c0001t0008g0061 a0001c0002t0004g0203 a0001c0002t0006g0045 others(2): Show |
5 | HG01346.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-16539dupG | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69489239 | ||||||
| chr17:69489239 | A | G | 19 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(16): Show |
19 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.17-16541A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69489239 | |||||||
| chr17:69489292 | A | G | 1 | a0001c0001t0008g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.17-16488A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69489292 | |||||||
| chr17:69489326 | C | T | 2 | a0001c0001t0065g0149 a0001c0002t0057g0214 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.17-16454C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69489326 | |||||||
| chr17:69489415 | G | A | 3 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0002t0063g0078 |
3 | HG02280.hp1 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.17-16365G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69489415 | |||||||
| chr17:69489800 | T | C | 2 | a0001c0001t0028g0072 a0001c0001t0028g0096 |
2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.17-15980T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69489800 | |||||||
| chr17:69489877 | A | C | 1 | a0001c0002t0004g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.17-15903A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69489877 | |||||||
| chr17:69489898 | T | G | 2 | a0001c0001t0004g0050 a0001c0001t0010g0016 |
2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.17-15882T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69489898 | |||||||
| chr17:69489913 | G | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0243 a0001c0001t0002g0180 |
3 | NA18945.hp2 NA18978.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.17-15867G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69489913 | |||||||
| chr17:69490010 | G | A | 8 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-15770G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69490010 | |||||||
| chr17:69490079 | G | A | 3 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0002t0063g0078 |
3 | HG02280.hp1 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.17-15701G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69490079 | |||||||
| chr17:69490080 | C | T | 122 | a0001c0001t0001g0089 a0001c0001t0001g0156 a0001c0001t0001g0178 others(119): Show |
122 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.17-15700C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69490080 | |||||||
| chr17:69490110 | T | C | 162 | a0001c0001t0001g0089 a0001c0001t0001g0119 a0001c0001t0001g0148 others(159): Show |
162 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.17-15670T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69490110 | |||||||
| chr17:69490248 | TGCTCCAC others(6): Show |
T | 2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.17-15529_17-15517d others(15): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69490248 | ||||||
| chr17:69490292 | T | A | 23 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(20): Show |
23 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.17-15488T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69490292 | |||||||
| chr17:69490343 | A | G | 2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.17-15437A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69490343 | |||||||
| chr17:69490596 | T | C | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-15184T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69490596 | |||||||
| chr17:69490687 | A | G | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-15093A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69490687 | |||||||
| chr17:69490789 | A | G | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-14991A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69490789 | |||||||
| chr17:69490805 | A | G | 1 | a0001c0002t0001g0018 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.17-14975A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69490805 | |||||||
| chr17:69490868 | C | T | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-14912C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69490868 | |||||||
| chr17:69490869 | C | G | 4 | a0001c0002t0001g0144 a0001c0002t0003g0123 a0001c0002t0003g0139 others(1): Show |
4 | NA18975.hp1 NA19002.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-14911C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69490869 | |||||||
| chr17:69491078 | T | G | 3 | a0001c0001t0065g0149 a0001c0002t0002g0026 a0001c0002t0057g0214 |
3 | HG02622.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.17-14702T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491078 | |||||||
| chr17:69491108 | T | TTTCC | 4 | a0001c0001t0002g0008 a0001c0001t0005g0032 a0001c0001t0008g0104 others(1): Show |
4 | HG00140.hp2 HG00738.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-14649_17-14646d others(6): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491108 | ||||||
| chr17:69491108 | T | TTTCCTTC others(5): Show |
2 | a0001c0001t0028g0072 a0001c0002t0064g0199 |
2 | HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.17-14657_17-14646d others(14): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491108 | ||||||
| chr17:69491108 | T | TTTCCTTC others(33): Show |
1 | a0001c0001t0008g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.17-14661_17-14660i others(42): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491108 | ||||||
| chr17:69491108 | T | TTTCCTTC others(41): Show |
6 | a0001c0001t0002g0047 a0001c0002t0004g0203 a0001c0002t0006g0045 others(3): Show |
6 | HG01346.hp2 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.17-14661_17-14660i others(50): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491108 | ||||||
| chr17:69491108 | T | TTTCCTTC others(45): Show |
5 | a0001c0001t0001g0119 a0001c0001t0003g0226 a0001c0001t0004g0050 others(2): Show |
5 | HG01243.hp2 HG02965.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-14661_17-14660i others(54): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491108 | ||||||
| chr17:69491108 | T | TTTCCTTC others(49): Show |
7 | a0001c0001t0001g0148 a0001c0001t0001g0181 a0001c0001t0003g0069 others(4): Show |
7 | HG00408.hp2 HG02109.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.17-14661_17-14660i others(58): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491108 | ||||||
| chr17:69491108 | T | TTTCCTTC others(53): Show |
4 | a0001c0001t0001g0211 a0001c0001t0001g0257 a0001c0001t0004g0228 others(1): Show |
4 | HG00438.hp2 HG03688.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-14661_17-14660i others(62): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491108 | ||||||
| chr17:69491108 | T | TTTCCTTC others(61): Show |
1 | a0001c0001t0001g0159 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.17-14661_17-14660i others(70): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491108 | ||||||
| chr17:69491120 | C | T | 3 | a0001c0001t0065g0149 a0001c0002t0002g0026 a0001c0002t0057g0214 |
3 | HG02622.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.17-14660C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491120 | |||||||
| chr17:69491123 | C | T | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-14657C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491123 | |||||||
| chr17:69491182 | C | T | 1 | a0001c0001t0008g0049 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.17-14598C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491182 | |||||||
| chr17:69491246 | C | A | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-14534C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491246 | |||||||
| chr17:69491290 | C | T | 2 | a0001c0001t0026g0191 a0001c0001t0026g0192 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.17-14490C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491290 | |||||||
| chr17:69491304 | C | T | 1 | a0001c0002t0003g0249 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.17-14476C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491304 | |||||||
| chr17:69491305 | G | A | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-14475G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491305 | |||||||
| chr17:69491390 | C | T | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-14390C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491390 | |||||||
| chr17:69491407 | G | A | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-14373G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491407 | |||||||
| chr17:69491582 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.17-14198C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491582 | |||||||
| chr17:69491668 | G | A | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-14112G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491668 | |||||||
| chr17:69491678 | C | T | 1 | a0001c0001t0016g0074 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.17-14102C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491678 | |||||||
| chr17:69491730 | G | GTTA | 9 | a0001c0001t0006g0023 a0001c0001t0006g0033 a0001c0001t0028g0072 others(6): Show |
9 | HG02257.hp2 HG02258.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.17-14026_17-14024d others(5): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491730 | ||||||
| chr17:69491730 | G | GTTATTA | 110 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0187 others(107): Show |
110 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.17-14029_17-14024d others(8): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491730 | ||||||
| chr17:69491730 | G | GTTATTAT others(2): Show |
87 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0043 others(84): Show |
87 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.17-14032_17-14024d others(11): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491730 | ||||||
| chr17:69491730 | G | GTTATTAT others(5): Show |
14 | a0001c0001t0001g0212 a0001c0001t0001g0222 a0001c0001t0008g0075 others(11): Show |
14 | HG00621.hp2 HG01099.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.17-14035_17-14024d others(14): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491730 | ||||||
| chr17:69491730 | G | GTTATTAT others(8): Show |
13 | a0001c0001t0001g0079 a0001c0001t0001g0112 a0001c0001t0001g0138 others(10): Show |
13 | HG00323.hp1 HG02109.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.17-14038_17-14024d others(17): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491730 | ||||||
| chr17:69491730 | G | GTTATTAT others(11): Show |
2 | a0001c0001t0004g0050 a0001c0001t0010g0016 |
2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.17-14041_17-14024d others(20): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491730 | ||||||
| chr17:69491730 | G | GTTATTAT others(14): Show |
16 | a0001c0001t0001g0119 a0001c0001t0001g0181 a0001c0001t0001g0211 others(13): Show |
16 | HG00408.hp2 HG00438.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.17-14044_17-14024d others(23): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491730 | ||||||
| chr17:69491730 | G | GTTATTAT others(17): Show |
4 | a0001c0001t0001g0159 a0001c0001t0008g0061 a0001c0001t0060g0224 others(1): Show |
4 | HG01346.hp2 HG02717.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-14047_17-14024d others(26): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491730 | ||||||
| chr17:69491730 | G | GTTATTAT others(20): Show |
1 | a0001c0001t0001g0148 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.17-14024_17-14023i others(29): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491730 | ||||||
| chr17:69491773 | A | C | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-14007A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491773 | |||||||
| chr17:69491779 | A | AGACTGGT others(37): Show |
1 | a0001c0002t0001g0163 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.17-13958_17-13957i others(46): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69491779 | ||||||
| chr17:69491823 | A | G | 168 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0119 others(165): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.17-13957A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491823 | |||||||
| chr17:69491845 | C | T | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-13935C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491845 | |||||||
| chr17:69491866 | C | T | 1 | a0001c0001t0004g0050 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.17-13914C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491866 | |||||||
| chr17:69491916 | G | A | 8 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-13864G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491916 | |||||||
| chr17:69491944 | T | C | 167 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0119 others(164): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.17-13836T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491944 | |||||||
| chr17:69491945 | G | A | 2 | a0001c0002t0003g0237 a0001c0002t0045g0152 |
2 | HG00609.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.17-13835G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69491945 | |||||||
| chr17:69492095 | G | A | 1 | a0001c0002t0004g0053 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.17-13685G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69492095 | |||||||
| chr17:69492559 | A | G | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-13221A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69492559 | |||||||
| chr17:69492697 | G | C | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-13083G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69492697 | |||||||
| chr17:69492777 | ATCT | A | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-12999_17-12997d others(5): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69492777 | ||||||
| chr17:69492892 | A | G | 120 | a0001c0001t0001g0089 a0001c0001t0001g0187 a0001c0001t0001g0193 others(117): Show |
120 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.17-12888A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69492892 | |||||||
| chr17:69492985 | AT | A | 25 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(22): Show |
25 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.17-12786delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69492985 | ||||||
| chr17:69493101 | A | G | 1 | a0001c0002t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.17-12679A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69493101 | |||||||
| chr17:69493300 | T | C | 1 | a0001c0002t0003g0239 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.17-12480T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69493300 | |||||||
| chr17:69493307 | T | TTG | 8 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-12453_17-12452d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69493307 | ||||||
| chr17:69493307 | T | TTGTG | 144 | a0001c0001t0001g0089 a0001c0001t0001g0119 a0001c0001t0001g0148 others(141): Show |
144 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.17-12455_17-12452d others(6): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69493307 | ||||||
| chr17:69493307 | T | TTGTGTG | 3 | a0001c0001t0001g0257 a0001c0001t0002g0047 a0001c0001t0048g0231 |
3 | HG01891.hp2 NA18968.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.17-12457_17-12452d others(8): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69493307 | ||||||
| chr17:69493351 | G | T | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.17-12429G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69493351 | |||||||
| chr17:69493401 | C | T | 122 | a0001c0001t0001g0089 a0001c0001t0001g0187 a0001c0001t0001g0193 others(119): Show |
122 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.17-12379C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69493401 | |||||||
| chr17:69493432 | A | C | 3 | a0001c0001t0001g0187 a0001c0001t0003g0185 a0001c0001t0036g0126 |
3 | HG01952.hp1 HG01975.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.17-12348A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69493432 | |||||||
| chr17:69493487 | G | A | 16 | a0001c0001t0001g0122 a0001c0001t0001g0156 a0001c0001t0001g0158 others(13): Show |
16 | HG00558.hp1 HG01074.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.17-12293G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69493487 | |||||||
| chr17:69493504 | T | A | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.17-12276T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69493504 | |||||||
| chr17:69493634 | G | A | 3 | a0001c0001t0008g0075 a0001c0002t0002g0026 a0001c0002t0062g0060 |
3 | HG01099.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.17-12146G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69493634 | |||||||
| chr17:69493691 | A | G | 169 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0119 others(166): Show |
169 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.17-12089A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69493691 | |||||||
| chr17:69493778 | A | T | 23 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(20): Show |
23 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.17-12002A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69493778 | |||||||
| chr17:69493780 | A | AAT | 120 | a0001c0001t0001g0089 a0001c0001t0001g0187 a0001c0001t0001g0193 others(117): Show |
120 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.17-11995_17-11994d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69493780 | ||||||
| chr17:69493780 | A | ATAT | 15 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(12): Show |
15 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.17-12000_17-11999i others(5): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69493780 | |||||||
| chr17:69493780 | A | T | 34 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0001g0148 others(31): Show |
34 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.17-12000A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69493780 | |||||||
| chr17:69493803 | T | A | 5 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0001t0030g0046 others(2): Show |
5 | HG02280.hp1 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.17-11977T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69493803 | |||||||
| chr17:69493997 | G | A | 1 | a0001c0001t0043g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.17-11783G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69493997 | |||||||
| chr17:69494089 | C | T | 168 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0119 others(165): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.17-11691C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69494089 | |||||||
| chr17:69494203 | AG | A | 3 | a0001c0001t0008g0075 a0001c0002t0002g0026 a0001c0002t0062g0060 |
3 | HG01099.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.17-11576delG | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69494203 | |||||||
| chr17:69494498 | T | TA | 12 | a0001c0001t0002g0106 a0001c0001t0003g0069 a0001c0001t0006g0133 others(9): Show |
12 | HG01099.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.17-11271dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69494498 | ||||||
| chr17:69494710 | C | T | 1 | a0001c0002t0032g0054 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.17-11070C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69494710 | |||||||
| chr17:69494832 | C | G | 8 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0001t0028g0072 others(5): Show |
8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-10948C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69494832 | |||||||
| chr17:69494871 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.17-10909G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69494871 | |||||||
| chr17:69494891 | G | C | 10 | a0001c0001t0001g0187 a0001c0001t0003g0058 a0001c0001t0003g0185 others(7): Show |
10 | HG00423.hp1 HG01952.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.17-10889G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69494891 | |||||||
| chr17:69494939 | A | C | 3 | a0001c0001t0008g0075 a0001c0002t0002g0026 a0001c0002t0062g0060 |
3 | HG01099.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.17-10841A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69494939 | |||||||
| chr17:69494954 | G | A | 3 | a0001c0001t0028g0072 a0001c0001t0028g0096 a0001c0002t0064g0199 |
3 | HG02258.hp2 HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.17-10826G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69494954 | |||||||
| chr17:69494960 | G | A | 8 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0001t0028g0072 others(5): Show |
8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-10820G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69494960 | |||||||
| chr17:69494963 | A | C | 8 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0001t0028g0072 others(5): Show |
8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-10817A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69494963 | |||||||
| chr17:69494993 | G | A | 2 | a0001c0001t0065g0149 a0001c0002t0057g0214 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.17-10787G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69494993 | |||||||
| chr17:69495006 | GA | G | 8 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0001t0028g0072 others(5): Show |
8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-10766delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69495006 | ||||||
| chr17:69495098 | T | TA | 6 | a0001c0001t0001g0089 a0001c0001t0001g0229 a0001c0001t0002g0180 others(3): Show |
6 | HG01099.hp1 HG02572.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.17-10665dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69495098 | ||||||
| chr17:69495098 | TA | T | 144 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0001g0148 others(141): Show |
144 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.17-10665delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69495098 | ||||||
| chr17:69495098 | TAA | T | 5 | a0001c0001t0002g0047 a0001c0001t0003g0069 a0001c0001t0065g0149 others(2): Show |
5 | HG01168.hp1 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.17-10666_17-10665d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69495098 | ||||||
| chr17:69495098 | TAAAA | T | 6 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0001t0030g0046 others(3): Show |
6 | HG02280.hp1 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.17-10668_17-10665d others(6): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69495098 | ||||||
| chr17:69495111 | A | C | 2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.17-10669A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69495111 | |||||||
| chr17:69495113 | A | C | 2 | a0001c0001t0043g0117 a0001c0002t0050g0087 |
2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.17-10667A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69495113 | |||||||
| chr17:69495130 | C | T | 7 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.17-10650C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69495130 | |||||||
| chr17:69495139 | G | A | 8 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0001t0028g0072 others(5): Show |
8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-10641G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69495139 | |||||||
| chr17:69495217 | A | C | 8 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0001t0028g0072 others(5): Show |
8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-10563A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69495217 | |||||||
| chr17:69495245 | AT | A | 17 | a0001c0001t0001g0201 a0001c0001t0005g0001 a0001c0001t0006g0080 others(14): Show |
17 | HG01071.hp1 HG01106.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.17-10525delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69495245 | ||||||
| chr17:69495249 | T | A | 8 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(5): Show |
8 | HG00558.hp2 HG01884.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.17-10531T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69495249 | |||||||
| chr17:69495257 | A | C | 3 | a0001c0001t0028g0072 a0001c0001t0028g0096 a0001c0002t0064g0199 |
3 | HG02258.hp2 HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.17-10523A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69495257 | |||||||
| chr17:69495293 | C | T | 8 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0001t0028g0072 others(5): Show |
8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-10487C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69495293 | |||||||
| chr17:69495344 | C | T | 8 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0001t0028g0072 others(5): Show |
8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-10436C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69495344 | |||||||
| chr17:69495471 | G | C | 2 | a0001c0001t0001g0247 a0001c0001t0047g0177 |
2 | NA18983.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.17-10309G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69495471 | |||||||
| chr17:69495726 | C | G | 1 | a0001c0001t0065g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.17-10054C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69495726 | |||||||
| chr17:69495729 | T | TA | 24 | a0001c0001t0001g0084 a0001c0001t0002g0006 a0001c0001t0002g0007 others(21): Show |
24 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-10041dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69495729 | ||||||
| chr17:69495729 | T | TAA | 7 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0001t0028g0072 others(4): Show |
7 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.17-10042_17-10041d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69495729 | ||||||
| chr17:69495791 | G | A | 5 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0001t0030g0046 others(2): Show |
5 | HG02280.hp1 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.17-9989G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69495791 | |||||||
| chr17:69495805 | A | G | 3 | a0001c0001t0008g0075 a0001c0002t0002g0026 a0001c0002t0062g0060 |
3 | HG01099.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.17-9975A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69495805 | |||||||
| chr17:69495929 | G | C | 23 | a0001c0001t0001g0084 a0001c0001t0002g0006 a0001c0001t0002g0007 others(20): Show |
23 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.17-9851G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69495929 | |||||||
| chr17:69496080 | A | AT | 4 | a0001c0001t0003g0069 a0001c0001t0008g0075 a0001c0002t0002g0026 others(1): Show |
4 | HG01099.hp1 HG02109.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-9700_17-9699ins others(1): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69496080 | |||||||
| chr17:69496080 | A | ATTT | 6 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0001t0028g0072 others(3): Show |
6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.17-9700_17-9699ins others(3): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69496080 | |||||||
| chr17:69496081 | C | T | 12 | a0001c0001t0003g0069 a0001c0001t0006g0133 a0001c0001t0008g0075 others(9): Show |
12 | HG01099.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.17-9699C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69496081 | |||||||
| chr17:69496100 | A | G | 2 | a0001c0002t0001g0182 a0001c0002t0001g0183 |
2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.17-9680A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69496100 | |||||||
| chr17:69496173 | G | A | 8 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0001t0028g0072 others(5): Show |
8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-9607G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69496173 | |||||||
| chr17:69496229 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.17-9551A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69496229 | |||||||
| chr17:69496232 | G | A | 1 | a0001c0001t0002g0254 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.17-9548G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69496232 | |||||||
| chr17:69496261 | G | A | 21 | a0001c0001t0001g0084 a0001c0001t0002g0006 a0001c0001t0002g0007 others(18): Show |
21 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.17-9519G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69496261 | |||||||
| chr17:69496274 | C | CT | 128 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0001g0148 others(125): Show |
128 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.17-9491dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69496274 | ||||||
| chr17:69496274 | C | CTT | 27 | a0001c0001t0001g0220 a0001c0001t0003g0069 a0001c0001t0006g0133 others(24): Show |
27 | HG00408.hp1 HG00609.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.17-9492_17-9491dup others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69496274 | ||||||
| chr17:69496601 | T | C | 1 | a0001c0002t0008g0081 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.17-9179T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69496601 | |||||||
| chr17:69496745 | C | G | 1 | a0001c0002t0002g0035 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.17-9035C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69496745 | |||||||
| chr17:69496806 | C | T | 3 | a0001c0001t0028g0072 a0001c0001t0028g0096 a0001c0002t0064g0199 |
3 | HG02258.hp2 HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.17-8974C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69496806 | |||||||
| chr17:69496816 | G | T | 1 | a0001c0001t0002g0106 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.17-8964G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69496816 | |||||||
| chr17:69496942 | T | C | 134 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0001g0220 others(131): Show |
134 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.17-8838T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69496942 | |||||||
| chr17:69496953 | T | C | 135 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0001g0220 others(132): Show |
135 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.17-8827T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69496953 | |||||||
| chr17:69497134 | T | C | 2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.17-8646T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69497134 | |||||||
| chr17:69497240 | C | T | 3 | a0001c0001t0028g0072 a0001c0001t0028g0096 a0001c0002t0064g0199 |
3 | HG02258.hp2 HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.17-8540C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69497240 | |||||||
| chr17:69497524 | C | CT | 119 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0001g0220 others(116): Show |
119 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.17-8245dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69497524 | ||||||
| chr17:69497524 | C | CTT | 46 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0001g0148 others(43): Show |
46 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.17-8246_17-8245dup others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69497524 | ||||||
| chr17:69497553 | C | T | 106 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0001g0220 others(103): Show |
106 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.17-8227C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69497553 | |||||||
| chr17:69497620 | G | T | 18 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(15): Show |
18 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-8160G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69497620 | |||||||
| chr17:69497844 | A | C | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.17-7936A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69497844 | |||||||
| chr17:69497889 | G | T | 3 | a0001c0001t0008g0075 a0001c0002t0002g0026 a0001c0002t0062g0060 |
3 | HG01099.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.17-7891G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69497889 | |||||||
| chr17:69498001 | TGCTTGTA others(19): Show |
T | 110 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0001g0220 others(107): Show |
110 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.17-7775_17-7750del others(26): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69498001 | ||||||
| chr17:69498027 | C | T | 46 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0001g0148 others(43): Show |
46 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.17-7753C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69498027 | |||||||
| chr17:69498223 | G | A | 4 | a0001c0001t0002g0204 a0001c0001t0020g0071 a0001c0001t0034g0027 others(1): Show |
4 | HG01517.hp1 HG01884.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-7557G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69498223 | |||||||
| chr17:69498284 | A | G | 8 | a0001c0001t0006g0133 a0001c0001t0008g0075 a0001c0001t0018g0132 others(5): Show |
8 | HG01099.hp1 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.17-7496A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69498284 | |||||||
| chr17:69498286 | G | GACAA | 3 | a0001c0001t0028g0072 a0001c0001t0028g0096 a0001c0002t0064g0199 |
3 | HG02258.hp2 HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.17-7474_17-7471dup others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69498286 | ||||||
| chr17:69498286 | GACAA | G | 116 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0043 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.17-7474_17-7471del others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69498286 | ||||||
| chr17:69498353 | A | G | 46 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0001g0148 others(43): Show |
46 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.17-7427A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69498353 | |||||||
| chr17:69498629 | C | CCA | 107 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0001g0220 others(104): Show |
107 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.17-7139_17-7138dup others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69498629 | ||||||
| chr17:69498650 | C | CCA | 37 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(34): Show |
37 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.17-7096_17-7095dup others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69498650 | ||||||
| chr17:69498650 | C | CCACA | 6 | a0001c0001t0001g0201 a0001c0001t0003g0004 a0001c0001t0012g0143 others(3): Show |
6 | HG02723.hp1 HG03540.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.17-7098_17-7095dup others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69498650 | ||||||
| chr17:69498650 | C | CCACACAC others(1): Show |
6 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0003g0069 others(3): Show |
6 | HG01099.hp1 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.17-7102_17-7095dup others(8): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69498650 | ||||||
| chr17:69498650 | C | CCACACAC others(3): Show |
16 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(13): Show |
16 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.17-7104_17-7095dup others(10): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69498650 | ||||||
| chr17:69498650 | C | CCACACAC others(7): Show |
4 | a0001c0001t0005g0032 a0001c0001t0005g0206 a0001c0001t0005g0207 others(1): Show |
4 | HG01257.hp1 HG01258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-7108_17-7095dup others(14): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69498650 | ||||||
| chr17:69498650 | C | CCACACAC others(9): Show |
1 | a0001c0001t0043g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.17-7110_17-7095dup others(16): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69498650 | ||||||
| chr17:69498650 | CCA | C | 5 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0002t0002g0077 others(2): Show |
5 | HG02155.hp1 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.17-7096_17-7095del others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69498650 | ||||||
| chr17:69498650 | CCACACA | C | 8 | a0001c0001t0036g0126 a0001c0002t0001g0195 a0001c0002t0004g0038 others(5): Show |
8 | HG01071.hp2 HG01517.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.17-7100_17-7095del others(6): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69498650 | ||||||
| chr17:69498650 | CCACACAC others(1): Show |
C | 98 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0002g0010 others(95): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.17-7102_17-7095del others(8): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69498650 | ||||||
| chr17:69498650 | CCACACAC others(3): Show |
C | 2 | a0001c0001t0001g0220 a0001c0002t0001g0255 |
2 | HG01169.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.17-7104_17-7095del others(10): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69498650 | ||||||
| chr17:69498762 | A | G | 110 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0001g0220 others(107): Show |
110 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.17-7018A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69498762 | |||||||
| chr17:69498763 | G | A | 3 | a0001c0001t0028g0072 a0001c0001t0028g0096 a0001c0002t0064g0199 |
3 | HG02258.hp2 HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.17-7017G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69498763 | |||||||
| chr17:69498819 | C | A | 1 | a0001c0002t0053g0146 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.17-6961C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69498819 | |||||||
| chr17:69498820 | G | A | 1 | a0001c0001t0040g0009 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.17-6960G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69498820 | |||||||
| chr17:69498946 | C | T | 18 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(15): Show |
18 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-6834C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69498946 | |||||||
| chr17:69498948 | A | G | 109 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0001g0220 others(106): Show |
109 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.17-6832A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69498948 | |||||||
| chr17:69498952 | G | C | 107 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0001g0220 others(104): Show |
107 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.17-6828G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69498952 | |||||||
| chr17:69498963 | A | C | 119 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0001g0220 others(116): Show |
119 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.17-6817A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69498963 | |||||||
| chr17:69499021 | G | A | 167 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0001g0148 others(164): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.17-6759G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69499021 | |||||||
| chr17:69499130 | C | G | 9 | a0001c0001t0003g0069 a0001c0001t0006g0133 a0001c0001t0008g0075 others(6): Show |
9 | HG01099.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.17-6650C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69499130 | |||||||
| chr17:69499136 | G | A | 1 | a0001c0001t0010g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.17-6644G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69499136 | |||||||
| chr17:69499147 | C | T | 1 | a0001c0002t0001g0018 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.17-6633C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69499147 | |||||||
| chr17:69499198 | G | A | 5 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0001t0030g0046 others(2): Show |
5 | HG02280.hp1 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.17-6582G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69499198 | |||||||
| chr17:69499199 | T | C | 166 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0001g0148 others(163): Show |
166 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.17-6581T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69499199 | |||||||
| chr17:69499265 | C | T | 1 | a0001c0001t0015g0118 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.17-6515C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69499265 | |||||||
| chr17:69499286 | T | A | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.17-6494T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69499286 | |||||||
| chr17:69499480 | G | A | 23 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(20): Show |
23 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.17-6300G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69499480 | |||||||
| chr17:69499669 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.17-6111G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69499669 | |||||||
| chr17:69499708 | G | C | 3 | a0001c0001t0001g0193 a0001c0001t0026g0191 a0001c0001t0026g0192 |
3 | HG01516.hp1 HG01517.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.17-6072G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69499708 | |||||||
| chr17:69499799 | C | G | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.17-5981C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69499799 | |||||||
| chr17:69499822 | G | A | 104 | a0001c0001t0001g0187 a0001c0001t0001g0220 a0001c0001t0002g0010 others(101): Show |
104 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.17-5958G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69499822 | |||||||
| chr17:69499862 | A | G | 1 | a0001c0002t0002g0026 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.17-5918A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69499862 | |||||||
| chr17:69499899 | A | G | 1 | a0001c0002t0008g0081 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.17-5881A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69499899 | |||||||
| chr17:69499997 | A | G | 4 | a0001c0002t0004g0203 a0001c0002t0006g0045 a0001c0002t0006g0051 others(1): Show |
4 | HG01346.hp2 HG02615.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-5783A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69499997 | |||||||
| chr17:69500255 | C | G | 1 | a0001c0001t0001g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.17-5525C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69500255 | |||||||
| chr17:69500371 | G | A | 23 | a0001c0001t0001g0084 a0001c0001t0002g0006 a0001c0001t0002g0007 others(20): Show |
23 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.17-5409G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69500371 | |||||||
| chr17:69500447 | C | CA | 30 | a0001c0001t0001g0031 a0001c0001t0001g0165 a0001c0001t0001g0193 others(27): Show |
30 | HG00438.hp1 HG00621.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.17-5306dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69500447 | ||||||
| chr17:69500447 | C | CAAAA | 15 | a0001c0001t0001g0084 a0001c0001t0002g0006 a0001c0001t0002g0007 others(12): Show |
15 | HG00323.hp2 HG00738.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.17-5309_17-5306dup others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69500447 | ||||||
| chr17:69500447 | C | CAAAAA | 6 | a0001c0001t0002g0048 a0001c0001t0002g0068 a0001c0001t0005g0032 others(3): Show |
6 | HG00140.hp2 HG00735.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.17-5310_17-5306dup others(5): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69500447 | ||||||
| chr17:69500447 | CA | C | 12 | a0001c0001t0001g0159 a0001c0001t0003g0069 a0001c0001t0003g0179 others(9): Show |
12 | HG00408.hp2 HG01243.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.17-5306delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69500447 | ||||||
| chr17:69500447 | CAAAAAA | C | 6 | a0001c0001t0007g0044 a0001c0002t0001g0195 a0001c0002t0002g0077 others(3): Show |
6 | HG01071.hp2 HG02738.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.17-5311_17-5306del others(6): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69500447 | ||||||
| chr17:69500447 | CAAAAAAA | C | 97 | a0001c0001t0001g0187 a0001c0001t0001g0220 a0001c0001t0002g0010 others(94): Show |
97 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.17-5312_17-5306del others(7): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69500447 | ||||||
| chr17:69500478 | C | T | 1 | a0001c0002t0003g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.17-5302C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69500478 | |||||||
| chr17:69500481 | C | G | 167 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0001g0148 others(164): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.17-5299C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69500481 | |||||||
| chr17:69500617 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.17-5163G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69500617 | |||||||
| chr17:69500674 | C | T | 7 | a0001c0002t0001g0258 a0001c0002t0004g0203 a0001c0002t0006g0045 others(4): Show |
7 | HG01346.hp2 HG02615.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.17-5106C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69500674 | |||||||
| chr17:69500678 | G | A | 3 | a0001c0001t0028g0072 a0001c0001t0028g0096 a0001c0002t0064g0199 |
3 | HG02258.hp2 HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.17-5102G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69500678 | |||||||
| chr17:69500755 | C | CA | 105 | a0001c0001t0001g0187 a0001c0001t0001g0220 a0001c0001t0002g0010 others(102): Show |
105 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.17-5015dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69500755 | ||||||
| chr17:69500766 | G | A | 37 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(34): Show |
37 | HG00408.hp2 HG00438.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.17-5014G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69500766 | |||||||
| chr17:69500767 | A | G | 37 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(34): Show |
37 | HG00408.hp2 HG00438.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.17-5013A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69500767 | |||||||
| chr17:69501226 | G | A | 36 | a0001c0001t0001g0187 a0001c0001t0003g0058 a0001c0001t0003g0185 others(33): Show |
36 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.17-4554G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69501226 | |||||||
| chr17:69501237 | C | T | 2 | a0001c0002t0009g0120 a0001c0002t0009g0121 |
2 | HG00639.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.17-4543C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69501237 | |||||||
| chr17:69501240 | C | T | 21 | a0001c0001t0001g0084 a0001c0001t0002g0006 a0001c0001t0002g0007 others(18): Show |
21 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.17-4540C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69501240 | |||||||
| chr17:69501270 | C | T | 3 | a0001c0001t0001g0134 a0001c0001t0009g0056 a0001c0001t0009g0057 |
3 | HG00323.hp1 HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.17-4510C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69501270 | |||||||
| chr17:69501342 | A | G | 1 | a0001c0002t0001g0041 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.17-4438A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69501342 | |||||||
| chr17:69501422 | T | G | 105 | a0001c0001t0001g0187 a0001c0001t0001g0220 a0001c0001t0002g0010 others(102): Show |
105 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.17-4358T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69501422 | |||||||
| chr17:69501425 | C | T | 2 | a0001c0002t0006g0076 a0001c0002t0006g0100 |
2 | HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.17-4355C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69501425 | |||||||
| chr17:69501689 | C | T | 2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.17-4091C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69501689 | |||||||
| chr17:69501810 | CT | C | 5 | a0001c0001t0005g0170 a0001c0002t0001g0144 a0001c0002t0003g0123 others(2): Show |
5 | NA18975.hp1 NA19002.hp1 NA19062.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-3959delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69501810 | ||||||
| chr17:69501918 | G | GT | 61 | a0001c0001t0001g0089 a0001c0001t0001g0112 a0001c0001t0001g0138 others(58): Show |
61 | HG00609.hp1 HG01123.hp1 HG01168.hp1 others(58): Show |
intron_variant | MODIFIER | c.17-3843dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69501918 | ||||||
| chr17:69501918 | G | GTT | 60 | a0001c0001t0001g0187 a0001c0001t0002g0010 a0001c0001t0002g0106 others(57): Show |
60 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.17-3844_17-3843dup others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69501918 | ||||||
| chr17:69502142 | G | T | 2 | a0001c0001t0006g0133 a0001c0001t0018g0132 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.17-3638G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69502142 | |||||||
| chr17:69502192 | A | G | 3 | a0001c0001t0003g0069 a0001c0001t0022g0101 a0001c0001t0022g0102 |
3 | HG02109.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.17-3588A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69502192 | |||||||
| chr17:69502262 | A | G | 1 | a0001c0001t0056g0059 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.17-3518A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69502262 | |||||||
| chr17:69502333 | T | A | 1 | a0001c0002t0064g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.17-3447T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69502333 | |||||||
| chr17:69502543 | T | C | 1 | a0001c0001t0018g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.17-3237T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69502543 | |||||||
| chr17:69502743 | G | C | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.17-3037G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69502743 | |||||||
| chr17:69502817 | C | T | 1 | a0001c0001t0010g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.17-2963C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69502817 | |||||||
| chr17:69502827 | A | C | 1 | a0001c0002t0004g0188 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.17-2953A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69502827 | |||||||
| chr17:69502886 | G | T | 1 | a0001c0001t0031g0252 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.17-2894G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69502886 | |||||||
| chr17:69503380 | A | G | 12 | a0001c0001t0006g0110 a0001c0001t0006g0129 a0001c0001t0006g0130 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.17-2400A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69503380 | |||||||
| chr17:69503503 | A | C | 1 | a0001c0001t0002g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.17-2277A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69503503 | |||||||
| chr17:69503510 | G | T | 1 | a0001c0001t0002g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.17-2270G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69503510 | |||||||
| chr17:69503530 | T | C | 2 | a0001c0001t0028g0072 a0001c0001t0028g0096 |
2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.17-2250T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69503530 | |||||||
| chr17:69503576 | C | T | 105 | a0001c0001t0001g0187 a0001c0001t0001g0220 a0001c0001t0002g0010 others(102): Show |
105 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.17-2204C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69503576 | |||||||
| chr17:69503816 | G | T | 24 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.17-1964G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69503816 | |||||||
| chr17:69503823 | A | T | 1 | a0001c0001t0007g0246 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.17-1957A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69503823 | |||||||
| chr17:69504082 | C | T | 3 | a0001c0001t0001g0201 a0001c0001t0005g0001 a0001c0001t0008g0104 |
3 | HG02723.hp1 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.17-1698C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69504082 | |||||||
| chr17:69504156 | A | T | 5 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.17-1624A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69504156 | |||||||
| chr17:69504161 | G | A | 26 | a0001c0001t0001g0084 a0001c0001t0002g0006 a0001c0001t0002g0007 others(23): Show |
26 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.17-1619G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69504161 | |||||||
| chr17:69504162 | T | TTTC | 133 | a0001c0001t0001g0084 a0001c0001t0001g0187 a0001c0001t0001g0220 others(130): Show |
133 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.17-1616_17-1615ins others(3): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69504162 | ||||||
| chr17:69504216 | T | C | 1 | a0001c0002t0057g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.17-1564T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69504216 | |||||||
| chr17:69504482 | G | A | 1 | a0001c0001t0002g0106 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.17-1298G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69504482 | |||||||
| chr17:69504547 | C | T | 2 | a0001c0001t0028g0072 a0001c0001t0028g0096 |
2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.17-1233C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69504547 | |||||||
| chr17:69504555 | A | G | 2 | a0001c0001t0028g0072 a0001c0001t0028g0096 |
2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.17-1225A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69504555 | |||||||
| chr17:69504732 | T | C | 1 | a0001c0001t0008g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.17-1048T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69504732 | |||||||
| chr17:69504801 | T | C | 1 | a0001c0001t0008g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.17-979T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69504801 | |||||||
| chr17:69504808 | C | G | 2 | a0001c0001t0014g0002 a0001c0001t0056g0059 |
2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.17-972C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69504808 | |||||||
| chr17:69504842 | C | T | 1 | a0001c0001t0054g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.17-938C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69504842 | |||||||
| chr17:69504992 | C | T | 19 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(16): Show |
19 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.17-788C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69504992 | |||||||
| chr17:69505033 | T | C | 17 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.17-747T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69505033 | |||||||
| chr17:69505138 | A | C | 1 | a0001c0002t0001g0022 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.17-642A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69505138 | |||||||
| chr17:69505143 | A | C | 18 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(15): Show |
18 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-637A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69505143 | |||||||
| chr17:69505177 | C | T | 17 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.17-603C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69505177 | |||||||
| chr17:69505418 | G | A | 1 | a0001c0002t0001g0151 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.17-362G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69505418 | |||||||
| chr17:69505442 | C | CA | 27 | a0001c0001t0001g0011 a0001c0001t0001g0084 a0001c0001t0001g0243 others(24): Show |
27 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.17-316dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69505442 | ||||||
| chr17:69505442 | CA | C | 107 | a0001c0001t0001g0159 a0001c0001t0001g0162 a0001c0001t0001g0171 others(104): Show |
107 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.17-316delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69505442 | ||||||
| chr17:69505442 | CAA | C | 18 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(15): Show |
18 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-317_17-316delAA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 69505442 | ||||||
| chr17:69505473 | G | A | 19 | a0001c0001t0001g0220 a0001c0002t0001g0082 a0001c0002t0001g0168 others(16): Show |
19 | HG00609.hp1 HG01123.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.17-307G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69505473 | |||||||
| chr17:69505496 | G | A | 1 | a0001c0001t0007g0246 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.17-284G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69505496 | |||||||
| chr17:69505740 | G | A | 2 | a0001c0001t0007g0114 a0001c0001t0058g0067 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.17-40G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | chr17 | 69505740 | |||||||
| chr17:69505997 | G | A | 174 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0001g0148 others(171): Show |
174 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.83+151G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69505997 | |||||||
| chr17:69506104 | A | G | 27 | a0001c0001t0001g0119 a0001c0001t0001g0148 a0001c0001t0001g0159 others(24): Show |
27 | HG00408.hp2 HG00438.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.83+258A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69506104 | |||||||
| chr17:69506301 | CTTT | C | 173 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0001g0148 others(170): Show |
173 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.83+462_83+464delTT others(1): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69506301 | ||||||
| chr17:69506401 | CCTT | C | 36 | a0001c0001t0001g0084 a0001c0001t0002g0006 a0001c0001t0002g0007 others(33): Show |
36 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.83+559_83+561delCT others(1): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69506401 | ||||||
| chr17:69506408 | GTT | G | 107 | a0001c0001t0001g0187 a0001c0001t0001g0220 a0001c0001t0002g0010 others(104): Show |
107 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.83+575_83+576delTT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69506408 | ||||||
| chr17:69506456 | A | G | 2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.83+610A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69506456 | |||||||
| chr17:69506473 | A | G | 19 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(16): Show |
19 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.83+627A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69506473 | |||||||
| chr17:69506771 | GCAGTATA others(4): Show |
G | 2 | a0001c0001t0028g0072 a0001c0001t0028g0096 |
2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.83+928_83+938delGT others(9): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69506771 | ||||||
| chr17:69506953 | CT | C | 19 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(16): Show |
19 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.83+1117delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69506953 | ||||||
| chr17:69506973 | T | C | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.83+1127T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69506973 | |||||||
| chr17:69507001 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.83+1155C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69507001 | |||||||
| chr17:69507067 | C | A | 5 | a0001c0001t0008g0075 a0001c0001t0065g0149 a0001c0002t0002g0026 others(2): Show |
5 | HG01099.hp1 HG02622.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+1221C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69507067 | |||||||
| chr17:69507072 | A | G | 2 | a0001c0001t0028g0072 a0001c0001t0028g0096 |
2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.83+1226A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69507072 | |||||||
| chr17:69507238 | A | C | 2 | a0001c0001t0005g0001 a0001c0001t0008g0104 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.83+1392A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69507238 | |||||||
| chr17:69507332 | T | TTG | 10 | a0001c0001t0002g0008 a0001c0001t0002g0048 a0001c0001t0002g0254 others(7): Show |
10 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.83+1509_83+1510dup others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69507332 | ||||||
| chr17:69507332 | TTG | T | 15 | a0001c0001t0001g0119 a0001c0001t0002g0047 a0001c0001t0003g0226 others(12): Show |
15 | HG01243.hp2 HG01346.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.83+1509_83+1510del others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69507332 | ||||||
| chr17:69507332 | TTGTG | T | 8 | a0001c0001t0003g0069 a0001c0001t0008g0075 a0001c0001t0022g0101 others(5): Show |
8 | HG01099.hp1 HG02109.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.83+1507_83+1510del others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69507332 | ||||||
| chr17:69507360 | G | A | 105 | a0001c0001t0001g0187 a0001c0001t0001g0220 a0001c0001t0002g0010 others(102): Show |
105 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.83+1514G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69507360 | |||||||
| chr17:69507501 | C | T | 5 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.83+1655C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69507501 | |||||||
| chr17:69507512 | A | G | 118 | a0001c0001t0001g0084 a0001c0001t0001g0187 a0001c0001t0001g0220 others(115): Show |
118 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.83+1666A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69507512 | |||||||
| chr17:69507519 | G | A | 1 | a0001c0001t0008g0075 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.83+1673G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69507519 | |||||||
| chr17:69507592 | GA | G | 15 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(12): Show |
15 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.83+1747delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69507592 | |||||||
| chr17:69507851 | T | A | 6 | a0001c0001t0006g0110 a0001c0001t0006g0129 a0001c0001t0006g0130 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.83+2005T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69507851 | |||||||
| chr17:69507913 | G | A | 20 | a0001c0002t0001g0041 a0001c0002t0001g0082 a0001c0002t0001g0168 others(17): Show |
20 | HG00408.hp1 HG00609.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.83+2067G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69507913 | |||||||
| chr17:69507930 | T | G | 2 | a0001c0001t0003g0069 a0001c0001t0008g0075 |
2 | HG01099.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.83+2084T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69507930 | |||||||
| chr17:69508041 | G | GT | 87 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(84): Show |
87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.83+2222dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69508041 | ||||||
| chr17:69508041 | G | GTT | 22 | a0001c0001t0001g0145 a0001c0001t0001g0181 a0001c0001t0001g0222 others(19): Show |
22 | HG00438.hp1 HG00621.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.83+2221_83+2222dup others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69508041 | ||||||
| chr17:69508041 | G | GTTT | 68 | a0001c0001t0014g0002 a0001c0001t0055g0169 a0001c0001t0056g0059 others(65): Show |
68 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.83+2220_83+2222dup others(3): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69508041 | ||||||
| chr17:69508041 | G | GTTTT | 27 | a0001c0001t0006g0033 a0001c0001t0008g0103 a0001c0001t0016g0052 others(24): Show |
27 | HG00733.hp1 HG00733.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.83+2219_83+2222dup others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69508041 | ||||||
| chr17:69508041 | G | GTTTTT | 7 | a0001c0002t0001g0183 a0001c0002t0002g0026 a0001c0002t0004g0038 others(4): Show |
7 | HG01192.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.83+2218_83+2222dup others(5): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69508041 | ||||||
| chr17:69508041 | GT | G | 19 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(16): Show |
19 | HG01099.hp1 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.83+2222delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69508041 | ||||||
| chr17:69508041 | GTTTTTTT others(2): Show |
G | 5 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.83+2214_83+2222del others(9): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69508041 | ||||||
| chr17:69508041 | GTTTTTTT others(4): Show |
G | 6 | a0001c0001t0006g0110 a0001c0001t0006g0129 a0001c0001t0006g0130 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.83+2212_83+2222del others(11): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69508041 | ||||||
| chr17:69508077 | G | GTT | 111 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(108): Show |
111 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.83+2233_83+2234dup others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69508077 | ||||||
| chr17:69508081 | C | T | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.83+2235C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69508081 | |||||||
| chr17:69508112 | C | A | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.83+2266C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69508112 | |||||||
| chr17:69508121 | G | A | 117 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(114): Show |
117 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.83+2275G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69508121 | |||||||
| chr17:69508143 | C | G | 1 | a0001c0002t0057g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.83+2297C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69508143 | |||||||
| chr17:69508218 | AT | A | 9 | a0001c0001t0005g0001 a0001c0001t0006g0080 a0001c0001t0007g0114 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+2384delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69508218 | ||||||
| chr17:69508556 | G | A | 1 | a0001c0002t0057g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.83+2710G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69508556 | |||||||
| chr17:69508559 | A | G | 2 | a0001c0002t0012g0024 a0001c0002t0012g0208 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.83+2713A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69508559 | |||||||
| chr17:69508599 | G | T | 1 | a0001c0001t0018g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.83+2753G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69508599 | |||||||
| chr17:69508643 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.83+2797G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69508643 | |||||||
| chr17:69508825 | C | G | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.83+2979C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69508825 | |||||||
| chr17:69508909 | C | G | 1 | a0001c0001t0010g0016 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.83+3063C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69508909 | |||||||
| chr17:69508940 | C | T | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.83+3094C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69508940 | |||||||
| chr17:69508972 | G | A | 3 | a0001c0001t0008g0075 a0001c0001t0022g0101 a0001c0001t0022g0102 |
3 | HG01099.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.83+3126G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69508972 | |||||||
| chr17:69509365 | A | G | 18 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.83+3519A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69509365 | |||||||
| chr17:69509501 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.83+3655T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69509501 | |||||||
| chr17:69509603 | T | C | 18 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.83+3757T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69509603 | |||||||
| chr17:69509633 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.83+3787T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69509633 | |||||||
| chr17:69509673 | C | G | 145 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0002g0010 others(142): Show |
145 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.83+3827C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69509673 | |||||||
| chr17:69509684 | G | C | 18 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.83+3838G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69509684 | |||||||
| chr17:69509838 | G | A | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.83+3992G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69509838 | |||||||
| chr17:69509951 | T | A | 1 | a0001c0002t0029g0227 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.83+4105T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69509951 | |||||||
| chr17:69510003 | C | T | 2 | a0001c0002t0001g0184 a0001c0002t0017g0232 |
2 | HG02273.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.83+4157C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69510003 | |||||||
| chr17:69510017 | T | G | 1 | a0001c0002t0062g0060 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.83+4171T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69510017 | |||||||
| chr17:69510127 | C | T | 1 | a0001c0002t0002g0026 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.83+4281C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69510127 | |||||||
| chr17:69510247 | A | G | 1 | a0001c0001t0010g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.83+4401A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69510247 | |||||||
| chr17:69510281 | G | T | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.83+4435G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69510281 | |||||||
| chr17:69510299 | G | T | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.83+4453G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69510299 | |||||||
| chr17:69510541 | A | C | 137 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0002g0010 others(134): Show |
137 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.83+4695A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69510541 | |||||||
| chr17:69510587 | A | AT | 38 | a0001c0001t0001g0011 a0001c0001t0001g0089 a0001c0001t0001g0112 others(35): Show |
38 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.83+4751dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69510587 | ||||||
| chr17:69510801 | CT | C | 19 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(16): Show |
19 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.83+4966delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69510801 | ||||||
| chr17:69510862 | C | T | 1 | a0001c0001t0004g0050 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.83+5016C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69510862 | |||||||
| chr17:69510880 | T | C | 4 | a0001c0002t0001g0144 a0001c0002t0003g0123 a0001c0002t0003g0139 others(1): Show |
4 | NA18975.hp1 NA19002.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+5034T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69510880 | |||||||
| chr17:69511163 | C | G | 3 | a0001c0001t0008g0075 a0001c0001t0022g0101 a0001c0001t0022g0102 |
3 | HG01099.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.83+5317C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69511163 | |||||||
| chr17:69511165 | C | G | 2 | a0001c0001t0004g0050 a0001c0001t0010g0016 |
2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.83+5319C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69511165 | |||||||
| chr17:69511306 | T | G | 18 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.83+5460T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69511306 | |||||||
| chr17:69511403 | T | C | 4 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0001t0028g0072 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-5452T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69511403 | |||||||
| chr17:69511439 | A | G | 1 | a0001c0002t0062g0060 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.84-5416A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69511439 | |||||||
| chr17:69511462 | C | T | 13 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(10): Show |
13 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.84-5393C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69511462 | |||||||
| chr17:69511463 | G | A | 1 | a0001c0001t0003g0004 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.84-5392G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69511463 | |||||||
| chr17:69511499 | T | C | 3 | a0001c0001t0008g0075 a0001c0001t0022g0101 a0001c0001t0022g0102 |
3 | HG01099.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.84-5356T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69511499 | |||||||
| chr17:69511537 | T | C | 16 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(13): Show |
16 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.84-5318T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69511537 | |||||||
| chr17:69511657 | C | T | 4 | a0001c0001t0006g0133 a0001c0001t0018g0132 a0001c0001t0028g0072 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-5198C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69511657 | |||||||
| chr17:69511980 | A | G | 2 | a0001c0001t0027g0020 a0001c0001t0027g0021 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.84-4875A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69511980 | |||||||
| chr17:69512204 | G | C | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.84-4651G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69512204 | |||||||
| chr17:69512326 | GTGTTTTT others(4): Show |
G | 20 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(17): Show |
20 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.84-4516_84-4506del others(11): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69512326 | ||||||
| chr17:69512328 | G | GTTTTTT | 26 | a0001c0001t0002g0204 a0001c0001t0024g0097 a0001c0001t0056g0059 others(23): Show |
26 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.84-4522_84-4517dup others(6): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69512328 | ||||||
| chr17:69512328 | G | GTTTTTTT | 38 | a0001c0001t0002g0068 a0001c0001t0006g0033 a0001c0001t0008g0103 others(35): Show |
38 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.84-4523_84-4517dup others(7): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69512328 | ||||||
| chr17:69512328 | G | GTTTTTTT others(1): Show |
13 | a0001c0001t0001g0084 a0001c0001t0065g0149 a0001c0002t0001g0005 others(10): Show |
13 | HG00558.hp2 HG00733.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.84-4524_84-4517dup others(8): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69512328 | ||||||
| chr17:69512328 | G | GTTTTTTT others(2): Show |
9 | a0001c0002t0001g0041 a0001c0002t0001g0168 a0001c0002t0001g0223 others(6): Show |
9 | HG02056.hp1 HG02486.hp1 HG04228.hp2 others(6): Show |
intron_variant | MODIFIER | c.84-4525_84-4517dup others(9): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69512328 | ||||||
| chr17:69512328 | G | GTTTTTTT others(3): Show |
2 | a0001c0001t0008g0061 a0001c0002t0032g0054 |
2 | HG01123.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.84-4526_84-4517dup others(10): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69512328 | ||||||
| chr17:69512328 | G | GTTTTTTT others(4): Show |
1 | a0001c0002t0001g0195 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.84-4517_84-4516ins others(11): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69512328 | ||||||
| chr17:69512328 | GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.84-4516_84-4503del others(14): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69512328 | ||||||
| chr17:69512328 | GTTTTTTT others(8): Show |
G | 3 | a0001c0001t0008g0075 a0001c0001t0022g0101 a0001c0001t0022g0102 |
3 | HG01099.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.84-4516_84-4502del others(15): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69512328 | ||||||
| chr17:69512329 | TTTTTTTT others(3): Show |
T | 1 | a0001c0002t0023g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.84-4516_84-4507del others(10): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69512329 | ||||||
| chr17:69512332 | TTTTTTTG | T | 5 | a0001c0002t0001g0258 a0001c0002t0006g0045 a0001c0002t0006g0051 others(2): Show |
5 | HG01346.hp2 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-4516_84-4510del others(7): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69512332 | ||||||
| chr17:69512333 | TTTTTTG | T | 16 | a0001c0001t0002g0047 a0001c0001t0004g0050 a0001c0001t0007g0111 others(13): Show |
16 | HG00609.hp2 HG01243.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.84-4516_84-4511del others(6): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69512333 | ||||||
| chr17:69512334 | TTTTTG | T | 12 | a0001c0001t0002g0010 a0001c0001t0002g0106 a0001c0001t0003g0226 others(9): Show |
12 | HG01891.hp1 HG02451.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.84-4516_84-4512del others(5): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69512334 | ||||||
| chr17:69512339 | G | GT | 11 | a0001c0001t0001g0134 a0001c0001t0001g0229 a0001c0001t0001g0243 others(8): Show |
11 | HG02257.hp1 HG02970.hp2 HG03516.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-4498dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69512339 | ||||||
| chr17:69512339 | G | T | 95 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(92): Show |
95 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.84-4516G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69512339 | |||||||
| chr17:69512426 | G | A | 16 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(13): Show |
16 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.84-4429G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69512426 | |||||||
| chr17:69512449 | C | T | 18 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.84-4406C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69512449 | |||||||
| chr17:69512573 | G | A | 3 | a0001c0001t0008g0075 a0001c0001t0022g0101 a0001c0001t0022g0102 |
3 | HG01099.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.84-4282G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69512573 | |||||||
| chr17:69512596 | C | T | 2 | a0001c0002t0004g0203 a0001c0002t0033g0109 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.84-4259C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69512596 | |||||||
| chr17:69512616 | C | T | 1 | a0001c0002t0053g0146 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.84-4239C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69512616 | |||||||
| chr17:69512865 | G | A | 1 | a0001c0001t0002g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.84-3990G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69512865 | |||||||
| chr17:69512918 | A | G | 145 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0002g0010 others(142): Show |
145 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.84-3937A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69512918 | |||||||
| chr17:69513397 | C | T | 1 | a0001c0002t0003g0239 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.84-3458C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69513397 | |||||||
| chr17:69513526 | A | G | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.84-3329A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69513526 | |||||||
| chr17:69513538 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.84-3317G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69513538 | |||||||
| chr17:69513544 | G | A | 2 | a0001c0001t0020g0128 a0001c0002t0062g0060 |
2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.84-3311G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69513544 | |||||||
| chr17:69513577 | G | A | 2 | a0001c0002t0032g0054 a0001c0002t0041g0125 |
2 | HG01123.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.84-3278G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69513577 | |||||||
| chr17:69513633 | G | GT | 18 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.84-3215dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69513633 | ||||||
| chr17:69513889 | C | T | 16 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(13): Show |
16 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.84-2966C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69513889 | |||||||
| chr17:69514108 | T | TA | 6 | a0001c0001t0003g0069 a0001c0001t0013g0137 a0001c0001t0015g0118 others(3): Show |
6 | HG02109.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-2730dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69514108 | ||||||
| chr17:69514108 | TA | T | 122 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(119): Show |
122 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.84-2730delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 69514108 | ||||||
| chr17:69514183 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.84-2672A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69514183 | |||||||
| chr17:69514350 | A | G | 1 | a0001c0001t0006g0023 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.84-2505A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69514350 | |||||||
| chr17:69514859 | C | T | 3 | a0001c0001t0008g0075 a0001c0001t0022g0101 a0001c0001t0022g0102 |
3 | HG01099.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.84-1996C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69514859 | |||||||
| chr17:69515098 | G | A | 18 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.84-1757G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69515098 | |||||||
| chr17:69515151 | C | T | 5 | a0001c0001t0006g0110 a0001c0001t0006g0129 a0001c0001t0006g0130 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.84-1704C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69515151 | |||||||
| chr17:69515226 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.84-1629G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69515226 | |||||||
| chr17:69515228 | C | T | 1 | a0001c0002t0062g0060 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.84-1627C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69515228 | |||||||
| chr17:69515358 | C | T | 1 | a0001c0002t0001g0168 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.84-1497C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69515358 | |||||||
| chr17:69515386 | A | C | 5 | a0001c0002t0001g0258 a0001c0002t0006g0045 a0001c0002t0006g0051 others(2): Show |
5 | HG01346.hp2 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-1469A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69515386 | |||||||
| chr17:69515414 | C | G | 1 | a0001c0002t0045g0152 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.84-1441C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69515414 | |||||||
| chr17:69515577 | A | G | 1 | a0001c0002t0062g0060 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.84-1278A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69515577 | |||||||
| chr17:69515578 | C | T | 1 | a0001c0002t0001g0197 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.84-1277C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69515578 | |||||||
| chr17:69515728 | T | A | 146 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0002g0010 others(143): Show |
146 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.84-1127T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69515728 | |||||||
| chr17:69515787 | C | G | 146 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0002g0010 others(143): Show |
146 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.84-1068C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69515787 | |||||||
| chr17:69515822 | A | G | 18 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.84-1033A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69515822 | |||||||
| chr17:69515836 | G | A | 1 | a0001c0001t0004g0166 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.84-1019G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69515836 | |||||||
| chr17:69515953 | T | C | 3 | a0001c0001t0005g0001 a0001c0001t0006g0080 a0001c0001t0010g0200 |
3 | HG02257.hp1 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.84-902T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69515953 | |||||||
| chr17:69515990 | A | G | 2 | a0001c0001t0003g0069 a0001c0001t0006g0023 |
2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.84-865A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69515990 | |||||||
| chr17:69516081 | A | T | 1 | a0001c0001t0017g0140 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.84-774A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69516081 | |||||||
| chr17:69516107 | T | C | 18 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.84-748T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69516107 | |||||||
| chr17:69516186 | A | G | 117 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(114): Show |
117 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.84-669A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69516186 | |||||||
| chr17:69516195 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.84-660C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69516195 | |||||||
| chr17:69516251 | A | G | 146 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0002g0010 others(143): Show |
146 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.84-604A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69516251 | |||||||
| chr17:69516299 | C | T | 18 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.84-556C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69516299 | |||||||
| chr17:69516311 | C | T | 18 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.84-544C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69516311 | |||||||
| chr17:69516529 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.84-326C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69516529 | |||||||
| chr17:69516594 | T | C | 13 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(10): Show |
13 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.84-261T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69516594 | |||||||
| chr17:69516783 | G | GTT | 119 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0204 others(116): Show |
119 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.84-72_84-71insTT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 2/11 | chr17 | 69516783 | |||||||
| chr17:69516914 | A | G | 100 | a0001c0002t0001g0005 a0001c0002t0001g0018 a0001c0002t0001g0022 others(97): Show |
100 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.132+11A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 3/11 | chr17 | 69516914 | |||||||
| chr17:69517714 | G | A | 2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.246+101G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 4/11 | chr17 | 69517714 | |||||||
| chr17:69517761 | C | T | 6 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0005g0108 others(3): Show |
6 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.246+148C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 4/11 | chr17 | 69517761 | |||||||
| chr17:69517970 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.246+357C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 4/11 | chr17 | 69517970 | |||||||
| chr17:69518051 | A | G | 17 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(14): Show |
17 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.246+438A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 4/11 | chr17 | 69518051 | |||||||
| chr17:69518132 | G | A | 4 | a0001c0001t0006g0133 a0001c0001t0028g0072 a0001c0001t0028g0096 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+519G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 4/11 | chr17 | 69518132 | |||||||
| chr17:69518159 | C | T | 1 | a0001c0002t0019g0167 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.246+546C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 4/11 | chr17 | 69518159 | |||||||
| chr17:69518183 | C | G | 2 | a0001c0001t0001g0222 a0001c0001t0003g0042 |
2 | HG00621.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.246+570C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 4/11 | chr17 | 69518183 | |||||||
| chr17:69518198 | T | TTAA | 114 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0106 others(111): Show |
114 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.246+605_246+607dup others(3): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 69518198 | ||||||
| chr17:69518423 | C | T | 1 | a0001c0002t0002g0036 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.246+810C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 4/11 | chr17 | 69518423 | |||||||
| chr17:69518504 | G | A | 5 | a0001c0002t0001g0082 a0001c0002t0003g0124 a0001c0002t0003g0248 others(2): Show |
5 | NA18978.hp1 NA18997.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.247-809G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 4/11 | chr17 | 69518504 | |||||||
| chr17:69518532 | A | G | 1 | a0001c0002t0062g0060 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.247-781A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 4/11 | chr17 | 69518532 | |||||||
| chr17:69518537 | A | G | 17 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(14): Show |
17 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.247-776A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 4/11 | chr17 | 69518537 | |||||||
| chr17:69518551 | T | C | 158 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0002g0006 others(155): Show |
158 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.247-762T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 4/11 | chr17 | 69518551 | |||||||
| chr17:69518675 | T | G | 2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.247-638T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 4/11 | chr17 | 69518675 | |||||||
| chr17:69518967 | C | T | 3 | a0001c0001t0006g0133 a0001c0001t0028g0072 a0001c0001t0028g0096 |
3 | HG02258.hp2 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.247-346C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 4/11 | chr17 | 69518967 | |||||||
| chr17:69519702 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.366+270G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 5/11 | chr17 | 69519702 | |||||||
| chr17:69519706 | A | G | 1 | a0001c0002t0062g0060 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.366+274A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 5/11 | chr17 | 69519706 | |||||||
| chr17:69519914 | G | C | 1 | a0001c0001t0001g0011 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.367-356G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 5/11 | chr17 | 69519914 | |||||||
| chr17:69520089 | G | T | 1 | a0001c0001t0065g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.367-181G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 5/11 | chr17 | 69520089 | |||||||
| chr17:69520199 | G | GT | 7 | a0001c0001t0022g0101 a0001c0001t0022g0102 a0001c0002t0006g0045 others(4): Show |
7 | HG01346.hp2 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.367-59dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 69520199 | ||||||
| chr17:69520493 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.483+107C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 6/11 | chr17 | 69520493 | |||||||
| chr17:69520660 | C | G | 13 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(10): Show |
13 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.483+274C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 6/11 | chr17 | 69520660 | |||||||
| chr17:69520968 | G | C | 1 | a0001c0002t0005g0240 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.484-81G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 6/11 | chr17 | 69520968 | |||||||
| chr17:69521181 | C | G | 6 | a0001c0002t0001g0086 a0001c0002t0001g0260 a0001c0002t0002g0173 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.535+81C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69521181 | |||||||
| chr17:69521284 | G | A | 15 | a0001c0001t0001g0043 a0001c0002t0001g0086 a0001c0002t0001g0116 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.535+184G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69521284 | |||||||
| chr17:69521339 | G | A | 2 | a0001c0001t0003g0069 a0001c0001t0008g0075 |
2 | HG01099.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.535+239G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69521339 | |||||||
| chr17:69521408 | T | C | 164 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(161): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.535+308T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69521408 | |||||||
| chr17:69521806 | C | CA | 26 | a0001c0001t0001g0098 a0001c0001t0001g0148 a0001c0001t0001g0156 others(23): Show |
26 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.535+733dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 69521806 | ||||||
| chr17:69521806 | CA | C | 36 | a0001c0001t0001g0089 a0001c0001t0002g0010 a0001c0001t0003g0226 others(33): Show |
36 | HG00733.hp1 HG01099.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.535+733delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 69521806 | ||||||
| chr17:69521806 | CAA | C | 90 | a0001c0001t0001g0043 a0001c0001t0005g0001 a0001c0001t0006g0033 others(87): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.535+732_535+733del others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 69521806 | ||||||
| chr17:69521806 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0002g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.535+719_535+733del others(15): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 69521806 | ||||||
| chr17:69521806 | CAAAAAAA others(9): Show |
C | 6 | a0001c0001t0001g0084 a0001c0001t0002g0068 a0001c0001t0002g0106 others(3): Show |
6 | HG01884.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.535+718_535+733del others(16): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 69521806 | ||||||
| chr17:69521807 | A | AAAAAC | 12 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.535+711_535+712ins others(5): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 69521807 | ||||||
| chr17:69521812 | A | C | 12 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.535+712A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69521812 | |||||||
| chr17:69521813 | A | C | 1 | a0001c0001t0005g0032 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.535+713A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69521813 | |||||||
| chr17:69521818 | A | C | 13 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(10): Show |
13 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.535+718A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69521818 | |||||||
| chr17:69521819 | A | C | 39 | a0001c0001t0005g0032 a0001c0002t0001g0005 a0001c0002t0001g0022 others(36): Show |
39 | HG00408.hp1 HG00621.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.535+719A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69521819 | |||||||
| chr17:69521822 | A | C | 1 | a0001c0002t0002g0241 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.535+722A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69521822 | |||||||
| chr17:69521823 | A | C | 1 | a0001c0002t0001g0029 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.535+723A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69521823 | |||||||
| chr17:69521825 | A | C | 1 | a0001c0001t0005g0032 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.535+725A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69521825 | |||||||
| chr17:69521916 | G | A | 6 | a0001c0001t0006g0110 a0001c0001t0006g0129 a0001c0001t0006g0130 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.535+816G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69521916 | |||||||
| chr17:69521925 | A | G | 166 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(163): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.535+825A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69521925 | |||||||
| chr17:69522071 | T | C | 17 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(14): Show |
17 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.535+971T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69522071 | |||||||
| chr17:69522209 | C | T | 166 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(163): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.535+1109C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69522209 | |||||||
| chr17:69522435 | T | G | 4 | a0001c0001t0006g0133 a0001c0001t0028g0072 a0001c0001t0028g0096 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.536-1079T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69522435 | |||||||
| chr17:69522507 | T | A | 19 | a0001c0001t0001g0119 a0001c0001t0001g0201 a0001c0001t0002g0010 others(16): Show |
19 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.536-1007T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69522507 | |||||||
| chr17:69522578 | G | A | 1 | a0001c0002t0003g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.536-936G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69522578 | |||||||
| chr17:69522643 | A | C | 3 | a0001c0001t0005g0206 a0001c0001t0005g0207 a0001c0001t0025g0094 |
3 | HG01257.hp1 HG01258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.536-871A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69522643 | |||||||
| chr17:69522699 | G | A | 110 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0002g0068 others(107): Show |
110 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.536-815G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69522699 | |||||||
| chr17:69522701 | G | A | 1 | a0001c0002t0003g0237 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.536-813G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69522701 | |||||||
| chr17:69522706 | T | C | 1 | a0001c0001t0006g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.536-808T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69522706 | |||||||
| chr17:69522779 | G | T | 2 | a0001c0001t0001g0201 a0001c0001t0008g0104 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.536-735G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69522779 | |||||||
| chr17:69522890 | C | CA | 33 | a0001c0001t0001g0243 a0001c0001t0003g0069 a0001c0001t0004g0166 others(30): Show |
33 | HG00408.hp1 HG01099.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.536-604dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 69522890 | ||||||
| chr17:69522890 | CA | C | 37 | a0001c0001t0001g0201 a0001c0001t0002g0006 a0001c0001t0002g0007 others(34): Show |
37 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.536-604delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 69522890 | ||||||
| chr17:69522984 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0008g0104 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.536-530C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69522984 | |||||||
| chr17:69523028 | A | T | 1 | a0001c0001t0001g0221 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.536-486A>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69523028 | |||||||
| chr17:69523202 | T | G | 5 | a0001c0002t0006g0045 a0001c0002t0006g0051 a0001c0002t0014g0062 others(2): Show |
5 | HG01346.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.536-312T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69523202 | |||||||
| chr17:69523401 | G | A | 148 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0201 others(145): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.536-113G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 7/11 | chr17 | 69523401 | |||||||
| chr17:69523786 | T | G | 1 | a0001c0002t0046g0242 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.663+145T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 8/11 | chr17 | 69523786 | |||||||
| chr17:69523805 | C | T | 2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.663+164C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 8/11 | chr17 | 69523805 | |||||||
| chr17:69523817 | G | A | 165 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(162): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.663+176G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 8/11 | chr17 | 69523817 | |||||||
| chr17:69523894 | C | T | 165 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(162): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.663+253C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 8/11 | chr17 | 69523894 | |||||||
| chr17:69523951 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0013g0137 |
2 | HG01346.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.663+310C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 8/11 | chr17 | 69523951 | |||||||
| chr17:69524046 | T | A | 8 | a0001c0001t0006g0080 a0001c0001t0007g0114 a0001c0001t0008g0049 others(5): Show |
8 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.663+405T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 8/11 | chr17 | 69524046 | |||||||
| chr17:69524180 | T | TTA | 2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.663+549_663+550dup others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 69524180 | ||||||
| chr17:69524259 | G | A | 4 | a0001c0001t0006g0133 a0001c0001t0028g0072 a0001c0001t0028g0096 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.663+618G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 8/11 | chr17 | 69524259 | |||||||
| chr17:69524814 | G | A | 10 | a0001c0001t0001g0201 a0001c0001t0003g0069 a0001c0001t0006g0133 others(7): Show |
10 | HG01099.hp1 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.664-87G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 8/11 | chr17 | 69524814 | |||||||
| chr17:69525042 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.741+64G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69525042 | |||||||
| chr17:69525100 | C | A | 167 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(164): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.741+122C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69525100 | |||||||
| chr17:69525192 | A | G | 2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.741+214A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69525192 | |||||||
| chr17:69525258 | C | T | 1 | a0001c0001t0008g0075 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.741+280C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69525258 | |||||||
| chr17:69525358 | C | T | 2 | a0001c0002t0007g0037 a0001c0002t0052g0115 |
2 | HG03704.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.741+380C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69525358 | |||||||
| chr17:69525359 | G | A | 1 | a0001c0002t0063g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.741+381G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69525359 | |||||||
| chr17:69525465 | G | A | 1 | a0001c0002t0062g0060 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.741+487G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69525465 | |||||||
| chr17:69525521 | G | A | 2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.741+543G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69525521 | |||||||
| chr17:69525563 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.741+585C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69525563 | |||||||
| chr17:69525576 | A | G | 140 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0002g0006 others(137): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.741+598A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69525576 | |||||||
| chr17:69525583 | A | G | 1 | a0001c0001t0018g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.741+605A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69525583 | |||||||
| chr17:69525661 | A | G | 17 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(14): Show |
17 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.741+683A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69525661 | |||||||
| chr17:69525734 | A | G | 2 | a0001c0001t0007g0155 a0001c0001t0007g0246 |
2 | NA18955.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.741+756A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69525734 | |||||||
| chr17:69525797 | G | A | 2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.742-773G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69525797 | |||||||
| chr17:69525823 | G | A | 148 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0201 others(145): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.742-747G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69525823 | |||||||
| chr17:69526127 | T | C | 1 | a0001c0002t0001g0197 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.742-443T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69526127 | |||||||
| chr17:69526192 | C | T | 3 | a0001c0001t0006g0133 a0001c0001t0028g0072 a0001c0001t0028g0096 |
3 | HG02258.hp2 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.742-378C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69526192 | |||||||
| chr17:69526232 | C | G | 140 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0002g0006 others(137): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.742-338C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69526232 | |||||||
| chr17:69526466 | A | G | 11 | a0001c0001t0001g0187 a0001c0001t0001g0220 a0001c0001t0003g0058 others(8): Show |
11 | HG00423.hp1 HG01169.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.742-104A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69526466 | |||||||
| chr17:69526507 | G | A | 2 | a0001c0002t0001g0182 a0001c0002t0001g0183 |
2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.742-63G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 9/11 | chr17 | 69526507 | |||||||
| chr17:69526762 | C | T | 13 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(10): Show |
13 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.881+53C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69526762 | |||||||
| chr17:69526778 | C | T | 138 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0002g0006 others(135): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.881+69C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69526778 | |||||||
| chr17:69526834 | T | C | 99 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0002g0068 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.881+125T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69526834 | |||||||
| chr17:69526884 | A | G | 107 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0002g0068 others(104): Show |
107 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.881+175A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69526884 | |||||||
| chr17:69527119 | G | A | 155 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(152): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.881+410G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69527119 | |||||||
| chr17:69527297 | G | A | 1 | a0001c0001t0015g0118 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.881+588G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69527297 | |||||||
| chr17:69527349 | T | C | 4 | a0001c0001t0006g0133 a0001c0001t0028g0072 a0001c0001t0028g0096 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+640T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69527349 | |||||||
| chr17:69527385 | A | G | 1 | a0001c0002t0062g0060 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.881+676A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69527385 | |||||||
| chr17:69527491 | C | T | 1 | a0001c0001t0058g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.881+782C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69527491 | |||||||
| chr17:69527496 | C | T | 138 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0002g0006 others(135): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.881+787C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69527496 | |||||||
| chr17:69527821 | G | C | 155 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(152): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.881+1112G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69527821 | |||||||
| chr17:69527906 | A | C | 1 | a0001c0001t0001g0171 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.881+1197A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69527906 | |||||||
| chr17:69527952 | C | T | 155 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(152): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.881+1243C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69527952 | |||||||
| chr17:69527961 | CA | C | 4 | a0001c0001t0006g0023 a0001c0001t0014g0002 a0001c0001t0016g0052 others(1): Show |
4 | HG02896.hp2 HG02976.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+1258delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69527961 | ||||||
| chr17:69528057 | C | T | 138 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0002g0006 others(135): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.881+1348C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69528057 | |||||||
| chr17:69528065 | C | T | 17 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(14): Show |
17 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.881+1356C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69528065 | |||||||
| chr17:69528066 | G | A | 2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.881+1357G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69528066 | |||||||
| chr17:69528109 | C | CAA | 13 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(10): Show |
13 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.881+1416_881+1417d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69528109 | ||||||
| chr17:69528109 | C | CAAAAAA | 18 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(15): Show |
18 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.881+1412_881+1417d others(8): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69528109 | ||||||
| chr17:69528109 | C | CAAAAAAA | 111 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0201 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.881+1411_881+1417d others(9): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69528109 | ||||||
| chr17:69528109 | C | CAAAAAAA others(1): Show |
12 | a0001c0001t0003g0069 a0001c0001t0008g0049 a0001c0001t0008g0075 others(9): Show |
12 | HG01099.hp1 HG01346.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.881+1410_881+1417d others(10): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69528109 | ||||||
| chr17:69528109 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.881+1408_881+1417d others(12): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69528109 | ||||||
| chr17:69528109 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0006g0133 a0001c0001t0028g0072 a0001c0001t0028g0096 |
3 | HG02258.hp2 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.881+1407_881+1417d others(13): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69528109 | ||||||
| chr17:69528194 | T | C | 1 | a0001c0002t0064g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.881+1485T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69528194 | |||||||
| chr17:69528216 | C | G | 1 | a0001c0002t0003g0250 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.881+1507C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69528216 | |||||||
| chr17:69528244 | T | C | 155 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(152): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.881+1535T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69528244 | |||||||
| chr17:69528276 | G | A | 1 | a0001c0001t0058g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.881+1567G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69528276 | |||||||
| chr17:69528307 | G | A | 1 | a0001c0001t0039g0012 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.881+1598G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69528307 | |||||||
| chr17:69528397 | C | T | 1 | a0001c0001t0043g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.881+1688C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69528397 | |||||||
| chr17:69528597 | G | A | 155 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(152): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.881+1888G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69528597 | |||||||
| chr17:69528634 | G | A | 155 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(152): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.881+1925G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69528634 | |||||||
| chr17:69528694 | G | T | 1 | a0001c0002t0003g0142 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.881+1985G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69528694 | |||||||
| chr17:69528702 | T | A | 155 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(152): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.881+1993T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69528702 | |||||||
| chr17:69528737 | T | C | 2 | a0001c0001t0022g0101 a0001c0001t0022g0102 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.881+2028T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69528737 | |||||||
| chr17:69528769 | G | T | 137 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0002g0006 others(134): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.881+2060G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69528769 | |||||||
| chr17:69528846 | A | G | 1 | a0001c0002t0014g0062 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.881+2137A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69528846 | |||||||
| chr17:69528859 | C | CA | 16 | a0001c0001t0001g0039 a0001c0001t0001g0145 a0001c0001t0001g0181 others(13): Show |
16 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(13): Show |
intron_variant | MODIFIER | c.881+2179dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69528859 | ||||||
| chr17:69528859 | CA | C | 11 | a0001c0001t0001g0119 a0001c0001t0002g0047 a0001c0001t0002g0210 others(8): Show |
11 | HG00323.hp1 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+2179delA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69528859 | ||||||
| chr17:69528859 | CAA | C | 24 | a0001c0001t0001g0201 a0001c0001t0002g0010 a0001c0001t0004g0050 others(21): Show |
24 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.881+2178_881+2179d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69528859 | ||||||
| chr17:69528859 | CAAA | C | 122 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0002g0006 others(119): Show |
122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.881+2177_881+2179d others(5): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69528859 | ||||||
| chr17:69528859 | CAAAA | C | 9 | a0001c0001t0006g0133 a0001c0002t0001g0082 a0001c0002t0004g0099 others(6): Show |
9 | HG02109.hp2 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.881+2176_881+2179d others(6): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69528859 | ||||||
| chr17:69528887 | A | G | 137 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0002g0006 others(134): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.881+2178A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69528887 | |||||||
| chr17:69529181 | G | A | 137 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0002g0006 others(134): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.881+2472G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69529181 | |||||||
| chr17:69529344 | T | C | 163 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(160): Show |
163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.881+2635T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69529344 | |||||||
| chr17:69529364 | T | TA | 9 | a0001c0001t0006g0080 a0001c0001t0007g0114 a0001c0001t0008g0049 others(6): Show |
9 | HG02257.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.881+2663dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69529364 | ||||||
| chr17:69529434 | G | A | 155 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(152): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.881+2725G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69529434 | |||||||
| chr17:69529449 | T | C | 1 | a0001c0002t0013g0085 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.881+2740T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69529449 | |||||||
| chr17:69529504 | A | AT | 12 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0001g0181 others(9): Show |
12 | HG00423.hp1 HG01168.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.881+2818dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69529504 | ||||||
| chr17:69529504 | AT | A | 26 | a0001c0001t0001g0201 a0001c0001t0005g0032 a0001c0001t0008g0075 others(23): Show |
26 | HG01099.hp1 HG01192.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.881+2818delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69529504 | ||||||
| chr17:69529504 | ATT | A | 118 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0002g0006 others(115): Show |
118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.881+2817_881+2818d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69529504 | ||||||
| chr17:69529504 | ATTT | A | 20 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(17): Show |
20 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.881+2816_881+2818d others(5): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69529504 | ||||||
| chr17:69529534 | G | A | 24 | a0001c0002t0001g0041 a0001c0002t0001g0082 a0001c0002t0001g0168 others(21): Show |
24 | HG00408.hp1 HG01123.hp1 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.881+2825G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69529534 | |||||||
| chr17:69529541 | T | G | 2 | a0001c0001t0001g0201 a0001c0001t0008g0104 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.881+2832T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69529541 | |||||||
| chr17:69529573 | C | T | 2 | a0001c0002t0044g0003 a0001c0002t0049g0230 |
2 | HG02135.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.881+2864C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69529573 | |||||||
| chr17:69529591 | A | C | 13 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(10): Show |
13 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.881+2882A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69529591 | |||||||
| chr17:69529745 | C | T | 1 | a0001c0002t0062g0060 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.881+3036C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69529745 | |||||||
| chr17:69529752 | T | C | 169 | a0001c0001t0001g0043 a0001c0001t0001g0079 a0001c0001t0001g0084 others(166): Show |
169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.881+3043T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69529752 | |||||||
| chr17:69529789 | G | A | 18 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.881+3080G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69529789 | |||||||
| chr17:69529791 | T | A | 155 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(152): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.881+3082T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69529791 | |||||||
| chr17:69529852 | C | T | 18 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.881+3143C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69529852 | |||||||
| chr17:69530075 | G | A | 13 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(10): Show |
13 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.881+3366G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69530075 | |||||||
| chr17:69530141 | T | C | 157 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(154): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.881+3432T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69530141 | |||||||
| chr17:69530145 | T | C | 1 | a0001c0002t0003g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.881+3436T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69530145 | |||||||
| chr17:69530204 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.881+3495A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69530204 | |||||||
| chr17:69530265 | T | C | 18 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.881+3556T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69530265 | |||||||
| chr17:69530279 | C | T | 13 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(10): Show |
13 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.881+3570C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69530279 | |||||||
| chr17:69530372 | ACTAT | A | 18 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.881+3667_881+3670d others(6): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69530372 | ||||||
| chr17:69530452 | T | G | 2 | a0001c0001t0001g0119 a0001c0001t0003g0226 |
2 | NA19010.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.881+3743T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69530452 | |||||||
| chr17:69530472 | A | G | 137 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0002g0006 others(134): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.881+3763A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69530472 | |||||||
| chr17:69530608 | C | A | 137 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0002g0006 others(134): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.881+3899C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69530608 | |||||||
| chr17:69531064 | T | C | 1 | a0001c0001t0043g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.881+4355T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69531064 | |||||||
| chr17:69531328 | T | C | 157 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(154): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.881+4619T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69531328 | |||||||
| chr17:69531351 | A | G | 18 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0047 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.881+4642A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69531351 | |||||||
| chr17:69531374 | T | C | 38 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0029 others(35): Show |
38 | HG00408.hp1 HG00621.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.881+4665T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69531374 | |||||||
| chr17:69531377 | C | G | 1 | a0001c0002t0003g0139 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.881+4668C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69531377 | |||||||
| chr17:69531380 | T | TG | 4 | a0001c0001t0006g0133 a0001c0001t0028g0072 a0001c0001t0028g0096 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+4672dupG | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69531380 | ||||||
| chr17:69531453 | C | T | 137 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0002g0006 others(134): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.882-4662C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69531453 | |||||||
| chr17:69531485 | T | C | 163 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0119 others(160): Show |
163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.882-4630T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69531485 | |||||||
| chr17:69531543 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0008g0104 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.882-4572G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69531543 | |||||||
| chr17:69531672 | C | T | 4 | a0001c0001t0001g0201 a0001c0001t0008g0104 a0001c0002t0005g0164 others(1): Show |
4 | HG02602.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882-4443C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69531672 | |||||||
| chr17:69531755 | G | T | 2 | a0001c0001t0003g0069 a0001c0001t0008g0075 |
2 | HG01099.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.882-4360G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69531755 | |||||||
| chr17:69531786 | T | A | 1 | a0001c0002t0057g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.882-4329T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69531786 | |||||||
| chr17:69531794 | G | A | 28 | a0001c0001t0001g0119 a0001c0001t0001g0201 a0001c0001t0002g0010 others(25): Show |
28 | HG01099.hp1 HG01243.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.882-4321G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69531794 | |||||||
| chr17:69532109 | G | A | 1 | a0001c0002t0006g0076 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.882-4006G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69532109 | |||||||
| chr17:69532169 | AG | A | 9 | a0001c0001t0001g0148 a0001c0001t0001g0159 a0001c0001t0001g0181 others(6): Show |
9 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(6): Show |
intron_variant | MODIFIER | c.882-3945delG | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69532169 | |||||||
| chr17:69532255 | C | T | 2 | a0001c0001t0010g0017 a0001c0002t0057g0214 |
2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.882-3860C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69532255 | |||||||
| chr17:69532290 | G | A | 66 | a0001c0001t0001g0084 a0001c0001t0001g0257 a0001c0001t0002g0047 others(63): Show |
66 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.882-3825G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69532290 | |||||||
| chr17:69532291 | T | C | 1 | a0001c0001t0002g0106 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882-3824T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69532291 | |||||||
| chr17:69532422 | C | T | 3 | a0001c0001t0008g0075 a0001c0001t0008g0104 a0001c0002t0001g0041 |
3 | HG01099.hp1 HG02886.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.882-3693C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69532422 | |||||||
| chr17:69532472 | G | A | 2 | a0001c0001t0001g0193 a0001c0002t0032g0054 |
2 | HG01123.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.882-3643G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69532472 | |||||||
| chr17:69532537 | T | G | 24 | a0001c0001t0002g0010 a0001c0001t0002g0068 a0001c0001t0002g0204 others(21): Show |
24 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.882-3578T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69532537 | |||||||
| chr17:69532581 | C | G | 78 | a0001c0001t0001g0011 a0001c0001t0001g0043 a0001c0001t0001g0089 others(75): Show |
78 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.882-3534C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69532581 | |||||||
| chr17:69532703 | C | A | 28 | a0001c0001t0001g0148 a0001c0001t0003g0004 a0001c0001t0003g0042 others(25): Show |
28 | HG00408.hp2 HG00609.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.882-3412C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69532703 | |||||||
| chr17:69532866 | T | C | 14 | a0001c0001t0010g0017 a0001c0001t0022g0101 a0001c0001t0022g0102 others(11): Show |
14 | HG00099.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.882-3249T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69532866 | |||||||
| chr17:69533016 | C | T | 1 | a0001c0002t0062g0060 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.882-3099C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69533016 | |||||||
| chr17:69533125 | C | T | 2 | a0001c0002t0057g0214 a0001c0002t0063g0078 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.882-2990C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69533125 | |||||||
| chr17:69533129 | G | A | 70 | a0001c0001t0001g0236 a0001c0001t0003g0004 a0001c0001t0003g0042 others(67): Show |
70 | HG00099.hp2 HG00408.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.882-2986G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69533129 | |||||||
| chr17:69533229 | G | A | 1 | a0001c0002t0045g0152 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.882-2886G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69533229 | |||||||
| chr17:69533378 | A | G | 1 | a0001c0002t0001g0005 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.882-2737A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69533378 | |||||||
| chr17:69533423 | T | C | 1 | a0001c0002t0064g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.882-2692T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69533423 | |||||||
| chr17:69533506 | G | A | 1 | a0001c0001t0001g0253 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.882-2609G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69533506 | |||||||
| chr17:69533645 | C | T | 1 | a0001c0001t0058g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.882-2470C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69533645 | |||||||
| chr17:69533731 | G | GT | 9 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0002g0063 others(6): Show |
9 | HG01069.hp2 HG02698.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.882-2381dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69533731 | ||||||
| chr17:69533735 | G | GT | 90 | a0001c0001t0001g0031 a0001c0001t0001g0043 a0001c0001t0001g0098 others(87): Show |
90 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.882-2362dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69533735 | ||||||
| chr17:69533735 | G | GTT | 6 | a0001c0001t0001g0011 a0001c0001t0001g0089 a0001c0001t0001g0236 others(3): Show |
6 | HG03017.hp2 HG03139.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.882-2363_882-2362d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69533735 | ||||||
| chr17:69533735 | G | T | 17 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0002g0063 others(14): Show |
17 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.882-2380G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69533735 | |||||||
| chr17:69533735 | GT | G | 6 | a0001c0001t0006g0080 a0001c0001t0028g0072 a0001c0001t0028g0096 others(3): Show |
6 | HG02257.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.882-2362delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69533735 | ||||||
| chr17:69533735 | GTT | G | 63 | a0001c0001t0003g0004 a0001c0001t0003g0042 a0001c0001t0003g0058 others(60): Show |
63 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.882-2363_882-2362d others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69533735 | ||||||
| chr17:69533832 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.882-2283C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69533832 | |||||||
| chr17:69533874 | G | T | 2 | a0001c0001t0020g0128 a0001c0001t0040g0009 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.882-2241G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69533874 | |||||||
| chr17:69533981 | A | G | 1 | a0001c0002t0005g0240 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.882-2134A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69533981 | |||||||
| chr17:69534192 | C | A | 70 | a0001c0001t0003g0004 a0001c0001t0003g0042 a0001c0001t0003g0058 others(67): Show |
70 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.882-1923C>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69534192 | |||||||
| chr17:69534213 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.882-1902C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69534213 | |||||||
| chr17:69534249 | C | T | 21 | a0001c0001t0006g0023 a0001c0001t0006g0033 a0001c0001t0006g0080 others(18): Show |
21 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.882-1866C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69534249 | |||||||
| chr17:69534562 | CT | C | 5 | a0001c0001t0004g0228 a0001c0001t0006g0023 a0001c0001t0025g0094 others(2): Show |
5 | HG02572.hp1 HG02735.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.882-1539delT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69534562 | ||||||
| chr17:69534563 | T | TC | 98 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(95): Show |
98 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.882-1552_882-1551i others(3): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69534563 | |||||||
| chr17:69534564 | T | C | 2 | a0001c0002t0001g0065 a0001c0002t0005g0164 |
2 | HG01168.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.882-1551T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69534564 | |||||||
| chr17:69534565 | T | C | 1 | a0001c0002t0001g0259 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.882-1550T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69534565 | |||||||
| chr17:69534576 | T | A | 1 | a0001c0001t0020g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.882-1539T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69534576 | |||||||
| chr17:69534784 | A | C | 5 | a0001c0001t0001g0134 a0001c0001t0001g0145 a0001c0002t0001g0182 others(2): Show |
5 | HG01099.hp2 HG01192.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.882-1331A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69534784 | |||||||
| chr17:69535094 | C | T | 100 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(97): Show |
100 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.882-1021C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69535094 | |||||||
| chr17:69535122 | T | G | 1 | a0001c0001t0001g0253 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.882-993T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69535122 | |||||||
| chr17:69535241 | T | C | 1 | a0001c0002t0001g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.882-874T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69535241 | |||||||
| chr17:69535391 | G | A | 45 | a0001c0001t0003g0004 a0001c0001t0003g0042 a0001c0001t0003g0058 others(42): Show |
45 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.882-724G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69535391 | |||||||
| chr17:69535398 | G | T | 1 | a0001c0001t0020g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.882-717G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69535398 | |||||||
| chr17:69535477 | A | G | 1 | a0001c0002t0057g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.882-638A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69535477 | |||||||
| chr17:69535494 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.882-621G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69535494 | |||||||
| chr17:69535540 | C | T | 1 | a0001c0002t0001g0018 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.882-575C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69535540 | |||||||
| chr17:69535875 | A | C | 101 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(98): Show |
101 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.882-240A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | chr17 | 69535875 | |||||||
| chr17:69535879 | T | TAC | 86 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(83): Show |
86 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.882-206_882-205dup others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69535879 | ||||||
| chr17:69535879 | T | TACAC | 3 | a0001c0001t0001g0222 a0001c0001t0007g0044 a0001c0002t0001g0116 |
3 | HG00621.hp2 HG02738.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.882-208_882-205dup others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69535879 | ||||||
| chr17:69535879 | TAC | T | 26 | a0001c0001t0001g0098 a0001c0001t0001g0187 a0001c0001t0001g0220 others(23): Show |
26 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.882-206_882-205del others(2): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69535879 | ||||||
| chr17:69535879 | TACAC | T | 50 | a0001c0001t0003g0004 a0001c0001t0003g0042 a0001c0001t0003g0058 others(47): Show |
50 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.882-208_882-205del others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69535879 | ||||||
| chr17:69535879 | TACACAC | T | 9 | a0001c0001t0008g0049 a0001c0001t0008g0061 a0001c0001t0008g0075 others(6): Show |
9 | HG00408.hp1 HG00733.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.882-210_882-205del others(6): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 69535879 | ||||||
| chr17:69536178 | C | T | 1 | a0001c0001t0010g0200 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.927+18C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69536178 | |||||||
| chr17:69536247 | A | G | 71 | a0001c0001t0003g0004 a0001c0001t0003g0042 a0001c0001t0003g0058 others(68): Show |
71 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.927+87A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69536247 | |||||||
| chr17:69536593 | T | C | 1 | a0001c0002t0019g0215 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.927+433T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69536593 | |||||||
| chr17:69536714 | A | G | 96 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(93): Show |
96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.927+554A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69536714 | |||||||
| chr17:69536747 | G | A | 1 | a0001c0001t0010g0016 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.927+587G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69536747 | |||||||
| chr17:69536931 | A | G | 5 | a0001c0001t0008g0061 a0001c0001t0008g0075 a0001c0001t0008g0103 others(2): Show |
5 | HG00733.hp1 HG01099.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+771A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69536931 | |||||||
| chr17:69536966 | C | T | 1 | a0001c0001t0048g0231 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.927+806C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69536966 | |||||||
| chr17:69537087 | A | AAAAC | 72 | a0001c0001t0003g0004 a0001c0001t0003g0042 a0001c0001t0003g0058 others(69): Show |
72 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.927+947_927+950dup others(4): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 69537087 | ||||||
| chr17:69537118 | T | C | 73 | a0001c0001t0003g0004 a0001c0001t0003g0042 a0001c0001t0003g0058 others(70): Show |
73 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.927+958T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69537118 | |||||||
| chr17:69537346 | G | A | 2 | a0001c0002t0057g0214 a0001c0002t0063g0078 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.927+1186G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69537346 | |||||||
| chr17:69537801 | T | C | 13 | a0001c0001t0006g0033 a0001c0001t0006g0080 a0001c0001t0006g0110 others(10): Show |
13 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.927+1641T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69537801 | |||||||
| chr17:69538096 | G | C | 70 | a0001c0001t0003g0004 a0001c0001t0003g0042 a0001c0001t0003g0058 others(67): Show |
70 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.927+1936G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69538096 | |||||||
| chr17:69538129 | C | G | 1 | a0001c0002t0063g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.927+1969C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69538129 | |||||||
| chr17:69538316 | C | G | 1 | a0001c0001t0058g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.927+2156C>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69538316 | |||||||
| chr17:69538369 | C | T | 2 | a0001c0002t0057g0214 a0001c0002t0063g0078 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.927+2209C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69538369 | |||||||
| chr17:69538379 | T | C | 4 | a0001c0001t0028g0072 a0001c0001t0028g0096 a0001c0002t0062g0060 others(1): Show |
4 | HG02258.hp2 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+2219T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69538379 | |||||||
| chr17:69538384 | A | G | 1 | a0001c0002t0001g0184 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.927+2224A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69538384 | |||||||
| chr17:69538477 | C | T | 1 | a0001c0002t0002g0035 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.927+2317C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69538477 | |||||||
| chr17:69538595 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.927+2435G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69538595 | |||||||
| chr17:69538713 | G | T | 3 | a0001c0001t0024g0097 a0001c0001t0056g0059 a0001c0002t0024g0105 |
3 | HG02922.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.927+2553G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69538713 | |||||||
| chr17:69538746 | G | T | 31 | a0001c0001t0003g0004 a0001c0001t0003g0042 a0001c0001t0003g0058 others(28): Show |
31 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.927+2586G>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69538746 | |||||||
| chr17:69538932 | T | TA | 9 | a0001c0001t0004g0166 a0001c0001t0004g0205 a0001c0001t0004g0228 others(6): Show |
9 | HG00438.hp1 HG00558.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.928-2734dupA | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 69538932 | ||||||
| chr17:69539041 | A | G | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.928-2635A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69539041 | |||||||
| chr17:69539110 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.928-2566T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69539110 | |||||||
| chr17:69539219 | G | A | 1 | a0001c0002t0005g0240 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.928-2457G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69539219 | |||||||
| chr17:69539248 | G | A | 1 | a0001c0002t0021g0196 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.928-2428G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69539248 | |||||||
| chr17:69539513 | A | G | 1 | a0001c0001t0047g0177 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.928-2163A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69539513 | |||||||
| chr17:69539542 | C | T | 1 | a0001c0002t0057g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.928-2134C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69539542 | |||||||
| chr17:69539552 | C | T | 40 | a0001c0001t0003g0004 a0001c0001t0003g0042 a0001c0001t0003g0058 others(37): Show |
40 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.928-2124C>T | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69539552 | |||||||
| chr17:69539959 | T | C | 1 | a0001c0002t0064g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.928-1717T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69539959 | |||||||
| chr17:69539982 | G | C | 75 | a0001c0001t0003g0004 a0001c0001t0003g0042 a0001c0001t0003g0058 others(72): Show |
75 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.928-1694G>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69539982 | |||||||
| chr17:69540079 | T | G | 2 | a0001c0002t0001g0065 a0001c0002t0001g0259 |
2 | HG01168.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.928-1597T>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69540079 | |||||||
| chr17:69540104 | T | C | 25 | a0001c0001t0006g0023 a0001c0001t0006g0033 a0001c0001t0006g0080 others(22): Show |
25 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.928-1572T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69540104 | |||||||
| chr17:69540159 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.928-1517G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69540159 | |||||||
| chr17:69540181 | T | C | 175 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(172): Show |
175 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.928-1495T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69540181 | |||||||
| chr17:69540476 | A | G | 1 | a0001c0002t0057g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.928-1200A>G | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69540476 | |||||||
| chr17:69540530 | T | C | 3 | a0001c0001t0005g0108 a0001c0001t0005g0206 a0001c0001t0005g0207 |
3 | HG01123.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.928-1146T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69540530 | |||||||
| chr17:69540611 | G | A | 2 | a0001c0002t0057g0214 a0001c0002t0063g0078 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.928-1065G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69540611 | |||||||
| chr17:69540656 | GACTTGTT others(15): Show |
G | 1 | a0001c0001t0001g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.928-1012_928-991de others(23): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 69540656 | ||||||
| chr17:69540795 | G | A | 6 | a0001c0001t0004g0166 a0001c0001t0004g0205 a0001c0001t0004g0228 others(3): Show |
6 | HG00438.hp1 HG00558.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-881G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69540795 | |||||||
| chr17:69541334 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0047g0177 |
2 | NA18983.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.928-342G>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69541334 | |||||||
| chr17:69541395 | T | C | 4 | a0001c0001t0002g0068 a0001c0001t0002g0106 a0001c0001t0002g0204 others(1): Show |
4 | HG02451.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-281T>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69541395 | |||||||
| chr17:69541428 | C | CT | 22 | a0001c0001t0006g0023 a0001c0001t0006g0033 a0001c0001t0006g0080 others(19): Show |
22 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.928-240dupT | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 69541428 | ||||||
| chr17:69541436 | T | A | 96 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0039 others(93): Show |
96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.928-240T>A | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69541436 | |||||||
| chr17:69541469 | A | C | 4 | a0001c0001t0028g0072 a0001c0001t0028g0096 a0001c0002t0062g0060 others(1): Show |
4 | HG02258.hp2 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-207A>C | MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 11/11 | chr17 | 69541469 |