Item | Value |
---|---|
geneid | 65125 |
ensemblid | ENSG00000060237.19 |
hgncid | 14540 |
symbol | WNK1 |
name | WNK lysine deficient protein kinase 1 |
refseq_nuc | NM_018979.4 |
refseq_prot | NP_061852.3 |
ensembl_nuc | ENST00000315939.11 |
ensembl_prot | ENSP00000313059.6 |
mane_status | MANE Select |
chr | chr12 |
start | 752579 |
end | 911452 |
strand | + |
ver | v1.2 |
region | chr12:752579-911452 |
region5000 | chr12:747579-916452 |
regionname0 | WNK1_chr12_752579_911452 |
regionname5000 | WNK1_chr12_747579_916452 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 2382 | 96 | 27 | 31 | 26 | 5 | 6 | 15 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0002 | 0/0 | 2382 | 89 | 38 | 14 | 20 | 2 | 15 | 14 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0003 | 0/0 | 2382 | 22 | 0 | 5 | 13 | 3 | 1 | 9 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0004 | 0/0 | 2382 | 22 | 0 | 4 | 10 | 2 | 6 | 5 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0005 | 0/0 | 2382 | 16 | 1 | 5 | 10 | 0 | 0 | 8 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0006 | 0/0 | 2382 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0007 | 1/0 | 2382 | 7 | 6 | 0 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0008 | 0/0 | 2382 | 4 | 0 | 1 | 2 | 0 | 1 | 1 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0009 | 0/0 | 2382 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0010 | 0/0 | 2382 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0011 | 0/0 | 2382 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0012 | 0/0 | 2382 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0013 | 0/0 | 2382 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0014 | 0/0 | 2382 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0015 | 0/0 | 2382 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0016 | 0/0 | 2382 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0017 | 0/0 | 2382 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0018 | 0/0 | 2382 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0019 | 0/0 | 2382 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0020 | 0/0 | 2382 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0021 | 0/0 | 2382 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0022 | 0/0 | 2382 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0023 | 0/0 | 2382 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
a0024 | 0/0 | 2382 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | MSGGA others(2377): Show |
chr12 | 747579 | 916452 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 7146 | 79 | 19 | 24 | 25 | 5 | 5 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0001c0008 | 0/0 | 7146 | 6 | 0 | 6 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0001c0012 | 0/0 | 7146 | 4 | 4 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0001c0018 | 0/0 | 7146 | 2 | 2 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0001c0022 | 0/0 | 7146 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0001c0032 | 0/0 | 7146 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0001c0035 | 0/0 | 7146 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0001c0037 | 0/0 | 7146 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0001c0041 | 0/0 | 7146 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0002c0002 | 0/0 | 7146 | 46 | 22 | 10 | 5 | 0 | 9 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0002c0003 | 0/0 | 7146 | 26 | 6 | 3 | 10 | 2 | 5 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0002c0009 | 0/0 | 7146 | 6 | 1 | 1 | 4 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0002c0011 | 0/0 | 7146 | 5 | 5 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0002c0015 | 0/0 | 7146 | 3 | 3 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0002c0023 | 0/0 | 7146 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0002c0024 | 0/0 | 7146 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0002c0029 | 0/0 | 7146 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0003c0005 | 0/0 | 7146 | 21 | 0 | 5 | 12 | 3 | 1 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0003c0026 | 0/0 | 7146 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0004c0004 | 0/0 | 7146 | 21 | 0 | 4 | 9 | 2 | 6 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0004c0020 | 0/0 | 7146 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0005c0006 | 0/0 | 7146 | 15 | 1 | 4 | 10 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0005c0027 | 0/0 | 7146 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0006c0007 | 0/0 | 7146 | 8 | 6 | 2 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0007c0010 | 0/0 | 7146 | 5 | 5 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0007c0030 | 0/0 | 7146 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0007c0043 | 1/0 | 7146 | 1 | 0 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0008c0013 | 0/0 | 7146 | 4 | 0 | 1 | 2 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0009c0014 | 0/0 | 7146 | 3 | 0 | 0 | 3 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0010c0016 | 0/0 | 7146 | 2 | 0 | 2 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0011c0017 | 0/0 | 7146 | 2 | 2 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0012c0033 | 0/0 | 7146 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0013c0040 | 0/0 | 7146 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0014c0028 | 0/0 | 7146 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0015c0039 | 0/0 | 7146 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0016c0044 | 0/0 | 7146 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0017c0031 | 0/0 | 7146 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0018c0019 | 0/0 | 7146 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0019c0025 | 0/0 | 7146 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0020c0021 | 0/0 | 7146 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0021c0038 | 0/0 | 7146 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0022c0034 | 0/0 | 7146 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0023c0036 | 0/0 | 7146 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 | ||
a0024c0042 | 0/0 | 7146 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | ATGTC others(7141): Show |
chr12 | 747579 | 916452 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 10796 | 3 | 1 | 0 | 0 | 2 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0001c0001t0002 | 0/0 | 10799 | 22 | 7 | 5 | 7 | 2 | 1 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0001c0001t0004 | 0/1 | 10799 | 19 | 3 | 9 | 3 | 1 | 2 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0001c0001t0006 | 0/0 | 10796 | 7 | 5 | 2 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0001c0001t0007 | 0/0 | 10803 | 13 | 0 | 0 | 13 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10798): Show |
chr12 | 747579 | 916452 |
a0001c0001t0011 | 0/0 | 10799 | 5 | 0 | 5 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0001c0001t0012 | 0/0 | 10803 | 2 | 0 | 0 | 2 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10798): Show |
chr12 | 747579 | 916452 |
a0001c0001t0016 | 0/0 | 10799 | 2 | 0 | 0 | 0 | 0 | 2 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0001c0001t0018 | 0/0 | 10799 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0001c0001t0020 | 0/0 | 10799 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0001c0001t0021 | 0/0 | 10799 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0001c0001t0023 | 0/0 | 10799 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0001c0001t0025 | 0/0 | 10799 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0001c0001t0026 | 0/0 | 10799 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0001c0008t0002 | 0/0 | 10799 | 6 | 0 | 6 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0001c0012t0002 | 0/0 | 10799 | 3 | 3 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0001c0012t0028 | 0/0 | 10799 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0001c0018t0006 | 0/0 | 10796 | 2 | 2 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0001c0022t0001 | 0/0 | 10796 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0001c0032t0002 | 0/0 | 10799 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0001c0035t0004 | 0/0 | 10799 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0001c0037t0002 | 0/0 | 10799 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0001c0041t0006 | 0/0 | 10796 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0002c0002t0001 | 0/0 | 10796 | 39 | 20 | 10 | 3 | 0 | 6 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0002c0002t0006 | 0/0 | 10796 | 2 | 0 | 0 | 2 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0002c0002t0017 | 0/0 | 10800 | 2 | 0 | 0 | 0 | 0 | 2 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10795): Show |
chr12 | 747579 | 916452 |
a0002c0002t0019 | 0/0 | 10796 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0002c0002t0029 | 0/0 | 10796 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0002c0002t0035 | 0/0 | 10796 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0002c0003t0001 | 0/0 | 10796 | 22 | 6 | 3 | 7 | 2 | 4 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0002c0003t0006 | 0/0 | 10796 | 2 | 0 | 0 | 2 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0002c0003t0032 | 0/0 | 10796 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0002c0003t0034 | 0/0 | 10796 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0002c0009t0001 | 0/0 | 10796 | 4 | 1 | 1 | 2 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0002c0009t0005 | 0/0 | 10796 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0002c0009t0006 | 0/0 | 10796 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0002c0011t0001 | 0/0 | 10796 | 5 | 5 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0002c0015t0001 | 0/0 | 10796 | 3 | 3 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0002c0023t0001 | 0/0 | 10796 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0002c0024t0014 | 0/0 | 10796 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0002c0029t0001 | 0/0 | 10796 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0003c0005t0001 | 0/0 | 10796 | 6 | 0 | 2 | 2 | 2 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0003c0005t0005 | 0/0 | 10796 | 15 | 0 | 3 | 10 | 1 | 1 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0003c0026t0005 | 0/0 | 10796 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0004c0004t0003 | 0/0 | 10796 | 20 | 0 | 4 | 9 | 2 | 5 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0004c0004t0022 | 0/0 | 10796 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0004c0020t0003 | 0/0 | 10796 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0005c0006t0003 | 0/0 | 10796 | 9 | 0 | 3 | 6 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0005c0006t0009 | 0/0 | 10796 | 6 | 1 | 1 | 4 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0005c0027t0003 | 0/0 | 10796 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0006c0007t0008 | 0/0 | 10799 | 7 | 5 | 2 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0006c0007t0031 | 0/0 | 10799 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0007c0010t0010 | 0/0 | 10796 | 4 | 4 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0007c0010t0030 | 0/0 | 10811 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10806): Show |
chr12 | 747579 | 916452 |
a0007c0030t0002 | 0/0 | 10799 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0007c0043t0010 | 1/0 | 10796 | 1 | 0 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0008c0013t0013 | 0/0 | 10799 | 3 | 0 | 1 | 1 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0008c0013t0027 | 0/0 | 10799 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0009c0014t0002 | 0/0 | 10799 | 3 | 0 | 0 | 3 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0010c0016t0015 | 0/0 | 10800 | 2 | 0 | 2 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10795): Show |
chr12 | 747579 | 916452 |
a0011c0017t0014 | 0/0 | 10796 | 2 | 2 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0012c0033t0006 | 0/0 | 10796 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0013c0040t0006 | 0/0 | 10796 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0014c0028t0001 | 0/0 | 10796 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0015c0039t0001 | 0/0 | 10796 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0016c0044t0001 | 0/0 | 10796 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0017c0031t0033 | 0/0 | 10796 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0018c0019t0003 | 0/0 | 10796 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0019c0025t0001 | 0/0 | 10796 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
a0020c0021t0024 | 0/0 | 10799 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0021c0038t0012 | 0/0 | 10803 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10798): Show |
chr12 | 747579 | 916452 |
a0022c0034t0004 | 0/0 | 10799 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10794): Show |
chr12 | 747579 | 916452 |
a0023c0036t0007 | 0/0 | 10803 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10798): Show |
chr12 | 747579 | 916452 |
a0024c0042t0001 | 0/0 | 10796 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | AGACT others(10791): Show |
chr12 | 747579 | 916452 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0004g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0006g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0006g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0007g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0007g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0007g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0007g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0007g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0007g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0007g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0007g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0011g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0011g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0011g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0011g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0011g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0012g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0012g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0016g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0016g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0018g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0020g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0021g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0023g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0025g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0001t0026g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0008t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0008t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0008t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0008t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0008t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0008t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0012t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0012t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0012t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0012t0028g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0018t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0018t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0022t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0032t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0035t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0037t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0001c0041t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0017g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0017g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0019g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0029g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0002t0035g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0032g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0003t0034g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0009t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0009t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0009t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0009t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0009t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0009t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0011t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0011t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0011t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0011t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0011t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0015t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0015t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0015t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0023t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0024t0014g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0002c0029t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0005g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0005g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0005t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0003c0026t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0004t0022g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0004c0020t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0005c0006t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0005c0006t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0005c0006t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0005c0006t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0005c0006t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0005c0006t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0005c0006t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0005c0006t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0005c0006t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0005c0006t0009g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0005c0006t0009g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0005c0006t0009g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0005c0006t0009g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0005c0006t0009g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0005c0006t0009g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0005c0027t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0006c0007t0008g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0006c0007t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0006c0007t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0006c0007t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0006c0007t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0006c0007t0008g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0006c0007t0008g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0006c0007t0031g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0007c0010t0010g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0007c0010t0010g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0007c0010t0010g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0007c0010t0010g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0007c0010t0030g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0007c0030t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0007c0043t0010g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0008c0013t0013g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0008c0013t0013g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0008c0013t0013g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0008c0013t0027g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0009c0014t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0009c0014t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0009c0014t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0010c0016t0015g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0010c0016t0015g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0011c0017t0014g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0011c0017t0014g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0012c0033t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0013c0040t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0014c0028t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0015c0039t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0016c0044t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0017c0031t0033g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0018c0019t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0019c0025t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0020c0021t0024g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0021c0038t0012g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0022c0034t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0023c0036t0007g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
a0024c0042t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0004 | g0155 | EUR | FIN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00280 | hp2 | a0002 | c0003 | t0001 | g0131 | EUR | FIN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00323 | hp1 | a0003 | c0005 | t0005 | g0209 | EUR | FIN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0051 | EUR | FIN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | CHS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00408 | hp2 | a0004 | c0004 | t0003 | g0088 | EAS | CHS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00423 | hp1 | a0004 | c0020 | t0003 | g0084 | EAS | CHS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00423 | hp2 | a0002 | c0003 | t0001 | g0133 | EAS | CHS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00438 | hp1 | a0001 | c0001 | t0007 | g0041 | EAS | CHS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00438 | hp2 | a0003 | c0005 | t0001 | g0036 | EAS | CHS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00544 | hp1 | a0001 | c0001 | t0007 | g0054 | EAS | CHS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00544 | hp2 | a0003 | c0005 | t0005 | g0203 | EAS | CHS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00609 | hp1 | a0008 | c0013 | t0013 | g0033 | EAS | CHS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00609 | hp2 | a0003 | c0005 | t0005 | g0234 | EAS | CHS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00673 | hp1 | a0001 | c0001 | t0007 | g0035 | EAS | CHS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | CHS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00735 | hp1 | a0001 | c0001 | t0011 | g0169 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00741 | hp1 | a0001 | c0008 | t0002 | g0266 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01069 | hp1 | a0002 | c0003 | t0001 | g0117 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01069 | hp2 | a0004 | c0004 | t0003 | g0081 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01071 | hp2 | a0002 | c0003 | t0001 | g0118 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01074 | hp1 | a0002 | c0003 | t0001 | g0115 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01081 | hp1 | a0004 | c0004 | t0003 | g0080 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0251 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01106 | hp2 | a0005 | c0006 | t0009 | g0021 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01109 | hp1 | a0001 | c0032 | t0002 | g0050 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01109 | hp2 | a0006 | c0007 | t0008 | g0011 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0257 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0166 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0154 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01175 | hp1 | a0003 | c0005 | t0001 | g0248 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0183 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01192 | hp1 | a0005 | c0027 | t0003 | g0075 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01192 | hp2 | a0002 | c0009 | t0001 | g0126 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0172 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01243 | hp2 | a0008 | c0013 | t0013 | g0149 | AMR | PUR | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0252 | AMR | CLM | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01255 | hp2 | a0001 | c0001 | t0026 | g0167 | AMR | CLM | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01261 | hp1 | a0010 | c0016 | t0015 | g0093 | AMR | CLM | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0144 | AMR | CLM | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0258 | AMR | CLM | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0175 | AMR | CLM | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01358 | hp1 | a0006 | c0007 | t0008 | g0283 | AMR | CLM | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01358 | hp2 | a0003 | c0005 | t0001 | g0193 | AMR | CLM | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01361 | hp1 | a0001 | c0001 | t0023 | g0171 | AMR | CLM | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01361 | hp2 | a0001 | c0001 | t0006 | g0003 | AMR | CLM | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0219 | AMR | CLM | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01515 | hp1 | a0004 | c0004 | t0003 | g0079 | EUR | IBS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | IBS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01516 | hp1 | a0003 | c0005 | t0001 | g0240 | EUR | IBS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0109 | EUR | IBS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01517 | hp2 | a0003 | c0005 | t0001 | g0241 | EUR | IBS | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01884 | hp1 | a0012 | c0033 | t0006 | g0007 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01884 | hp2 | a0001 | c0012 | t0002 | g0267 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0150 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01928 | hp2 | a0001 | c0008 | t0002 | g0273 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0181 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01934 | hp2 | a0001 | c0008 | t0002 | g0274 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0250 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01943 | hp2 | a0001 | c0001 | t0011 | g0159 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0191 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01952 | hp2 | a0003 | c0005 | t0005 | g0235 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01978 | hp1 | a0001 | c0008 | t0002 | g0275 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01978 | hp2 | a0001 | c0001 | t0011 | g0162 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01981 | hp1 | a0001 | c0001 | t0011 | g0187 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01981 | hp2 | a0004 | c0004 | t0003 | g0082 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01993 | hp1 | a0005 | c0006 | t0003 | g0156 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0226 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02004 | hp1 | a0001 | c0008 | t0002 | g0276 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02004 | hp2 | a0005 | c0006 | t0003 | g0158 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02040 | hp1 | a0002 | c0009 | t0001 | g0122 | EAS | KHV | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02040 | hp2 | a0002 | c0003 | t0006 | g0147 | EAS | KHV | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | KHV | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02056 | hp2 | a0004 | c0004 | t0003 | g0072 | EAS | KHV | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02071 | hp1 | a0001 | c0001 | t0007 | g0032 | EAS | KHV | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02071 | hp2 | a0004 | c0004 | t0003 | g0078 | EAS | KHV | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02074 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | KHV | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02074 | hp2 | a0009 | c0014 | t0002 | g0061 | EAS | KHV | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02083 | hp1 | a0001 | c0001 | t0007 | g0042 | EAS | KHV | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02083 | hp2 | a0005 | c0006 | t0003 | g0163 | EAS | KHV | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02129 | hp1 | a0002 | c0003 | t0001 | g0022 | EAS | KHV | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02129 | hp2 | a0003 | c0005 | t0001 | g0037 | EAS | KHV | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02132 | hp1 | a0004 | c0004 | t0003 | g0074 | EAS | KHV | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02132 | hp2 | a0001 | c0001 | t0007 | g0040 | EAS | KHV | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0107 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02145 | hp2 | a0001 | c0012 | t0028 | g0269 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02148 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02148 | hp2 | a0003 | c0005 | t0005 | g0236 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02165 | hp1 | a0005 | c0006 | t0009 | g0047 | EAS | CDX | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | CDX | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02257 | hp1 | a0002 | c0003 | t0001 | g0228 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02257 | hp2 | a0002 | c0003 | t0001 | g0199 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02258 | hp1 | a0001 | c0041 | t0006 | g0010 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02258 | hp2 | a0011 | c0017 | t0014 | g0197 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02273 | hp1 | a0001 | c0001 | t0011 | g0170 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02273 | hp2 | a0010 | c0016 | t0015 | g0092 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02280 | hp2 | a0001 | c0012 | t0002 | g0268 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02293 | hp1 | a0001 | c0008 | t0002 | g0272 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02293 | hp2 | a0001 | c0001 | t0020 | g0168 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02300 | hp1 | a0003 | c0005 | t0005 | g0260 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02300 | hp2 | a0005 | c0006 | t0003 | g0182 | AMR | PEL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02451 | hp1 | a0002 | c0009 | t0001 | g0278 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02451 | hp2 | a0013 | c0040 | t0006 | g0016 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02523 | hp1 | a0001 | c0035 | t0004 | g0127 | EAS | KHV | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02523 | hp2 | a0002 | c0029 | t0001 | g0125 | EAS | KHV | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02572 | hp1 | a0001 | c0018 | t0006 | g0009 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02572 | hp2 | a0002 | c0003 | t0001 | g0201 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02602 | hp1 | a0002 | c0002 | t0017 | g0139 | SAS | PJL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0262 | SAS | PJL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0223 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02622 | hp1 | a0015 | c0039 | t0001 | g0151 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02622 | hp2 | a0002 | c0002 | t0035 | g0208 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02630 | hp1 | a0002 | c0023 | t0001 | g0212 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02630 | hp2 | a0016 | c0044 | t0001 | g0245 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02698 | hp1 | a0002 | c0003 | t0001 | g0108 | SAS | PJL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0218 | SAS | PJL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02717 | hp2 | a0001 | c0012 | t0002 | g0270 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02735 | hp1 | a0017 | c0031 | t0033 | g0099 | SAS | PJL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02735 | hp2 | a0004 | c0004 | t0003 | g0096 | SAS | PJL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0238 | SAS | PJL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02738 | hp2 | a0001 | c0001 | t0016 | g0056 | SAS | PJL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02809 | hp1 | a0007 | c0010 | t0010 | g0104 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02809 | hp2 | a0005 | c0006 | t0009 | g0277 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0265 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0190 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02895 | hp2 | a0006 | c0007 | t0008 | g0018 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02896 | hp1 | a0001 | c0001 | t0025 | g0024 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0216 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02897 | hp1 | a0006 | c0007 | t0008 | g0017 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02922 | hp1 | a0002 | c0015 | t0001 | g0244 | AFR | ESN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0141 | AFR | ESN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02965 | hp1 | a0006 | c0007 | t0008 | g0281 | AFR | ESN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02965 | hp2 | a0002 | c0015 | t0001 | g0211 | AFR | ESN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02976 | hp1 | a0002 | c0003 | t0001 | g0280 | AFR | ESN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03041 | hp2 | a0007 | c0010 | t0030 | g0102 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0138 | AFR | MSL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | MSL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03130 | hp1 | a0007 | c0010 | t0010 | g0103 | AFR | ESN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0136 | AFR | ESN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03139 | hp1 | a0002 | c0003 | t0001 | g0202 | AFR | ESN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03139 | hp2 | a0002 | c0011 | t0001 | g0222 | AFR | ESN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03195 | hp1 | a0007 | c0010 | t0010 | g0101 | AFR | ESN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03195 | hp2 | a0001 | c0018 | t0006 | g0005 | AFR | ESN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03209 | hp1 | a0002 | c0003 | t0001 | g0279 | AFR | MSL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03209 | hp2 | a0007 | c0010 | t0010 | g0100 | AFR | MSL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0224 | AFR | MSL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | MSL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03239 | hp1 | a0003 | c0005 | t0005 | g0229 | SAS | PJL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03239 | hp2 | a0002 | c0003 | t0001 | g0105 | SAS | PJL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0207 | AFR | MSL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03453 | hp2 | a0002 | c0011 | t0001 | g0253 | AFR | MSL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0143 | AFR | MSL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03486 | hp2 | a0001 | c0037 | t0002 | g0129 | AFR | MSL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03490 | hp1 | a0002 | c0003 | t0001 | g0124 | SAS | PJL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03490 | hp2 | a0004 | c0004 | t0003 | g0087 | SAS | PJL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ESN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03516 | hp2 | a0002 | c0011 | t0001 | g0254 | AFR | ESN | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0142 | AFR | GWD | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03579 | hp1 | a0001 | c0001 | t0021 | g0176 | AFR | MSL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0206 | AFR | MSL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03688 | hp1 | a0002 | c0003 | t0034 | g0130 | SAS | STU | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03688 | hp2 | a0002 | c0002 | t0017 | g0140 | SAS | STU | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0030 | SAS | PJL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03710 | hp1 | a0004 | c0004 | t0003 | g0076 | SAS | PJL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03710 | hp2 | a0002 | c0002 | t0029 | g0237 | SAS | PJL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03927 | hp1 | a0018 | c0019 | t0003 | g0091 | SAS | BEB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03927 | hp2 | a0019 | c0025 | t0001 | g0214 | SAS | BEB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0261 | SAS | BEB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03942 | hp2 | a0002 | c0024 | t0014 | g0196 | SAS | BEB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG04115 | hp1 | a0008 | c0013 | t0013 | g0180 | SAS | STU | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0264 | SAS | STU | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0179 | SAS | BEB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG04184 | hp2 | a0004 | c0004 | t0003 | g0094 | SAS | BEB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG04199 | hp1 | a0004 | c0004 | t0003 | g0086 | SAS | STU | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG04199 | hp2 | a0002 | c0003 | t0001 | g0110 | SAS | STU | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0205 | SAS | STU | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG04204 | hp2 | a0001 | c0022 | t0001 | g0263 | SAS | STU | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG04228 | hp1 | a0001 | c0001 | t0016 | g0049 | SAS | STU | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG04228 | hp2 | a0004 | c0004 | t0022 | g0085 | SAS | STU | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18522 | hp1 | a0006 | c0007 | t0031 | g0282 | AFR | YRI | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | YRI | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | YRI | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18906 | hp2 | a0006 | c0007 | t0008 | g0013 | AFR | YRI | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18941 | hp1 | a0001 | c0001 | t0007 | g0192 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18941 | hp2 | a0003 | c0026 | t0005 | g0204 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18944 | hp1 | a0005 | c0006 | t0003 | g0039 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18944 | hp2 | a0021 | c0038 | t0012 | g0135 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18945 | hp1 | a0004 | c0004 | t0003 | g0073 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18945 | hp2 | a0002 | c0003 | t0032 | g0123 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18948 | hp1 | a0002 | c0009 | t0001 | g0064 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18948 | hp2 | a0005 | c0006 | t0003 | g0148 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18950 | hp1 | a0022 | c0034 | t0004 | g0095 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18950 | hp2 | a0001 | c0001 | t0007 | g0069 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18951 | hp1 | a0003 | c0005 | t0005 | g0231 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18951 | hp2 | a0005 | c0006 | t0009 | g0153 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18959 | hp1 | a0001 | c0001 | t0012 | g0121 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18959 | hp2 | a0005 | c0006 | t0009 | g0038 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18960 | hp1 | a0009 | c0014 | t0002 | g0046 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18960 | hp2 | a0001 | c0001 | t0007 | g0063 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18962 | hp1 | a0002 | c0009 | t0005 | g0043 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18962 | hp2 | a0009 | c0014 | t0002 | g0053 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18963 | hp1 | a0004 | c0004 | t0003 | g0077 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18965 | hp1 | a0003 | c0005 | t0005 | g0232 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18965 | hp2 | a0005 | c0006 | t0003 | g0152 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18972 | hp1 | a0003 | c0005 | t0005 | g0246 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18972 | hp2 | a0001 | c0001 | t0007 | g0058 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18984 | hp1 | a0008 | c0013 | t0027 | g0128 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18984 | hp2 | a0002 | c0003 | t0001 | g0065 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18992 | hp1 | a0003 | c0005 | t0005 | g0225 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18992 | hp2 | a0001 | c0001 | t0007 | g0055 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18993 | hp1 | a0003 | c0005 | t0005 | g0230 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA18993 | hp2 | a0002 | c0003 | t0001 | g0114 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19007 | hp1 | a0002 | c0002 | t0006 | g0178 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19007 | hp2 | a0023 | c0036 | t0007 | g0062 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19009 | hp1 | a0003 | c0005 | t0005 | g0247 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0174 | AFR | LWK | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | LWK | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0137 | AFR | LWK | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19043 | hp2 | a0002 | c0002 | t0019 | g0106 | AFR | LWK | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19054 | hp1 | a0004 | c0004 | t0003 | g0083 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19054 | hp2 | a0002 | c0009 | t0006 | g0146 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19056 | hp1 | a0003 | c0005 | t0005 | g0242 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19056 | hp2 | a0002 | c0003 | t0001 | g0116 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19058 | hp2 | a0005 | c0006 | t0003 | g0161 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19068 | hp1 | a0005 | c0006 | t0003 | g0160 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19077 | hp1 | a0001 | c0001 | t0012 | g0185 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19077 | hp2 | a0005 | c0006 | t0009 | g0052 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19078 | hp1 | a0002 | c0002 | t0006 | g0145 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19078 | hp2 | a0024 | c0042 | t0001 | g0120 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19080 | hp1 | a0004 | c0004 | t0003 | g0098 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19080 | hp2 | a0001 | c0001 | t0007 | g0044 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19083 | hp1 | a0001 | c0001 | t0007 | g0070 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19084 | hp1 | a0003 | c0005 | t0005 | g0210 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19084 | hp2 | a0002 | c0003 | t0001 | g0186 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19086 | hp2 | a0002 | c0003 | t0006 | g0132 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19091 | hp1 | a0002 | c0003 | t0001 | g0113 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19091 | hp2 | a0004 | c0004 | t0003 | g0097 | EAS | JPT | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | YRI | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0213 | AFR | YRI | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA20752 | hp1 | a0004 | c0004 | t0003 | g0089 | EUR | TSI | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA20752 | hp2 | a0002 | c0003 | t0001 | g0119 | EUR | TSI | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01123 | hp1 | a0004 | c0004 | t0003 | g0090 | AMR | CLM | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02109 | hp1 | a0002 | c0011 | t0001 | g0255 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02486 | hp1 | a0011 | c0017 | t0014 | g0195 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0173 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02559 | hp1 | a0014 | c0028 | t0001 | g0200 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG02559 | hp2 | a0002 | c0015 | t0001 | g0243 | AFR | ACB | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03471 | hp1 | a0006 | c0007 | t0008 | g0019 | AFR | MSL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG03471 | hp2 | a0002 | c0011 | t0001 | g0220 | AFR | MSL | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG06807 | hp1 | a0020 | c0021 | t0024 | g0189 | AFR | USA | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0217 | AFR | USA | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA20300 | hp1 | a0007 | c0030 | t0002 | g0271 | AFR | USA | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0233 | AFR | USA | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA21309 | hp1 | a0001 | c0001 | t0018 | g0112 | AFR | LWK | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0259 | AFR | LWK | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0188 | REF | REF | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
homoSapiens | grch38p0 | a0007 | c0043 | t0010 | g0221 | REF | REF | WNK1_chr12_747579_916452 | WNK1 | chr12 | 747579 | 916452 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:753986 | G | A | 4 | a0004 a0010 a0018 others(1): Show |
26 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(23): Show |
missense_variant | MODERATE | c.421G>A | p.Ala141Thr | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/28 | 1408/10796 | 421/7149 | 141/2382 | chr12 | 753986 | |||
chr12:754011 | C | T | 1 | a0009 | 3 | HG02074.hp2 NA18960.hp1 NA18962.hp2 |
missense_variant | MODERATE | c.446C>T | p.Ala149Val | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/28 | 1433/10796 | 446/7149 | 149/2382 | chr12 | 754011 | |||
chr12:754076 | C | T | 1 | a0024 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.511C>T | p.Leu171Phe | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/28 | 1498/10796 | 511/7149 | 171/2382 | chr12 | 754076 | |||
chr12:859370 | T | C | 3 | a0006 a0013 a0020 |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
missense_variant | MODERATE | c.1526T>C | p.Ile509Thr | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/28 | 2513/10796 | 1526/7149 | 509/2382 | chr12 | 859370 | |||
chr12:862125 | C | T | 1 | a0003 | 22 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(19): Show |
missense_variant | MODERATE | c.1994C>T | p.Thr665Ile | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/28 | 2981/10796 | 1994/7149 | 665/2382 | chr12 | 862125 | |||
chr12:862151 | A | G | 1 | a0016 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.2020A>G | p.Thr674Ala | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/28 | 3007/10796 | 2020/7149 | 674/2382 | chr12 | 862151 | |||
chr12:862212 | T | C | 3 | a0006 a0013 a0020 |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
missense_variant | MODERATE | c.2081T>C | p.Ile694Thr | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/28 | 3068/10796 | 2081/7149 | 694/2382 | chr12 | 862212 | |||
chr12:871331 | A | G | 1 | a0019 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.2206A>G | p.Ile736Val | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/28 | 3193/10796 | 2206/7149 | 736/2382 | chr12 | 871331 | |||
chr12:879855 | C | G | 1 | a0015 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.2656C>G | p.Pro886Ala | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 11/28 | 3643/10796 | 2656/7149 | 886/2382 | chr12 | 879855 | |||
chr12:881746 | A | C | 17 | a0001 a0002 a0003 others(14): Show |
227 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(224): Show |
missense_variant | MODERATE | c.3166A>C | p.Thr1056Pro | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 13/28 | 4153/10796 | 3166/7149 | 1056/2382 | chr12 | 881746 | |||
chr12:883421 | A | G | 1 | a0021 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.3516A>G | p.Ile1172Met | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 16/28 | 4503/10796 | 3516/7149 | 1172/2382 | chr12 | 883421 | |||
chr12:883483 | G | A | 1 | a0018 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.3578G>A | p.Ser1193Asn | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 16/28 | 4565/10796 | 3578/7149 | 1193/2382 | chr12 | 883483 | |||
chr12:884902 | T | G | 1 | a0014 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.4098T>G | p.Ile1366Met | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/28 | 5085/10796 | 4098/7149 | 1366/2382 | chr12 | 884902 | |||
chr12:885158 | A | G | 1 | a0017 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.4354A>G | p.Thr1452Ala | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/28 | 5341/10796 | 4354/7149 | 1452/2382 | chr12 | 885158 | |||
chr12:885321 | G | C | 23 | a0001 a0002 a0003 others(20): Show |
276 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(273): Show |
missense_variant | MODERATE | c.4517G>C | p.Cys1506Ser | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/28 | 5504/10796 | 4517/7149 | 1506/2382 | chr12 | 885321 | |||
chr12:885540 | C | T | 1 | a0023 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.4736C>T | p.Thr1579Ile | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/28 | 5723/10796 | 4736/7149 | 1579/2382 | chr12 | 885540 | |||
chr12:889199 | G | T | 9 | a0002 a0003 a0010 others(6): Show |
120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
missense_variant | MODERATE | c.5424G>T | p.Met1808Ile | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 21/28 | 6411/10796 | 5424/7149 | 1808/2382 | chr12 | 889199 | |||
chr12:890472 | C | T | 1 | a0008 | 4 | HG00609.hp1 HG01243.hp2 HG04115.hp1 others(1): Show |
missense_variant | MODERATE | c.5468C>T | p.Pro1823Leu | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/28 | 6455/10796 | 5468/7149 | 1823/2382 | chr12 | 890472 | |||
chr12:896320 | C | T | 1 | a0022 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.5833C>T | p.Arg1945Cys | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/28 | 6820/10796 | 5833/7149 | 1945/2382 | chr12 | 896320 | |||
chr12:896356 | C | T | 1 | a0012 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.5869C>T | p.Arg1957Cys | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/28 | 6856/10796 | 5869/7149 | 1957/2382 | chr12 | 896356 | |||
chr12:900651 | C | A | 1 | a0011 | 2 | HG02258.hp2 HG02486.hp1 |
missense_variant | MODERATE | c.6624C>A | p.Ser2208Arg | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/28 | 7611/10796 | 6624/7149 | 2208/2382 | chr12 | 900651 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:753823 | T | C | 40 | a0001c0001 a0001c0008 a0001c0012 others(37): Show |
273 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(270): Show |
synonymous_variant | LOW | c.258T>C | p.Cys86Cys | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/28 | 1245/10796 | 258/7149 | 86/2382 | chr12 | 753823 | |||
chr12:754249 | C | T | 1 | a0001c0018 | 2 | HG02572.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.684C>T | p.Gly228Gly | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/28 | 1671/10796 | 684/7149 | 228/2382 | chr12 | 754249 | |||
chr12:830061 | C | T | 1 | a0001c0041 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.1212C>T | p.Asp404Asp | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/28 | 2199/10796 | 1212/7149 | 404/2382 | chr12 | 830061 | |||
chr12:830136 | A | G | 32 | a0001c0001 a0001c0008 a0001c0012 others(29): Show |
199 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
synonymous_variant | LOW | c.1287A>G | p.Ala429Ala | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/28 | 2274/10796 | 1287/7149 | 429/2382 | chr12 | 830136 | |||
chr12:859323 | T | C | 3 | a0004c0004 a0005c0027 a0018c0019 |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
synonymous_variant | LOW | c.1479T>C | p.Asp493Asp | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/28 | 2466/10796 | 1479/7149 | 493/2382 | chr12 | 859323 | |||
chr12:859356 | A | G | 3 | a0006c0007 a0013c0040 a0020c0021 |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
synonymous_variant | LOW | c.1512A>G | p.Leu504Leu | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/28 | 2499/10796 | 1512/7149 | 504/2382 | chr12 | 859356 | |||
chr12:878316 | G | A | 30 | a0001c0001 a0001c0008 a0001c0012 others(27): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
synonymous_variant | LOW | c.2328G>A | p.Gln776Gln | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/28 | 3315/10796 | 2328/7149 | 776/2382 | chr12 | 878316 | |||
chr12:879728 | G | A | 6 | a0001c0008 a0001c0012 a0002c0003 others(3): Show |
39 | HG00280.hp2 HG00423.hp2 HG00741.hp1 others(36): Show |
synonymous_variant | LOW | c.2529G>A | p.Gln843Gln | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 11/28 | 3516/10796 | 2529/7149 | 843/2382 | chr12 | 879728 | |||
chr12:879857 | G | A | 1 | a0003c0026 | 1 | NA18941.hp2 | synonymous_variant | LOW | c.2658G>A | p.Pro886Pro | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 11/28 | 3645/10796 | 2658/7149 | 886/2382 | chr12 | 879857 | |||
chr12:883487 | G | A | 1 | a0011c0017 | 2 | HG02258.hp2 HG02486.hp1 |
synonymous_variant | LOW | c.3582G>A | p.Glu1194Glu | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 16/28 | 4569/10796 | 3582/7149 | 1194/2382 | chr12 | 883487 | |||
chr12:883559 | A | G | 2 | a0002c0024 a0011c0017 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
synonymous_variant | LOW | c.3654A>G | p.Ser1218Ser | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 16/28 | 4641/10796 | 3654/7149 | 1218/2382 | chr12 | 883559 | |||
chr12:884764 | C | T | 13 | a0001c0001 a0001c0018 a0001c0032 others(10): Show |
96 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
synonymous_variant | LOW | c.3960C>T | p.Asn1320Asn | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/28 | 4947/10796 | 3960/7149 | 1320/2382 | chr12 | 884764 | |||
chr12:884848 | C | T | 5 | a0004c0004 a0004c0020 a0005c0006 others(2): Show |
39 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(36): Show |
synonymous_variant | LOW | c.4044C>T | p.Thr1348Thr | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/28 | 5031/10796 | 4044/7149 | 1348/2382 | chr12 | 884848 | |||
chr12:884908 | A | G | 1 | a0001c0037 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.4104A>G | p.Thr1368Thr | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/28 | 5091/10796 | 4104/7149 | 1368/2382 | chr12 | 884908 | |||
chr12:885787 | T | C | 1 | a0017c0031 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.4983T>C | p.Ser1661Ser | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/28 | 5970/10796 | 4983/7149 | 1661/2382 | chr12 | 885787 | |||
chr12:885805 | C | T | 1 | a0001c0035 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.5001C>T | p.Ser1667Ser | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/28 | 5988/10796 | 5001/7149 | 1667/2382 | chr12 | 885805 | |||
chr12:889172 | A | G | 1 | a0001c0008 | 6 | HG00741.hp1 HG01928.hp2 HG01934.hp2 others(3): Show |
synonymous_variant | LOW | c.5397A>G | p.Gln1799Gln | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 21/28 | 6384/10796 | 5397/7149 | 1799/2382 | chr12 | 889172 | |||
chr12:890485 | A | G | 1 | a0002c0015 | 3 | HG02559.hp2 HG02922.hp1 HG02965.hp2 |
synonymous_variant | LOW | c.5481A>G | p.Thr1827Thr | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/28 | 6468/10796 | 5481/7149 | 1827/2382 | chr12 | 890485 | |||
chr12:890497 | A | T | 1 | a0002c0029 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.5493A>T | p.Thr1831Thr | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/28 | 6480/10796 | 5493/7149 | 1831/2382 | chr12 | 890497 | |||
chr12:896610 | T | A | 1 | a0001c0032 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.6123T>A | p.Leu2041Leu | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/28 | 7110/10796 | 6123/7149 | 2041/2382 | chr12 | 896610 | |||
chr12:900651 | C | T | 1 | a0002c0023 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.6624C>T | p.Ser2208Ser | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/28 | 7611/10796 | 6624/7149 | 2208/2382 | chr12 | 900651 | |||
chr12:908031 | C | T | 42 | a0001c0001 a0001c0008 a0001c0012 others(39): Show |
277 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(274): Show |
synonymous_variant | LOW | c.6828C>T | p.Tyr2276Tyr | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 27/28 | 7815/10796 | 6828/7149 | 2276/2382 | chr12 | 908031 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:752851 | C | T | 1 | a0002c0002t0035 | 1 | HG02622.hp2 | 5_prime_UTR_variant | MODIFIER | c.-715C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/28 | 715 | chr12 | 752851 | ||||||
chr12:752873 | G | A | 2 | a0001c0001t0018 a0002c0002t0019 |
2 | NA19043.hp2 NA21309.hp1 |
5_prime_UTR_variant | MODIFIER | c.-693G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/28 | 693 | chr12 | 752873 | ||||||
chr12:752957 | G | A | 1 | a0001c0001t0020 | 1 | HG02293.hp2 | 5_prime_UTR_variant | MODIFIER | c.-609G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/28 | 609 | chr12 | 752957 | ||||||
chr12:752968 | C | G | 2 | a0002c0002t0017 a0002c0003t0034 |
3 | HG02602.hp1 HG03688.hp1 HG03688.hp2 |
5_prime_UTR_variant | MODIFIER | c.-598C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/28 | 598 | chr12 | 752968 | ||||||
chr12:753114 | G | A | 3 | a0002c0009t0005 a0003c0005t0005 a0003c0026t0005 |
17 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-452G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/28 | 452 | chr12 | 753114 | ||||||
chr12:753353 | G | T | 2 | a0002c0024t0014 a0011c0017t0014 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
5_prime_UTR_variant | MODIFIER | c.-213G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/28 | 213 | chr12 | 753353 | ||||||
chr12:753363 | C | G | 1 | a0001c0001t0011 | 5 | HG00735.hp1 HG01943.hp2 HG01978.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-203C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/28 | chr12 | 753363 | |||||||
chr12:753444 | C | T | 1 | a0017c0031t0033 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-122C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/28 | 122 | chr12 | 753444 | ||||||
chr12:753475 | T | G | 29 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0011 others(26): Show |
94 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
5_prime_UTR_variant | MODIFIER | c.-91T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/28 | 91 | chr12 | 753475 | ||||||
chr12:753495 | G | A | 1 | a0017c0031t0033 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-71G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/28 | 71 | chr12 | 753495 | ||||||
chr12:753541 | C | G | 1 | a0001c0001t0026 | 1 | HG01255.hp2 | 5_prime_UTR_variant | MODIFIER | c.-25C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/28 | 25 | chr12 | 753541 | ||||||
chr12:753543 | C | T | 1 | a0002c0003t0032 | 1 | NA18945.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-23C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/28 | chr12 | 753543 | |||||||
chr12:909356 | A | G | 1 | a0001c0001t0025 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*564A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 564 | chr12 | 909356 | ||||||
chr12:909550 | C | G | 3 | a0006c0007t0008 a0006c0007t0031 a0020c0021t0024 |
9 | HG01109.hp2 HG01358.hp1 HG02895.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*758C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 758 | chr12 | 909550 | ||||||
chr12:909826 | T | C | 1 | a0001c0001t0026 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1034T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 1034 | chr12 | 909826 | ||||||
chr12:909938 | G | A | 2 | a0006c0007t0008 a0006c0007t0031 |
8 | HG01109.hp2 HG01358.hp1 HG02895.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1146G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 1146 | chr12 | 909938 | ||||||
chr12:910078 | G | T | 1 | a0020c0021t0024 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1286G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 1286 | chr12 | 910078 | ||||||
chr12:910134 | G | T | 1 | a0001c0001t0023 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1342G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 1342 | chr12 | 910134 | ||||||
chr12:910287 | T | TATC | 25 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(22): Show |
92 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*1496_*1498dupATC | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 1499 | INFO_REALIGN_3_PRIME | chr12 | 910287 | |||||
chr12:910448 | C | A | 1 | a0001c0001t0016 | 2 | HG02738.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1656C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 1656 | chr12 | 910448 | ||||||
chr12:910673 | C | T | 1 | a0004c0004t0022 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1881C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 1881 | chr12 | 910673 | ||||||
chr12:910714 | T | C | 1 | a0008c0013t0027 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1922T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 1922 | chr12 | 910714 | ||||||
chr12:910778 | G | A | 71 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(68): Show |
277 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*1986G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 1986 | chr12 | 910778 | ||||||
chr12:910799 | C | T | 1 | a0001c0012t0028 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2007C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 2007 | chr12 | 910799 | ||||||
chr12:910894 | T | TCTCTGCT others(8): Show |
1 | a0007c0010t0030 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2103_*2117dupCTCT others(11): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 2118 | INFO_REALIGN_3_PRIME | chr12 | 910894 | |||||
chr12:911100 | T | C | 8 | a0004c0004t0003 a0004c0004t0022 a0004c0020t0003 others(5): Show |
40 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2308T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 2308 | chr12 | 911100 | ||||||
chr12:911205 | G | T | 2 | a0008c0013t0013 a0008c0013t0027 |
4 | HG00609.hp1 HG01243.hp2 HG04115.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2413G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 2413 | chr12 | 911205 | ||||||
chr12:911266 | A | G | 1 | a0001c0001t0021 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2474A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 2474 | chr12 | 911266 | ||||||
chr12:911289 | T | C | 1 | a0002c0002t0029 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2497T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 2497 | chr12 | 911289 | ||||||
chr12:911340 | C | CACTA | 4 | a0001c0001t0007 a0001c0001t0012 a0021c0038t0012 others(1): Show |
17 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2552_*2555dupAACT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 2556 | INFO_REALIGN_3_PRIME | chr12 | 911340 | |||||
chr12:911343 | T | TAAC | 3 | a0006c0007t0008 a0006c0007t0031 a0020c0021t0024 |
9 | HG01109.hp2 HG01358.hp1 HG02895.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2552_*2554dupAAC | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 2555 | INFO_REALIGN_3_PRIME | chr12 | 911343 | |||||
chr12:911405 | G | GACTT | 2 | a0002c0002t0017 a0010c0016t0015 |
4 | HG01261.hp1 HG02273.hp2 HG02602.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2615_*2618dupCTTA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 28/28 | 2619 | INFO_REALIGN_3_PRIME | chr12 | 911405 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:754339 | A | ACTT | 20 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0006g0003 others(17): Show |
20 | HG00735.hp2 HG01074.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.759+16_759+18dupCT others(1): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 754339 | ||||||
chr12:754339 | A | C | 18 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(15): Show |
18 | HG00741.hp1 HG01358.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.759+15A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 754339 | |||||||
chr12:754351 | G | A | 171 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(168): Show |
172 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.759+27G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 754351 | |||||||
chr12:754425 | G | A | 1 | a0003c0005t0001g0193 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.759+101G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 754425 | |||||||
chr12:754436 | G | A | 1 | a0002c0003t0001g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.759+112G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 754436 | |||||||
chr12:754488 | T | C | 2 | a0001c0001t0004g0023 a0001c0001t0025g0024 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.759+164T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 754488 | |||||||
chr12:754569 | T | C | 1 | a0002c0002t0001g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.759+245T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 754569 | |||||||
chr12:754664 | T | G | 5 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 others(2): Show |
5 | HG02109.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+340T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 754664 | |||||||
chr12:754667 | A | G | 176 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(173): Show |
177 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.759+343A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 754667 | |||||||
chr12:754942 | T | A | 1 | a0001c0001t0004g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.759+618T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 754942 | |||||||
chr12:754943 | C | T | 2 | a0001c0001t0004g0030 a0003c0005t0005g0260 |
2 | HG02300.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.759+619C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 754943 | |||||||
chr12:754945 | C | G | 1 | a0001c0001t0004g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.759+621C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 754945 | |||||||
chr12:754988 | T | G | 1 | a0001c0001t0002g0031 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.759+664T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 754988 | |||||||
chr12:755014 | C | T | 1 | a0001c0001t0007g0192 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.759+690C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 755014 | |||||||
chr12:755014 | CATT | C | 4 | a0002c0002t0001g0256 a0002c0002t0001g0257 a0002c0002t0001g0258 others(1): Show |
4 | HG01168.hp1 HG01169.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+691_759+693del others(3): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 755014 | |||||||
chr12:755311 | T | C | 46 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0031 others(43): Show |
46 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.759+987T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 755311 | |||||||
chr12:755354 | G | A | 2 | a0001c0001t0004g0002 a0001c0001t0006g0003 |
2 | HG01074.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.759+1030G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 755354 | |||||||
chr12:755555 | C | G | 1 | a0002c0002t0001g0191 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.759+1231C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 755555 | |||||||
chr12:755559 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.759+1235G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 755559 | |||||||
chr12:755582 | CATTA | C | 3 | a0002c0011t0001g0253 a0002c0011t0001g0254 a0002c0011t0001g0255 |
3 | HG02109.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.759+1262_759+1265d others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 755582 | ||||||
chr12:755626 | TA | T | 25 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0006g0003 others(22): Show |
25 | HG00735.hp2 HG01074.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.759+1314delA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 755626 | ||||||
chr12:755721 | A | C | 1 | a0005c0006t0009g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.759+1397A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 755721 | |||||||
chr12:755795 | G | A | 1 | a0001c0001t0007g0032 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.759+1471G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 755795 | |||||||
chr12:755998 | C | A | 28 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(25): Show |
28 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.759+1674C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 755998 | |||||||
chr12:756223 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.759+1899A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 756223 | |||||||
chr12:756248 | CTTCTGAG others(24): Show |
C | 1 | a0004c0004t0003g0072 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.759+1928_759+1958d others(33): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 756248 | ||||||
chr12:756260 | C | G | 6 | a0001c0001t0006g0006 a0001c0001t0006g0008 a0001c0018t0006g0005 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.759+1936C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 756260 | |||||||
chr12:756383 | A | G | 2 | a0001c0001t0007g0070 a0001c0001t0007g0192 |
2 | NA18941.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.759+2059A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 756383 | |||||||
chr12:756449 | T | C | 8 | a0001c0001t0002g0198 a0002c0003t0001g0199 a0002c0003t0001g0201 others(5): Show |
8 | HG01081.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.759+2125T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 756449 | |||||||
chr12:756681 | G | T | 1 | a0001c0001t0006g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.759+2357G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 756681 | |||||||
chr12:756744 | T | C | 2 | a0003c0005t0005g0203 a0003c0026t0005g0204 |
2 | HG00544.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.759+2420T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 756744 | |||||||
chr12:756797 | G | A | 1 | a0002c0002t0001g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.759+2473G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 756797 | |||||||
chr12:756804 | C | G | 195 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.759+2480C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 756804 | |||||||
chr12:756834 | G | A | 1 | a0002c0002t0001g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.759+2510G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 756834 | |||||||
chr12:756854 | G | A | 1 | a0002c0002t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.759+2530G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 756854 | |||||||
chr12:756915 | G | C | 1 | a0002c0002t0035g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.759+2591G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 756915 | |||||||
chr12:757042 | C | T | 23 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0006g0003 others(20): Show |
23 | HG00735.hp2 HG01074.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.759+2718C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757042 | |||||||
chr12:757128 | CTTA | C | 23 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0006g0003 others(20): Show |
23 | HG00735.hp2 HG01074.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.759+2806_759+2808d others(5): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 757128 | ||||||
chr12:757242 | T | C | 1 | a0008c0013t0013g0033 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.759+2918T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757242 | |||||||
chr12:757309 | C | CT | 7 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0007g0069 others(4): Show |
7 | HG01106.hp1 HG01255.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.759+3009dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 757309 | ||||||
chr12:757309 | CTT | C | 24 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(21): Show |
24 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.759+3008_759+3009d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 757309 | ||||||
chr12:757309 | CTTTTT | C | 7 | a0001c0001t0006g0006 a0001c0001t0006g0008 a0001c0018t0006g0005 others(4): Show |
7 | HG01169.hp1 HG01884.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.759+3005_759+3009d others(7): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 757309 | ||||||
chr12:757309 | CTTTTTTT others(5): Show |
C | 1 | a0001c0008t0002g0266 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.759+2998_759+3009d others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 757309 | ||||||
chr12:757320 | TTTTTTTT others(8): Show |
T | 1 | a0001c0001t0002g0025 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.759+2997_759+3011d others(17): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757320 | |||||||
chr12:757332 | TTAA | T | 15 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(12): Show |
15 | HG01261.hp2 HG01952.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.759+3009_759+3011d others(5): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757332 | |||||||
chr12:757333 | T | A | 51 | a0001c0001t0002g0198 a0001c0001t0006g0006 a0001c0001t0006g0008 others(48): Show |
51 | HG00408.hp2 HG00423.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.759+3009T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757333 | |||||||
chr12:757333 | T | TAA | 7 | a0006c0007t0008g0011 a0006c0007t0008g0017 a0006c0007t0008g0018 others(4): Show |
7 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.759+3019_759+3020d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 757333 | ||||||
chr12:757333 | T | TTA | 8 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0006g0003 others(5): Show |
8 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.759+3009_759+3010i others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757333 | |||||||
chr12:757333 | TA | T | 20 | a0001c0001t0002g0034 a0001c0001t0002g0060 a0001c0001t0004g0154 others(17): Show |
20 | HG00735.hp1 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.759+3020delA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 757333 | ||||||
chr12:757333 | TAA | T | 43 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(40): Show |
44 | HG00280.hp1 HG00673.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.759+3019_759+3020d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 757333 | ||||||
chr12:757334 | A | T | 70 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0031 others(67): Show |
70 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.759+3010A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757334 | |||||||
chr12:757335 | A | T | 87 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0031 others(84): Show |
87 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.759+3011A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757335 | |||||||
chr12:757336 | A | T | 7 | a0001c0001t0002g0066 a0001c0001t0002g0071 a0001c0001t0004g0023 others(4): Show |
7 | HG00408.hp1 HG00741.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.759+3012A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757336 | |||||||
chr12:757337 | A | T | 1 | a0001c0001t0002g0071 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.759+3013A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757337 | |||||||
chr12:757352 | A | T | 176 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(173): Show |
177 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.759+3028A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757352 | |||||||
chr12:757353 | G | T | 176 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(173): Show |
177 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.759+3029G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757353 | |||||||
chr12:757354 | T | TTTA | 176 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(173): Show |
177 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.759+3030_759+3031i others(5): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757354 | |||||||
chr12:757357 | T | C | 176 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(173): Show |
177 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.759+3033T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757357 | |||||||
chr12:757358 | G | C | 176 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(173): Show |
177 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.759+3034G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757358 | |||||||
chr12:757359 | C | G | 176 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(173): Show |
177 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.759+3035C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757359 | |||||||
chr12:757363 | A | G | 2 | a0001c0001t0004g0023 a0001c0001t0025g0024 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.759+3039A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757363 | |||||||
chr12:757412 | G | A | 5 | a0001c0012t0002g0267 a0001c0012t0002g0268 a0001c0012t0002g0270 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.759+3088G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757412 | |||||||
chr12:757470 | C | T | 1 | a0002c0003t0001g0186 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.759+3146C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757470 | |||||||
chr12:757516 | A | G | 1 | a0004c0004t0003g0094 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.759+3192A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757516 | |||||||
chr12:757634 | GGTTGTCT others(7976): Show |
G | 27 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(24): Show |
27 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.759+3316_759+11298 others(3): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 757634 | ||||||
chr12:757790 | C | A | 1 | a0003c0005t0005g0209 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.759+3466C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757790 | |||||||
chr12:757803 | C | T | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.759+3479C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757803 | |||||||
chr12:757857 | G | A | 144 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(141): Show |
145 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.759+3533G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 757857 | |||||||
chr12:758035 | T | TA | 25 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0006g0003 others(22): Show |
25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.759+3730dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 758035 | ||||||
chr12:758035 | TAAAA | T | 149 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(146): Show |
150 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.759+3727_759+3730d others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 758035 | ||||||
chr12:758051 | A | G | 1 | a0001c0001t0002g0066 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.759+3727A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 758051 | |||||||
chr12:758187 | A | G | 2 | a0006c0007t0008g0017 a0006c0007t0008g0018 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.759+3863A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 758187 | |||||||
chr12:758269 | C | G | 1 | a0002c0002t0001g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.759+3945C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 758269 | |||||||
chr12:758373 | C | CT | 81 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(78): Show |
82 | HG00323.hp1 HG00609.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.759+4074dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 758373 | ||||||
chr12:758373 | C | CTT | 38 | a0001c0001t0002g0111 a0001c0001t0002g0165 a0001c0001t0004g0150 others(35): Show |
38 | HG00280.hp1 HG00544.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.759+4073_759+4074d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 758373 | ||||||
chr12:758373 | C | CTTT | 76 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0031 others(73): Show |
76 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.759+4072_759+4074d others(5): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 758373 | ||||||
chr12:758373 | C | CTTTT | 27 | a0001c0001t0002g0051 a0001c0001t0004g0002 a0001c0001t0006g0003 others(24): Show |
27 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.759+4071_759+4074d others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 758373 | ||||||
chr12:758373 | C | CTTTTT | 6 | a0001c0001t0006g0012 a0001c0001t0006g0014 a0001c0001t0006g0015 others(3): Show |
6 | HG00735.hp2 HG01358.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.759+4070_759+4074d others(7): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 758373 | ||||||
chr12:758425 | G | C | 140 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(137): Show |
141 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.759+4101G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 758425 | |||||||
chr12:758542 | C | T | 154 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(151): Show |
155 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.759+4218C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 758542 | |||||||
chr12:758544 | T | C | 178 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(175): Show |
179 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.759+4220T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 758544 | |||||||
chr12:758548 | C | T | 155 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(152): Show |
156 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.759+4224C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 758548 | |||||||
chr12:758552 | T | C | 6 | a0001c0001t0012g0121 a0005c0006t0003g0152 a0005c0006t0003g0156 others(3): Show |
6 | HG01993.hp1 HG02004.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+4228T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 758552 | |||||||
chr12:758578 | G | A | 1 | a0002c0002t0001g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.759+4254G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 758578 | |||||||
chr12:758749 | G | T | 13 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(10): Show |
13 | HG01261.hp2 HG01952.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.759+4425G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 758749 | |||||||
chr12:758924 | T | C | 1 | a0001c0001t0018g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.759+4600T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 758924 | |||||||
chr12:758927 | A | G | 1 | a0002c0003t0001g0108 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.759+4603A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 758927 | |||||||
chr12:759009 | C | CA | 23 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0006g0003 others(20): Show |
23 | HG00735.hp2 HG01074.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.759+4691dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 759009 | ||||||
chr12:759245 | C | A | 194 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.759+4921C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 759245 | |||||||
chr12:759400 | G | A | 3 | a0002c0002t0001g0194 a0002c0002t0001g0213 a0002c0002t0001g0224 |
3 | HG03225.hp1 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.759+5076G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 759400 | |||||||
chr12:759491 | C | A | 1 | a0002c0002t0001g0191 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.759+5167C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 759491 | |||||||
chr12:759538 | C | T | 1 | a0001c0032t0002g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.759+5214C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 759538 | |||||||
chr12:759653 | T | C | 1 | a0002c0002t0001g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.759+5329T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 759653 | |||||||
chr12:759687 | G | C | 2 | a0001c0001t0004g0002 a0001c0001t0006g0003 |
2 | HG01074.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.759+5363G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 759687 | |||||||
chr12:759856 | G | C | 1 | a0001c0001t0004g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.759+5532G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 759856 | |||||||
chr12:760294 | G | A | 2 | a0001c0001t0004g0023 a0001c0001t0025g0024 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.759+5970G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 760294 | |||||||
chr12:760455 | A | C | 1 | a0002c0002t0001g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.759+6131A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 760455 | |||||||
chr12:760508 | A | C | 1 | a0001c0001t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.759+6184A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 760508 | |||||||
chr12:760593 | T | C | 1 | a0001c0001t0002g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.759+6269T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 760593 | |||||||
chr12:760809 | A | G | 3 | a0006c0007t0008g0017 a0006c0007t0008g0018 a0006c0007t0008g0019 |
3 | HG02895.hp2 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.759+6485A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 760809 | |||||||
chr12:760847 | C | T | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.759+6523C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 760847 | |||||||
chr12:760936 | G | A | 3 | a0001c0001t0007g0040 a0001c0001t0007g0041 a0001c0001t0007g0042 |
3 | HG00438.hp1 HG02083.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.759+6612G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 760936 | |||||||
chr12:760940 | A | AT | 25 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0006g0003 others(22): Show |
25 | HG00735.hp2 HG01074.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.759+6632dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 760940 | ||||||
chr12:760940 | AT | A | 45 | a0001c0001t0002g0198 a0001c0001t0002g0227 a0001c0001t0004g0150 others(42): Show |
45 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.759+6632delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 760940 | ||||||
chr12:760981 | C | G | 6 | a0001c0001t0002g0001 a0001c0037t0002g0129 a0007c0010t0010g0101 others(3): Show |
7 | HG01496.hp1 HG02809.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.759+6657C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 760981 | |||||||
chr12:761445 | G | A | 20 | a0003c0005t0001g0193 a0003c0005t0001g0240 a0003c0005t0001g0241 others(17): Show |
20 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.759+7121G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 761445 | |||||||
chr12:761446 | T | C | 13 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0006g0003 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.759+7122T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 761446 | |||||||
chr12:761559 | C | T | 3 | a0002c0003t0001g0113 a0002c0003t0001g0114 a0024c0042t0001g0120 |
3 | NA18993.hp2 NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.759+7235C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 761559 | |||||||
chr12:761804 | C | T | 13 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(10): Show |
13 | HG01261.hp2 HG01952.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.759+7480C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 761804 | |||||||
chr12:761939 | T | C | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.759+7615T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 761939 | |||||||
chr12:762045 | G | C | 154 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(151): Show |
155 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.759+7721G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 762045 | |||||||
chr12:762062 | AT | A | 173 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(170): Show |
174 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.759+7753delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 762062 | ||||||
chr12:762273 | T | C | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.759+7949T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 762273 | |||||||
chr12:762306 | T | A | 150 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(147): Show |
151 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.759+7982T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 762306 | |||||||
chr12:762324 | C | T | 1 | a0011c0017t0014g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.759+8000C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 762324 | |||||||
chr12:762475 | G | T | 3 | a0001c0001t0012g0185 a0005c0006t0003g0161 a0005c0006t0003g0163 |
3 | HG02083.hp2 NA19058.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.759+8151G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 762475 | |||||||
chr12:762651 | T | C | 1 | a0005c0006t0009g0277 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.759+8327T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 762651 | |||||||
chr12:762730 | G | A | 1 | a0003c0026t0005g0204 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.759+8406G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 762730 | |||||||
chr12:762925 | T | C | 23 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0006g0003 others(20): Show |
23 | HG00735.hp2 HG01074.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.759+8601T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 762925 | |||||||
chr12:762938 | G | A | 1 | a0001c0001t0007g0063 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.759+8614G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 762938 | |||||||
chr12:762989 | G | A | 1 | a0001c0001t0002g0045 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.759+8665G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 762989 | |||||||
chr12:762993 | G | A | 3 | a0001c0001t0007g0040 a0001c0001t0007g0041 a0001c0001t0007g0042 |
3 | HG00438.hp1 HG02083.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.759+8669G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 762993 | |||||||
chr12:763217 | A | G | 1 | a0002c0003t0001g0279 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.759+8893A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 763217 | |||||||
chr12:763321 | C | T | 12 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(9): Show |
12 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.759+8997C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 763321 | |||||||
chr12:763443 | G | A | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+9119G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 763443 | |||||||
chr12:763446 | G | A | 1 | a0002c0002t0029g0237 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.759+9122G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 763446 | |||||||
chr12:763589 | C | CA | 141 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(138): Show |
142 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.759+9275dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 763589 | ||||||
chr12:764110 | G | C | 2 | a0001c0001t0004g0002 a0001c0001t0006g0003 |
2 | HG01074.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.759+9786G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 764110 | |||||||
chr12:764225 | C | A | 1 | a0001c0001t0002g0071 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.759+9901C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 764225 | |||||||
chr12:764434 | G | C | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.759+10110G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 764434 | |||||||
chr12:764510 | C | G | 1 | a0003c0005t0005g0246 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.759+10186C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 764510 | |||||||
chr12:764634 | C | CA | 144 | a0001c0001t0001g0067 a0001c0001t0002g0001 a0001c0001t0002g0034 others(141): Show |
145 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.759+10330dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 764634 | ||||||
chr12:764634 | C | CAA | 12 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0028 others(9): Show |
12 | HG00438.hp2 HG02109.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.759+10329_759+1033 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 764634 | ||||||
chr12:764856 | A | G | 1 | a0002c0002t0017g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.759+10532A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 764856 | |||||||
chr12:764975 | A | G | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.759+10651A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 764975 | |||||||
chr12:764980 | C | T | 1 | a0001c0008t0002g0266 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.759+10656C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 764980 | |||||||
chr12:765598 | A | G | 178 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(175): Show |
179 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.759+11274A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 765598 | |||||||
chr12:765610 | T | G | 2 | a0002c0003t0001g0131 a0002c0003t0001g0228 |
2 | HG00280.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.759+11286T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 765610 | |||||||
chr12:765624 | C | G | 1 | a0002c0002t0001g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.759+11300C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 765624 | |||||||
chr12:765697 | C | T | 1 | a0002c0009t0001g0064 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.759+11373C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 765697 | |||||||
chr12:765698 | G | A | 1 | a0003c0005t0005g0209 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.759+11374G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 765698 | |||||||
chr12:765928 | A | G | 22 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0006g0003 others(19): Show |
22 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.759+11604A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 765928 | |||||||
chr12:766079 | G | C | 1 | a0004c0004t0003g0073 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.759+11755G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 766079 | |||||||
chr12:766120 | T | C | 1 | a0001c0001t0002g0034 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.759+11796T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 766120 | |||||||
chr12:766137 | G | T | 1 | a0001c0001t0012g0185 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.759+11813G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 766137 | |||||||
chr12:766157 | G | A | 1 | a0001c0001t0007g0035 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.759+11833G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 766157 | |||||||
chr12:766487 | C | CT | 52 | a0001c0001t0002g0060 a0001c0001t0002g0165 a0001c0001t0004g0023 others(49): Show |
52 | HG00280.hp1 HG00673.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.759+12174dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 766487 | ||||||
chr12:766564 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.759+12240C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 766564 | |||||||
chr12:766620 | A | T | 27 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(24): Show |
27 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.759+12296A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 766620 | |||||||
chr12:766636 | G | A | 6 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(3): Show |
6 | HG00741.hp1 HG01928.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+12312G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 766636 | |||||||
chr12:766773 | G | A | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+12449G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 766773 | |||||||
chr12:766897 | C | T | 1 | a0002c0003t0001g0280 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.759+12573C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 766897 | |||||||
chr12:767057 | G | A | 1 | a0002c0003t0001g0105 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.759+12733G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 767057 | |||||||
chr12:767122 | T | C | 15 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(12): Show |
15 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.759+12798T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 767122 | |||||||
chr12:767188 | G | A | 1 | a0002c0002t0001g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.759+12864G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 767188 | |||||||
chr12:767234 | G | GT | 12 | a0001c0008t0002g0276 a0002c0002t0001g0233 a0002c0002t0001g0259 others(9): Show |
12 | HG01358.hp2 HG02004.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.759+12945dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 767234 | ||||||
chr12:767234 | G | GTT | 17 | a0002c0002t0001g0207 a0002c0002t0001g0238 a0002c0002t0001g0239 others(14): Show |
17 | HG00544.hp2 HG00609.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.759+12944_759+1294 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 767234 | ||||||
chr12:767234 | G | GTTT | 6 | a0002c0002t0001g0252 a0002c0003t0001g0279 a0003c0005t0001g0248 others(3): Show |
6 | HG01175.hp1 HG01255.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+12943_759+1294 others(7): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 767234 | ||||||
chr12:767234 | G | GTTTTTTT others(3): Show |
2 | a0002c0002t0001g0141 a0002c0002t0001g0190 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.759+12936_759+1294 others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 767234 | ||||||
chr12:767234 | G | GTTTTTTT others(4): Show |
2 | a0002c0002t0001g0142 a0002c0002t0001g0143 |
2 | HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.759+12935_759+1294 others(15): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 767234 | ||||||
chr12:767234 | G | GTTTTTTT others(11): Show |
1 | a0002c0002t0001g0144 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.759+12928_759+1294 others(22): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 767234 | ||||||
chr12:767234 | GT | G | 15 | a0001c0008t0002g0275 a0001c0012t0002g0270 a0001c0012t0028g0269 others(12): Show |
15 | HG01169.hp1 HG01496.hp2 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.759+12945delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 767234 | ||||||
chr12:767234 | GTT | G | 8 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(5): Show |
8 | HG00741.hp1 HG01168.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.759+12944_759+1294 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 767234 | ||||||
chr12:767234 | GTTTT | G | 12 | a0001c0001t0001g0004 a0001c0001t0006g0003 a0001c0001t0006g0014 others(9): Show |
12 | HG00735.hp2 HG01358.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.759+12942_759+1294 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 767234 | ||||||
chr12:767234 | GTTTTT | G | 13 | a0001c0001t0004g0002 a0001c0001t0006g0006 a0001c0001t0006g0008 others(10): Show |
13 | HG01074.hp2 HG01109.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.759+12941_759+1294 others(9): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 767234 | ||||||
chr12:767234 | GTTTTTTT others(2): Show |
G | 10 | a0004c0004t0003g0086 a0004c0004t0003g0087 a0004c0004t0003g0088 others(7): Show |
10 | HG00408.hp2 HG01123.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.759+12937_759+1294 others(13): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 767234 | ||||||
chr12:767234 | GTTTTTTT others(3): Show |
G | 17 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(14): Show |
17 | HG00423.hp1 HG01069.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.759+12936_759+1294 others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 767234 | ||||||
chr12:767234 | GTTTTTTT others(4): Show |
G | 9 | a0001c0001t0002g0057 a0001c0001t0002g0071 a0001c0001t0007g0055 others(6): Show |
9 | HG00408.hp1 HG00609.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.759+12935_759+1294 others(15): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 767234 | ||||||
chr12:767234 | GTTTTTTT others(5): Show |
G | 45 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0031 others(42): Show |
45 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.759+12934_759+1294 others(16): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 767234 | ||||||
chr12:767234 | GTTTTTTT others(6): Show |
G | 84 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 others(81): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.759+12933_759+1294 others(17): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 767234 | ||||||
chr12:767234 | GTTTTTTT others(7): Show |
G | 4 | a0001c0001t0002g0001 a0002c0002t0001g0107 a0002c0002t0001g0191 others(1): Show |
5 | HG01496.hp1 HG01952.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+12932_759+1294 others(18): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 767234 | ||||||
chr12:767234 | GTTTTTTT others(9): Show |
G | 1 | a0003c0005t0005g0210 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.759+12930_759+1294 others(20): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 767234 | ||||||
chr12:767246 | T | G | 1 | a0002c0002t0001g0226 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.759+12922T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 767246 | |||||||
chr12:767269 | T | A | 1 | a0002c0002t0019g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.759+12945T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 767269 | |||||||
chr12:767386 | G | A | 1 | a0002c0011t0001g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.759+13062G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 767386 | |||||||
chr12:767494 | A | G | 21 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0006g0003 others(18): Show |
21 | HG00735.hp2 HG01074.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.759+13170A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 767494 | |||||||
chr12:767922 | A | C | 4 | a0002c0002t0001g0207 a0002c0015t0001g0211 a0002c0015t0001g0243 others(1): Show |
4 | HG02559.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.759+13598A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 767922 | |||||||
chr12:768163 | C | T | 9 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(6): Show |
9 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.759+13839C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 768163 | |||||||
chr12:768281 | G | T | 1 | a0005c0006t0009g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.759+13957G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 768281 | |||||||
chr12:768319 | A | G | 1 | a0002c0003t0001g0280 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.759+13995A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 768319 | |||||||
chr12:768690 | A | C | 6 | a0001c0001t0006g0008 a0007c0010t0010g0100 a0007c0010t0010g0101 others(3): Show |
6 | HG02615.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+14366A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 768690 | |||||||
chr12:768763 | A | G | 1 | a0002c0002t0001g0219 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.759+14439A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 768763 | |||||||
chr12:768824 | T | C | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.759+14500T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 768824 | |||||||
chr12:768921 | T | C | 1 | a0001c0001t0002g0031 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.759+14597T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 768921 | |||||||
chr12:769177 | C | A | 2 | a0001c0001t0004g0023 a0001c0001t0025g0024 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.759+14853C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 769177 | |||||||
chr12:769481 | T | C | 6 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(3): Show |
6 | HG00741.hp1 HG01928.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+15157T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 769481 | |||||||
chr12:769490 | C | T | 1 | a0001c0001t0002g0031 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.759+15166C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 769490 | |||||||
chr12:769498 | A | G | 213 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(210): Show |
214 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.759+15174A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 769498 | |||||||
chr12:769532 | T | C | 1 | a0003c0005t0005g0203 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.759+15208T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 769532 | |||||||
chr12:769707 | C | T | 2 | a0001c0001t0007g0058 a0001c0001t0007g0069 |
2 | NA18950.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.759+15383C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 769707 | |||||||
chr12:769738 | G | A | 1 | a0005c0006t0009g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.759+15414G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 769738 | |||||||
chr12:770138 | C | G | 1 | a0001c0001t0007g0192 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.759+15814C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 770138 | |||||||
chr12:770380 | T | C | 14 | a0001c0001t0001g0004 a0001c0001t0002g0227 a0001c0001t0004g0002 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.759+16056T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 770380 | |||||||
chr12:770701 | G | A | 1 | a0002c0003t0001g0108 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.759+16377G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 770701 | |||||||
chr12:770970 | G | A | 13 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0006g0003 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.759+16646G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 770970 | |||||||
chr12:771159 | G | A | 155 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(152): Show |
156 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.759+16835G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 771159 | |||||||
chr12:771196 | A | G | 1 | a0005c0006t0009g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.759+16872A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 771196 | |||||||
chr12:771244 | G | A | 5 | a0001c0012t0002g0267 a0001c0012t0002g0268 a0001c0012t0002g0270 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.759+16920G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 771244 | |||||||
chr12:771270 | G | T | 1 | a0002c0023t0001g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.759+16946G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 771270 | |||||||
chr12:771292 | C | T | 3 | a0002c0002t0017g0139 a0002c0002t0017g0140 a0002c0023t0001g0212 |
3 | HG02602.hp1 HG02630.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.759+16968C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 771292 | |||||||
chr12:771565 | G | A | 2 | a0002c0002t0001g0261 a0002c0002t0001g0262 |
2 | HG02602.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.759+17241G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 771565 | |||||||
chr12:771644 | C | T | 18 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(15): Show |
18 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.759+17320C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 771644 | |||||||
chr12:771645 | G | T | 1 | a0001c0001t0002g0071 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.759+17321G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 771645 | |||||||
chr12:771654 | C | T | 15 | a0001c0001t0001g0004 a0001c0001t0002g0057 a0001c0001t0002g0227 others(12): Show |
15 | HG00735.hp2 HG01074.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.759+17330C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 771654 | |||||||
chr12:771735 | T | G | 2 | a0002c0002t0001g0194 a0002c0002t0001g0213 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.759+17411T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 771735 | |||||||
chr12:771939 | C | T | 8 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(5): Show |
8 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.759+17615C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 771939 | |||||||
chr12:772103 | C | CA | 3 | a0001c0008t0002g0272 a0001c0008t0002g0273 a0001c0008t0002g0275 |
3 | HG01928.hp2 HG01978.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.759+17785dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 772103 | ||||||
chr12:772184 | A | C | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.759+17860A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 772184 | |||||||
chr12:772404 | G | GGT | 6 | a0001c0001t0004g0173 a0001c0001t0004g0174 a0001c0001t0004g0175 others(3): Show |
6 | HG01346.hp2 HG02074.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+18099_759+1810 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 772404 | ||||||
chr12:772406 | T | G | 3 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0013c0040t0006g0016 |
3 | HG01109.hp2 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.759+18082T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 772406 | |||||||
chr12:772421 | G | A | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.759+18097G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 772421 | |||||||
chr12:772431 | G | GTA | 201 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(198): Show |
202 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.759+18108_759+1810 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 772431 | ||||||
chr12:772560 | C | T | 1 | a0002c0003t0001g0131 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.759+18236C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 772560 | |||||||
chr12:772596 | A | C | 4 | a0007c0010t0010g0101 a0007c0010t0010g0103 a0007c0010t0010g0104 others(1): Show |
4 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+18272A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 772596 | |||||||
chr12:772886 | T | A | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.759+18562T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 772886 | |||||||
chr12:773198 | C | T | 1 | a0001c0001t0004g0184 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.759+18874C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 773198 | |||||||
chr12:773258 | CA | C | 11 | a0001c0001t0025g0024 a0006c0007t0008g0011 a0006c0007t0008g0013 others(8): Show |
11 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.759+18946delA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 773258 | ||||||
chr12:773275 | T | G | 37 | a0001c0001t0004g0177 a0004c0004t0003g0072 a0004c0004t0003g0073 others(34): Show |
37 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.759+18951T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 773275 | |||||||
chr12:773587 | A | C | 1 | a0002c0023t0001g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.759+19263A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 773587 | |||||||
chr12:773589 | A | G | 4 | a0007c0010t0010g0101 a0007c0010t0010g0103 a0007c0010t0010g0104 others(1): Show |
4 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+19265A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 773589 | |||||||
chr12:773661 | A | C | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0142 others(2): Show |
5 | HG01261.hp2 HG03098.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+19337A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 773661 | |||||||
chr12:773708 | T | A | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.759+19384T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 773708 | |||||||
chr12:773759 | A | G | 15 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(12): Show |
15 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.759+19435A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 773759 | |||||||
chr12:774007 | T | C | 3 | a0006c0007t0008g0017 a0006c0007t0008g0018 a0006c0007t0008g0019 |
3 | HG02895.hp2 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.759+19683T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 774007 | |||||||
chr12:774012 | A | T | 199 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(196): Show |
200 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.759+19688A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 774012 | |||||||
chr12:774207 | C | T | 1 | a0003c0005t0005g0242 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.759+19883C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 774207 | |||||||
chr12:774330 | T | C | 1 | a0002c0002t0035g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.759+20006T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 774330 | |||||||
chr12:774566 | T | C | 1 | a0001c0001t0004g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.759+20242T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 774566 | |||||||
chr12:774688 | T | C | 1 | a0001c0001t0004g0177 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.759+20364T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 774688 | |||||||
chr12:775115 | T | A | 37 | a0001c0001t0004g0177 a0004c0004t0003g0072 a0004c0004t0003g0073 others(34): Show |
37 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.759+20791T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 775115 | |||||||
chr12:775123 | T | C | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.759+20799T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 775123 | |||||||
chr12:775287 | C | T | 1 | a0005c0006t0009g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.759+20963C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 775287 | |||||||
chr12:775312 | A | G | 1 | a0002c0003t0001g0105 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.759+20988A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 775312 | |||||||
chr12:775377 | G | A | 1 | a0001c0001t0006g0003 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.759+21053G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 775377 | |||||||
chr12:775448 | G | A | 15 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(12): Show |
15 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.759+21124G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 775448 | |||||||
chr12:775631 | G | A | 1 | a0005c0006t0009g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.759+21307G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 775631 | |||||||
chr12:775723 | T | A | 219 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(216): Show |
220 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.759+21399T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 775723 | |||||||
chr12:775926 | A | G | 1 | a0001c0001t0004g0177 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.759+21602A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 775926 | |||||||
chr12:776161 | G | C | 1 | a0001c0001t0007g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.759+21837G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 776161 | |||||||
chr12:776280 | T | C | 1 | a0002c0002t0001g0259 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.759+21956T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 776280 | |||||||
chr12:776412 | T | TTG | 42 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(39): Show |
42 | HG00408.hp2 HG00438.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.759+22120_759+2212 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 776412 | ||||||
chr12:776412 | T | TTGTG | 23 | a0001c0001t0021g0176 a0001c0008t0002g0266 a0001c0008t0002g0272 others(20): Show |
23 | HG00741.hp1 HG01106.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.759+22118_759+2212 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 776412 | ||||||
chr12:776412 | T | TTGTGTG | 8 | a0001c0001t0004g0172 a0001c0001t0004g0177 a0002c0002t0001g0190 others(5): Show |
8 | HG01243.hp1 HG02148.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.759+22116_759+2212 others(10): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 776412 | ||||||
chr12:776412 | T | TTGTGTGT others(1): Show |
11 | a0001c0001t0004g0023 a0001c0001t0007g0032 a0001c0001t0007g0054 others(8): Show |
11 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.759+22114_759+2212 others(12): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 776412 | ||||||
chr12:776412 | T | TTGTGTGT others(3): Show |
71 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(68): Show |
72 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.759+22112_759+2212 others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 776412 | ||||||
chr12:776412 | T | TTGTGTGT others(5): Show |
28 | a0001c0001t0002g0025 a0001c0001t0002g0034 a0001c0001t0002g0045 others(25): Show |
28 | HG00423.hp2 HG00741.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.759+22110_759+2212 others(16): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 776412 | ||||||
chr12:776412 | T | TTGTGTGT others(7): Show |
14 | a0001c0001t0002g0109 a0001c0001t0002g0111 a0001c0001t0004g0173 others(11): Show |
14 | HG00438.hp1 HG01243.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.759+22108_759+2212 others(18): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 776412 | ||||||
chr12:776412 | T | TTGTGTGT others(9): Show |
1 | a0005c0006t0003g0039 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.759+22106_759+2212 others(20): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 776412 | ||||||
chr12:776412 | T | TTGTGTGT others(11): Show |
1 | a0002c0009t0006g0146 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.759+22104_759+2212 others(22): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 776412 | ||||||
chr12:776412 | TTG | T | 56 | a0001c0001t0002g0227 a0002c0002t0001g0029 a0002c0002t0001g0194 others(53): Show |
56 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.759+22120_759+2212 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 776412 | ||||||
chr12:776412 | TTGTG | T | 13 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0006g0003 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.759+22118_759+2212 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 776412 | ||||||
chr12:776445 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0004g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.759+22121_759+2212 others(15): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 776445 | |||||||
chr12:776453 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.759+22129G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 776453 | |||||||
chr12:776545 | T | C | 1 | a0004c0004t0003g0074 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.759+22221T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 776545 | |||||||
chr12:776577 | C | T | 26 | a0001c0001t0004g0177 a0004c0004t0003g0072 a0004c0004t0003g0073 others(23): Show |
26 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.759+22253C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 776577 | |||||||
chr12:776686 | T | C | 1 | a0001c0022t0001g0263 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.759+22362T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 776686 | |||||||
chr12:776749 | G | A | 1 | a0009c0014t0002g0046 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.759+22425G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 776749 | |||||||
chr12:776887 | C | G | 1 | a0004c0004t0003g0094 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.759+22563C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 776887 | |||||||
chr12:776988 | T | G | 1 | a0001c0001t0004g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.759+22664T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 776988 | |||||||
chr12:777075 | C | T | 2 | a0003c0005t0001g0036 a0003c0005t0001g0037 |
2 | HG00438.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.759+22751C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 777075 | |||||||
chr12:777158 | G | GT | 37 | a0001c0001t0001g0004 a0001c0001t0002g0025 a0001c0001t0002g0028 others(34): Show |
37 | HG00735.hp2 HG01074.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.759+22845dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 777158 | ||||||
chr12:777337 | C | T | 193 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(190): Show |
194 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.759+23013C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 777337 | |||||||
chr12:777444 | C | T | 1 | a0001c0001t0007g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.759+23120C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 777444 | |||||||
chr12:777450 | G | A | 1 | a0005c0006t0009g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.759+23126G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 777450 | |||||||
chr12:777584 | A | G | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.759+23260A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 777584 | |||||||
chr12:777679 | A | C | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.759+23355A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 777679 | |||||||
chr12:777800 | A | G | 4 | a0001c0022t0001g0263 a0002c0002t0001g0261 a0002c0002t0001g0262 others(1): Show |
4 | HG02602.hp2 HG03942.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.759+23476A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 777800 | |||||||
chr12:777818 | A | G | 1 | a0001c0001t0002g0198 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.759+23494A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 777818 | |||||||
chr12:777844 | A | G | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+23520A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 777844 | |||||||
chr12:777855 | T | G | 2 | a0001c0001t0002g0048 a0005c0006t0009g0047 |
2 | HG02165.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.759+23531T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 777855 | |||||||
chr12:777961 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0002g0227 a0001c0001t0004g0002 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.759+23637C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 777961 | |||||||
chr12:778180 | A | G | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0060 |
3 | HG01515.hp2 HG01517.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.759+23856A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 778180 | |||||||
chr12:778181 | A | C | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0060 |
3 | HG01515.hp2 HG01517.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.759+23857A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 778181 | |||||||
chr12:778394 | G | A | 1 | a0001c0001t0004g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.759+24070G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 778394 | |||||||
chr12:778510 | C | G | 1 | a0002c0011t0001g0255 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.759+24186C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 778510 | |||||||
chr12:778626 | C | T | 1 | a0001c0001t0002g0001 | 2 | HG01496.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.759+24302C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 778626 | |||||||
chr12:778637 | C | CT | 56 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(53): Show |
57 | HG00280.hp1 HG00609.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.759+24331dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 778637 | ||||||
chr12:778637 | CT | C | 10 | a0001c0001t0001g0067 a0001c0001t0002g0109 a0001c0001t0002g0227 others(7): Show |
10 | HG00323.hp1 HG01074.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.759+24331delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 778637 | ||||||
chr12:778664 | T | G | 1 | a0002c0002t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.759+24340T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 778664 | |||||||
chr12:778760 | A | G | 37 | a0001c0001t0004g0177 a0004c0004t0003g0072 a0004c0004t0003g0073 others(34): Show |
37 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.759+24436A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 778760 | |||||||
chr12:779051 | G | T | 1 | a0008c0013t0013g0149 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.759+24727G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 779051 | |||||||
chr12:779154 | G | A | 195 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.759+24830G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 779154 | |||||||
chr12:779262 | C | T | 194 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.759+24938C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 779262 | |||||||
chr12:779281 | T | C | 3 | a0004c0004t0003g0076 a0004c0004t0003g0086 a0004c0004t0003g0096 |
3 | HG02735.hp2 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.759+24957T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 779281 | |||||||
chr12:779317 | T | G | 2 | a0001c0001t0002g0026 a0001c0001t0002g0028 |
2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.759+24993T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 779317 | |||||||
chr12:779338 | C | T | 33 | a0001c0001t0001g0004 a0001c0001t0002g0227 a0001c0001t0004g0002 others(30): Show |
33 | HG00735.hp2 HG01074.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.759+25014C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 779338 | |||||||
chr12:779382 | TTTCTTTT others(8): Show |
T | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.759+25061_759+2507 others(19): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 779382 | ||||||
chr12:779397 | G | GT | 6 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(3): Show |
6 | HG01106.hp1 HG01255.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.759+25085dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 779397 | ||||||
chr12:779397 | GT | G | 181 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(178): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.759+25085delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 779397 | ||||||
chr12:779398 | T | G | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.759+25074T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 779398 | |||||||
chr12:779409 | T | C | 14 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0006g0003 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.759+25085T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 779409 | |||||||
chr12:779410 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0006g0003 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.759+25086C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 779410 | |||||||
chr12:779411 | T | C | 1 | a0005c0006t0003g0152 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.759+25087T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 779411 | |||||||
chr12:779467 | C | T | 1 | a0002c0002t0001g0138 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.759+25143C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 779467 | |||||||
chr12:779490 | T | C | 202 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(199): Show |
203 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.759+25166T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 779490 | |||||||
chr12:779682 | G | A | 197 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(194): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.759+25358G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 779682 | |||||||
chr12:779882 | C | A | 1 | a0007c0010t0010g0100 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.759+25558C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 779882 | |||||||
chr12:780009 | A | G | 1 | a0001c0001t0002g0025 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.759+25685A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 780009 | |||||||
chr12:780171 | C | A | 1 | a0002c0002t0001g0264 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.759+25847C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 780171 | |||||||
chr12:780428 | C | A | 1 | a0002c0003t0001g0280 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.759+26104C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 780428 | |||||||
chr12:780580 | G | T | 1 | a0001c0001t0004g0184 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.759+26256G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 780580 | |||||||
chr12:780667 | A | G | 160 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(157): Show |
161 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.759+26343A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 780667 | |||||||
chr12:780736 | T | G | 62 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(59): Show |
63 | HG00280.hp1 HG00609.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.759+26412T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 780736 | |||||||
chr12:780902 | C | A | 1 | a0002c0002t0001g0144 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.759+26578C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 780902 | |||||||
chr12:780950 | A | G | 1 | a0005c0006t0009g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.759+26626A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 780950 | |||||||
chr12:781026 | G | A | 1 | a0002c0002t0001g0264 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.759+26702G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 781026 | |||||||
chr12:781039 | G | T | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+26715G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 781039 | |||||||
chr12:781089 | T | A | 2 | a0003c0005t0001g0036 a0003c0005t0001g0037 |
2 | HG00438.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.759+26765T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 781089 | |||||||
chr12:781100 | T | TAAC | 3 | a0004c0004t0003g0073 a0004c0004t0003g0097 a0004c0004t0003g0098 |
3 | NA18945.hp1 NA19080.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.759+26797_759+2679 others(7): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 781100 | ||||||
chr12:781100 | TAACAACA others(2): Show |
T | 123 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(120): Show |
124 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.759+26791_759+2679 others(13): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 781100 | ||||||
chr12:781190 | T | C | 37 | a0001c0001t0004g0177 a0004c0004t0003g0072 a0004c0004t0003g0073 others(34): Show |
37 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.759+26866T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 781190 | |||||||
chr12:781199 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.759+26875C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 781199 | |||||||
chr12:781287 | A | C | 5 | a0002c0002t0001g0219 a0002c0002t0001g0233 a0002c0002t0001g0249 others(2): Show |
5 | HG01496.hp2 NA19007.hp1 NA19078.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+26963A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 781287 | |||||||
chr12:781412 | ATATAGTG others(2): Show |
A | 12 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(9): Show |
12 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.759+27093_759+2710 others(13): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 781412 | ||||||
chr12:781558 | G | A | 1 | a0022c0034t0004g0095 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.759+27234G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 781558 | |||||||
chr12:781713 | T | C | 1 | a0002c0002t0035g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.759+27389T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 781713 | |||||||
chr12:781859 | A | C | 27 | a0001c0001t0004g0177 a0004c0004t0003g0072 a0004c0004t0003g0073 others(24): Show |
27 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.759+27535A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 781859 | |||||||
chr12:782069 | A | G | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.759+27745A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 782069 | |||||||
chr12:782092 | A | G | 2 | a0001c0001t0002g0001 a0001c0037t0002g0129 |
3 | HG01496.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.759+27768A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 782092 | |||||||
chr12:782286 | C | A | 1 | a0001c0001t0002g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.759+27962C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 782286 | |||||||
chr12:782496 | A | G | 27 | a0001c0001t0004g0177 a0004c0004t0003g0072 a0004c0004t0003g0073 others(24): Show |
27 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.759+28172A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 782496 | |||||||
chr12:782629 | C | T | 3 | a0003c0005t0001g0240 a0003c0005t0001g0241 a0003c0005t0001g0248 |
3 | HG01175.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.759+28305C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 782629 | |||||||
chr12:782796 | G | A | 1 | a0001c0001t0007g0044 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.759+28472G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 782796 | |||||||
chr12:782991 | A | C | 1 | a0002c0002t0001g0141 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.759+28667A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 782991 | |||||||
chr12:783006 | C | A | 160 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(157): Show |
161 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.759+28682C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 783006 | |||||||
chr12:783125 | C | T | 5 | a0001c0012t0002g0267 a0001c0012t0002g0268 a0001c0012t0002g0270 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.759+28801C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 783125 | |||||||
chr12:783490 | C | CA | 160 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(157): Show |
161 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.759+29176dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783490 | ||||||
chr12:783490 | C | T | 1 | a0002c0002t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.759+29166C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 783490 | |||||||
chr12:783554 | CGGAGGCT others(130): Show |
C | 8 | a0001c0001t0004g0155 a0001c0018t0006g0005 a0002c0003t0001g0113 others(5): Show |
8 | HG00280.hp1 HG02809.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.759+29325_759+2946 others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783554 | ||||||
chr12:783572 | G | A | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.759+29248G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 783572 | |||||||
chr12:783633 | CAAAAAAA others(131): Show |
C | 137 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(134): Show |
138 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.759+29463_759+2960 others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783633 | ||||||
chr12:783664 | G | A | 1 | a0002c0002t0001g0213 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.759+29340G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 783664 | |||||||
chr12:783770 | C | CA | 6 | a0002c0002t0001g0029 a0002c0002t0001g0194 a0002c0002t0001g0213 others(3): Show |
6 | HG02615.hp2 HG03225.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+29462dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783770 | ||||||
chr12:783770 | C | CAAAAAAA others(4): Show |
20 | a0004c0004t0003g0073 a0004c0004t0003g0076 a0004c0004t0003g0079 others(17): Show |
20 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.759+29452_759+2946 others(15): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783770 | ||||||
chr12:783770 | C | CAAAAAAA others(5): Show |
21 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(18): Show |
21 | HG00741.hp1 HG01192.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.759+29451_759+2946 others(16): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783770 | ||||||
chr12:783770 | C | CAAAAAAA others(6): Show |
3 | a0001c0012t0028g0269 a0002c0003t0001g0201 a0014c0028t0001g0200 |
3 | HG02145.hp2 HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.759+29450_759+2946 others(17): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783770 | ||||||
chr12:783770 | C | CAAAAAAA others(156): Show |
5 | a0006c0007t0008g0017 a0006c0007t0008g0018 a0006c0007t0008g0019 others(2): Show |
5 | HG01358.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+29462_759+2946 others(167): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783770 | ||||||
chr12:783770 | C | CAAAAAAA others(154): Show |
1 | a0013c0040t0006g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.759+29462_759+2946 others(165): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783770 | ||||||
chr12:783770 | C | CAAAAAAA others(155): Show |
1 | a0006c0007t0008g0013 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.759+29462_759+2946 others(166): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783770 | ||||||
chr12:783770 | C | CAAAAAAA others(156): Show |
1 | a0006c0007t0008g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.759+29462_759+2946 others(167): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783770 | ||||||
chr12:783770 | CAAAAAAA others(133): Show |
C | 1 | a0008c0013t0013g0180 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.759+29463_759+2960 others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783770 | ||||||
chr12:783770 | CAAAAAAA others(139): Show |
C | 1 | a0002c0003t0001g0186 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.759+29463_759+2960 others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783770 | ||||||
chr12:783771 | AAAAAAAA others(130): Show |
A | 12 | a0001c0001t0002g0031 a0001c0001t0007g0069 a0001c0001t0016g0049 others(9): Show |
12 | HG00423.hp2 HG01106.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.759+29463_759+2959 others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783771 | ||||||
chr12:783772 | AAAAAAAA others(129): Show |
A | 1 | a0002c0009t0001g0064 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.759+29463_759+2959 others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783772 | ||||||
chr12:783787 | T | G | 49 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(46): Show |
49 | HG00408.hp2 HG00423.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.759+29463T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 783787 | |||||||
chr12:783908 | C | CA | 35 | a0001c0012t0028g0269 a0002c0002t0001g0206 a0002c0002t0001g0218 others(32): Show |
35 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.759+29611dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783908 | ||||||
chr12:783908 | CA | C | 84 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 others(81): Show |
84 | HG00280.hp1 HG00609.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.759+29611delA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783908 | ||||||
chr12:783908 | CAAAAAAA others(3): Show |
C | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.759+29602_759+2961 others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783908 | ||||||
chr12:783977 | G | GGGGAGGC others(129): Show |
3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.760-29557_760-2955 others(140): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783977 | ||||||
chr12:783977 | G | GGGGAGGC others(129): Show |
5 | a0002c0002t0001g0219 a0002c0002t0001g0233 a0002c0002t0001g0249 others(2): Show |
5 | HG01496.hp2 NA19007.hp1 NA19078.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-29624_760-2948 others(140): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 783977 | ||||||
chr12:783977 | G | T | 194 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.759+29653G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 783977 | |||||||
chr12:784057 | CAA | C | 36 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(33): Show |
36 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.760-29572_760-2957 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 784057 | ||||||
chr12:784086 | T | C | 1 | a0002c0002t0001g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.760-29556T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 784086 | |||||||
chr12:784108 | C | A | 1 | a0002c0002t0001g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.760-29534C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 784108 | |||||||
chr12:784114 | G | C | 1 | a0004c0004t0003g0087 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.760-29528G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 784114 | |||||||
chr12:784308 | A | G | 19 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(16): Show |
19 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.760-29334A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 784308 | |||||||
chr12:784446 | G | A | 26 | a0001c0001t0002g0165 a0001c0001t0004g0157 a0001c0001t0004g0164 others(23): Show |
26 | HG00673.hp2 HG00735.hp1 HG01943.hp2 others(23): Show |
intron_variant | MODIFIER | c.760-29196G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 784446 | |||||||
chr12:784447 | T | C | 60 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(57): Show |
61 | HG00280.hp1 HG00609.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.760-29195T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 784447 | |||||||
chr12:784452 | G | C | 14 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0004g0173 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.760-29190G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 784452 | |||||||
chr12:784472 | A | G | 1 | a0002c0003t0001g0279 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.760-29170A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 784472 | |||||||
chr12:784801 | C | A | 137 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(134): Show |
138 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.760-28841C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 784801 | |||||||
chr12:784826 | A | G | 12 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(9): Show |
12 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.760-28816A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 784826 | |||||||
chr12:784882 | C | T | 1 | a0002c0002t0001g0233 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.760-28760C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 784882 | |||||||
chr12:785012 | C | T | 1 | a0004c0004t0022g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.760-28630C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785012 | |||||||
chr12:785077 | T | C | 2 | a0001c0018t0006g0005 a0001c0018t0006g0009 |
2 | HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.760-28565T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785077 | |||||||
chr12:785321 | A | G | 2 | a0001c0001t0004g0023 a0001c0001t0025g0024 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.760-28321A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785321 | |||||||
chr12:785363 | T | C | 3 | a0006c0007t0008g0281 a0006c0007t0008g0283 a0006c0007t0031g0282 |
3 | HG01358.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.760-28279T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785363 | |||||||
chr12:785377 | T | C | 2 | a0001c0001t0006g0012 a0002c0002t0001g0207 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.760-28265T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785377 | |||||||
chr12:785384 | T | C | 1 | a0002c0002t0001g0250 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.760-28258T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785384 | |||||||
chr12:785398 | T | TC | 17 | a0001c0001t0004g0183 a0001c0001t0006g0015 a0001c0001t0016g0049 others(14): Show |
17 | HG00735.hp2 HG01175.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.760-28233dupC | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 785398 | ||||||
chr12:785403 | C | A | 1 | a0001c0001t0004g0181 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.760-28239C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785403 | |||||||
chr12:785405 | C | A | 20 | a0002c0002t0001g0215 a0002c0002t0006g0145 a0002c0024t0014g0196 others(17): Show |
20 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.760-28237C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785405 | |||||||
chr12:785405 | C | CA | 215 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(212): Show |
216 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.760-28237_760-2823 others(5): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785405 | |||||||
chr12:785406 | C | G | 1 | a0007c0010t0010g0104 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.760-28236C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785406 | |||||||
chr12:785410 | A | AC | 75 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0031 others(72): Show |
75 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.760-28227dupC | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 785410 | ||||||
chr12:785421 | G | A | 130 | a0001c0001t0001g0004 a0001c0001t0002g0001 a0001c0001t0002g0025 others(127): Show |
131 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.760-28221G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785421 | |||||||
chr12:785587 | C | T | 1 | a0001c0001t0002g0045 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.760-28055C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785587 | |||||||
chr12:785638 | C | T | 1 | a0002c0002t0001g0251 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.760-28004C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785638 | |||||||
chr12:785639 | C | T | 1 | a0019c0025t0001g0214 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.760-28003C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785639 | |||||||
chr12:785640 | A | G | 1 | a0019c0025t0001g0214 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.760-28002A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785640 | |||||||
chr12:785643 | C | T | 4 | a0002c0002t0001g0216 a0002c0002t0001g0217 a0002c0002t0001g0251 others(1): Show |
4 | HG01106.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.760-27999C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785643 | |||||||
chr12:785676 | C | T | 1 | a0005c0006t0003g0148 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.760-27966C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785676 | |||||||
chr12:785677 | G | A | 1 | a0002c0002t0001g0223 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.760-27965G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785677 | |||||||
chr12:785758 | A | C | 1 | a0009c0014t0002g0053 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.760-27884A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785758 | |||||||
chr12:785845 | G | A | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.760-27797G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785845 | |||||||
chr12:785883 | G | A | 2 | a0002c0003t0001g0280 a0002c0009t0001g0278 |
2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.760-27759G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 785883 | |||||||
chr12:786469 | C | CT | 120 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(117): Show |
121 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.760-27158dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 786469 | ||||||
chr12:786657 | G | C | 2 | a0001c0001t0004g0002 a0001c0001t0006g0003 |
2 | HG01074.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.760-26985G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 786657 | |||||||
chr12:786764 | G | T | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.760-26878G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 786764 | |||||||
chr12:786792 | T | A | 1 | a0006c0007t0008g0013 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.760-26850T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 786792 | |||||||
chr12:786922 | C | T | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.760-26720C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 786922 | |||||||
chr12:787165 | T | C | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.760-26477T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 787165 | |||||||
chr12:787388 | A | C | 2 | a0006c0007t0008g0017 a0006c0007t0008g0018 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.760-26254A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 787388 | |||||||
chr12:787415 | G | A | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.760-26227G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 787415 | |||||||
chr12:787571 | T | C | 1 | a0004c0004t0003g0096 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.760-26071T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 787571 | |||||||
chr12:787598 | T | C | 1 | a0001c0001t0002g0059 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.760-26044T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 787598 | |||||||
chr12:787759 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0004g0002 a0001c0001t0006g0003 others(9): Show |
12 | HG01074.hp2 HG01361.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.760-25883C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 787759 | |||||||
chr12:787799 | A | G | 215 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(212): Show |
216 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.760-25843A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 787799 | |||||||
chr12:788116 | A | G | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.760-25526A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 788116 | |||||||
chr12:788136 | C | G | 2 | a0001c0001t0004g0023 a0001c0001t0025g0024 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.760-25506C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 788136 | |||||||
chr12:788145 | A | T | 148 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(145): Show |
149 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.760-25497A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 788145 | |||||||
chr12:788237 | G | A | 215 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(212): Show |
216 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.760-25405G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 788237 | |||||||
chr12:788296 | G | A | 3 | a0004c0004t0003g0076 a0004c0004t0003g0086 a0004c0004t0003g0096 |
3 | HG02735.hp2 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.760-25346G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 788296 | |||||||
chr12:788398 | G | C | 187 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.760-25244G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 788398 | |||||||
chr12:788506 | G | A | 2 | a0005c0006t0009g0052 a0023c0036t0007g0062 |
2 | NA19007.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.760-25136G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 788506 | |||||||
chr12:788608 | A | G | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-25034A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 788608 | |||||||
chr12:788692 | G | A | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.760-24950G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 788692 | |||||||
chr12:788886 | CG | C | 21 | a0001c0001t0004g0155 a0001c0008t0002g0266 a0001c0008t0002g0272 others(18): Show |
21 | HG00280.hp1 HG00741.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.760-24749delG | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 788886 | ||||||
chr12:788893 | G | A | 157 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(154): Show |
158 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.760-24749G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 788893 | |||||||
chr12:788899 | G | A | 215 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(212): Show |
216 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.760-24743G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 788899 | |||||||
chr12:788899 | G | T | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.760-24743G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 788899 | |||||||
chr12:788902 | AGGTAAGT others(16): Show |
A | 2 | a0001c0001t0004g0023 a0001c0001t0025g0024 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.760-24736_760-2471 others(27): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 788902 | ||||||
chr12:789234 | C | A | 199 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(196): Show |
200 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.760-24408C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 789234 | |||||||
chr12:789272 | A | G | 2 | a0011c0017t0014g0195 a0011c0017t0014g0197 |
2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.760-24370A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 789272 | |||||||
chr12:789321 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.760-24321T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 789321 | |||||||
chr12:789534 | C | CT | 46 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(43): Show |
46 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.760-24088dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 789534 | ||||||
chr12:789534 | C | CTT | 7 | a0001c0001t0004g0177 a0002c0002t0001g0226 a0004c0004t0003g0076 others(4): Show |
7 | HG01261.hp1 HG01993.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.760-24089_760-2408 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 789534 | ||||||
chr12:789534 | CT | C | 11 | a0001c0001t0004g0179 a0001c0001t0016g0049 a0001c0001t0016g0056 others(8): Show |
11 | HG01074.hp1 HG02258.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.760-24088delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 789534 | ||||||
chr12:789555 | G | A | 3 | a0002c0002t0001g0216 a0002c0002t0001g0217 a0002c0002t0035g0208 |
3 | HG02622.hp2 HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.760-24087G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 789555 | |||||||
chr12:789927 | G | T | 1 | a0001c0001t0004g0175 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.760-23715G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 789927 | |||||||
chr12:790079 | T | A | 1 | a0002c0002t0019g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.760-23563T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 790079 | |||||||
chr12:790090 | G | A | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.760-23552G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 790090 | |||||||
chr12:790130 | C | T | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.760-23512C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 790130 | |||||||
chr12:790391 | A | G | 1 | a0006c0007t0008g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.760-23251A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 790391 | |||||||
chr12:790647 | A | G | 19 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(16): Show |
19 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.760-22995A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 790647 | |||||||
chr12:790649 | G | A | 6 | a0002c0003t0001g0065 a0002c0003t0001g0113 a0002c0003t0001g0114 others(3): Show |
6 | NA18984.hp2 NA18993.hp2 NA19056.hp2 others(3): Show |
intron_variant | MODIFIER | c.760-22993G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 790649 | |||||||
chr12:790875 | C | A | 2 | a0001c0001t0002g0165 a0001c0001t0004g0164 |
2 | HG00673.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.760-22767C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 790875 | |||||||
chr12:791051 | C | A | 3 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 |
3 | HG02109.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.760-22591C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 791051 | |||||||
chr12:791225 | C | CCA | 25 | a0001c0001t0002g0031 a0001c0001t0002g0111 a0001c0001t0002g0198 others(22): Show |
25 | HG00438.hp2 HG00544.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.760-22386_760-2238 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 791225 | ||||||
chr12:791225 | C | CCACA | 12 | a0001c0001t0001g0004 a0001c0001t0004g0175 a0001c0001t0006g0003 others(9): Show |
12 | HG01346.hp2 HG01361.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.760-22388_760-2238 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 791225 | ||||||
chr12:791225 | C | CCACACA | 24 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0004g0002 others(21): Show |
24 | HG00408.hp2 HG00735.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.760-22390_760-2238 others(10): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 791225 | ||||||
chr12:791225 | C | CCACACAC others(3): Show |
2 | a0004c0004t0003g0079 a0004c0004t0003g0096 |
2 | HG01515.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.760-22394_760-2238 others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 791225 | ||||||
chr12:791225 | CCA | C | 18 | a0001c0001t0002g0227 a0001c0008t0002g0266 a0001c0008t0002g0272 others(15): Show |
18 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.760-22386_760-2238 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 791225 | ||||||
chr12:791225 | CCACA | C | 5 | a0002c0015t0001g0211 a0002c0015t0001g0243 a0002c0015t0001g0244 others(2): Show |
5 | HG01106.hp2 HG02523.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-22388_760-2238 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 791225 | ||||||
chr12:791225 | CCACACA | C | 3 | a0002c0003t0032g0123 a0002c0009t0001g0122 a0005c0006t0009g0153 |
3 | HG02040.hp1 NA18945.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.760-22390_760-2238 others(10): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 791225 | ||||||
chr12:791375 | C | T | 1 | a0003c0005t0005g0231 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.760-22267C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 791375 | |||||||
chr12:791512 | G | A | 4 | a0002c0002t0017g0139 a0002c0002t0017g0140 a0010c0016t0015g0092 others(1): Show |
4 | HG01261.hp1 HG02273.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.760-22130G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 791512 | |||||||
chr12:791561 | TA | T | 181 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(178): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.760-22068delA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 791561 | ||||||
chr12:791562 | A | T | 4 | a0002c0002t0001g0206 a0002c0024t0014g0196 a0011c0017t0014g0195 others(1): Show |
4 | HG02258.hp2 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-22080A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 791562 | |||||||
chr12:791563 | A | T | 7 | a0001c0032t0002g0050 a0004c0004t0003g0081 a0007c0010t0010g0100 others(4): Show |
7 | HG01069.hp2 HG01109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.760-22079A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 791563 | |||||||
chr12:791775 | AT | A | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-21859delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 791775 | ||||||
chr12:791795 | T | C | 19 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(16): Show |
19 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.760-21847T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 791795 | |||||||
chr12:791842 | A | G | 1 | a0005c0006t0009g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.760-21800A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 791842 | |||||||
chr12:791982 | T | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(12): Show |
15 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.760-21660T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 791982 | |||||||
chr12:792103 | C | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(12): Show |
15 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.760-21539C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 792103 | |||||||
chr12:792112 | C | T | 22 | a0003c0005t0001g0036 a0003c0005t0001g0037 a0003c0005t0001g0193 others(19): Show |
22 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.760-21530C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 792112 | |||||||
chr12:792308 | CT | C | 131 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(128): Show |
132 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.760-21312delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 792308 | ||||||
chr12:792308 | CTT | C | 43 | a0001c0001t0002g0109 a0001c0001t0002g0111 a0001c0001t0011g0159 others(40): Show |
43 | HG00408.hp2 HG00423.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.760-21313_760-2131 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 792308 | ||||||
chr12:792365 | C | T | 147 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(144): Show |
148 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.760-21277C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 792365 | |||||||
chr12:792393 | G | A | 181 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(178): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.760-21249G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 792393 | |||||||
chr12:792399 | G | A | 181 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(178): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.760-21243G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 792399 | |||||||
chr12:792828 | A | T | 2 | a0001c0001t0004g0174 a0001c0001t0004g0175 |
2 | HG01346.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.760-20814A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 792828 | |||||||
chr12:792830 | T | A | 18 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(15): Show |
18 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.760-20812T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 792830 | |||||||
chr12:793241 | C | T | 1 | a0002c0003t0001g0133 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.760-20401C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 793241 | |||||||
chr12:793799 | C | T | 1 | a0002c0002t0001g0233 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.760-19843C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 793799 | |||||||
chr12:793913 | T | C | 184 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(181): Show |
185 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.760-19729T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 793913 | |||||||
chr12:794154 | A | G | 1 | a0001c0001t0004g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.760-19488A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 794154 | |||||||
chr12:794184 | G | A | 1 | a0006c0007t0008g0013 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.760-19458G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 794184 | |||||||
chr12:794279 | G | A | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.760-19363G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 794279 | |||||||
chr12:794445 | G | A | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.760-19197G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 794445 | |||||||
chr12:794470 | A | G | 1 | a0001c0001t0004g0155 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.760-19172A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 794470 | |||||||
chr12:794502 | A | AT | 19 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(16): Show |
19 | HG01261.hp2 HG01952.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.760-19125dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 794502 | ||||||
chr12:794502 | A | ATG | 162 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(159): Show |
163 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.760-19139_760-1913 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 794502 | ||||||
chr12:794502 | A | ATGT | 36 | a0002c0003t0001g0280 a0002c0009t0001g0278 a0004c0004t0003g0072 others(33): Show |
36 | HG00408.hp2 HG00423.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.760-19139_760-1913 others(7): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 794502 | ||||||
chr12:794505 | T | G | 1 | a0001c0001t0026g0167 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.760-19137T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 794505 | |||||||
chr12:794518 | A | T | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.760-19124A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 794518 | |||||||
chr12:794536 | C | T | 1 | a0001c0001t0007g0069 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.760-19106C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 794536 | |||||||
chr12:794570 | G | T | 2 | a0001c0001t0002g0227 a0005c0006t0009g0021 |
2 | HG01106.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.760-19072G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 794570 | |||||||
chr12:794692 | T | C | 184 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(181): Show |
185 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.760-18950T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 794692 | |||||||
chr12:794702 | G | A | 1 | a0002c0002t0001g0144 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.760-18940G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 794702 | |||||||
chr12:794925 | T | A | 2 | a0004c0004t0003g0097 a0004c0004t0003g0098 |
2 | NA19080.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.760-18717T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 794925 | |||||||
chr12:795117 | C | T | 11 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(8): Show |
11 | HG01261.hp2 HG01952.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.760-18525C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 795117 | |||||||
chr12:795295 | TG | T | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.760-18346delG | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 795295 | |||||||
chr12:795296 | GT | G | 143 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(140): Show |
144 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.760-18330delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 795296 | ||||||
chr12:795297 | T | G | 2 | a0002c0002t0001g0217 a0002c0002t0035g0208 |
2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.760-18345T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 795297 | |||||||
chr12:795299 | T | G | 1 | a0002c0002t0001g0216 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.760-18343T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 795299 | |||||||
chr12:795303 | T | G | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.760-18339T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 795303 | |||||||
chr12:795663 | AACTG | A | 149 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(146): Show |
150 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.760-17975_760-1797 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 795663 | ||||||
chr12:795708 | C | G | 1 | a0002c0003t0034g0130 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.760-17934C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 795708 | |||||||
chr12:795775 | T | C | 275 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(272): Show |
276 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.760-17867T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 795775 | |||||||
chr12:795803 | T | C | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.760-17839T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 795803 | |||||||
chr12:795930 | A | G | 1 | a0003c0005t0005g0229 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.760-17712A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 795930 | |||||||
chr12:796115 | C | G | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.760-17527C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 796115 | |||||||
chr12:796158 | G | A | 1 | a0001c0001t0004g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.760-17484G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 796158 | |||||||
chr12:796411 | C | T | 1 | a0001c0001t0002g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.760-17231C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 796411 | |||||||
chr12:796416 | T | C | 23 | a0001c0022t0001g0263 a0002c0002t0001g0215 a0002c0002t0001g0218 others(20): Show |
23 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.760-17226T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 796416 | |||||||
chr12:796529 | G | A | 1 | a0002c0002t0001g0239 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.760-17113G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 796529 | |||||||
chr12:796537 | A | G | 1 | a0001c0032t0002g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.760-17105A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 796537 | |||||||
chr12:796593 | T | G | 3 | a0002c0002t0017g0139 a0002c0002t0017g0140 a0002c0003t0034g0130 |
3 | HG02602.hp1 HG03688.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.760-17049T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 796593 | |||||||
chr12:796809 | T | A | 2 | a0005c0006t0009g0021 a0005c0006t0009g0277 |
2 | HG01106.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.760-16833T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 796809 | |||||||
chr12:796882 | TATGAAGA others(3): Show |
T | 122 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(119): Show |
123 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.760-16758_760-1674 others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 796882 | ||||||
chr12:796894 | A | C | 122 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(119): Show |
123 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.760-16748A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 796894 | |||||||
chr12:796965 | G | GT | 15 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(12): Show |
15 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.760-16675dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 796965 | ||||||
chr12:796974 | A | C | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.760-16668A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 796974 | |||||||
chr12:797084 | A | C | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.760-16558A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 797084 | |||||||
chr12:797133 | A | G | 1 | a0002c0015t0001g0244 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.760-16509A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 797133 | |||||||
chr12:797255 | T | C | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.760-16387T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 797255 | |||||||
chr12:797455 | G | A | 1 | a0022c0034t0004g0095 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.760-16187G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 797455 | |||||||
chr12:797602 | G | A | 5 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 others(2): Show |
5 | HG02109.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-16040G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 797602 | |||||||
chr12:797704 | C | G | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.760-15938C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 797704 | |||||||
chr12:797723 | A | T | 3 | a0002c0015t0001g0211 a0002c0015t0001g0243 a0002c0015t0001g0244 |
3 | HG02559.hp2 HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.760-15919A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 797723 | |||||||
chr12:797874 | G | A | 1 | a0018c0019t0003g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.760-15768G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 797874 | |||||||
chr12:797918 | C | T | 1 | a0001c0001t0004g0164 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.760-15724C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 797918 | |||||||
chr12:797948 | C | CA | 10 | a0002c0002t0001g0217 a0002c0002t0001g0223 a0002c0002t0001g0261 others(7): Show |
10 | HG00544.hp2 HG02615.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.760-15676dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 797948 | ||||||
chr12:797948 | CA | C | 37 | a0001c0001t0001g0004 a0001c0001t0002g0198 a0001c0001t0006g0006 others(34): Show |
37 | HG01069.hp1 HG01081.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.760-15676delA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 797948 | ||||||
chr12:797948 | CAA | C | 151 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(148): Show |
152 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.760-15677_760-1567 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 797948 | ||||||
chr12:797948 | CAAA | C | 18 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(15): Show |
18 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.760-15678_760-1567 others(7): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 797948 | ||||||
chr12:798065 | A | G | 1 | a0003c0005t0005g0230 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.760-15577A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 798065 | |||||||
chr12:798123 | A | G | 1 | a0015c0039t0001g0151 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.760-15519A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 798123 | |||||||
chr12:798143 | G | C | 1 | a0002c0003t0034g0130 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.760-15499G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 798143 | |||||||
chr12:798144 | G | T | 181 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(178): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.760-15498G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 798144 | |||||||
chr12:798192 | C | CT | 25 | a0001c0001t0004g0183 a0002c0002t0001g0144 a0004c0004t0003g0072 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.760-15439dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 798192 | ||||||
chr12:798204 | G | T | 1 | a0001c0001t0002g0045 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.760-15438G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 798204 | |||||||
chr12:798277 | C | T | 6 | a0001c0001t0006g0006 a0001c0001t0006g0008 a0001c0018t0006g0005 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.760-15365C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 798277 | |||||||
chr12:798284 | C | T | 5 | a0002c0003t0001g0199 a0002c0003t0001g0201 a0002c0003t0001g0202 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-15358C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 798284 | |||||||
chr12:798349 | G | A | 1 | a0001c0022t0001g0263 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.760-15293G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 798349 | |||||||
chr12:798365 | A | G | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.760-15277A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 798365 | |||||||
chr12:798455 | G | A | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.760-15187G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 798455 | |||||||
chr12:798495 | C | G | 1 | a0002c0002t0001g0191 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.760-15147C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 798495 | |||||||
chr12:798593 | T | G | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.760-15049T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 798593 | |||||||
chr12:798635 | TTTAA | T | 164 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(161): Show |
165 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.760-15004_760-1500 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 798635 | ||||||
chr12:798820 | G | A | 2 | a0002c0003t0001g0124 a0002c0009t0001g0126 |
2 | HG01192.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.760-14822G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 798820 | |||||||
chr12:799015 | A | G | 2 | a0005c0006t0009g0021 a0005c0006t0009g0277 |
2 | HG01106.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.760-14627A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 799015 | |||||||
chr12:799048 | T | C | 2 | a0002c0003t0032g0123 a0002c0009t0001g0122 |
2 | HG02040.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.760-14594T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 799048 | |||||||
chr12:799117 | C | T | 197 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(194): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.760-14525C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 799117 | |||||||
chr12:799267 | C | T | 33 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(30): Show |
33 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.760-14375C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 799267 | |||||||
chr12:799297 | A | AT | 11 | a0001c0001t0004g0173 a0001c0001t0004g0174 a0001c0001t0004g0175 others(8): Show |
11 | HG01346.hp2 HG02486.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.760-14331dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 799297 | ||||||
chr12:799297 | AT | A | 5 | a0001c0001t0002g0001 a0001c0037t0002g0129 a0002c0024t0014g0196 others(2): Show |
6 | HG01358.hp1 HG01496.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.760-14331delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 799297 | ||||||
chr12:799595 | A | G | 1 | a0002c0002t0035g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.760-14047A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 799595 | |||||||
chr12:799694 | A | G | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.760-13948A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 799694 | |||||||
chr12:799925 | T | C | 16 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(13): Show |
16 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.760-13717T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 799925 | |||||||
chr12:799985 | T | C | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.760-13657T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 799985 | |||||||
chr12:800152 | A | T | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.760-13490A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 800152 | |||||||
chr12:800153 | T | A | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.760-13489T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 800153 | |||||||
chr12:800228 | C | A | 16 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(13): Show |
16 | HG01261.hp2 HG01952.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.760-13414C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 800228 | |||||||
chr12:800565 | A | G | 34 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(31): Show |
34 | HG00735.hp2 HG00741.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.760-13077A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 800565 | |||||||
chr12:800601 | G | A | 1 | a0002c0003t0001g0280 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.760-13041G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 800601 | |||||||
chr12:801278 | G | C | 1 | a0002c0003t0001g0228 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.760-12364G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 801278 | |||||||
chr12:801325 | T | G | 1 | a0001c0001t0002g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.760-12317T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 801325 | |||||||
chr12:801420 | T | C | 17 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(14): Show |
17 | HG01261.hp2 HG01952.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.760-12222T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 801420 | |||||||
chr12:801423 | T | TTG | 35 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0004g0002 others(32): Show |
35 | HG00423.hp2 HG00735.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.760-12179_760-1217 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 801423 | ||||||
chr12:801423 | T | TTGTG | 3 | a0002c0002t0001g0141 a0002c0002t0001g0217 a0005c0006t0009g0021 |
3 | HG01106.hp2 HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.760-12181_760-1217 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 801423 | ||||||
chr12:801423 | TTG | T | 63 | a0001c0001t0001g0004 a0001c0001t0002g0045 a0001c0001t0002g0051 others(60): Show |
63 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.760-12179_760-1217 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 801423 | ||||||
chr12:801423 | TTGTG | T | 62 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 others(59): Show |
62 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.760-12181_760-1217 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 801423 | ||||||
chr12:801423 | TTGTGTG | T | 12 | a0001c0001t0002g0111 a0001c0001t0004g0023 a0001c0001t0004g0030 others(9): Show |
12 | HG01516.hp1 HG01934.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.760-12183_760-1217 others(10): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 801423 | ||||||
chr12:801423 | TTGTGTGT others(1): Show |
T | 4 | a0001c0035t0004g0127 a0005c0027t0003g0075 a0010c0016t0015g0092 others(1): Show |
4 | HG01192.hp1 HG01261.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-12185_760-1217 others(12): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 801423 | ||||||
chr12:801423 | TTGTGTGT others(3): Show |
T | 20 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(17): Show |
20 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.760-12187_760-1217 others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 801423 | ||||||
chr12:801423 | TTGTGTGT others(5): Show |
T | 1 | a0006c0007t0008g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.760-12189_760-1217 others(16): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 801423 | ||||||
chr12:801429 | G | T | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.760-12213G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 801429 | |||||||
chr12:801574 | A | AT | 26 | a0001c0001t0007g0069 a0002c0024t0014g0196 a0004c0004t0003g0072 others(23): Show |
26 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.760-12053dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 801574 | ||||||
chr12:801574 | AT | A | 21 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(18): Show |
21 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.760-12053delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 801574 | ||||||
chr12:801683 | T | C | 1 | a0001c0001t0004g0150 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.760-11959T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 801683 | |||||||
chr12:801738 | A | G | 1 | a0002c0002t0001g0238 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.760-11904A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 801738 | |||||||
chr12:801857 | C | T | 4 | a0001c0022t0001g0263 a0002c0002t0001g0261 a0002c0002t0001g0262 others(1): Show |
4 | HG02602.hp2 HG03942.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-11785C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 801857 | |||||||
chr12:802035 | T | G | 1 | a0002c0015t0001g0244 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.760-11607T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 802035 | |||||||
chr12:802336 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.760-11306C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 802336 | |||||||
chr12:803061 | G | A | 2 | a0002c0002t0001g0256 a0002c0002t0001g0257 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.760-10581G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 803061 | |||||||
chr12:803178 | C | T | 1 | a0004c0004t0003g0094 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.760-10464C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 803178 | |||||||
chr12:803407 | G | T | 1 | a0013c0040t0006g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.760-10235G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 803407 | |||||||
chr12:803575 | G | A | 1 | a0004c0004t0003g0094 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.760-10067G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 803575 | |||||||
chr12:803658 | A | G | 25 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.760-9984A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 803658 | |||||||
chr12:803712 | G | A | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-9930G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 803712 | |||||||
chr12:803889 | T | G | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.760-9753T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 803889 | |||||||
chr12:803964 | C | G | 1 | a0004c0004t0003g0072 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.760-9678C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 803964 | |||||||
chr12:804184 | CT | C | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.760-9457delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 804184 | |||||||
chr12:804187 | T | C | 14 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(11): Show |
14 | HG01261.hp2 HG01952.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.760-9455T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 804187 | |||||||
chr12:804333 | G | C | 1 | a0005c0006t0003g0156 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.760-9309G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 804333 | |||||||
chr12:804370 | T | C | 1 | a0001c0001t0002g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.760-9272T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 804370 | |||||||
chr12:804416 | G | GT | 18 | a0001c0001t0002g0048 a0001c0001t0004g0164 a0001c0001t0016g0056 others(15): Show |
18 | HG00423.hp1 HG01123.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.760-9212dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 804416 | ||||||
chr12:804441 | CAGCTCAC others(8): Show |
C | 25 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.760-9199_760-9185d others(17): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 804441 | ||||||
chr12:804471 | C | T | 1 | a0005c0006t0009g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.760-9171C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 804471 | |||||||
chr12:804530 | G | A | 1 | a0005c0006t0009g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.760-9112G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 804530 | |||||||
chr12:804630 | C | A | 56 | a0001c0001t0002g0031 a0001c0001t0002g0045 a0001c0001t0002g0048 others(53): Show |
56 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.760-9012C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 804630 | |||||||
chr12:804772 | A | G | 1 | a0002c0003t0001g0065 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.760-8870A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 804772 | |||||||
chr12:804787 | C | T | 1 | a0005c0006t0009g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.760-8855C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 804787 | |||||||
chr12:804897 | A | ATATTTTT others(6): Show |
211 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(208): Show |
212 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.760-8741_760-8729d others(15): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 804897 | ||||||
chr12:804918 | A | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(208): Show |
212 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.760-8724A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 804918 | |||||||
chr12:804939 | TTA | T | 118 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(115): Show |
118 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.760-8692_760-8691d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 804939 | ||||||
chr12:804939 | TTATA | T | 121 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(118): Show |
122 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.760-8694_760-8691d others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 804939 | ||||||
chr12:804957 | A | T | 1 | a0001c0001t0004g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.760-8685A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 804957 | |||||||
chr12:805321 | C | T | 11 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(8): Show |
11 | HG01261.hp2 HG01952.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.760-8321C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 805321 | |||||||
chr12:805715 | T | C | 1 | a0020c0021t0024g0189 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.760-7927T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 805715 | |||||||
chr12:805852 | A | G | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.760-7790A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 805852 | |||||||
chr12:806094 | T | C | 1 | a0002c0002t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.760-7548T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 806094 | |||||||
chr12:806139 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.760-7503C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 806139 | |||||||
chr12:806604 | G | T | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.760-7038G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 806604 | |||||||
chr12:806668 | G | T | 2 | a0002c0003t0006g0147 a0002c0009t0006g0146 |
2 | HG02040.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.760-6974G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 806668 | |||||||
chr12:806714 | G | A | 2 | a0001c0001t0016g0049 a0001c0001t0016g0056 |
2 | HG02738.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.760-6928G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 806714 | |||||||
chr12:806747 | T | C | 1 | a0001c0001t0023g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.760-6895T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 806747 | |||||||
chr12:807144 | G | A | 120 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(117): Show |
121 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.760-6498G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 807144 | |||||||
chr12:807291 | CTGTTT | C | 11 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(8): Show |
11 | HG01261.hp2 HG01952.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.760-6349_760-6345d others(7): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 807291 | ||||||
chr12:807293 | G | GT | 10 | a0001c0001t0004g0174 a0001c0001t0004g0179 a0002c0002t0001g0206 others(7): Show |
10 | HG01261.hp1 HG02273.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.760-6331dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 807293 | ||||||
chr12:807293 | G | T | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.760-6349G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 807293 | |||||||
chr12:807293 | GT | G | 203 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(200): Show |
204 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.760-6331delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 807293 | ||||||
chr12:807525 | A | G | 1 | a0001c0001t0023g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.760-6117A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 807525 | |||||||
chr12:807643 | C | T | 1 | a0002c0003t0001g0279 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.760-5999C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 807643 | |||||||
chr12:807645 | C | T | 2 | a0011c0017t0014g0195 a0011c0017t0014g0197 |
2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.760-5997C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 807645 | |||||||
chr12:807695 | G | A | 1 | a0002c0015t0001g0244 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.760-5947G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 807695 | |||||||
chr12:807711 | C | CT | 27 | a0002c0002t0001g0136 a0002c0002t0001g0137 a0002c0002t0001g0141 others(24): Show |
27 | HG00323.hp1 HG00438.hp2 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.760-5905dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 807711 | ||||||
chr12:807711 | C | CTT | 7 | a0002c0002t0001g0107 a0002c0002t0001g0138 a0002c0002t0001g0143 others(4): Show |
7 | HG01261.hp2 HG02145.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.760-5906_760-5905d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 807711 | ||||||
chr12:807711 | CT | C | 22 | a0001c0001t0002g0001 a0001c0001t0002g0027 a0001c0001t0002g0111 others(19): Show |
23 | HG01243.hp1 HG01243.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.760-5905delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 807711 | ||||||
chr12:807711 | CTT | C | 106 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0028 others(103): Show |
106 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.760-5906_760-5905d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 807711 | ||||||
chr12:807711 | CTTT | C | 18 | a0001c0001t0002g0034 a0001c0008t0002g0266 a0001c0008t0002g0273 others(15): Show |
18 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.760-5907_760-5905d others(5): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 807711 | ||||||
chr12:807711 | CTTTTTTT others(1): Show |
C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(12): Show |
15 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.760-5912_760-5905d others(10): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 807711 | ||||||
chr12:807711 | CTTTTTTT others(5): Show |
C | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.760-5916_760-5905d others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 807711 | ||||||
chr12:807783 | A | C | 1 | a0001c0001t0002g0045 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.760-5859A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 807783 | |||||||
chr12:807805 | C | A | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.760-5837C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 807805 | |||||||
chr12:807832 | G | T | 1 | a0002c0003t0001g0228 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.760-5810G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 807832 | |||||||
chr12:807911 | G | A | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.760-5731G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 807911 | |||||||
chr12:807933 | A | G | 1 | a0001c0001t0002g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.760-5709A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 807933 | |||||||
chr12:807971 | G | A | 5 | a0002c0002t0001g0194 a0002c0002t0001g0213 a0002c0002t0001g0223 others(2): Show |
5 | HG02615.hp2 HG03225.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-5671G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 807971 | |||||||
chr12:808130 | A | AG | 35 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0045 others(32): Show |
36 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.760-5511dupG | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 808130 | ||||||
chr12:808206 | A | G | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.760-5436A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 808206 | |||||||
chr12:808455 | C | T | 1 | a0002c0003t0001g0279 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.760-5187C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 808455 | |||||||
chr12:808500 | G | GT | 17 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(14): Show |
17 | HG00735.hp2 HG01074.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.760-5132dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 808500 | ||||||
chr12:808553 | A | G | 15 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(12): Show |
15 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.760-5089A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 808553 | |||||||
chr12:808722 | C | T | 1 | a0005c0006t0009g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.760-4920C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 808722 | |||||||
chr12:808761 | C | CT | 6 | a0002c0002t0001g0136 a0002c0002t0001g0256 a0002c0002t0001g0257 others(3): Show |
6 | HG01168.hp1 HG01169.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.760-4862dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 808761 | ||||||
chr12:808761 | CT | C | 175 | a0001c0001t0001g0004 a0001c0001t0001g0068 a0001c0001t0002g0001 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.760-4862delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 808761 | ||||||
chr12:808761 | CTT | C | 32 | a0001c0001t0001g0067 a0001c0001t0002g0109 a0001c0001t0004g0023 others(29): Show |
32 | HG00408.hp2 HG01081.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.760-4863_760-4862d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 808761 | ||||||
chr12:808763 | T | C | 3 | a0006c0007t0008g0011 a0006c0007t0008g0281 a0006c0007t0031g0282 |
3 | HG01109.hp2 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.760-4879T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 808763 | |||||||
chr12:808764 | T | C | 6 | a0006c0007t0008g0013 a0006c0007t0008g0017 a0006c0007t0008g0019 others(3): Show |
6 | HG01358.hp1 HG02451.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.760-4878T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 808764 | |||||||
chr12:808765 | T | C | 1 | a0006c0007t0008g0018 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.760-4877T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 808765 | |||||||
chr12:809010 | C | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(12): Show |
15 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.760-4632C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809010 | |||||||
chr12:809013 | C | T | 4 | a0001c0001t0004g0173 a0001c0001t0004g0174 a0001c0001t0004g0175 others(1): Show |
4 | HG01346.hp2 HG02486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.760-4629C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809013 | |||||||
chr12:809053 | C | T | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.760-4589C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809053 | |||||||
chr12:809130 | T | C | 1 | a0001c0001t0002g0034 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.760-4512T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809130 | |||||||
chr12:809225 | GAA | G | 21 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(18): Show |
21 | HG00408.hp2 HG01081.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.760-4400_760-4399d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 809225 | ||||||
chr12:809226 | A | G | 2 | a0003c0005t0001g0036 a0003c0005t0001g0037 |
2 | HG00438.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.760-4416A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809226 | |||||||
chr12:809241 | A | AT | 3 | a0001c0001t0018g0112 a0007c0010t0030g0102 a0024c0042t0001g0120 |
3 | HG03041.hp2 NA19078.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.760-4401_760-4400i others(3): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809241 | |||||||
chr12:809242 | A | AT | 124 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(121): Show |
125 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.760-4400_760-4399i others(3): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809242 | |||||||
chr12:809242 | A | ATT | 5 | a0001c0001t0004g0183 a0001c0001t0011g0162 a0001c0001t0011g0187 others(2): Show |
5 | HG01175.hp2 HG01978.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-4400_760-4399i others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809242 | |||||||
chr12:809242 | A | T | 18 | a0001c0001t0002g0045 a0001c0001t0018g0112 a0001c0008t0002g0266 others(15): Show |
18 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.760-4400A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809242 | |||||||
chr12:809243 | A | AAT | 12 | a0002c0002t0001g0136 a0002c0002t0001g0137 a0002c0002t0001g0138 others(9): Show |
12 | HG01261.hp2 HG01952.hp1 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.760-4399_760-4398i others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809243 | |||||||
chr12:809243 | A | ATT | 19 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(16): Show |
19 | HG00735.hp2 HG00741.hp2 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.760-4386_760-4385d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 809243 | ||||||
chr12:809243 | A | T | 177 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0027 others(174): Show |
178 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.760-4399A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809243 | |||||||
chr12:809250 | T | TC | 4 | a0002c0003t0001g0199 a0002c0003t0001g0201 a0002c0003t0001g0202 others(1): Show |
4 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-4392_760-4391i others(3): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809250 | |||||||
chr12:809323 | G | A | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.760-4319G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809323 | |||||||
chr12:809367 | C | T | 1 | a0002c0003t0001g0110 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.760-4275C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809367 | |||||||
chr12:809439 | C | T | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.760-4203C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809439 | |||||||
chr12:809502 | G | C | 6 | a0001c0001t0006g0006 a0001c0001t0006g0008 a0001c0018t0006g0005 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.760-4140G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809502 | |||||||
chr12:809727 | C | A | 158 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(155): Show |
159 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.760-3915C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809727 | |||||||
chr12:809814 | T | C | 4 | a0002c0003t0006g0147 a0002c0009t0005g0043 a0002c0009t0006g0146 others(1): Show |
4 | HG02040.hp2 NA18948.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.760-3828T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809814 | |||||||
chr12:809825 | G | A | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-3817G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809825 | |||||||
chr12:809974 | G | C | 173 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(170): Show |
174 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.760-3668G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 809974 | |||||||
chr12:810195 | A | C | 214 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(211): Show |
215 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.760-3447A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 810195 | |||||||
chr12:810226 | G | A | 173 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(170): Show |
174 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.760-3416G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 810226 | |||||||
chr12:810237 | A | C | 1 | a0003c0005t0005g0229 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.760-3405A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 810237 | |||||||
chr12:810246 | C | CA | 25 | a0001c0001t0002g0109 a0001c0008t0002g0266 a0001c0008t0002g0272 others(22): Show |
25 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.760-3384dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 810246 | ||||||
chr12:810316 | G | A | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.760-3326G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 810316 | |||||||
chr12:810407 | G | A | 1 | a0001c0001t0004g0183 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.760-3235G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 810407 | |||||||
chr12:810603 | CGAAT | C | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.760-3038_760-3035d others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 810603 | |||||||
chr12:810725 | G | A | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.760-2917G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 810725 | |||||||
chr12:810791 | G | A | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.760-2851G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 810791 | |||||||
chr12:810850 | A | G | 3 | a0002c0002t0001g0261 a0002c0002t0001g0262 a0002c0002t0001g0264 |
3 | HG02602.hp2 HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.760-2792A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 810850 | |||||||
chr12:810881 | C | T | 1 | a0001c0001t0007g0040 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.760-2761C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 810881 | |||||||
chr12:810931 | G | A | 1 | a0004c0004t0003g0081 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.760-2711G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 810931 | |||||||
chr12:811033 | A | G | 1 | a0002c0002t0001g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.760-2609A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 811033 | |||||||
chr12:811298 | G | C | 11 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(8): Show |
11 | HG01261.hp2 HG01952.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.760-2344G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 811298 | |||||||
chr12:811449 | T | G | 1 | a0021c0038t0012g0135 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.760-2193T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 811449 | |||||||
chr12:811556 | A | G | 1 | a0007c0010t0010g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.760-2086A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 811556 | |||||||
chr12:811654 | T | A | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-1988T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 811654 | |||||||
chr12:811814 | A | T | 2 | a0001c0001t0004g0172 a0008c0013t0013g0149 |
2 | HG01243.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.760-1828A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 811814 | |||||||
chr12:812041 | C | T | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.760-1601C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 812041 | |||||||
chr12:812269 | T | A | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.760-1373T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 812269 | |||||||
chr12:812305 | A | G | 34 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(31): Show |
34 | HG00735.hp2 HG00741.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.760-1337A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 812305 | |||||||
chr12:812527 | T | C | 18 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(15): Show |
18 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.760-1115T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 812527 | |||||||
chr12:812626 | C | T | 1 | a0002c0023t0001g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.760-1016C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 812626 | |||||||
chr12:812627 | G | A | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.760-1015G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 812627 | |||||||
chr12:812692 | A | G | 25 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.760-950A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 812692 | |||||||
chr12:812792 | T | C | 1 | a0001c0022t0001g0263 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.760-850T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 812792 | |||||||
chr12:812899 | T | C | 1 | a0004c0004t0003g0082 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.760-743T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 812899 | |||||||
chr12:812908 | G | C | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.760-734G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 812908 | |||||||
chr12:813011 | TAGG | T | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-626_760-624del others(3): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 813011 | ||||||
chr12:813116 | C | T | 1 | a0002c0003t0001g0105 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.760-526C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 813116 | |||||||
chr12:813242 | C | T | 146 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(143): Show |
147 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.760-400C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 813242 | |||||||
chr12:813269 | T | C | 1 | a0001c0001t0006g0003 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.760-373T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 813269 | |||||||
chr12:813449 | A | G | 1 | a0001c0001t0007g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.760-193A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 1/27 | chr12 | 813449 | |||||||
chr12:813910 | C | T | 1 | a0002c0002t0001g0224 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.932+96C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 813910 | |||||||
chr12:813933 | A | G | 1 | a0001c0018t0006g0009 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.932+119A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 813933 | |||||||
chr12:814058 | A | G | 1 | a0002c0003t0001g0119 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.932+244A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 814058 | |||||||
chr12:814079 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.932+265C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 814079 | |||||||
chr12:814126 | C | T | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.932+312C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 814126 | |||||||
chr12:814127 | G | A | 4 | a0002c0003t0001g0199 a0002c0003t0001g0201 a0002c0003t0001g0202 others(1): Show |
4 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.932+313G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 814127 | |||||||
chr12:814132 | CAGCCTGG others(42): Show |
C | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.932+323_932+371del others(49): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 814132 | ||||||
chr12:814143 | A | T | 2 | a0005c0006t0009g0021 a0005c0006t0009g0277 |
2 | HG01106.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.932+329A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 814143 | |||||||
chr12:814145 | G | A | 141 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(138): Show |
142 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.932+331G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 814145 | |||||||
chr12:814321 | C | CA | 7 | a0001c0001t0002g0111 a0001c0001t0004g0023 a0001c0001t0025g0024 others(4): Show |
7 | HG02258.hp2 HG02486.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.932+522dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 814321 | ||||||
chr12:814321 | CA | C | 24 | a0001c0001t0007g0055 a0004c0004t0003g0072 a0004c0004t0003g0073 others(21): Show |
24 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.932+522delA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 814321 | ||||||
chr12:814401 | G | T | 1 | a0002c0003t0001g0065 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.932+587G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 814401 | |||||||
chr12:814446 | C | G | 1 | a0002c0003t0001g0279 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.932+632C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 814446 | |||||||
chr12:814711 | C | T | 5 | a0002c0002t0001g0194 a0002c0002t0001g0213 a0002c0002t0001g0223 others(2): Show |
5 | HG02615.hp2 HG03225.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.932+897C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 814711 | |||||||
chr12:814801 | A | G | 1 | a0001c0001t0004g0175 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.932+987A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 814801 | |||||||
chr12:814809 | T | C | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.932+995T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 814809 | |||||||
chr12:814917 | G | C | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.932+1103G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 814917 | |||||||
chr12:814961 | C | T | 4 | a0001c0001t0006g0006 a0001c0001t0006g0008 a0001c0041t0006g0010 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.932+1147C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 814961 | |||||||
chr12:815169 | T | C | 2 | a0002c0002t0001g0205 a0002c0002t0001g0226 |
2 | HG01993.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.932+1355T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 815169 | |||||||
chr12:815308 | A | G | 60 | a0001c0001t0002g0031 a0001c0001t0002g0045 a0001c0001t0002g0048 others(57): Show |
60 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.932+1494A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 815308 | |||||||
chr12:815739 | A | G | 34 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(31): Show |
34 | HG00735.hp2 HG00741.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.932+1925A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 815739 | |||||||
chr12:815833 | A | G | 1 | a0002c0002t0001g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.932+2019A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 815833 | |||||||
chr12:816054 | A | G | 1 | a0001c0001t0002g0031 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.932+2240A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 816054 | |||||||
chr12:816078 | G | A | 25 | a0001c0001t0002g0109 a0001c0001t0002g0134 a0002c0003t0001g0022 others(22): Show |
25 | HG00280.hp2 HG00423.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.932+2264G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 816078 | |||||||
chr12:816113 | C | T | 4 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.932+2299C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 816113 | |||||||
chr12:816116 | T | G | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.932+2302T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 816116 | |||||||
chr12:816304 | C | T | 3 | a0004c0004t0003g0078 a0004c0004t0003g0083 a0004c0004t0003g0088 |
3 | HG00408.hp2 HG02071.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.932+2490C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 816304 | |||||||
chr12:816447 | A | AT | 28 | a0001c0001t0002g0026 a0001c0001t0002g0028 a0004c0004t0003g0072 others(25): Show |
28 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.932+2646dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 816447 | ||||||
chr12:816447 | A | G | 1 | a0002c0002t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.932+2633A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 816447 | |||||||
chr12:816493 | T | C | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.932+2679T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 816493 | |||||||
chr12:816494 | G | A | 1 | a0002c0003t0001g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.932+2680G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 816494 | |||||||
chr12:816495 | C | T | 1 | a0002c0003t0001g0108 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.932+2681C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 816495 | |||||||
chr12:816674 | A | G | 1 | a0002c0023t0001g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.932+2860A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 816674 | |||||||
chr12:816857 | C | T | 1 | a0002c0002t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.932+3043C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 816857 | |||||||
chr12:816914 | A | T | 1 | a0001c0001t0002g0045 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.932+3100A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 816914 | |||||||
chr12:817077 | C | G | 1 | a0001c0001t0002g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.932+3263C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 817077 | |||||||
chr12:817082 | T | C | 147 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(144): Show |
148 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.932+3268T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 817082 | |||||||
chr12:817127 | A | G | 198 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(195): Show |
199 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.932+3313A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 817127 | |||||||
chr12:817501 | A | G | 60 | a0001c0001t0002g0031 a0001c0001t0002g0045 a0001c0001t0002g0048 others(57): Show |
60 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.932+3687A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 817501 | |||||||
chr12:817536 | G | A | 196 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(193): Show |
197 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.932+3722G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 817536 | |||||||
chr12:817555 | A | C | 22 | a0003c0005t0001g0036 a0003c0005t0001g0037 a0003c0005t0001g0193 others(19): Show |
22 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.932+3741A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 817555 | |||||||
chr12:817562 | A | G | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.932+3748A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 817562 | |||||||
chr12:817716 | A | C | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.932+3902A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 817716 | |||||||
chr12:817732 | A | G | 1 | a0002c0002t0001g0223 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.932+3918A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 817732 | |||||||
chr12:817749 | C | T | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.932+3935C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 817749 | |||||||
chr12:817829 | T | C | 1 | a0004c0004t0003g0088 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.932+4015T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 817829 | |||||||
chr12:817832 | A | ACCCATCA others(1): Show |
162 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(159): Show |
163 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.932+4018_932+4019i others(10): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 817832 | |||||||
chr12:817833 | A | C | 162 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(159): Show |
163 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.932+4019A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 817833 | |||||||
chr12:818199 | C | T | 1 | a0001c0001t0018g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.932+4385C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 818199 | |||||||
chr12:818325 | G | A | 1 | a0002c0002t0001g0250 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.932+4511G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 818325 | |||||||
chr12:818411 | A | G | 1 | a0002c0002t0035g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.932+4597A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 818411 | |||||||
chr12:818436 | G | A | 2 | a0001c0001t0002g0057 a0001c0032t0002g0050 |
2 | HG01109.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.932+4622G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 818436 | |||||||
chr12:818493 | T | TA | 5 | a0002c0002t0001g0194 a0002c0002t0001g0213 a0002c0002t0001g0223 others(2): Show |
5 | HG02615.hp2 HG03225.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.932+4685dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 818493 | ||||||
chr12:818601 | A | G | 1 | a0001c0001t0004g0184 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.932+4787A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 818601 | |||||||
chr12:818634 | C | G | 1 | a0022c0034t0004g0095 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.932+4820C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 818634 | |||||||
chr12:818706 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.932+4892A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 818706 | |||||||
chr12:818747 | G | A | 1 | a0019c0025t0001g0214 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.932+4933G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 818747 | |||||||
chr12:818950 | G | C | 4 | a0006c0007t0008g0281 a0006c0007t0008g0283 a0006c0007t0031g0282 others(1): Show |
4 | HG01358.hp1 HG02965.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.932+5136G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 818950 | |||||||
chr12:819354 | T | C | 1 | a0002c0003t0034g0130 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.932+5540T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 819354 | |||||||
chr12:819443 | A | C | 7 | a0001c0001t0007g0040 a0001c0001t0007g0041 a0001c0001t0007g0042 others(4): Show |
7 | HG00438.hp1 HG02083.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.932+5629A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 819443 | |||||||
chr12:819660 | A | G | 1 | a0001c0001t0004g0184 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.932+5846A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 819660 | |||||||
chr12:819745 | G | A | 183 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(180): Show |
184 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.932+5931G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 819745 | |||||||
chr12:819752 | G | A | 19 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(16): Show |
19 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.932+5938G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 819752 | |||||||
chr12:819787 | G | A | 1 | a0015c0039t0001g0151 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.932+5973G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 819787 | |||||||
chr12:819794 | A | G | 8 | a0002c0003t0001g0065 a0002c0003t0001g0113 a0002c0003t0001g0114 others(5): Show |
8 | HG02040.hp1 NA18945.hp2 NA18984.hp2 others(5): Show |
intron_variant | MODIFIER | c.932+5980A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 819794 | |||||||
chr12:819919 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.932+6105A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 819919 | |||||||
chr12:819934 | T | G | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.932+6120T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 819934 | |||||||
chr12:820339 | T | G | 1 | a0001c0001t0012g0121 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.932+6525T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 820339 | |||||||
chr12:820442 | C | CTG | 26 | a0001c0001t0006g0012 a0004c0004t0003g0072 a0004c0004t0003g0073 others(23): Show |
26 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.933-6590_933-6589d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 820442 | ||||||
chr12:820466 | G | GT | 11 | a0002c0002t0001g0238 a0002c0002t0001g0249 a0002c0002t0001g0252 others(8): Show |
11 | HG00609.hp2 HG01175.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.933-6552dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 820466 | ||||||
chr12:820466 | GT | G | 120 | a0001c0001t0001g0004 a0001c0001t0001g0068 a0001c0001t0002g0001 others(117): Show |
121 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.933-6552delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 820466 | ||||||
chr12:820466 | GTT | G | 72 | a0001c0001t0001g0067 a0001c0001t0002g0025 a0001c0001t0002g0026 others(69): Show |
72 | HG00280.hp1 HG00609.hp1 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.933-6553_933-6552d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 820466 | ||||||
chr12:820690 | G | A | 1 | a0019c0025t0001g0214 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.933-6352G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 820690 | |||||||
chr12:820899 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.933-6143A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 820899 | |||||||
chr12:821042 | G | GT | 21 | a0002c0002t0001g0215 a0002c0002t0001g0218 a0002c0002t0001g0219 others(18): Show |
21 | HG01168.hp1 HG01169.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.933-5975dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 821042 | ||||||
chr12:821042 | G | GTT | 8 | a0001c0022t0001g0263 a0002c0002t0001g0194 a0002c0002t0001g0205 others(5): Show |
8 | HG01993.hp2 HG02615.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.933-5976_933-5975d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 821042 | ||||||
chr12:821042 | GT | G | 16 | a0001c0012t0002g0268 a0002c0002t0001g0143 a0002c0002t0001g0207 others(13): Show |
16 | HG01109.hp2 HG01358.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.933-5975delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 821042 | ||||||
chr12:821042 | GTT | G | 47 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(44): Show |
47 | HG00735.hp2 HG00741.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.933-5976_933-5975d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 821042 | ||||||
chr12:821042 | GTTT | G | 65 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0028 others(62): Show |
65 | HG00280.hp1 HG00423.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.933-5977_933-5975d others(5): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 821042 | ||||||
chr12:821042 | GTTTT | G | 58 | a0001c0001t0002g0001 a0001c0001t0002g0045 a0001c0001t0002g0048 others(55): Show |
59 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.933-5978_933-5975d others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 821042 | ||||||
chr12:821042 | GTTTTTTT others(7): Show |
G | 25 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.933-5988_933-5975d others(16): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 821042 | ||||||
chr12:821043 | T | G | 1 | a0002c0024t0014g0196 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.933-5999T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 821043 | |||||||
chr12:821278 | A | T | 5 | a0002c0002t0001g0194 a0002c0002t0001g0213 a0002c0002t0001g0223 others(2): Show |
5 | HG02615.hp2 HG03225.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.933-5764A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 821278 | |||||||
chr12:821375 | T | A | 1 | a0001c0001t0002g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.933-5667T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 821375 | |||||||
chr12:821443 | C | T | 13 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(10): Show |
13 | HG01261.hp2 HG01952.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.933-5599C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 821443 | |||||||
chr12:821459 | C | T | 5 | a0004c0004t0003g0079 a0004c0004t0003g0080 a0004c0004t0003g0081 others(2): Show |
5 | HG01069.hp2 HG01081.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.933-5583C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 821459 | |||||||
chr12:821725 | G | A | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.933-5317G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 821725 | |||||||
chr12:821829 | T | C | 2 | a0001c0001t0011g0159 a0001c0001t0011g0162 |
2 | HG01943.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.933-5213T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 821829 | |||||||
chr12:821862 | A | G | 25 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.933-5180A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 821862 | |||||||
chr12:821877 | C | G | 25 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.933-5165C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 821877 | |||||||
chr12:821978 | A | G | 5 | a0001c0012t0002g0267 a0001c0012t0002g0268 a0001c0012t0002g0270 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.933-5064A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 821978 | |||||||
chr12:822060 | G | C | 12 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(9): Show |
12 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.933-4982G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 822060 | |||||||
chr12:822082 | T | G | 1 | a0001c0001t0004g0164 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.933-4960T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 822082 | |||||||
chr12:822087 | C | CT | 133 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(130): Show |
134 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.933-4931dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 822087 | ||||||
chr12:822087 | C | CTT | 27 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0048 others(24): Show |
27 | HG00423.hp2 HG00735.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.933-4932_933-4931d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 822087 | ||||||
chr12:822089 | T | C | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.933-4953T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 822089 | |||||||
chr12:822117 | G | A | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.933-4925G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 822117 | |||||||
chr12:822186 | C | T | 13 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(10): Show |
13 | HG01261.hp2 HG01952.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.933-4856C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 822186 | |||||||
chr12:822295 | C | T | 183 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(180): Show |
184 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.933-4747C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 822295 | |||||||
chr12:822373 | G | T | 1 | a0001c0001t0002g0048 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.933-4669G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 822373 | |||||||
chr12:822392 | C | T | 124 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(121): Show |
125 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.933-4650C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 822392 | |||||||
chr12:822393 | G | T | 1 | a0002c0003t0001g0280 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.933-4649G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 822393 | |||||||
chr12:822398 | A | T | 4 | a0007c0010t0010g0101 a0007c0010t0010g0103 a0007c0010t0010g0104 others(1): Show |
4 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.933-4644A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 822398 | |||||||
chr12:822493 | A | G | 1 | a0002c0002t0001g0138 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.933-4549A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 822493 | |||||||
chr12:822614 | C | T | 2 | a0002c0002t0001g0258 a0002c0002t0001g0259 |
2 | HG01346.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.933-4428C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 822614 | |||||||
chr12:822702 | G | C | 25 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.933-4340G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 822702 | |||||||
chr12:822740 | A | C | 198 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(195): Show |
199 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.933-4302A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 822740 | |||||||
chr12:822775 | A | G | 11 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(8): Show |
11 | HG01261.hp2 HG01952.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.933-4267A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 822775 | |||||||
chr12:823055 | T | G | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.933-3987T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 823055 | |||||||
chr12:823107 | C | T | 3 | a0008c0013t0013g0033 a0008c0013t0013g0180 a0008c0013t0027g0128 |
3 | HG00609.hp1 HG04115.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.933-3935C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 823107 | |||||||
chr12:823121 | C | G | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.933-3921C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 823121 | |||||||
chr12:823176 | A | G | 1 | a0001c0001t0020g0168 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.933-3866A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 823176 | |||||||
chr12:823191 | C | T | 121 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(118): Show |
122 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.933-3851C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 823191 | |||||||
chr12:823193 | T | G | 1 | a0001c0032t0002g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.933-3849T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 823193 | |||||||
chr12:823374 | C | A | 1 | a0002c0002t0001g0249 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.933-3668C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 823374 | |||||||
chr12:823389 | T | C | 11 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(8): Show |
11 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.933-3653T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 823389 | |||||||
chr12:823566 | G | A | 2 | a0006c0007t0008g0281 a0006c0007t0031g0282 |
2 | HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.933-3476G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 823566 | |||||||
chr12:823642 | G | A | 1 | a0003c0005t0001g0193 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.933-3400G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 823642 | |||||||
chr12:823871 | A | C | 243 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(240): Show |
244 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.933-3171A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 823871 | |||||||
chr12:823900 | C | CT | 6 | a0002c0002t0029g0237 a0003c0005t0005g0203 a0003c0005t0005g0236 others(3): Show |
6 | HG00544.hp2 HG02148.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.933-3121dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 823900 | ||||||
chr12:823900 | CT | C | 11 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0227 others(8): Show |
12 | HG01255.hp1 HG01261.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.933-3121delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 823900 | ||||||
chr12:823900 | CTT | C | 162 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(159): Show |
162 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.933-3122_933-3121d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 823900 | ||||||
chr12:823900 | CTTT | C | 40 | a0001c0012t0002g0267 a0001c0032t0002g0050 a0002c0003t0006g0147 others(37): Show |
40 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.933-3123_933-3121d others(5): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 823900 | ||||||
chr12:823954 | C | T | 181 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(178): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.933-3088C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 823954 | |||||||
chr12:823967 | C | T | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.933-3075C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 823967 | |||||||
chr12:823975 | C | T | 1 | a0002c0024t0014g0196 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.933-3067C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 823975 | |||||||
chr12:824044 | C | T | 1 | a0002c0002t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.933-2998C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 824044 | |||||||
chr12:824216 | C | CT | 32 | a0001c0001t0002g0134 a0001c0001t0002g0227 a0001c0001t0004g0172 others(29): Show |
32 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.933-2808dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 824216 | ||||||
chr12:824259 | A | G | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.933-2783A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 824259 | |||||||
chr12:824316 | G | A | 181 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(178): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.933-2726G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 824316 | |||||||
chr12:824351 | T | A | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.933-2691T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 824351 | |||||||
chr12:824380 | T | C | 15 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(12): Show |
15 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.933-2662T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 824380 | |||||||
chr12:824396 | A | C | 1 | a0002c0003t0001g0124 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.933-2646A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 824396 | |||||||
chr12:824397 | T | C | 1 | a0003c0005t0005g0234 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.933-2645T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 824397 | |||||||
chr12:824535 | T | A | 8 | a0001c0001t0004g0154 a0001c0001t0004g0155 a0001c0001t0004g0166 others(5): Show |
8 | HG00280.hp1 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.933-2507T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 824535 | |||||||
chr12:824535 | T | G | 190 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(187): Show |
191 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.933-2507T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 824535 | |||||||
chr12:824675 | A | AAGAG | 196 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(193): Show |
197 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.933-2363_933-2360d others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 824675 | ||||||
chr12:824681 | G | A | 1 | a0002c0002t0001g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.933-2361G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 824681 | |||||||
chr12:824865 | CT | C | 18 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(15): Show |
18 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.933-2172delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 824865 | ||||||
chr12:825085 | C | T | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.933-1957C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 825085 | |||||||
chr12:825086 | G | A | 2 | a0003c0005t0005g0203 a0003c0026t0005g0204 |
2 | HG00544.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.933-1956G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 825086 | |||||||
chr12:825116 | C | T | 1 | a0007c0010t0030g0102 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.933-1926C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 825116 | |||||||
chr12:825229 | A | C | 1 | a0001c0001t0004g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.933-1813A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 825229 | |||||||
chr12:825229 | A | G | 4 | a0001c0022t0001g0263 a0002c0002t0001g0261 a0002c0002t0001g0262 others(1): Show |
4 | HG02602.hp2 HG03942.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.933-1813A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 825229 | |||||||
chr12:825242 | C | T | 121 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(118): Show |
122 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.933-1800C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 825242 | |||||||
chr12:825243 | A | G | 25 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.933-1799A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 825243 | |||||||
chr12:825306 | T | G | 1 | a0002c0015t0001g0244 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.933-1736T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 825306 | |||||||
chr12:825369 | T | G | 3 | a0002c0015t0001g0211 a0002c0015t0001g0243 a0002c0015t0001g0244 |
3 | HG02559.hp2 HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.933-1673T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 825369 | |||||||
chr12:825489 | C | G | 1 | a0001c0001t0023g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.933-1553C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 825489 | |||||||
chr12:825501 | A | G | 15 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(12): Show |
15 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.933-1541A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 825501 | |||||||
chr12:825603 | G | A | 1 | a0002c0002t0001g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.933-1439G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 825603 | |||||||
chr12:825671 | A | C | 1 | a0002c0003t0001g0280 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.933-1371A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 825671 | |||||||
chr12:825679 | C | G | 215 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(212): Show |
216 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.933-1363C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 825679 | |||||||
chr12:825815 | A | G | 2 | a0004c0004t0003g0078 a0004c0004t0003g0083 |
2 | HG02071.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.933-1227A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 825815 | |||||||
chr12:825817 | CAT | C | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.933-1224_933-1223d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 825817 | |||||||
chr12:826220 | G | A | 1 | a0002c0002t0001g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.933-822G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 826220 | |||||||
chr12:826323 | C | T | 2 | a0005c0006t0009g0021 a0005c0006t0009g0277 |
2 | HG01106.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.933-719C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 826323 | |||||||
chr12:826405 | G | T | 1 | a0001c0001t0023g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.933-637G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 826405 | |||||||
chr12:826851 | CTT | C | 11 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(8): Show |
11 | HG01261.hp2 HG01952.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.933-190_933-189del others(2): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 826851 | |||||||
chr12:826903 | A | G | 2 | a0001c0001t0016g0049 a0001c0001t0016g0056 |
2 | HG02738.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.933-139A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 2/27 | chr12 | 826903 | |||||||
chr12:827302 | C | G | 198 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(195): Show |
199 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1153+40C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 3/27 | chr12 | 827302 | |||||||
chr12:827480 | A | G | 1 | a0001c0018t0006g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1153+218A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 3/27 | chr12 | 827480 | |||||||
chr12:827498 | A | G | 1 | a0004c0004t0003g0080 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1153+236A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 3/27 | chr12 | 827498 | |||||||
chr12:827520 | TTTG | T | 199 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(196): Show |
200 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1153+283_1153+285d others(5): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 827520 | ||||||
chr12:827614 | C | T | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1153+352C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 3/27 | chr12 | 827614 | |||||||
chr12:827619 | A | G | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1153+357A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 3/27 | chr12 | 827619 | |||||||
chr12:827659 | G | C | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1153+397G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 3/27 | chr12 | 827659 | |||||||
chr12:827894 | A | AT | 163 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(160): Show |
164 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1153+633dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 827894 | ||||||
chr12:828143 | C | CA | 26 | a0001c0001t0002g0057 a0001c0032t0002g0050 a0004c0004t0003g0072 others(23): Show |
26 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1153+894dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 828143 | ||||||
chr12:828280 | T | C | 3 | a0001c0001t0002g0227 a0005c0006t0009g0021 a0005c0006t0009g0277 |
3 | HG01106.hp2 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1153+1018T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 3/27 | chr12 | 828280 | |||||||
chr12:828633 | C | A | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1154-1370C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 3/27 | chr12 | 828633 | |||||||
chr12:829074 | T | C | 1 | a0001c0001t0004g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1154-929T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 3/27 | chr12 | 829074 | |||||||
chr12:829256 | G | T | 1 | a0015c0039t0001g0151 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1154-747G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 3/27 | chr12 | 829256 | |||||||
chr12:829324 | A | G | 1 | a0002c0002t0001g0144 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1154-679A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 3/27 | chr12 | 829324 | |||||||
chr12:829554 | A | G | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1154-449A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 3/27 | chr12 | 829554 | |||||||
chr12:829744 | T | A | 183 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(180): Show |
184 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1154-259T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 3/27 | chr12 | 829744 | |||||||
chr12:830314 | G | T | 60 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 others(57): Show |
60 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1311+154G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 830314 | |||||||
chr12:830361 | T | C | 3 | a0004c0004t0022g0085 a0010c0016t0015g0092 a0010c0016t0015g0093 |
3 | HG01261.hp1 HG02273.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1311+201T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 830361 | |||||||
chr12:830547 | T | C | 1 | a0002c0002t0035g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1311+387T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 830547 | |||||||
chr12:830758 | A | G | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1311+598A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 830758 | |||||||
chr12:830954 | T | C | 1 | a0001c0008t0002g0276 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1311+794T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 830954 | |||||||
chr12:831039 | C | T | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1311+879C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 831039 | |||||||
chr12:831102 | G | T | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1311+942G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 831102 | |||||||
chr12:831148 | G | A | 1 | a0007c0030t0002g0271 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1311+988G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 831148 | |||||||
chr12:831262 | G | A | 1 | a0001c0001t0012g0185 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1311+1102G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 831262 | |||||||
chr12:831263 | C | T | 1 | a0002c0002t0001g0238 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1311+1103C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 831263 | |||||||
chr12:831444 | C | T | 1 | a0002c0002t0001g0264 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1311+1284C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 831444 | |||||||
chr12:831463 | G | A | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1311+1303G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 831463 | |||||||
chr12:831635 | T | C | 2 | a0001c0001t0007g0035 a0001c0001t0007g0063 |
2 | HG00673.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1311+1475T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 831635 | |||||||
chr12:831711 | C | T | 183 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(180): Show |
184 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1311+1551C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 831711 | |||||||
chr12:831776 | A | T | 126 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(123): Show |
127 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1311+1616A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 831776 | |||||||
chr12:831958 | T | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(12): Show |
15 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1311+1798T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 831958 | |||||||
chr12:832071 | T | A | 1 | a0003c0005t0001g0037 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1311+1911T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 832071 | |||||||
chr12:832078 | T | C | 1 | a0008c0013t0013g0180 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1311+1918T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 832078 | |||||||
chr12:832098 | C | T | 1 | a0004c0004t0003g0082 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1311+1938C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 832098 | |||||||
chr12:832279 | G | A | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1311+2119G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 832279 | |||||||
chr12:832309 | T | C | 61 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0045 others(58): Show |
62 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.1311+2149T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 832309 | |||||||
chr12:833008 | TTC | T | 2 | a0011c0017t0014g0195 a0011c0017t0014g0197 |
2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1311+2854_1311+285 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 833008 | ||||||
chr12:833014 | C | CT | 25 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1311+2865dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 833014 | ||||||
chr12:833070 | T | C | 1 | a0001c0001t0004g0164 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1311+2910T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 833070 | |||||||
chr12:833180 | A | C | 198 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(195): Show |
199 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1311+3020A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 833180 | |||||||
chr12:833352 | C | T | 1 | a0002c0003t0001g0202 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1311+3192C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 833352 | |||||||
chr12:833504 | A | G | 1 | a0006c0007t0008g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1311+3344A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 833504 | |||||||
chr12:833568 | CCTCCATG others(9): Show |
C | 2 | a0001c0001t0002g0060 a0001c0001t0002g0066 |
2 | HG00741.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1311+3411_1311+342 others(20): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 833568 | ||||||
chr12:833669 | A | G | 5 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 others(2): Show |
5 | HG02109.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1311+3509A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 833669 | |||||||
chr12:833796 | A | G | 1 | a0001c0001t0023g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1311+3636A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 833796 | |||||||
chr12:834461 | G | A | 1 | a0003c0005t0005g0242 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1311+4301G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 834461 | |||||||
chr12:834787 | G | T | 183 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(180): Show |
184 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1311+4627G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 834787 | |||||||
chr12:834884 | C | T | 1 | a0002c0002t0001g0252 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1311+4724C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 834884 | |||||||
chr12:834890 | G | C | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1311+4730G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 834890 | |||||||
chr12:835019 | T | A | 1 | a0001c0001t0004g0164 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1311+4859T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 835019 | |||||||
chr12:835262 | G | A | 3 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 |
3 | HG01106.hp1 HG01255.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1311+5102G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 835262 | |||||||
chr12:835635 | T | TA | 6 | a0001c0001t0006g0006 a0001c0001t0006g0008 a0001c0018t0006g0005 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1311+5488dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 835635 | ||||||
chr12:835834 | G | A | 1 | a0003c0005t0001g0193 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1311+5674G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 835834 | |||||||
chr12:836156 | T | C | 25 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1311+5996T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 836156 | |||||||
chr12:836249 | C | T | 275 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(272): Show |
276 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1311+6089C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 836249 | |||||||
chr12:836297 | T | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(12): Show |
15 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1311+6137T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 836297 | |||||||
chr12:836307 | T | C | 1 | a0020c0021t0024g0189 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1311+6147T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 836307 | |||||||
chr12:836433 | T | A | 6 | a0001c0001t0011g0159 a0001c0001t0011g0162 a0001c0001t0011g0169 others(3): Show |
6 | HG00735.hp1 HG01943.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1311+6273T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 836433 | |||||||
chr12:836871 | C | T | 183 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(180): Show |
184 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1311+6711C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 836871 | |||||||
chr12:836899 | TA | T | 4 | a0003c0005t0005g0225 a0003c0005t0005g0229 a0003c0005t0005g0232 others(1): Show |
4 | HG03239.hp1 NA18965.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1311+6740delA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 836899 | |||||||
chr12:836900 | AT | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(12): Show |
15 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1311+6750delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 836900 | ||||||
chr12:836932 | A | ACATTTAG others(6142): Show |
1 | a0009c0014t0002g0053 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1311+6789_1311+679 others(6153): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 836932 | ||||||
chr12:836977 | C | T | 183 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(180): Show |
184 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1311+6817C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 836977 | |||||||
chr12:837100 | C | T | 1 | a0002c0002t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1311+6940C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 837100 | |||||||
chr12:837446 | C | G | 1 | a0002c0029t0001g0125 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1311+7286C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 837446 | |||||||
chr12:837530 | C | T | 25 | a0002c0002t0001g0216 a0002c0002t0001g0217 a0002c0002t0035g0208 others(22): Show |
25 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1311+7370C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 837530 | |||||||
chr12:837572 | T | TA | 6 | a0002c0002t0001g0107 a0002c0002t0001g0206 a0002c0024t0014g0196 others(3): Show |
6 | HG01981.hp2 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1311+7432dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 837572 | ||||||
chr12:837572 | TAAAA | T | 8 | a0001c0001t0002g0060 a0001c0001t0004g0023 a0001c0001t0004g0173 others(5): Show |
8 | HG01346.hp2 HG02486.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1311+7429_1311+743 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 837572 | ||||||
chr12:837572 | TAAAAAAA others(3): Show |
T | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1311+7423_1311+743 others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 837572 | ||||||
chr12:837588 | A | AG | 113 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(110): Show |
114 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1311+7428_1311+742 others(5): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 837588 | |||||||
chr12:837588 | A | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(14): Show |
17 | HG00735.hp2 HG01069.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1311+7428A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 837588 | |||||||
chr12:837594 | A | T | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1311+7434A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 837594 | |||||||
chr12:837692 | A | G | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1311+7532A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 837692 | |||||||
chr12:837708 | T | G | 4 | a0001c0001t0006g0006 a0001c0001t0006g0008 a0001c0041t0006g0010 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1311+7548T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 837708 | |||||||
chr12:837712 | A | G | 148 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(145): Show |
149 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.1311+7552A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 837712 | |||||||
chr12:837734 | T | C | 1 | a0001c0008t0002g0273 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1311+7574T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 837734 | |||||||
chr12:837962 | T | A | 1 | a0002c0002t0035g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1311+7802T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 837962 | |||||||
chr12:837972 | G | A | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1311+7812G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 837972 | |||||||
chr12:838066 | G | GAGT | 181 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(178): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.1311+7908_1311+791 others(7): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 838066 | ||||||
chr12:838078 | A | AGT | 15 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(12): Show |
15 | HG00735.hp2 HG01074.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.1311+7949_1311+795 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 838078 | ||||||
chr12:838078 | A | AGTGT | 48 | a0001c0001t0006g0003 a0001c0018t0006g0009 a0001c0022t0001g0263 others(45): Show |
48 | HG00323.hp1 HG00609.hp2 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.1311+7947_1311+795 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 838078 | ||||||
chr12:838078 | A | AGTGTGT | 23 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(20): Show |
23 | HG00438.hp2 HG00544.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.1311+7945_1311+795 others(10): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 838078 | ||||||
chr12:838078 | A | AGTGTGTG others(1): Show |
5 | a0002c0002t0001g0138 a0002c0002t0001g0141 a0002c0002t0001g0217 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1311+7943_1311+795 others(12): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 838078 | ||||||
chr12:838078 | A | AGTGTGTG others(3): Show |
1 | a0002c0002t0001g0216 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1311+7941_1311+795 others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 838078 | ||||||
chr12:838078 | AGT | A | 49 | a0001c0001t0002g0025 a0001c0001t0002g0051 a0001c0001t0002g0057 others(46): Show |
49 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.1311+7949_1311+795 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 838078 | ||||||
chr12:838078 | AGTGT | A | 119 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0028 others(116): Show |
120 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1311+7947_1311+795 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 838078 | ||||||
chr12:838177 | T | C | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1311+8017T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 838177 | |||||||
chr12:838197 | C | T | 122 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(119): Show |
123 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1311+8037C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 838197 | |||||||
chr12:838206 | T | C | 15 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(12): Show |
15 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.1311+8046T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 838206 | |||||||
chr12:838306 | A | G | 15 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(12): Show |
15 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.1311+8146A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 838306 | |||||||
chr12:838479 | A | G | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1311+8319A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 838479 | |||||||
chr12:838565 | C | T | 1 | a0001c0001t0020g0168 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1311+8405C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 838565 | |||||||
chr12:838598 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1311+8438T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 838598 | |||||||
chr12:838607 | GGTTTTGT others(3): Show |
G | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1311+8451_1311+846 others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 838607 | ||||||
chr12:838614 | T | A | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1311+8454T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 838614 | |||||||
chr12:838803 | T | G | 143 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(140): Show |
144 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.1311+8643T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 838803 | |||||||
chr12:838978 | T | TA | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1311+8819dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 838978 | ||||||
chr12:839041 | C | T | 1 | a0002c0003t0001g0105 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1311+8881C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 839041 | |||||||
chr12:839160 | G | A | 1 | a0001c0001t0002g0045 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1311+9000G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 839160 | |||||||
chr12:839373 | A | G | 2 | a0001c0001t0004g0174 a0001c0001t0004g0175 |
2 | HG01346.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1311+9213A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 839373 | |||||||
chr12:839617 | T | C | 4 | a0002c0003t0001g0199 a0002c0003t0001g0201 a0002c0003t0001g0202 others(1): Show |
4 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1311+9457T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 839617 | |||||||
chr12:839643 | A | G | 5 | a0001c0022t0001g0263 a0002c0002t0001g0261 a0002c0002t0001g0262 others(2): Show |
5 | HG02602.hp2 HG03927.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1311+9483A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 839643 | |||||||
chr12:839884 | A | AT | 26 | a0002c0002t0001g0261 a0004c0004t0003g0072 a0004c0004t0003g0073 others(23): Show |
26 | HG00408.hp2 HG01081.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.1311+9746dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 839884 | ||||||
chr12:839884 | AT | A | 22 | a0001c0001t0004g0023 a0001c0001t0006g0020 a0001c0001t0023g0171 others(19): Show |
22 | HG00323.hp1 HG01169.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.1311+9746delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 839884 | ||||||
chr12:839906 | T | A | 137 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(134): Show |
138 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.1311+9746T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 839906 | |||||||
chr12:839906 | T | TA | 7 | a0001c0001t0004g0179 a0001c0001t0011g0159 a0001c0001t0011g0162 others(4): Show |
7 | HG00735.hp1 HG01943.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.1311+9748dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 839906 | ||||||
chr12:839952 | T | G | 1 | a0001c0001t0023g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1311+9792T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 839952 | |||||||
chr12:839975 | A | G | 183 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(180): Show |
184 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1311+9815A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 839975 | |||||||
chr12:840100 | C | T | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1311+9940C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 840100 | |||||||
chr12:840190 | C | A | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1311+10030C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 840190 | |||||||
chr12:840291 | C | CT | 21 | a0001c0001t0001g0004 a0001c0001t0006g0012 a0001c0001t0006g0014 others(18): Show |
21 | HG01175.hp1 HG01261.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.1311+10152dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 840291 | ||||||
chr12:840291 | CTTTTTTT | C | 156 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(153): Show |
157 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1311+10146_1311+10 others(13): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 840291 | ||||||
chr12:840446 | T | TA | 25 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1311+10288dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 840446 | ||||||
chr12:840636 | C | T | 25 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1311+10476C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 840636 | |||||||
chr12:840645 | A | G | 1 | a0001c0001t0018g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1311+10485A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 840645 | |||||||
chr12:841013 | A | G | 2 | a0002c0015t0001g0211 a0002c0015t0001g0243 |
2 | HG02559.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1311+10853A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 841013 | |||||||
chr12:841233 | G | A | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1311+11073G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 841233 | |||||||
chr12:841421 | T | C | 1 | a0002c0002t0001g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1311+11261T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 841421 | |||||||
chr12:841517 | T | A | 25 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1311+11357T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 841517 | |||||||
chr12:841810 | G | A | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1311+11650G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 841810 | |||||||
chr12:841893 | A | G | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1311+11733A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 841893 | |||||||
chr12:841915 | G | A | 181 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(178): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.1311+11755G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 841915 | |||||||
chr12:841921 | T | C | 1 | a0002c0003t0001g0279 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1311+11761T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 841921 | |||||||
chr12:842293 | A | G | 1 | a0001c0012t0002g0268 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1311+12133A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 842293 | |||||||
chr12:842442 | A | G | 1 | a0004c0004t0003g0074 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1311+12282A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 842442 | |||||||
chr12:842522 | T | C | 1 | a0003c0005t0005g0260 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1311+12362T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 842522 | |||||||
chr12:842609 | G | C | 183 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(180): Show |
184 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1311+12449G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 842609 | |||||||
chr12:842788 | G | C | 1 | a0002c0024t0014g0196 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1311+12628G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 842788 | |||||||
chr12:842858 | G | C | 2 | a0002c0002t0001g0216 a0002c0002t0001g0217 |
2 | HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1311+12698G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 842858 | |||||||
chr12:842923 | T | TTTTA | 9 | a0003c0005t0001g0193 a0003c0005t0001g0240 a0003c0005t0001g0241 others(6): Show |
9 | HG01175.hp1 HG01358.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1311+12787_1311+12 others(10): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 842923 | ||||||
chr12:842943 | A | C | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1311+12783A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 842943 | |||||||
chr12:842969 | G | A | 181 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(178): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.1311+12809G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 842969 | |||||||
chr12:843154 | C | T | 1 | a0004c0004t0022g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1311+12994C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 843154 | |||||||
chr12:843228 | C | T | 1 | a0001c0001t0012g0121 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1311+13068C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 843228 | |||||||
chr12:843344 | G | A | 3 | a0002c0003t0001g0115 a0002c0003t0001g0117 a0002c0003t0001g0118 |
3 | HG01069.hp1 HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.1311+13184G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 843344 | |||||||
chr12:843466 | A | G | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1311+13306A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 843466 | |||||||
chr12:843473 | C | A | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1311+13313C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 843473 | |||||||
chr12:843473 | C | T | 200 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(197): Show |
201 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1311+13313C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 843473 | |||||||
chr12:843506 | T | G | 1 | a0002c0002t0001g0259 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1311+13346T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 843506 | |||||||
chr12:843922 | C | T | 1 | a0001c0001t0018g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1312-13239C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 843922 | |||||||
chr12:843968 | C | T | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1312-13193C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 843968 | |||||||
chr12:844024 | CATT | C | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-13134_1312-13 others(9): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 844024 | ||||||
chr12:844093 | C | A | 1 | a0006c0007t0008g0283 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1312-13068C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 844093 | |||||||
chr12:844126 | C | G | 1 | a0003c0005t0005g0236 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1312-13035C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 844126 | |||||||
chr12:844140 | A | AT | 7 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0281 others(4): Show |
7 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1312-13012dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 844140 | ||||||
chr12:844258 | A | G | 4 | a0002c0002t0017g0139 a0002c0002t0017g0140 a0010c0016t0015g0092 others(1): Show |
4 | HG01261.hp1 HG02273.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-12903A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 844258 | |||||||
chr12:844308 | A | T | 1 | a0002c0003t0001g0065 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1312-12853A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 844308 | |||||||
chr12:844634 | G | A | 3 | a0004c0004t0003g0078 a0004c0004t0003g0083 a0004c0004t0003g0088 |
3 | HG00408.hp2 HG02071.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1312-12527G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 844634 | |||||||
chr12:844674 | C | G | 1 | a0004c0004t0003g0072 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1312-12487C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 844674 | |||||||
chr12:844757 | G | C | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1312-12404G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 844757 | |||||||
chr12:844890 | CT | C | 197 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(194): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1312-12248delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 844890 | ||||||
chr12:844890 | CTT | C | 7 | a0001c0001t0004g0173 a0001c0001t0004g0175 a0001c0001t0021g0176 others(4): Show |
7 | HG01346.hp2 HG02486.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.1312-12249_1312-12 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 844890 | ||||||
chr12:844918 | C | T | 1 | a0002c0002t0001g0191 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1312-12243C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 844918 | |||||||
chr12:844998 | C | A | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-12163C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 844998 | |||||||
chr12:845021 | A | G | 22 | a0003c0005t0001g0036 a0003c0005t0001g0037 a0003c0005t0001g0193 others(19): Show |
22 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.1312-12140A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 845021 | |||||||
chr12:845053 | G | A | 5 | a0002c0002t0001g0194 a0002c0002t0001g0213 a0002c0002t0001g0223 others(2): Show |
5 | HG02615.hp2 HG03225.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-12108G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 845053 | |||||||
chr12:845096 | C | T | 1 | a0001c0001t0023g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1312-12065C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 845096 | |||||||
chr12:845105 | C | T | 2 | a0005c0006t0009g0021 a0005c0006t0009g0277 |
2 | HG01106.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1312-12056C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 845105 | |||||||
chr12:845190 | C | T | 1 | a0001c0008t0002g0276 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1312-11971C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 845190 | |||||||
chr12:845256 | A | G | 1 | a0004c0004t0003g0082 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1312-11905A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 845256 | |||||||
chr12:845268 | T | C | 1 | a0002c0002t0001g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1312-11893T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 845268 | |||||||
chr12:845354 | C | A | 1 | a0006c0007t0008g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1312-11807C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 845354 | |||||||
chr12:845434 | A | G | 1 | a0002c0009t0005g0043 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1312-11727A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 845434 | |||||||
chr12:845517 | A | G | 1 | a0001c0001t0018g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1312-11644A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 845517 | |||||||
chr12:845629 | C | G | 1 | a0005c0006t0003g0152 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1312-11532C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 845629 | |||||||
chr12:845666 | G | A | 4 | a0001c0012t0002g0267 a0001c0012t0002g0268 a0001c0012t0002g0270 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312-11495G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 845666 | |||||||
chr12:846128 | C | T | 1 | a0001c0001t0002g0165 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1312-11033C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 846128 | |||||||
chr12:846342 | C | A | 214 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(211): Show |
215 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.1312-10819C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 846342 | |||||||
chr12:846422 | A | G | 1 | a0001c0001t0002g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1312-10739A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 846422 | |||||||
chr12:846713 | A | C | 1 | a0006c0007t0008g0013 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1312-10448A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 846713 | |||||||
chr12:846732 | T | G | 4 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-10429T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 846732 | |||||||
chr12:846811 | T | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(12): Show |
15 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1312-10350T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 846811 | |||||||
chr12:847217 | C | T | 1 | a0002c0002t0001g0239 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1312-9944C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 847217 | |||||||
chr12:847275 | C | G | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1312-9886C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 847275 | |||||||
chr12:847405 | C | G | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1312-9756C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 847405 | |||||||
chr12:847713 | GGTGC | G | 11 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(8): Show |
11 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1312-9447_1312-944 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 847713 | |||||||
chr12:847741 | T | C | 1 | a0001c0001t0004g0002 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1312-9420T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 847741 | |||||||
chr12:847801 | C | CT | 59 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 others(56): Show |
59 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1312-9336dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 847801 | ||||||
chr12:847801 | C | CTT | 29 | a0001c0001t0002g0165 a0001c0001t0002g0227 a0001c0001t0004g0150 others(26): Show |
29 | HG00280.hp1 HG00673.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1312-9337_1312-933 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 847801 | ||||||
chr12:847801 | CT | C | 20 | a0001c0001t0002g0198 a0001c0001t0004g0002 a0002c0002t0001g0107 others(17): Show |
20 | HG00609.hp2 HG01074.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.1312-9336delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 847801 | ||||||
chr12:847801 | CTT | C | 9 | a0002c0002t0017g0140 a0006c0007t0008g0011 a0006c0007t0008g0013 others(6): Show |
9 | HG01109.hp2 HG01358.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1312-9337_1312-933 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 847801 | ||||||
chr12:847803 | TTTTTTTT others(34): Show |
T | 1 | a0002c0002t0001g0141 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1312-9356_1312-931 others(45): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 847803 | ||||||
chr12:847932 | C | T | 25 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1312-9229C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 847932 | |||||||
chr12:848084 | C | T | 3 | a0003c0005t0005g0210 a0003c0005t0005g0242 a0003c0005t0005g0246 |
3 | NA18972.hp1 NA19056.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1312-9077C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 848084 | |||||||
chr12:848225 | G | A | 1 | a0005c0006t0009g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1312-8936G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 848225 | |||||||
chr12:848432 | T | G | 1 | a0004c0004t0003g0073 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1312-8729T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 848432 | |||||||
chr12:848433 | T | TTGA | 3 | a0002c0002t0001g0261 a0002c0002t0001g0262 a0002c0002t0001g0264 |
3 | HG02602.hp2 HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1312-8725_1312-872 others(7): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 848433 | ||||||
chr12:848439 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(12): Show |
15 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1312-8722G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 848439 | |||||||
chr12:848452 | T | C | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1312-8709T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 848452 | |||||||
chr12:848496 | C | CT | 10 | a0002c0002t0001g0207 a0002c0002t0001g0238 a0002c0015t0001g0211 others(7): Show |
10 | HG00609.hp2 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1312-8645dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 848496 | ||||||
chr12:848496 | C | CTT | 12 | a0002c0002t0001g0136 a0002c0002t0001g0137 a0002c0002t0001g0138 others(9): Show |
12 | HG01261.hp2 HG01952.hp1 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.1312-8646_1312-864 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 848496 | ||||||
chr12:848496 | C | CTTT | 18 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(15): Show |
18 | HG00323.hp2 HG00735.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1312-8647_1312-864 others(7): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 848496 | ||||||
chr12:848496 | C | CTTTT | 123 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(120): Show |
124 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1312-8648_1312-864 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 848496 | ||||||
chr12:848496 | C | CTTTTT | 47 | a0001c0001t0002g0066 a0001c0001t0004g0154 a0001c0001t0004g0181 others(44): Show |
47 | HG00408.hp2 HG00741.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.1312-8649_1312-864 others(9): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 848496 | ||||||
chr12:848496 | CTTT | C | 6 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(3): Show |
6 | HG02451.hp2 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1312-8647_1312-864 others(7): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 848496 | ||||||
chr12:848642 | T | C | 1 | a0002c0003t0001g0228 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1312-8519T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 848642 | |||||||
chr12:848649 | G | T | 1 | a0001c0001t0007g0042 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1312-8512G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 848649 | |||||||
chr12:849000 | C | T | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1312-8161C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 849000 | |||||||
chr12:849150 | A | G | 1 | a0008c0013t0013g0180 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1312-8011A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 849150 | |||||||
chr12:849602 | A | G | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1312-7559A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 849602 | |||||||
chr12:849706 | A | G | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1312-7455A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 849706 | |||||||
chr12:849836 | C | T | 1 | a0002c0015t0001g0211 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1312-7325C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 849836 | |||||||
chr12:849913 | C | T | 2 | a0001c0018t0006g0005 a0001c0018t0006g0009 |
2 | HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1312-7248C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 849913 | |||||||
chr12:850100 | G | C | 1 | a0005c0006t0009g0277 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1312-7061G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 850100 | |||||||
chr12:850210 | C | G | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1312-6951C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 850210 | |||||||
chr12:850339 | T | C | 4 | a0002c0002t0001g0256 a0002c0002t0001g0257 a0002c0002t0001g0258 others(1): Show |
4 | HG01168.hp1 HG01169.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-6822T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 850339 | |||||||
chr12:850390 | C | A | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1312-6771C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 850390 | |||||||
chr12:850520 | G | A | 15 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(12): Show |
15 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.1312-6641G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 850520 | |||||||
chr12:850524 | G | C | 180 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(177): Show |
181 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.1312-6637G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 850524 | |||||||
chr12:850666 | C | A | 22 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(19): Show |
22 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.1312-6495C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 850666 | |||||||
chr12:850768 | A | G | 1 | a0021c0038t0012g0135 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1312-6393A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 850768 | |||||||
chr12:850947 | G | T | 1 | a0003c0005t0005g0209 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1312-6214G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 850947 | |||||||
chr12:851177 | C | G | 24 | a0001c0022t0001g0263 a0002c0002t0001g0205 a0002c0002t0001g0215 others(21): Show |
24 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1312-5984C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 851177 | |||||||
chr12:851187 | T | C | 2 | a0002c0002t0017g0139 a0002c0002t0017g0140 |
2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1312-5974T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 851187 | |||||||
chr12:851223 | C | T | 1 | a0001c0001t0004g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1312-5938C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 851223 | |||||||
chr12:851224 | A | C | 1 | a0005c0006t0009g0277 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1312-5937A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 851224 | |||||||
chr12:851257 | A | G | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-5904A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 851257 | |||||||
chr12:852005 | A | G | 1 | a0002c0011t0001g0222 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1312-5156A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 852005 | |||||||
chr12:852019 | T | C | 1 | a0006c0007t0008g0013 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1312-5142T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 852019 | |||||||
chr12:852085 | C | T | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1312-5076C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 852085 | |||||||
chr12:852170 | C | T | 240 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(237): Show |
241 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1312-4991C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 852170 | |||||||
chr12:852292 | A | G | 1 | a0002c0002t0001g0265 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1312-4869A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 852292 | |||||||
chr12:852386 | G | T | 4 | a0001c0022t0001g0263 a0002c0002t0001g0261 a0002c0002t0001g0262 others(1): Show |
4 | HG02602.hp2 HG03942.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312-4775G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 852386 | |||||||
chr12:852397 | A | C | 15 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(12): Show |
15 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.1312-4764A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 852397 | |||||||
chr12:852429 | C | A | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1312-4732C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 852429 | |||||||
chr12:852537 | G | C | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1312-4624G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 852537 | |||||||
chr12:852663 | T | C | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1312-4498T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 852663 | |||||||
chr12:852703 | C | G | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1312-4458C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 852703 | |||||||
chr12:852793 | C | T | 4 | a0002c0002t0017g0139 a0002c0002t0017g0140 a0010c0016t0015g0092 others(1): Show |
4 | HG01261.hp1 HG02273.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-4368C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 852793 | |||||||
chr12:852876 | G | A | 1 | a0002c0003t0001g0131 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1312-4285G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 852876 | |||||||
chr12:853295 | G | T | 60 | a0001c0001t0002g0227 a0001c0008t0002g0266 a0001c0008t0002g0272 others(57): Show |
60 | HG00408.hp2 HG00741.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1312-3866G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 853295 | |||||||
chr12:853355 | A | G | 2 | a0002c0002t0006g0145 a0002c0002t0006g0178 |
2 | NA19007.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1312-3806A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 853355 | |||||||
chr12:853506 | G | A | 1 | a0002c0002t0001g0262 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1312-3655G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 853506 | |||||||
chr12:853520 | G | T | 2 | a0001c0001t0004g0023 a0001c0001t0025g0024 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1312-3641G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 853520 | |||||||
chr12:853523 | G | C | 14 | a0001c0001t0002g0227 a0002c0003t0001g0199 a0002c0003t0001g0201 others(11): Show |
14 | HG01106.hp2 HG02257.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1312-3638G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 853523 | |||||||
chr12:853694 | A | T | 1 | a0001c0001t0018g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1312-3467A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 853694 | |||||||
chr12:853812 | A | G | 1 | a0006c0007t0008g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1312-3349A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 853812 | |||||||
chr12:853903 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0006g0012 a0001c0001t0006g0014 others(1): Show |
4 | HG02280.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-3258C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 853903 | |||||||
chr12:853939 | A | AC | 22 | a0003c0005t0001g0036 a0003c0005t0001g0037 a0003c0005t0001g0193 others(19): Show |
22 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.1312-3221dupC | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 853939 | ||||||
chr12:854013 | A | G | 2 | a0001c0001t0002g0001 a0001c0037t0002g0129 |
3 | HG01496.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1312-3148A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 854013 | |||||||
chr12:854016 | G | A | 15 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(12): Show |
15 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.1312-3145G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 854016 | |||||||
chr12:854029 | C | G | 214 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(211): Show |
215 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.1312-3132C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 854029 | |||||||
chr12:854053 | A | T | 7 | a0002c0003t0001g0199 a0002c0003t0001g0201 a0002c0003t0001g0202 others(4): Show |
7 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1312-3108A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 854053 | |||||||
chr12:854094 | G | T | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1312-3067G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 854094 | |||||||
chr12:854155 | C | A | 1 | a0001c0001t0004g0155 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1312-3006C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 854155 | |||||||
chr12:854179 | G | C | 1 | a0005c0006t0009g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1312-2982G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 854179 | |||||||
chr12:854215 | A | G | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1312-2946A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 854215 | |||||||
chr12:854355 | C | CT | 29 | a0001c0001t0006g0012 a0002c0002t0001g0107 a0002c0002t0001g0136 others(26): Show |
29 | HG01109.hp2 HG01261.hp1 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.1312-2795dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 854355 | ||||||
chr12:854355 | C | CTT | 39 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(36): Show |
39 | HG00408.hp2 HG00735.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.1312-2796_1312-279 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 854355 | ||||||
chr12:854355 | C | CTTT | 10 | a0001c0001t0002g0034 a0001c0001t0007g0069 a0002c0003t0001g0199 others(7): Show |
10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1312-2797_1312-279 others(7): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 854355 | ||||||
chr12:854355 | C | CTTTT | 96 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 others(93): Show |
96 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1312-2798_1312-279 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 854355 | ||||||
chr12:854355 | C | CTTTTT | 20 | a0001c0001t0002g0001 a0001c0001t0002g0060 a0001c0001t0002g0066 others(17): Show |
21 | HG00423.hp1 HG00423.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1312-2799_1312-279 others(9): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 854355 | ||||||
chr12:854355 | C | CTTTTTT | 20 | a0001c0001t0002g0109 a0002c0003t0001g0022 a0002c0003t0001g0105 others(17): Show |
20 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1312-2800_1312-279 others(10): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 854355 | ||||||
chr12:854366 | TG | T | 3 | a0002c0002t0001g0207 a0003c0005t0005g0229 a0016c0044t0001g0245 |
3 | HG02630.hp2 HG03239.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1312-2794delG | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 854366 | |||||||
chr12:854367 | G | T | 278 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(275): Show |
279 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.1312-2794G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 854367 | |||||||
chr12:854458 | A | C | 1 | a0002c0002t0001g0190 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1312-2703A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 854458 | |||||||
chr12:854801 | A | G | 7 | a0002c0003t0001g0199 a0002c0003t0001g0201 a0002c0003t0001g0202 others(4): Show |
7 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1312-2360A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 854801 | |||||||
chr12:854859 | C | T | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1312-2302C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 854859 | |||||||
chr12:854886 | G | A | 1 | a0002c0002t0001g0141 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1312-2275G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 854886 | |||||||
chr12:854993 | C | T | 4 | a0002c0002t0017g0139 a0002c0002t0017g0140 a0010c0016t0015g0092 others(1): Show |
4 | HG01261.hp1 HG02273.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-2168C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 854993 | |||||||
chr12:855053 | C | A | 1 | a0002c0015t0001g0244 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1312-2108C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 855053 | |||||||
chr12:855098 | T | C | 1 | a0001c0001t0002g0198 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1312-2063T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 855098 | |||||||
chr12:855340 | G | A | 158 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(155): Show |
159 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1312-1821G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 855340 | |||||||
chr12:855367 | C | G | 181 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(178): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.1312-1794C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 855367 | |||||||
chr12:855385 | T | A | 158 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(155): Show |
159 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1312-1776T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 855385 | |||||||
chr12:855394 | C | T | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1312-1767C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 855394 | |||||||
chr12:855504 | T | C | 181 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(178): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.1312-1657T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 855504 | |||||||
chr12:855628 | C | A | 2 | a0001c0001t0004g0023 a0001c0001t0025g0024 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1312-1533C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 855628 | |||||||
chr12:855806 | T | C | 5 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-1355T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 855806 | |||||||
chr12:856029 | G | A | 1 | a0003c0005t0005g0242 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1312-1132G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 856029 | |||||||
chr12:856042 | G | C | 6 | a0001c0001t0006g0006 a0001c0001t0006g0008 a0001c0018t0006g0005 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1312-1119G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 856042 | |||||||
chr12:856102 | G | A | 1 | a0005c0006t0009g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1312-1059G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 856102 | |||||||
chr12:856125 | C | T | 2 | a0001c0001t0004g0023 a0001c0001t0025g0024 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1312-1036C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 856125 | |||||||
chr12:856130 | C | T | 1 | a0019c0025t0001g0214 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1312-1031C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 856130 | |||||||
chr12:856197 | C | T | 34 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0045 others(31): Show |
35 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.1312-964C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 856197 | |||||||
chr12:856283 | A | G | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1312-878A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 856283 | |||||||
chr12:856334 | T | C | 211 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(208): Show |
212 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.1312-827T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 856334 | |||||||
chr12:856379 | A | G | 1 | a0002c0003t0001g0228 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1312-782A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 856379 | |||||||
chr12:856455 | AG | A | 35 | a0002c0009t0001g0278 a0004c0004t0003g0072 a0004c0004t0003g0073 others(32): Show |
35 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1312-703delG | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 856455 | ||||||
chr12:856457 | GGA | G | 13 | a0001c0001t0002g0227 a0002c0003t0001g0199 a0002c0003t0001g0201 others(10): Show |
13 | HG01106.hp2 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1312-703_1312-702d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 856457 | |||||||
chr12:856458 | GA | G | 59 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0045 others(56): Show |
60 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.1312-692delA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 856458 | ||||||
chr12:856470 | T | A | 48 | a0001c0001t0002g0227 a0002c0003t0001g0199 a0002c0003t0001g0201 others(45): Show |
48 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.1312-691T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 856470 | |||||||
chr12:856503 | T | C | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1312-658T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 856503 | |||||||
chr12:856576 | T | A | 1 | a0002c0002t0017g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1312-585T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 856576 | |||||||
chr12:856619 | A | G | 2 | a0002c0002t0017g0139 a0002c0002t0017g0140 |
2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1312-542A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 856619 | |||||||
chr12:856638 | G | A | 158 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(155): Show |
159 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1312-523G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 856638 | |||||||
chr12:856931 | A | G | 181 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(178): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.1312-230A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 856931 | |||||||
chr12:856958 | T | C | 211 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(208): Show |
212 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.1312-203T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 856958 | |||||||
chr12:857042 | G | A | 147 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(144): Show |
148 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.1312-119G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 857042 | |||||||
chr12:857048 | G | GA | 10 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(7): Show |
10 | HG01109.hp2 HG01358.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1312-106dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 857048 | ||||||
chr12:857058 | C | T | 2 | a0002c0002t0001g0219 a0002c0002t0001g0233 |
2 | HG01496.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1312-103C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 4/27 | chr12 | 857058 | |||||||
chr12:857376 | A | G | 1 | a0001c0001t0002g0025 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1400+127A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 5/27 | chr12 | 857376 | |||||||
chr12:857544 | A | G | 1 | a0001c0001t0002g0028 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1400+295A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 5/27 | chr12 | 857544 | |||||||
chr12:857627 | T | C | 22 | a0003c0005t0001g0036 a0003c0005t0001g0037 a0003c0005t0001g0193 others(19): Show |
22 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.1400+378T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 5/27 | chr12 | 857627 | |||||||
chr12:857816 | T | C | 1 | a0009c0014t0002g0046 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1400+567T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 5/27 | chr12 | 857816 | |||||||
chr12:857827 | T | C | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1400+578T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 5/27 | chr12 | 857827 | |||||||
chr12:857891 | C | G | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1400+642C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 5/27 | chr12 | 857891 | |||||||
chr12:857997 | C | T | 2 | a0004c0004t0003g0076 a0004c0004t0003g0096 |
2 | HG02735.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1400+748C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 5/27 | chr12 | 857997 | |||||||
chr12:858006 | G | A | 126 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(123): Show |
127 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1400+757G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 5/27 | chr12 | 858006 | |||||||
chr12:858194 | C | CT | 16 | a0001c0001t0002g0227 a0002c0002t0001g0107 a0002c0002t0001g0136 others(13): Show |
16 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1400+959dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr12 | 858194 | ||||||
chr12:858228 | C | G | 1 | a0002c0002t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1400+979C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 5/27 | chr12 | 858228 | |||||||
chr12:858531 | T | C | 1 | a0002c0002t0001g0142 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1401-714T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 5/27 | chr12 | 858531 | |||||||
chr12:858612 | A | G | 1 | a0001c0001t0011g0187 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1401-633A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 5/27 | chr12 | 858612 | |||||||
chr12:858639 | T | G | 1 | a0004c0004t0003g0072 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1401-606T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 5/27 | chr12 | 858639 | |||||||
chr12:858724 | G | C | 1 | a0004c0004t0003g0074 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1401-521G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 5/27 | chr12 | 858724 | |||||||
chr12:858779 | A | G | 24 | a0002c0002t0001g0207 a0004c0004t0003g0072 a0004c0004t0003g0073 others(21): Show |
24 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1401-466A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 5/27 | chr12 | 858779 | |||||||
chr12:858857 | G | A | 1 | a0004c0004t0003g0082 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1401-388G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 5/27 | chr12 | 858857 | |||||||
chr12:859234 | C | A | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1401-11C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 5/27 | chr12 | 859234 | |||||||
chr12:859631 | T | TGTGTGTG others(4): Show |
22 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(19): Show |
22 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.1620+169_1620+170i others(13): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 859631 | ||||||
chr12:859631 | T | TGTGTGTG others(6): Show |
3 | a0001c0001t0002g0198 a0001c0001t0012g0121 a0005c0006t0009g0021 |
3 | HG01081.hp2 HG01106.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1620+169_1620+170i others(15): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 859631 | ||||||
chr12:859632 | G | GTGTGTGT others(5): Show |
1 | a0004c0004t0003g0082 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1620+169_1620+170i others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 859632 | ||||||
chr12:859632 | G | GTGTGTGT others(7): Show |
133 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(130): Show |
134 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1620+169_1620+170i others(16): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 859632 | ||||||
chr12:859632 | G | GTGTGTGT others(8): Show |
2 | a0001c0001t0007g0058 a0002c0003t0001g0065 |
2 | NA18972.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1620+169_1620+170i others(17): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 859632 | ||||||
chr12:859632 | G | GTGTGTGT others(9): Show |
8 | a0001c0001t0004g0030 a0001c0001t0007g0041 a0001c0001t0007g0042 others(5): Show |
8 | HG00438.hp1 HG02083.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1620+169_1620+170i others(18): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 859632 | ||||||
chr12:859632 | G | GTGTGTGT others(10): Show |
1 | a0007c0010t0010g0100 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1620+169_1620+170i others(19): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 859632 | ||||||
chr12:859632 | G | GTGTGTGT others(11): Show |
11 | a0001c0001t0007g0040 a0006c0007t0008g0011 a0006c0007t0008g0013 others(8): Show |
11 | HG01109.hp2 HG01358.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.1620+169_1620+170i others(20): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 859632 | ||||||
chr12:859633 | T | TGTGTGTG others(5): Show |
59 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(56): Show |
59 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1620+169_1620+170i others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | chr12 | 859633 | |||||||
chr12:859817 | G | A | 4 | a0001c0001t0004g0173 a0001c0001t0004g0174 a0001c0001t0004g0175 others(1): Show |
4 | HG01346.hp2 HG02486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1620+353G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | chr12 | 859817 | |||||||
chr12:860042 | G | GAT | 8 | a0002c0003t0001g0065 a0006c0007t0008g0017 a0006c0007t0008g0018 others(5): Show |
8 | HG01358.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1620+588_1620+589d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 860042 | ||||||
chr12:860067 | A | C | 1 | a0002c0002t0001g0259 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1620+603A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | chr12 | 860067 | |||||||
chr12:860104 | C | T | 3 | a0002c0002t0001g0219 a0002c0002t0001g0233 a0002c0002t0001g0249 |
3 | HG01496.hp2 NA19083.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1620+640C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | chr12 | 860104 | |||||||
chr12:860382 | G | C | 1 | a0001c0001t0007g0054 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1621-631G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | chr12 | 860382 | |||||||
chr12:860634 | G | T | 50 | a0001c0001t0002g0227 a0002c0003t0001g0199 a0002c0003t0001g0201 others(47): Show |
50 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.1621-379G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | chr12 | 860634 | |||||||
chr12:860677 | A | G | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1621-336A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | chr12 | 860677 | |||||||
chr12:860782 | C | T | 1 | a0005c0006t0009g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1621-231C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | chr12 | 860782 | |||||||
chr12:860901 | C | A | 1 | a0001c0001t0002g0071 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1621-112C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | chr12 | 860901 | |||||||
chr12:860927 | CT | C | 180 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(177): Show |
181 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.1621-74delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 860927 | ||||||
chr12:860927 | CTT | C | 13 | a0004c0020t0003g0084 a0005c0006t0003g0039 a0005c0006t0003g0148 others(10): Show |
13 | HG00423.hp1 HG01993.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.1621-75_1621-74del others(2): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 860927 | ||||||
chr12:860961 | G | T | 23 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(20): Show |
23 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.1621-52G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | chr12 | 860961 | |||||||
chr12:860984 | A | G | 2 | a0002c0009t0001g0122 a0002c0009t0006g0146 |
2 | HG02040.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1621-29A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 6/27 | chr12 | 860984 | |||||||
chr12:861552 | A | T | 121 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(118): Show |
122 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1951+209A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 7/27 | chr12 | 861552 | |||||||
chr12:861634 | C | T | 240 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(237): Show |
241 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1951+291C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 7/27 | chr12 | 861634 | |||||||
chr12:861638 | T | A | 243 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(240): Show |
244 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.1951+295T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 7/27 | chr12 | 861638 | |||||||
chr12:861997 | G | A | 1 | a0020c0021t0024g0189 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1952-86G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 7/27 | chr12 | 861997 | |||||||
chr12:862441 | G | A | 1 | a0004c0004t0003g0082 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2139+171G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 862441 | |||||||
chr12:862657 | A | G | 3 | a0006c0007t0008g0017 a0006c0007t0008g0018 a0006c0007t0008g0019 |
3 | HG02895.hp2 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2139+387A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 862657 | |||||||
chr12:862864 | G | C | 1 | a0004c0004t0003g0078 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2139+594G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 862864 | |||||||
chr12:862903 | T | C | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.2139+633T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 862903 | |||||||
chr12:863101 | TA | T | 10 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(7): Show |
10 | HG01261.hp2 HG01952.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.2139+833delA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 863101 | ||||||
chr12:863163 | CAGAA | C | 7 | a0001c0001t0007g0040 a0001c0001t0007g0041 a0001c0001t0007g0042 others(4): Show |
7 | HG00438.hp1 HG02083.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.2139+896_2139+899d others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 863163 | ||||||
chr12:863351 | C | G | 1 | a0002c0002t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2139+1081C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 863351 | |||||||
chr12:863517 | T | A | 60 | a0001c0001t0002g0227 a0001c0008t0002g0266 a0001c0008t0002g0272 others(57): Show |
60 | HG00408.hp2 HG00741.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.2139+1247T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 863517 | |||||||
chr12:863565 | A | T | 37 | a0001c0001t0002g0227 a0001c0008t0002g0266 a0001c0008t0002g0272 others(34): Show |
37 | HG00741.hp1 HG01106.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.2139+1295A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 863565 | |||||||
chr12:863566 | A | T | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2139+1296A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 863566 | |||||||
chr12:864110 | G | GTTTTTTT others(7): Show |
1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2139+1844_2139+185 others(18): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 864110 | ||||||
chr12:864110 | G | GTTTTTTT others(8): Show |
6 | a0005c0006t0009g0021 a0007c0010t0010g0101 a0007c0010t0010g0103 others(3): Show |
6 | HG01106.hp2 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2139+1843_2139+185 others(19): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 864110 | ||||||
chr12:864110 | G | GTTTTTTT others(9): Show |
7 | a0002c0003t0001g0199 a0002c0003t0001g0201 a0002c0003t0001g0202 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2139+1842_2139+185 others(20): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 864110 | ||||||
chr12:864110 | G | GTTTTTTT others(10): Show |
1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2139+1841_2139+185 others(21): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 864110 | ||||||
chr12:864110 | G | GTTTTTTT others(16): Show |
3 | a0006c0007t0008g0018 a0013c0040t0006g0016 a0020c0021t0024g0189 |
3 | HG02451.hp2 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2139+1857_2139+185 others(27): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 864110 | ||||||
chr12:864110 | G | GTTTTTTT others(17): Show |
5 | a0006c0007t0008g0017 a0006c0007t0008g0019 a0006c0007t0008g0281 others(2): Show |
5 | HG01358.hp1 HG02897.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2139+1857_2139+185 others(28): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 864110 | ||||||
chr12:864110 | G | GTTTTTTT others(21): Show |
1 | a0006c0007t0008g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2139+1857_2139+185 others(32): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 864110 | ||||||
chr12:864110 | G | GTTTTTTT others(25): Show |
1 | a0006c0007t0008g0013 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2139+1857_2139+185 others(36): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 864110 | ||||||
chr12:864123 | T | TTTTTTTT others(2): Show |
22 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(19): Show |
22 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.2139+1857_2139+185 others(13): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 864123 | ||||||
chr12:864134 | G | C | 60 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0045 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.2139+1864G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 864134 | |||||||
chr12:864623 | G | T | 1 | a0002c0002t0001g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2139+2353G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 864623 | |||||||
chr12:864729 | T | C | 2 | a0011c0017t0014g0195 a0011c0017t0014g0197 |
2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2139+2459T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 864729 | |||||||
chr12:864856 | A | G | 30 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(27): Show |
30 | HG00741.hp1 HG01109.hp2 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.2139+2586A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 864856 | |||||||
chr12:864909 | C | T | 10 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(7): Show |
10 | HG01261.hp2 HG01952.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.2139+2639C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 864909 | |||||||
chr12:864971 | C | CA | 197 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(194): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.2139+2711dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 864971 | ||||||
chr12:865142 | T | TC | 50 | a0001c0001t0002g0066 a0001c0001t0002g0071 a0001c0001t0002g0111 others(47): Show |
50 | HG00323.hp1 HG00408.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.2139+2875dupC | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 865142 | ||||||
chr12:865160 | G | C | 36 | a0001c0001t0001g0004 a0001c0001t0002g0034 a0001c0001t0004g0030 others(33): Show |
36 | HG00423.hp1 HG01175.hp2 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.2139+2890G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 865160 | |||||||
chr12:865189 | T | TC | 132 | a0001c0001t0002g0027 a0001c0001t0002g0034 a0001c0001t0002g0048 others(129): Show |
132 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.2139+2920dupC | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 865189 | ||||||
chr12:865238 | T | C | 193 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(190): Show |
194 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.2139+2968T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 865238 | |||||||
chr12:865240 | C | T | 1 | a0007c0010t0010g0100 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2139+2970C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 865240 | |||||||
chr12:865284 | T | C | 6 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(3): Show |
6 | HG00741.hp1 HG01928.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.2139+3014T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 865284 | |||||||
chr12:865601 | G | A | 3 | a0001c0001t0002g0001 a0001c0037t0002g0129 a0002c0002t0001g0107 |
4 | HG01496.hp1 HG02145.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2139+3331G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 865601 | |||||||
chr12:865621 | C | T | 16 | a0001c0001t0002g0198 a0001c0001t0018g0112 a0002c0002t0001g0136 others(13): Show |
16 | HG01081.hp2 HG01261.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.2139+3351C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 865621 | |||||||
chr12:865796 | CT | C | 7 | a0002c0002t0001g0224 a0007c0010t0010g0100 a0007c0010t0010g0101 others(4): Show |
7 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2139+3537delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 865796 | ||||||
chr12:866037 | T | G | 5 | a0003c0005t0001g0193 a0003c0005t0001g0240 a0003c0005t0001g0241 others(2): Show |
5 | HG00323.hp1 HG01175.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.2139+3767T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 866037 | |||||||
chr12:866068 | T | TTGC | 195 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.2139+3803_2139+380 others(7): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 866068 | ||||||
chr12:866110 | T | G | 165 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(162): Show |
166 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.2139+3840T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 866110 | |||||||
chr12:866209 | G | A | 9 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(6): Show |
9 | HG01109.hp2 HG01358.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.2139+3939G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 866209 | |||||||
chr12:866277 | G | A | 2 | a0002c0002t0001g0190 a0006c0007t0008g0013 |
2 | HG02895.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2139+4007G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 866277 | |||||||
chr12:866403 | G | A | 14 | a0006c0007t0008g0011 a0006c0007t0008g0017 a0006c0007t0008g0018 others(11): Show |
14 | HG01109.hp2 HG01358.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.2139+4133G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 866403 | |||||||
chr12:866481 | G | A | 26 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(23): Show |
26 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.2139+4211G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 866481 | |||||||
chr12:866483 | C | T | 1 | a0005c0006t0003g0163 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2139+4213C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 866483 | |||||||
chr12:866488 | G | A | 25 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.2139+4218G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 866488 | |||||||
chr12:866622 | A | G | 1 | a0002c0003t0001g0280 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2139+4352A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 866622 | |||||||
chr12:866730 | AG | A | 91 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(88): Show |
92 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.2139+4461delG | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 866730 | |||||||
chr12:866782 | T | G | 47 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(44): Show |
47 | HG00280.hp2 HG00423.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.2140-4483T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 866782 | |||||||
chr12:866890 | G | A | 37 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(34): Show |
37 | HG00280.hp2 HG00423.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.2140-4375G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 866890 | |||||||
chr12:866893 | G | T | 6 | a0005c0006t0003g0039 a0005c0006t0003g0152 a0005c0006t0003g0156 others(3): Show |
6 | HG01993.hp1 HG02004.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.2140-4372G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 866893 | |||||||
chr12:866907 | T | A | 1 | a0001c0001t0002g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2140-4358T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 866907 | |||||||
chr12:866992 | G | A | 1 | a0001c0001t0007g0063 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2140-4273G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 866992 | |||||||
chr12:866996 | G | A | 1 | a0006c0007t0008g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2140-4269G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 866996 | |||||||
chr12:867041 | T | G | 1 | a0001c0001t0002g0071 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2140-4224T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 867041 | |||||||
chr12:867162 | T | C | 1 | a0001c0001t0007g0069 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2140-4103T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 867162 | |||||||
chr12:867321 | C | T | 39 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(36): Show |
39 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.2140-3944C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 867321 | |||||||
chr12:868394 | G | A | 1 | a0003c0005t0005g0203 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2140-2871G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 868394 | |||||||
chr12:869015 | C | A | 1 | a0011c0017t0014g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2140-2250C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 869015 | |||||||
chr12:869386 | G | A | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2140-1879G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 869386 | |||||||
chr12:869442 | A | G | 1 | a0002c0002t0001g0259 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2140-1823A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 869442 | |||||||
chr12:869510 | A | T | 3 | a0002c0003t0001g0115 a0002c0003t0001g0117 a0002c0003t0001g0118 |
3 | HG01069.hp1 HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.2140-1755A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 869510 | |||||||
chr12:869563 | G | C | 1 | a0002c0003t0001g0105 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2140-1702G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 869563 | |||||||
chr12:869565 | A | T | 1 | a0002c0003t0001g0105 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2140-1700A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 869565 | |||||||
chr12:869566 | A | G | 1 | a0002c0003t0001g0105 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2140-1699A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 869566 | |||||||
chr12:869598 | C | T | 4 | a0001c0001t0006g0006 a0001c0001t0006g0008 a0001c0041t0006g0010 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2140-1667C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 869598 | |||||||
chr12:869795 | A | T | 2 | a0005c0006t0009g0021 a0005c0006t0009g0277 |
2 | HG01106.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2140-1470A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 869795 | |||||||
chr12:869893 | A | G | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2140-1372A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 869893 | |||||||
chr12:870037 | C | T | 33 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0045 others(30): Show |
34 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.2140-1228C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 870037 | |||||||
chr12:870191 | A | G | 1 | a0004c0004t0003g0087 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2140-1074A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 870191 | |||||||
chr12:870231 | G | A | 4 | a0008c0013t0013g0033 a0008c0013t0013g0149 a0008c0013t0013g0180 others(1): Show |
4 | HG00609.hp1 HG01243.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.2140-1034G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 870231 | |||||||
chr12:870233 | T | C | 1 | a0001c0001t0026g0167 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2140-1032T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 870233 | |||||||
chr12:870555 | G | A | 44 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(41): Show |
44 | HG00280.hp2 HG00423.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.2140-710G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 870555 | |||||||
chr12:870830 | A | G | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2140-435A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 870830 | |||||||
chr12:870883 | C | G | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2140-382C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 8/27 | chr12 | 870883 | |||||||
chr12:871707 | G | A | 130 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(127): Show |
131 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.2223+359G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 871707 | |||||||
chr12:871759 | C | A | 32 | a0001c0001t0002g0034 a0001c0001t0002g0109 a0001c0001t0002g0134 others(29): Show |
32 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.2223+411C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 871759 | |||||||
chr12:872083 | A | G | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2223+735A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 872083 | |||||||
chr12:872226 | A | G | 1 | a0005c0006t0003g0182 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2223+878A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 872226 | |||||||
chr12:872270 | C | T | 5 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(2): Show |
5 | HG00741.hp1 HG01928.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.2223+922C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 872270 | |||||||
chr12:872463 | G | T | 1 | a0001c0001t0004g0184 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2223+1115G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 872463 | |||||||
chr12:872515 | A | G | 20 | a0001c0001t0001g0004 a0001c0001t0006g0012 a0001c0001t0006g0014 others(17): Show |
20 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.2223+1167A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 872515 | |||||||
chr12:872614 | C | G | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2223+1266C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 872614 | |||||||
chr12:872771 | C | T | 2 | a0001c0001t0002g0060 a0001c0001t0002g0066 |
2 | HG00741.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2223+1423C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 872771 | |||||||
chr12:872828 | G | C | 31 | a0002c0003t0001g0022 a0002c0003t0001g0065 a0002c0003t0001g0105 others(28): Show |
31 | HG00280.hp2 HG00423.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.2223+1480G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 872828 | |||||||
chr12:872922 | A | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(13): Show |
16 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.2223+1574A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 872922 | |||||||
chr12:873155 | G | A | 38 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(35): Show |
38 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.2223+1807G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 873155 | |||||||
chr12:873187 | T | C | 1 | a0002c0011t0001g0222 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2223+1839T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 873187 | |||||||
chr12:873193 | T | G | 1 | a0002c0029t0001g0125 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2223+1845T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 873193 | |||||||
chr12:873352 | A | G | 106 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(103): Show |
107 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.2223+2004A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 873352 | |||||||
chr12:873501 | T | C | 31 | a0002c0003t0001g0022 a0002c0003t0001g0065 a0002c0003t0001g0105 others(28): Show |
31 | HG00280.hp2 HG00423.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.2223+2153T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 873501 | |||||||
chr12:873536 | T | C | 1 | a0005c0006t0009g0047 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2223+2188T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 873536 | |||||||
chr12:873598 | A | G | 1 | a0002c0002t0001g0141 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2223+2250A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 873598 | |||||||
chr12:873604 | G | A | 11 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(8): Show |
11 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.2223+2256G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 873604 | |||||||
chr12:873646 | A | C | 1 | a0002c0003t0032g0123 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2223+2298A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 873646 | |||||||
chr12:873880 | G | A | 35 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0045 others(32): Show |
36 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.2223+2532G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 873880 | |||||||
chr12:873881 | T | G | 1 | a0001c0001t0002g0059 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2223+2533T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 873881 | |||||||
chr12:873933 | C | A | 11 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(8): Show |
11 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.2223+2585C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 873933 | |||||||
chr12:873945 | T | C | 9 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(6): Show |
9 | HG01109.hp2 HG01358.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.2223+2597T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 873945 | |||||||
chr12:874032 | CACAGTGC others(5): Show |
C | 1 | a0001c0018t0006g0009 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2223+2687_2223+269 others(16): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr12 | 874032 | ||||||
chr12:874369 | CAGATGCT | C | 79 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(76): Show |
80 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.2223+3022_2223+302 others(11): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 874369 | |||||||
chr12:874384 | G | A | 136 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(133): Show |
137 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.2223+3036G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 874384 | |||||||
chr12:874554 | C | G | 41 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(38): Show |
41 | HG00280.hp2 HG00423.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.2223+3206C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 874554 | |||||||
chr12:874738 | A | G | 1 | a0007c0010t0010g0100 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2223+3390A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 874738 | |||||||
chr12:874855 | A | G | 39 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(36): Show |
39 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.2224-3357A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 874855 | |||||||
chr12:875205 | G | A | 6 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(3): Show |
6 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2224-3007G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 875205 | |||||||
chr12:875321 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(12): Show |
15 | HG00735.hp2 HG01361.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.2224-2891G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 875321 | |||||||
chr12:875430 | C | CTTCA | 15 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(12): Show |
15 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.2224-2781_2224-277 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr12 | 875430 | ||||||
chr12:875439 | A | C | 15 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(12): Show |
15 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.2224-2773A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 875439 | |||||||
chr12:875587 | G | A | 1 | a0001c0001t0007g0070 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2224-2625G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 875587 | |||||||
chr12:875599 | G | T | 95 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(92): Show |
96 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.2224-2613G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 875599 | |||||||
chr12:875670 | T | A | 5 | a0007c0010t0010g0101 a0007c0010t0010g0103 a0007c0010t0010g0104 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2224-2542T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 875670 | |||||||
chr12:875703 | A | G | 1 | a0002c0002t0001g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2224-2509A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 875703 | |||||||
chr12:875790 | T | C | 1 | a0001c0001t0007g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2224-2422T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 875790 | |||||||
chr12:875825 | T | A | 1 | a0004c0004t0003g0088 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2224-2387T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 875825 | |||||||
chr12:875862 | G | A | 95 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(92): Show |
96 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.2224-2350G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 875862 | |||||||
chr12:875970 | T | G | 2 | a0002c0002t0001g0216 a0002c0002t0001g0217 |
2 | HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2224-2242T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 875970 | |||||||
chr12:876032 | C | T | 2 | a0001c0001t0007g0058 a0001c0001t0007g0069 |
2 | NA18950.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.2224-2180C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 876032 | |||||||
chr12:876147 | C | T | 1 | a0002c0003t0001g0113 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2224-2065C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 876147 | |||||||
chr12:876364 | G | C | 95 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(92): Show |
96 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.2224-1848G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 876364 | |||||||
chr12:876413 | A | C | 1 | a0002c0003t0001g0110 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2224-1799A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 876413 | |||||||
chr12:876633 | G | A | 1 | a0005c0006t0003g0163 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2224-1579G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 876633 | |||||||
chr12:876638 | C | A | 1 | a0007c0010t0030g0102 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2224-1574C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 876638 | |||||||
chr12:876838 | A | G | 46 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(43): Show |
46 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.2224-1374A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 876838 | |||||||
chr12:876857 | C | G | 15 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(12): Show |
15 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.2224-1355C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 876857 | |||||||
chr12:877052 | A | AT | 16 | a0002c0002t0001g0226 a0002c0002t0001g0264 a0002c0002t0006g0145 others(13): Show |
16 | HG01175.hp1 HG01192.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.2224-1133dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr12 | 877052 | ||||||
chr12:877052 | AT | A | 37 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(34): Show |
37 | HG00423.hp2 HG00741.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.2224-1133delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr12 | 877052 | ||||||
chr12:877052 | ATT | A | 44 | a0001c0001t0001g0004 a0001c0001t0002g0057 a0001c0001t0002g0111 others(41): Show |
44 | HG00280.hp2 HG01081.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.2224-1134_2224-113 others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr12 | 877052 | ||||||
chr12:877052 | ATTT | A | 118 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(115): Show |
119 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2224-1135_2224-113 others(7): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr12 | 877052 | ||||||
chr12:877052 | ATTTT | A | 6 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(3): Show |
6 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2224-1136_2224-113 others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr12 | 877052 | ||||||
chr12:877137 | C | T | 6 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(3): Show |
6 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2224-1075C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 877137 | |||||||
chr12:877250 | C | A | 45 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(42): Show |
45 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.2224-962C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 877250 | |||||||
chr12:877984 | A | G | 1 | a0004c0004t0003g0078 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2224-228A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 9/27 | chr12 | 877984 | |||||||
chr12:878367 | C | CT | 183 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(180): Show |
184 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.2373+21dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 878367 | ||||||
chr12:878694 | C | G | 1 | a0002c0002t0001g0258 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2373+333C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/27 | chr12 | 878694 | |||||||
chr12:878786 | T | TTTTTTTT others(309): Show |
1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2373+436_2373+437i others(318): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 878786 | ||||||
chr12:878786 | T | TTTTTTTT others(300): Show |
35 | a0004c0004t0003g0073 a0004c0004t0003g0074 a0004c0004t0003g0076 others(32): Show |
35 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.2373+433_2373+434i others(309): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 878786 | ||||||
chr12:878786 | T | TTTTTTTT others(301): Show |
4 | a0004c0004t0003g0072 a0004c0004t0003g0077 a0004c0004t0003g0098 others(1): Show |
4 | HG02056.hp2 NA18959.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.2373+433_2373+434i others(310): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 878786 | ||||||
chr12:878889 | G | A | 1 | a0002c0003t0001g0279 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2373+528G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/27 | chr12 | 878889 | |||||||
chr12:878915 | C | G | 1 | a0002c0003t0001g0186 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2373+554C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/27 | chr12 | 878915 | |||||||
chr12:879053 | C | T | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2374-520C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/27 | chr12 | 879053 | |||||||
chr12:879103 | G | A | 40 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(37): Show |
40 | HG00280.hp2 HG00423.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2374-470G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/27 | chr12 | 879103 | |||||||
chr12:879392 | C | T | 150 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(147): Show |
151 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.2374-181C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/27 | chr12 | 879392 | |||||||
chr12:879446 | GT | G | 6 | a0007c0010t0010g0100 a0007c0010t0010g0101 a0007c0010t0010g0103 others(3): Show |
6 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2374-116delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 879446 | ||||||
chr12:879456 | T | G | 1 | a0001c0001t0002g0031 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2374-117T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/27 | chr12 | 879456 | |||||||
chr12:879457 | TG | T | 140 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(137): Show |
141 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.2374-115delG | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/27 | chr12 | 879457 | |||||||
chr12:879458 | G | T | 3 | a0001c0001t0007g0035 a0001c0001t0007g0063 a0001c0001t0018g0112 |
3 | HG00673.hp1 NA18960.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2374-115G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/27 | chr12 | 879458 | |||||||
chr12:879513 | C | CT | 17 | a0002c0002t0001g0107 a0002c0002t0001g0137 a0002c0002t0001g0138 others(14): Show |
17 | HG00423.hp2 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.2374-36dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 879513 | ||||||
chr12:879513 | CT | C | 125 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(122): Show |
126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.2374-36delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 879513 | ||||||
chr12:879513 | CTT | C | 21 | a0001c0001t0002g0051 a0001c0001t0004g0023 a0001c0001t0004g0157 others(18): Show |
21 | HG00323.hp2 HG01109.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.2374-37_2374-36del others(2): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 879513 | ||||||
chr12:880231 | A | G | 40 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(37): Show |
40 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.2832+200A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 11/27 | chr12 | 880231 | |||||||
chr12:880258 | C | T | 10 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(7): Show |
10 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.2832+227C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 11/27 | chr12 | 880258 | |||||||
chr12:880634 | CT | C | 117 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(114): Show |
118 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.2833-73delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr12 | 880634 | ||||||
chr12:880673 | T | C | 15 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(12): Show |
15 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.2833-48T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 11/27 | chr12 | 880673 | |||||||
chr12:880682 | C | G | 1 | a0001c0001t0020g0168 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2833-39C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 11/27 | chr12 | 880682 | |||||||
chr12:881235 | C | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(13): Show |
16 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.3111+236C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 12/27 | chr12 | 881235 | |||||||
chr12:881463 | T | C | 1 | a0001c0001t0004g0157 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3112-229T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 12/27 | chr12 | 881463 | |||||||
chr12:881831 | G | C | 1 | a0001c0001t0002g0165 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3209+42G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 13/27 | chr12 | 881831 | |||||||
chr12:881833 | C | T | 4 | a0002c0002t0017g0139 a0002c0002t0017g0140 a0010c0016t0015g0092 others(1): Show |
4 | HG01261.hp1 HG02273.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.3209+44C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 13/27 | chr12 | 881833 | |||||||
chr12:881843 | C | T | 71 | a0002c0002t0001g0029 a0002c0002t0001g0194 a0002c0002t0001g0205 others(68): Show |
71 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.3209+54C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 13/27 | chr12 | 881843 | |||||||
chr12:882140 | G | A | 37 | a0001c0001t0002g0034 a0001c0001t0002g0109 a0001c0001t0002g0134 others(34): Show |
37 | HG00280.hp1 HG00609.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.3372+67G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 14/27 | chr12 | 882140 | |||||||
chr12:882195 | C | T | 275 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(272): Show |
276 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.3372+122C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 14/27 | chr12 | 882195 | |||||||
chr12:882346 | G | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(11): Show |
14 | HG00735.hp2 HG01361.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.3372+273G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 14/27 | chr12 | 882346 | |||||||
chr12:882387 | C | G | 68 | a0001c0022t0001g0263 a0002c0002t0001g0029 a0002c0002t0001g0194 others(65): Show |
68 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.3372+314C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 14/27 | chr12 | 882387 | |||||||
chr12:882544 | T | C | 41 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(38): Show |
41 | HG00280.hp2 HG00423.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3373-399T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 14/27 | chr12 | 882544 | |||||||
chr12:883063 | C | T | 30 | a0002c0003t0001g0022 a0002c0003t0001g0065 a0002c0003t0001g0105 others(27): Show |
30 | HG00280.hp2 HG00423.hp2 HG01069.hp1 others(27): Show |
splice_region_variant&intron_variant | LOW | c.3489+4C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 15/27 | chr12 | 883063 | |||||||
chr12:883166 | T | C | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3489+107T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 15/27 | chr12 | 883166 | |||||||
chr12:883390 | T | A | 9 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(6): Show |
9 | HG01109.hp2 HG01358.hp1 HG02895.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.3490-5T>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 15/27 | chr12 | 883390 | |||||||
chr12:883598 | T | G | 1 | a0001c0001t0004g0002 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3663+30T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 16/27 | chr12 | 883598 | |||||||
chr12:883884 | C | A | 1 | a0002c0002t0001g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3721+53C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 17/27 | chr12 | 883884 | |||||||
chr12:883980 | A | G | 1 | a0003c0005t0005g0229 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3722-141A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 17/27 | chr12 | 883980 | |||||||
chr12:884096 | C | T | 1 | a0016c0044t0001g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3722-25C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 17/27 | chr12 | 884096 | |||||||
chr12:884285 | G | T | 1 | a0001c0001t0004g0184 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3844+42G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 18/27 | chr12 | 884285 | |||||||
chr12:884414 | A | G | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3844+171A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 18/27 | chr12 | 884414 | |||||||
chr12:884486 | T | G | 131 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(128): Show |
131 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.3845-163T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 18/27 | chr12 | 884486 | |||||||
chr12:884518 | A | G | 5 | a0001c0001t0011g0159 a0001c0001t0011g0162 a0001c0001t0011g0169 others(2): Show |
5 | HG00735.hp1 HG01943.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.3845-131A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 18/27 | chr12 | 884518 | |||||||
chr12:886125 | G | GT | 235 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(232): Show |
236 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.5280+49dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr12 | 886125 | ||||||
chr12:886212 | A | G | 41 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(38): Show |
42 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.5280+128A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/27 | chr12 | 886212 | |||||||
chr12:886440 | A | G | 140 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.5280+356A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/27 | chr12 | 886440 | |||||||
chr12:886452 | A | C | 10 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(7): Show |
10 | HG00741.hp1 HG01884.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.5280+368A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/27 | chr12 | 886452 | |||||||
chr12:886511 | G | C | 90 | a0002c0002t0001g0029 a0002c0002t0001g0107 a0002c0002t0001g0136 others(87): Show |
90 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.5280+427G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/27 | chr12 | 886511 | |||||||
chr12:886554 | GAAAT | G | 72 | a0002c0002t0001g0029 a0002c0002t0001g0194 a0002c0002t0001g0205 others(69): Show |
72 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.5280+477_5280+480d others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr12 | 886554 | ||||||
chr12:886646 | A | G | 1 | a0002c0002t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5280+562A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/27 | chr12 | 886646 | |||||||
chr12:886894 | A | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(13): Show |
16 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.5281-327A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/27 | chr12 | 886894 | |||||||
chr12:887039 | A | T | 275 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(272): Show |
276 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.5281-182A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/27 | chr12 | 887039 | |||||||
chr12:887191 | C | T | 29 | a0002c0003t0001g0022 a0002c0003t0001g0065 a0002c0003t0001g0105 others(26): Show |
29 | HG00280.hp2 HG00423.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.5281-30C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/27 | chr12 | 887191 | |||||||
chr12:887217 | G | A | 1 | a0008c0013t0013g0149 | 1 | HG01243.hp2 | splice_region_variant&intron_variant | LOW | c.5281-4G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 19/27 | chr12 | 887217 | |||||||
chr12:887505 | G | A | 72 | a0002c0002t0001g0029 a0002c0002t0001g0194 a0002c0002t0001g0205 others(69): Show |
72 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.5364+201G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 20/27 | chr12 | 887505 | |||||||
chr12:887628 | G | A | 1 | a0001c0001t0004g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5364+324G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 20/27 | chr12 | 887628 | |||||||
chr12:887690 | G | A | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5364+386G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 20/27 | chr12 | 887690 | |||||||
chr12:887805 | G | T | 1 | a0001c0001t0004g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5364+501G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 20/27 | chr12 | 887805 | |||||||
chr12:888200 | G | T | 4 | a0002c0002t0001g0206 a0002c0002t0001g0216 a0002c0002t0001g0217 others(1): Show |
4 | HG02622.hp2 HG02896.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.5364+896G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 20/27 | chr12 | 888200 | |||||||
chr12:888338 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(12): Show |
15 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.5365-802G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 20/27 | chr12 | 888338 | |||||||
chr12:888667 | G | A | 160 | a0002c0002t0001g0029 a0002c0002t0001g0107 a0002c0002t0001g0136 others(157): Show |
160 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.5365-473G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 20/27 | chr12 | 888667 | |||||||
chr12:888676 | T | C | 1 | a0002c0002t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5365-464T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 20/27 | chr12 | 888676 | |||||||
chr12:888924 | C | G | 2 | a0010c0016t0015g0092 a0010c0016t0015g0093 |
2 | HG01261.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.5365-216C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 20/27 | chr12 | 888924 | |||||||
chr12:889054 | A | C | 1 | a0001c0001t0002g0198 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.5365-86A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 20/27 | chr12 | 889054 | |||||||
chr12:889058 | A | T | 11 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(8): Show |
11 | HG01261.hp2 HG01952.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.5365-82A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 20/27 | chr12 | 889058 | |||||||
chr12:889328 | T | G | 1 | a0002c0009t0005g0043 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.5448+105T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 21/27 | chr12 | 889328 | |||||||
chr12:889590 | G | A | 89 | a0002c0002t0001g0029 a0002c0002t0001g0107 a0002c0002t0001g0136 others(86): Show |
89 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.5448+367G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 21/27 | chr12 | 889590 | |||||||
chr12:889615 | G | A | 1 | a0001c0032t0002g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5448+392G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 21/27 | chr12 | 889615 | |||||||
chr12:889634 | C | T | 96 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(93): Show |
97 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.5448+411C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 21/27 | chr12 | 889634 | |||||||
chr12:889653 | G | C | 81 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.5448+430G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 21/27 | chr12 | 889653 | |||||||
chr12:889735 | G | A | 3 | a0002c0015t0001g0211 a0002c0015t0001g0243 a0002c0015t0001g0244 |
3 | HG02559.hp2 HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.5448+512G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 21/27 | chr12 | 889735 | |||||||
chr12:889805 | C | T | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.5448+582C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 21/27 | chr12 | 889805 | |||||||
chr12:889951 | C | CT | 136 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(133): Show |
137 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.5449-484dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 889951 | ||||||
chr12:889951 | C | CTT | 12 | a0001c0001t0001g0004 a0001c0001t0004g0150 a0002c0003t0001g0279 others(9): Show |
12 | HG01109.hp2 HG01358.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.5449-485_5449-484d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 889951 | ||||||
chr12:890001 | G | A | 1 | a0016c0044t0001g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5449-452G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 21/27 | chr12 | 890001 | |||||||
chr12:890083 | GCTGGGAT others(189): Show |
G | 1 | a0007c0010t0010g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5449-367_5449-172d others(2): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 890083 | ||||||
chr12:890142 | G | A | 1 | a0001c0001t0018g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5449-311G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 21/27 | chr12 | 890142 | |||||||
chr12:890173 | G | A | 1 | a0001c0037t0002g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5449-280G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 21/27 | chr12 | 890173 | |||||||
chr12:890332 | G | A | 9 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(6): Show |
9 | HG01109.hp2 HG01358.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.5449-121G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 21/27 | chr12 | 890332 | |||||||
chr12:890347 | T | C | 1 | a0001c0001t0011g0187 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.5449-106T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 21/27 | chr12 | 890347 | |||||||
chr12:890596 | A | G | 172 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(169): Show |
172 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.5509+83A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 890596 | |||||||
chr12:891019 | A | G | 40 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(37): Show |
40 | HG00280.hp2 HG00423.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.5509+506A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 891019 | |||||||
chr12:891399 | G | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(11): Show |
14 | HG00735.hp2 HG01361.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.5509+886G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 891399 | |||||||
chr12:891532 | C | A | 3 | a0004c0004t0003g0078 a0004c0004t0003g0083 a0004c0004t0003g0088 |
3 | HG00408.hp2 HG02071.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.5509+1019C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 891532 | |||||||
chr12:891559 | A | G | 1 | a0007c0010t0030g0102 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5509+1046A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 891559 | |||||||
chr12:891602 | C | CT | 42 | a0001c0001t0007g0035 a0001c0001t0012g0185 a0002c0009t0001g0278 others(39): Show |
42 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.5509+1106dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | 891602 | ||||||
chr12:891602 | CT | C | 8 | a0001c0001t0001g0068 a0001c0001t0006g0012 a0002c0002t0001g0226 others(5): Show |
8 | HG01169.hp1 HG01515.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.5509+1106delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | 891602 | ||||||
chr12:891634 | T | C | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5509+1121T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 891634 | |||||||
chr12:891685 | G | A | 29 | a0002c0003t0001g0022 a0002c0003t0001g0065 a0002c0003t0001g0105 others(26): Show |
29 | HG00280.hp2 HG00423.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.5509+1172G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 891685 | |||||||
chr12:891724 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.5509+1211A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 891724 | |||||||
chr12:891779 | A | C | 1 | a0021c0038t0012g0135 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.5509+1266A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 891779 | |||||||
chr12:892035 | CT | C | 140 | a0001c0001t0002g0198 a0001c0001t0006g0014 a0001c0001t0006g0020 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.5509+1536delT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | 892035 | ||||||
chr12:892063 | C | CT | 72 | a0001c0022t0001g0263 a0002c0002t0001g0029 a0002c0002t0001g0194 others(69): Show |
72 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.5509+1562dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | 892063 | ||||||
chr12:892174 | C | T | 1 | a0002c0002t0001g0223 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5509+1661C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 892174 | |||||||
chr12:892182 | C | T | 1 | a0002c0002t0001g0223 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5509+1669C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 892182 | |||||||
chr12:892225 | C | T | 3 | a0009c0014t0002g0046 a0009c0014t0002g0053 a0009c0014t0002g0061 |
3 | HG02074.hp2 NA18960.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.5509+1712C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 892225 | |||||||
chr12:892266 | A | G | 1 | a0002c0002t0001g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5509+1753A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 892266 | |||||||
chr12:892289 | C | T | 2 | a0003c0005t0001g0036 a0003c0005t0001g0037 |
2 | HG00438.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.5509+1776C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 892289 | |||||||
chr12:892290 | G | A | 1 | a0004c0004t0003g0082 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.5509+1777G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 892290 | |||||||
chr12:892640 | C | T | 1 | a0006c0007t0008g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5510-1922C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 892640 | |||||||
chr12:892641 | G | A | 89 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(86): Show |
90 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.5510-1921G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 892641 | |||||||
chr12:892653 | C | T | 91 | a0001c0022t0001g0263 a0002c0002t0001g0029 a0002c0002t0001g0107 others(88): Show |
91 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.5510-1909C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 892653 | |||||||
chr12:892816 | A | G | 1 | a0002c0009t0005g0043 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.5510-1746A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 892816 | |||||||
chr12:892853 | G | A | 91 | a0001c0022t0001g0263 a0002c0002t0001g0029 a0002c0002t0001g0107 others(88): Show |
91 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.5510-1709G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 892853 | |||||||
chr12:892976 | C | T | 1 | a0002c0011t0001g0254 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5510-1586C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 892976 | |||||||
chr12:893072 | T | C | 1 | a0001c0001t0007g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.5510-1490T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 893072 | |||||||
chr12:893261 | A | G | 1 | a0004c0004t0003g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5510-1301A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 893261 | |||||||
chr12:893435 | G | A | 1 | a0004c0004t0003g0088 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.5510-1127G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 893435 | |||||||
chr12:893469 | A | G | 1 | a0002c0002t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5510-1093A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 893469 | |||||||
chr12:893595 | G | A | 4 | a0001c0012t0002g0267 a0001c0012t0002g0268 a0001c0012t0002g0270 others(1): Show |
4 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.5510-967G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 893595 | |||||||
chr12:893620 | G | A | 105 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(102): Show |
106 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.5510-942G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 893620 | |||||||
chr12:893637 | G | C | 197 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(194): Show |
198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.5510-925G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 893637 | |||||||
chr12:893680 | G | A | 92 | a0001c0022t0001g0263 a0002c0002t0001g0029 a0002c0002t0001g0107 others(89): Show |
92 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.5510-882G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 893680 | |||||||
chr12:893691 | T | C | 197 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(194): Show |
198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.5510-871T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 893691 | |||||||
chr12:893777 | C | T | 1 | a0002c0002t0001g0223 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5510-785C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 893777 | |||||||
chr12:893779 | C | CACCACTG others(7): Show |
1 | a0004c0004t0003g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5510-779_5510-766d others(16): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | 893779 | ||||||
chr12:893781 | C | T | 105 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(102): Show |
106 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.5510-781C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 893781 | |||||||
chr12:893823 | A | AAAT | 52 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(49): Show |
52 | HG00280.hp2 HG00423.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.5510-717_5510-715d others(5): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | 893823 | ||||||
chr12:893823 | A | AAATAAT | 71 | a0001c0001t0016g0049 a0001c0001t0016g0056 a0001c0022t0001g0263 others(68): Show |
71 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.5510-720_5510-715d others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | 893823 | ||||||
chr12:893823 | A | AAATAATA others(2): Show |
4 | a0002c0002t0001g0257 a0002c0002t0001g0261 a0002c0002t0001g0262 others(1): Show |
4 | HG01168.hp1 HG02602.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.5510-723_5510-715d others(11): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | 893823 | ||||||
chr12:893823 | A | AAATAATA others(5): Show |
31 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0045 others(28): Show |
32 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.5510-726_5510-715d others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | 893823 | ||||||
chr12:893823 | A | AAATAATA others(8): Show |
5 | a0001c0001t0002g0028 a0001c0001t0006g0020 a0001c0001t0007g0041 others(2): Show |
5 | HG00438.hp1 HG02109.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.5510-729_5510-715d others(17): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | 893823 | ||||||
chr12:893823 | A | AAATAATA others(11): Show |
17 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(14): Show |
17 | HG00735.hp1 HG00735.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.5510-732_5510-715d others(20): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | 893823 | ||||||
chr12:893823 | A | AAATAATA others(14): Show |
9 | a0001c0001t0002g0111 a0001c0001t0002g0198 a0001c0001t0004g0173 others(6): Show |
9 | HG01081.hp2 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.5510-735_5510-715d others(23): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | 893823 | ||||||
chr12:893823 | A | AAATAATA others(17): Show |
16 | a0001c0001t0002g0025 a0001c0001t0002g0027 a0001c0001t0002g0227 others(13): Show |
16 | HG00280.hp1 HG00741.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.5510-738_5510-715d others(26): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | 893823 | ||||||
chr12:893823 | A | AAATAATA others(20): Show |
6 | a0001c0001t0002g0109 a0001c0001t0004g0150 a0001c0008t0002g0273 others(3): Show |
6 | HG00609.hp1 HG01516.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.5510-715_5510-714i others(29): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | 893823 | ||||||
chr12:893823 | A | AAATAATA others(23): Show |
16 | a0001c0001t0002g0026 a0001c0001t0004g0023 a0001c0001t0004g0030 others(13): Show |
16 | HG01168.hp2 HG01169.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.5510-715_5510-714i others(32): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | 893823 | ||||||
chr12:893823 | A | AAATAATA others(26): Show |
3 | a0001c0001t0002g0034 a0001c0001t0002g0165 a0001c0001t0004g0179 |
3 | HG00673.hp2 HG04184.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.5510-715_5510-714i others(35): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | 893823 | ||||||
chr12:893889 | A | C | 1 | a0007c0010t0010g0104 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5510-673A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 893889 | |||||||
chr12:894010 | G | C | 1 | a0002c0003t0001g0280 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5510-552G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 894010 | |||||||
chr12:894033 | C | T | 29 | a0002c0003t0001g0022 a0002c0003t0001g0065 a0002c0003t0001g0105 others(26): Show |
29 | HG00280.hp2 HG00423.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.5510-529C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 894033 | |||||||
chr12:894172 | C | T | 1 | a0004c0004t0003g0096 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.5510-390C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 894172 | |||||||
chr12:894195 | C | T | 1 | a0008c0013t0013g0149 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5510-367C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 894195 | |||||||
chr12:894255 | A | G | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5510-307A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 894255 | |||||||
chr12:894273 | C | T | 29 | a0002c0003t0001g0022 a0002c0003t0001g0065 a0002c0003t0001g0105 others(26): Show |
29 | HG00280.hp2 HG00423.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.5510-289C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 894273 | |||||||
chr12:894371 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0006g0012 a0001c0001t0006g0014 others(2): Show |
5 | HG02280.hp1 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.5510-191G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 894371 | |||||||
chr12:894423 | G | A | 1 | a0002c0003t0001g0280 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5510-139G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 22/27 | chr12 | 894423 | |||||||
chr12:894671 | C | T | 73 | a0001c0022t0001g0263 a0002c0002t0001g0029 a0002c0002t0001g0194 others(70): Show |
73 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.5583+36C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | chr12 | 894671 | |||||||
chr12:894812 | T | C | 40 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(37): Show |
40 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.5583+177T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | chr12 | 894812 | |||||||
chr12:894822 | T | G | 5 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0004g0002 others(2): Show |
5 | HG00735.hp2 HG01074.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.5583+187T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | chr12 | 894822 | |||||||
chr12:894838 | C | T | 1 | a0002c0002t0001g0262 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5583+203C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | chr12 | 894838 | |||||||
chr12:894868 | C | T | 4 | a0002c0002t0001g0194 a0002c0002t0001g0213 a0002c0002t0001g0224 others(1): Show |
4 | HG03225.hp1 HG03540.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.5583+233C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | chr12 | 894868 | |||||||
chr12:894940 | A | T | 89 | a0001c0001t0002g0001 a0001c0001t0002g0025 a0001c0001t0002g0026 others(86): Show |
90 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.5583+305A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | chr12 | 894940 | |||||||
chr12:895008 | G | A | 1 | a0001c0001t0021g0176 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5583+373G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | chr12 | 895008 | |||||||
chr12:895014 | A | G | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5583+379A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | chr12 | 895014 | |||||||
chr12:895030 | T | C | 1 | a0001c0001t0007g0063 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.5583+395T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | chr12 | 895030 | |||||||
chr12:895041 | ATAAGT | A | 31 | a0001c0001t0002g0034 a0001c0001t0002g0109 a0001c0001t0002g0165 others(28): Show |
31 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.5583+412_5583+416d others(7): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 895041 | ||||||
chr12:895440 | A | C | 9 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(6): Show |
9 | HG01109.hp2 HG01358.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.5584-631A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | chr12 | 895440 | |||||||
chr12:895440 | A | G | 25 | a0002c0003t0001g0022 a0002c0003t0001g0065 a0002c0003t0001g0105 others(22): Show |
25 | HG00280.hp2 HG00423.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.5584-631A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | chr12 | 895440 | |||||||
chr12:895505 | C | T | 2 | a0002c0002t0001g0194 a0002c0002t0001g0213 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5584-566C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | chr12 | 895505 | |||||||
chr12:895599 | C | T | 9 | a0006c0007t0008g0011 a0006c0007t0008g0013 a0006c0007t0008g0017 others(6): Show |
9 | HG01109.hp2 HG01358.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.5584-472C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | chr12 | 895599 | |||||||
chr12:895649 | G | A | 4 | a0002c0002t0017g0139 a0002c0002t0017g0140 a0010c0016t0015g0092 others(1): Show |
4 | HG01261.hp1 HG02273.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.5584-422G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | chr12 | 895649 | |||||||
chr12:895851 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.5584-220G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | chr12 | 895851 | |||||||
chr12:895929 | A | G | 105 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(102): Show |
106 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.5584-142A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | chr12 | 895929 | |||||||
chr12:895996 | T | C | 31 | a0002c0003t0001g0022 a0002c0003t0001g0065 a0002c0003t0001g0105 others(28): Show |
31 | HG00280.hp2 HG00423.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.5584-75T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 23/27 | chr12 | 895996 | |||||||
chr12:896831 | G | A | 1 | a0002c0003t0001g0105 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.6245+99G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | chr12 | 896831 | |||||||
chr12:896886 | C | CCA | 4 | a0002c0003t0006g0132 a0006c0007t0008g0011 a0006c0007t0008g0283 others(1): Show |
4 | HG01109.hp2 HG01358.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.6245+206_6245+207d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 896886 | ||||||
chr12:896886 | C | CCACACAC others(1): Show |
4 | a0002c0002t0001g0216 a0006c0007t0008g0017 a0006c0007t0008g0018 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.6245+200_6245+207d others(10): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 896886 | ||||||
chr12:896886 | C | CCACACAC others(5): Show |
2 | a0002c0002t0001g0217 a0006c0007t0008g0019 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.6245+196_6245+207d others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 896886 | ||||||
chr12:896886 | C | CCACACAC others(7): Show |
1 | a0006c0007t0008g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.6245+194_6245+207d others(16): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 896886 | ||||||
chr12:896886 | CCACA | C | 7 | a0002c0003t0001g0113 a0002c0003t0001g0114 a0002c0003t0001g0131 others(4): Show |
7 | HG00280.hp2 HG02523.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.6245+204_6245+207d others(6): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 896886 | ||||||
chr12:896886 | CCACACA | C | 7 | a0002c0002t0035g0208 a0002c0003t0001g0124 a0002c0003t0001g0228 others(4): Show |
7 | HG01192.hp2 HG02257.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.6245+202_6245+207d others(8): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 896886 | ||||||
chr12:896886 | CCACACAC others(1): Show |
C | 17 | a0002c0002t0001g0206 a0002c0003t0001g0022 a0002c0003t0001g0105 others(14): Show |
17 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.6245+200_6245+207d others(10): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 896886 | ||||||
chr12:896886 | CCACACAC others(3): Show |
C | 12 | a0002c0002t0001g0107 a0002c0002t0001g0218 a0002c0002t0001g0226 others(9): Show |
12 | HG01358.hp2 HG01993.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.6245+198_6245+207d others(12): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 896886 | ||||||
chr12:896886 | CCACACAC others(5): Show |
C | 70 | a0001c0022t0001g0263 a0002c0002t0001g0029 a0002c0002t0001g0136 others(67): Show |
70 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.6245+196_6245+207d others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 896886 | ||||||
chr12:896886 | CCACACAC others(7): Show |
C | 5 | a0002c0002t0001g0142 a0002c0002t0001g0215 a0002c0015t0001g0244 others(2): Show |
5 | HG01261.hp1 HG02273.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.6245+194_6245+207d others(16): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 896886 | ||||||
chr12:896886 | CCACACAC others(9): Show |
C | 5 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(2): Show |
5 | HG01106.hp1 HG01255.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.6245+192_6245+207d others(18): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 896886 | ||||||
chr12:896886 | CCACACAC others(11): Show |
C | 3 | a0004c0004t0003g0076 a0004c0004t0003g0086 a0004c0004t0003g0096 |
3 | HG02735.hp2 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.6245+190_6245+207d others(20): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 896886 | ||||||
chr12:896886 | CCACACAC others(13): Show |
C | 33 | a0004c0004t0003g0073 a0004c0004t0003g0074 a0004c0004t0003g0077 others(30): Show |
33 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.6245+188_6245+207d others(22): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 896886 | ||||||
chr12:896886 | CCACACAC others(17): Show |
C | 5 | a0001c0001t0001g0004 a0001c0001t0004g0023 a0001c0001t0025g0024 others(2): Show |
5 | HG01106.hp2 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.6245+184_6245+207d others(26): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 896886 | ||||||
chr12:896886 | CCACACAC others(19): Show |
C | 48 | a0001c0001t0002g0034 a0001c0001t0002g0109 a0001c0001t0002g0134 others(45): Show |
48 | HG00280.hp1 HG00609.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.6245+182_6245+207d others(28): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 896886 | ||||||
chr12:896886 | CCACACAC others(21): Show |
C | 54 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0001 others(51): Show |
55 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.6245+180_6245+207d others(30): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 896886 | ||||||
chr12:896928 | ACACACAC others(5): Show |
A | 1 | a0002c0002t0001g0223 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.6245+197_6245+208d others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | chr12 | 896928 | |||||||
chr12:896938 | A | G | 1 | a0002c0002t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6245+206A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | chr12 | 896938 | |||||||
chr12:896939 | C | A | 1 | a0002c0002t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6245+207C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | chr12 | 896939 | |||||||
chr12:896958 | C | T | 15 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(12): Show |
15 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.6245+226C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | chr12 | 896958 | |||||||
chr12:897443 | A | T | 1 | a0002c0003t0001g0124 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.6246-36A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 24/27 | chr12 | 897443 | |||||||
chr12:897739 | G | C | 1 | a0004c0004t0003g0088 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.6448+58G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 897739 | |||||||
chr12:898256 | A | G | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.6448+575A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 898256 | |||||||
chr12:898361 | T | C | 1 | a0002c0015t0001g0244 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.6448+680T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 898361 | |||||||
chr12:898375 | C | G | 4 | a0001c0001t0004g0173 a0001c0001t0004g0174 a0001c0001t0004g0175 others(1): Show |
4 | HG01346.hp2 HG02486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.6448+694C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 898375 | |||||||
chr12:898409 | G | C | 1 | a0002c0002t0029g0237 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6448+728G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 898409 | |||||||
chr12:898482 | CA | C | 38 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0045 others(35): Show |
39 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.6448+818delA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr12 | 898482 | ||||||
chr12:898497 | A | G | 3 | a0009c0014t0002g0046 a0009c0014t0002g0053 a0009c0014t0002g0061 |
3 | HG02074.hp2 NA18960.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.6448+816A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 898497 | |||||||
chr12:898501 | A | G | 1 | a0004c0004t0003g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.6448+820A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 898501 | |||||||
chr12:898564 | A | G | 1 | a0002c0002t0001g0224 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.6448+883A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 898564 | |||||||
chr12:898664 | C | T | 1 | a0004c0004t0003g0074 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.6448+983C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 898664 | |||||||
chr12:898677 | G | A | 1 | a0002c0003t0001g0105 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.6448+996G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 898677 | |||||||
chr12:898747 | A | AT | 39 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(36): Show |
39 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.6448+1076dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr12 | 898747 | ||||||
chr12:898771 | G | A | 1 | a0001c0001t0004g0150 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.6448+1090G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 898771 | |||||||
chr12:898902 | G | A | 1 | a0003c0005t0005g0209 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.6448+1221G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 898902 | |||||||
chr12:898941 | A | G | 3 | a0004c0004t0003g0076 a0004c0004t0003g0086 a0004c0004t0003g0096 |
3 | HG02735.hp2 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.6448+1260A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 898941 | |||||||
chr12:899030 | G | A | 34 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0045 others(31): Show |
35 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.6448+1349G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 899030 | |||||||
chr12:899143 | T | C | 26 | a0002c0003t0001g0022 a0002c0003t0001g0065 a0002c0003t0001g0105 others(23): Show |
26 | HG00280.hp2 HG00423.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.6449-1333T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 899143 | |||||||
chr12:899190 | G | T | 1 | a0001c0001t0018g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6449-1286G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 899190 | |||||||
chr12:899300 | T | TTTTTTGT others(4): Show |
227 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(224): Show |
228 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.6449-1166_6449-116 others(15): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr12 | 899300 | ||||||
chr12:899445 | C | T | 31 | a0002c0003t0001g0022 a0002c0003t0001g0065 a0002c0003t0001g0105 others(28): Show |
31 | HG00280.hp2 HG00423.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.6449-1031C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 899445 | |||||||
chr12:899570 | T | C | 2 | a0001c0001t0004g0023 a0001c0001t0025g0024 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.6449-906T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 899570 | |||||||
chr12:899598 | C | T | 1 | a0001c0001t0007g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.6449-878C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 899598 | |||||||
chr12:899731 | G | T | 1 | a0001c0001t0004g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.6449-745G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 899731 | |||||||
chr12:899732 | T | G | 1 | a0001c0001t0004g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.6449-744T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 899732 | |||||||
chr12:899779 | G | A | 1 | a0001c0001t0004g0164 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.6449-697G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 899779 | |||||||
chr12:899856 | G | T | 1 | a0008c0013t0013g0149 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6449-620G>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 899856 | |||||||
chr12:899858 | T | TA | 96 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(93): Show |
97 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.6449-608dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr12 | 899858 | ||||||
chr12:899890 | G | A | 67 | a0002c0002t0001g0029 a0002c0002t0001g0194 a0002c0002t0001g0205 others(64): Show |
67 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.6449-586G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 899890 | |||||||
chr12:899927 | C | T | 1 | a0002c0002t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6449-549C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 899927 | |||||||
chr12:900015 | T | C | 1 | a0001c0001t0002g0198 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.6449-461T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 900015 | |||||||
chr12:900016 | C | CT | 179 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(176): Show |
180 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.6449-441dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr12 | 900016 | ||||||
chr12:900016 | C | CTT | 45 | a0001c0001t0002g0034 a0001c0001t0007g0032 a0001c0001t0007g0054 others(42): Show |
45 | HG00408.hp2 HG00544.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.6449-442_6449-441d others(4): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr12 | 900016 | ||||||
chr12:900020 | T | TTTC | 42 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(39): Show |
42 | HG00280.hp2 HG00423.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.6449-454_6449-453i others(5): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr12 | 900020 | ||||||
chr12:900206 | G | A | 95 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(92): Show |
96 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.6449-270G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 25/27 | chr12 | 900206 | |||||||
chr12:900806 | G | A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0006g0015 |
3 | HG00735.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.6643+136G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 900806 | |||||||
chr12:900927 | C | T | 2 | a0001c0001t0007g0040 a0001c0001t0007g0042 |
2 | HG02083.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.6643+257C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 900927 | |||||||
chr12:901311 | C | G | 1 | a0003c0005t0005g0209 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.6643+641C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 901311 | |||||||
chr12:901430 | C | T | 1 | a0003c0005t0005g0234 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.6643+760C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 901430 | |||||||
chr12:901708 | A | T | 1 | a0007c0010t0010g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.6643+1038A>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 901708 | |||||||
chr12:901746 | A | G | 1 | a0001c0001t0018g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6643+1076A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 901746 | |||||||
chr12:902032 | G | A | 1 | a0006c0007t0008g0013 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.6643+1362G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 902032 | |||||||
chr12:902132 | C | T | 1 | a0002c0024t0014g0196 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6643+1462C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 902132 | |||||||
chr12:902382 | A | AT | 5 | a0001c0001t0001g0004 a0001c0001t0006g0012 a0001c0001t0006g0014 others(2): Show |
5 | HG02280.hp1 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.6643+1719dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 902382 | ||||||
chr12:902448 | C | A | 1 | a0004c0004t0003g0094 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.6643+1778C>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 902448 | |||||||
chr12:902814 | A | G | 2 | a0001c0001t0007g0035 a0001c0001t0007g0063 |
2 | HG00673.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.6643+2144A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 902814 | |||||||
chr12:902983 | T | G | 1 | a0002c0003t0001g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.6643+2313T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 902983 | |||||||
chr12:903080 | C | T | 1 | a0001c0001t0007g0063 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.6643+2410C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 903080 | |||||||
chr12:903142 | A | G | 15 | a0002c0002t0001g0029 a0002c0009t0001g0064 a0002c0009t0001g0122 others(12): Show |
15 | HG02040.hp1 HG02109.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.6643+2472A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 903142 | |||||||
chr12:903276 | G | A | 1 | a0002c0002t0001g0223 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.6643+2606G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 903276 | |||||||
chr12:903289 | T | C | 4 | a0002c0002t0017g0139 a0002c0002t0017g0140 a0010c0016t0015g0092 others(1): Show |
4 | HG01261.hp1 HG02273.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.6643+2619T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 903289 | |||||||
chr12:903376 | G | A | 1 | a0002c0003t0001g0110 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.6643+2706G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 903376 | |||||||
chr12:903526 | G | C | 3 | a0001c0001t0007g0040 a0001c0001t0007g0041 a0001c0001t0007g0042 |
3 | HG00438.hp1 HG02083.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.6643+2856G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 903526 | |||||||
chr12:903733 | A | G | 276 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(273): Show |
277 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.6643+3063A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 903733 | |||||||
chr12:903774 | C | T | 1 | a0001c0001t0012g0121 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.6643+3104C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 903774 | |||||||
chr12:903824 | A | G | 1 | a0002c0009t0001g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.6643+3154A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 903824 | |||||||
chr12:903936 | G | C | 1 | a0003c0026t0005g0204 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.6643+3266G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 903936 | |||||||
chr12:903955 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.6643+3285G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 903955 | |||||||
chr12:903975 | A | C | 1 | a0001c0001t0002g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6643+3305A>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 903975 | |||||||
chr12:904010 | A | G | 132 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(129): Show |
132 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.6643+3340A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 904010 | |||||||
chr12:904057 | T | G | 23 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(20): Show |
23 | HG00408.hp2 HG00423.hp1 HG01993.hp1 others(20): Show |
intron_variant | MODIFIER | c.6643+3387T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 904057 | |||||||
chr12:904397 | A | G | 1 | a0002c0002t0001g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6644-3450A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 904397 | |||||||
chr12:904400 | T | C | 1 | a0006c0007t0008g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6644-3447T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 904400 | |||||||
chr12:904671 | G | C | 1 | a0002c0002t0001g0239 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.6644-3176G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 904671 | |||||||
chr12:904788 | A | G | 2 | a0002c0002t0001g0250 a0002c0002t0001g0252 |
2 | HG01255.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.6644-3059A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 904788 | |||||||
chr12:904978 | C | T | 1 | a0003c0005t0005g0231 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.6644-2869C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 904978 | |||||||
chr12:905251 | G | A | 72 | a0001c0022t0001g0263 a0002c0002t0001g0029 a0002c0002t0001g0194 others(69): Show |
72 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.6644-2596G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 905251 | |||||||
chr12:905372 | C | T | 3 | a0002c0024t0014g0196 a0011c0017t0014g0195 a0011c0017t0014g0197 |
3 | HG02258.hp2 HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.6644-2475C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 905372 | |||||||
chr12:905502 | A | G | 1 | a0002c0002t0001g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6644-2345A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 905502 | |||||||
chr12:906007 | G | A | 132 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(129): Show |
132 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.6644-1840G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 906007 | |||||||
chr12:906073 | G | A | 8 | a0002c0002t0001g0191 a0002c0011t0001g0220 a0002c0011t0001g0222 others(5): Show |
8 | HG01952.hp1 HG02109.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.6644-1774G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 906073 | |||||||
chr12:906218 | C | T | 1 | a0003c0005t0005g0231 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.6644-1629C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 906218 | |||||||
chr12:906220 | T | G | 1 | a0001c0001t0007g0040 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.6644-1627T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 906220 | |||||||
chr12:906303 | G | C | 25 | a0001c0001t0002g0034 a0001c0001t0002g0109 a0001c0001t0002g0134 others(22): Show |
25 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.6644-1544G>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 906303 | |||||||
chr12:906336 | G | A | 37 | a0004c0004t0003g0072 a0004c0004t0003g0073 a0004c0004t0003g0074 others(34): Show |
37 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.6644-1511G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 906336 | |||||||
chr12:906465 | T | G | 95 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(92): Show |
96 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.6644-1382T>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 906465 | |||||||
chr12:907024 | T | TAAAAAAA others(2): Show |
21 | a0001c0022t0001g0263 a0002c0002t0001g0205 a0002c0002t0001g0215 others(18): Show |
21 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.6644-817_6644-809d others(11): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 907024 | ||||||
chr12:907024 | T | TAAAAAAA others(3): Show |
3 | a0002c0002t0001g0238 a0002c0002t0006g0145 a0002c0002t0006g0178 |
3 | HG02738.hp1 NA19007.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.6644-818_6644-809d others(12): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 907024 | ||||||
chr12:907024 | T | TAAAAAAA others(5): Show |
41 | a0001c0001t0002g0227 a0001c0001t0004g0023 a0001c0001t0007g0192 others(38): Show |
41 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.6644-820_6644-809d others(14): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 907024 | ||||||
chr12:907024 | T | TAAAAAAA others(6): Show |
77 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(74): Show |
78 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.6644-821_6644-809d others(15): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 907024 | ||||||
chr12:907024 | T | TAAAAAAA others(7): Show |
19 | a0001c0001t0002g0057 a0001c0001t0002g0111 a0001c0001t0002g0134 others(16): Show |
19 | HG00735.hp1 HG01123.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.6644-822_6644-809d others(16): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 907024 | ||||||
chr12:907024 | T | TAAAAAAA others(8): Show |
2 | a0001c0001t0004g0173 a0011c0017t0014g0195 |
2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.6644-809_6644-808i others(17): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 907024 | ||||||
chr12:907024 | T | TAAAAAAA others(10): Show |
5 | a0002c0003t0001g0115 a0002c0003t0001g0117 a0002c0003t0001g0280 others(2): Show |
5 | HG01069.hp1 HG01074.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.6644-809_6644-808i others(19): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 907024 | ||||||
chr12:907024 | T | TAAAAAAA others(11): Show |
29 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(26): Show |
29 | HG00280.hp2 HG00741.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.6644-809_6644-808i others(20): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 907024 | ||||||
chr12:907024 | T | TAAAAAAA others(12): Show |
34 | a0001c0008t0002g0274 a0001c0008t0002g0275 a0001c0012t0028g0269 others(31): Show |
34 | HG00323.hp1 HG01516.hp1 HG01517.hp2 others(31): Show |
intron_variant | MODIFIER | c.6644-809_6644-808i others(21): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 907024 | ||||||
chr12:907024 | T | TAAAAAAA others(13): Show |
11 | a0002c0002t0001g0107 a0002c0002t0001g0206 a0002c0002t0001g0223 others(8): Show |
11 | HG00423.hp2 HG01175.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.6644-809_6644-808i others(22): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 907024 | ||||||
chr12:907024 | T | TAAAAAAA others(14): Show |
10 | a0002c0002t0001g0194 a0002c0002t0001g0213 a0003c0005t0001g0036 others(7): Show |
10 | HG00438.hp2 HG01952.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.6644-809_6644-808i others(23): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 907024 | ||||||
chr12:907024 | T | TAAAAAAA others(15): Show |
8 | a0002c0003t0001g0279 a0003c0005t0005g0203 a0003c0005t0005g0229 others(5): Show |
8 | HG00544.hp2 HG00609.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.6644-809_6644-808i others(24): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 907024 | ||||||
chr12:907024 | T | TAAAAAAA others(16): Show |
2 | a0003c0005t0005g0225 a0003c0005t0005g0247 |
2 | NA18992.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.6644-809_6644-808i others(25): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 907024 | ||||||
chr12:907024 | T | TTAAAAAA others(12): Show |
1 | a0003c0005t0001g0193 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.6644-823_6644-822i others(21): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 907024 | |||||||
chr12:907039 | G | A | 1 | a0002c0003t0001g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.6644-808G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 907039 | |||||||
chr12:907093 | G | A | 1 | a0002c0002t0001g0107 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.6644-754G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 907093 | |||||||
chr12:907107 | G | A | 3 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 |
3 | HG01106.hp1 HG01255.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.6644-740G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 907107 | |||||||
chr12:907320 | C | CA | 118 | a0001c0001t0016g0049 a0001c0001t0016g0056 a0001c0008t0002g0266 others(115): Show |
118 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.6644-512dupA | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 907320 | ||||||
chr12:907320 | C | CAAA | 15 | a0002c0002t0001g0107 a0002c0002t0001g0136 a0002c0002t0001g0137 others(12): Show |
15 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.6644-514_6644-512d others(5): Show |
WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 907320 | ||||||
chr12:907431 | A | G | 1 | a0003c0005t0005g0234 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.6644-416A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 907431 | |||||||
chr12:907555 | A | G | 1 | a0017c0031t0033g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.6644-292A>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 907555 | |||||||
chr12:907715 | C | CT | 131 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(128): Show |
131 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.6644-131dupT | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 907715 | ||||||
chr12:907744 | T | C | 42 | a0001c0008t0002g0266 a0001c0008t0002g0272 a0001c0008t0002g0273 others(39): Show |
42 | HG00280.hp2 HG00423.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.6644-103T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 907744 | |||||||
chr12:907825 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6644-22C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 26/27 | chr12 | 907825 | |||||||
chr12:908288 | G | A | 1 | a0005c0006t0009g0153 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.6832-187G>A | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 27/27 | chr12 | 908288 | |||||||
chr12:908351 | C | G | 2 | a0006c0007t0008g0283 a0020c0021t0024g0189 |
2 | HG01358.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.6832-124C>G | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 27/27 | chr12 | 908351 | |||||||
chr12:908449 | T | C | 1 | a0002c0002t0017g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.6832-26T>C | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 27/27 | chr12 | 908449 | |||||||
chr12:908453 | C | T | 1 | a0002c0003t0001g0124 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.6832-22C>T | WNK1 | ENSG00000060237.19 | transcript | ENST00000315939.11 | protein_coding | 27/27 | chr12 | 908453 |