Item | Value |
---|---|
geneid | 284434 |
ensemblid | ENSG00000188039.17 |
hgncid | 27619 |
symbol | NWD1 |
name | NACHT and WD repeat domain containing 1 |
refseq_nuc | NM_001007525.5 |
refseq_prot | NP_001007526.3 |
ensembl_nuc | ENST00000524140.7 |
ensembl_prot | ENSP00000428579.2 |
mane_status | MANE Select |
chr | chr19 |
start | 16719847 |
end | 16817953 |
strand | + |
ver | v1.2 |
region | chr19:16719847-16817953 |
region5000 | chr19:16714847-16822953 |
regionname0 | NWD1_chr19_16719847_16817953 |
regionname5000 | NWD1_chr19_16714847_16822953 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1432 | 62 | 6 | 29 | 19 | 1 | 7 | 13 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0002 | 0/0 | 1432 | 61 | 1 | 10 | 43 | 5 | 2 | 27 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0003 | 0/0 | 1432 | 41 | 2 | 11 | 14 | 3 | 11 | 7 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0004 | 0/0 | 1432 | 28 | 25 | 1 | 0 | 0 | 2 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0005 | 0/0 | 1432 | 21 | 0 | 6 | 8 | 2 | 5 | 5 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0006 | 0/0 | 1432 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0007 | 0/0 | 133 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(128): Show |
chr19 | 16714847 | 16822953 |
a0008 | 0/0 | 1432 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0009 | 0/0 | 1432 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0010 | 0/0 | 1432 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0011 | 0/0 | 1432 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0012 | 1/0 | 1432 | 3 | 0 | 0 | 2 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0013 | 0/0 | 1432 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0014 | 0/0 | 1432 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0015 | 0/0 | 133 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(128): Show |
chr19 | 16714847 | 16822953 |
a0016 | 0/0 | 1432 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0017 | 0/0 | 1432 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0018 | 0/0 | 1432 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0019 | 0/0 | 1432 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0020 | 0/0 | 1432 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0021 | 0/0 | 1432 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0022 | 0/0 | 1432 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0023 | 0/0 | 1432 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0024 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0025 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0026 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0027 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0028 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0029 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0030 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0031 | 0/0 | 1432 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0032 | 0/0 | 1432 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0033 | 0/0 | 1432 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0034 | 0/0 | 1432 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0035 | 0/0 | 1432 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0036 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0037 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0038 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0039 | 0/0 | 1432 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0040 | 0/0 | 1432 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0041 | 0/0 | 1432 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0042 | 0/0 | 1432 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0043 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0044 | 0/0 | 1432 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0045 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
a0046 | 0/1 | 1432 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | MQRGK others(1427): Show |
chr19 | 16714847 | 16822953 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4296 | 50 | 6 | 26 | 13 | 0 | 5 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0001c0007 | 0/0 | 4296 | 10 | 0 | 3 | 5 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0001c0046 | 0/0 | 4296 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0001c0047 | 0/0 | 4296 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0002c0002 | 0/0 | 4296 | 48 | 0 | 8 | 34 | 5 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0002c0008 | 0/0 | 4296 | 8 | 0 | 2 | 6 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0002c0023 | 0/0 | 4296 | 2 | 0 | 0 | 2 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0002c0031 | 0/0 | 4296 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0002c0033 | 0/0 | 4296 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0002c0036 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0003c0003 | 0/0 | 4296 | 26 | 2 | 4 | 13 | 2 | 5 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0003c0006 | 0/0 | 4296 | 13 | 0 | 6 | 1 | 1 | 5 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0003c0059 | 0/0 | 4296 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0003c0063 | 0/0 | 4296 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0004c0005 | 0/0 | 4296 | 15 | 12 | 1 | 0 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0004c0009 | 0/0 | 4296 | 8 | 8 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0004c0017 | 0/0 | 4296 | 4 | 4 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0004c0060 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0005c0004 | 0/0 | 4296 | 17 | 0 | 5 | 7 | 2 | 3 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0005c0016 | 0/0 | 4296 | 4 | 0 | 1 | 1 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0006c0014 | 0/0 | 4296 | 4 | 3 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0006c0015 | 0/0 | 4296 | 4 | 4 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0006c0044 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0007c0028 | 0/0 | 4296 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0007c0029 | 0/0 | 4296 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0007c0068 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0007c0069 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0008c0012 | 0/0 | 4296 | 5 | 5 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0008c0067 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0009c0010 | 0/0 | 4296 | 6 | 6 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0010c0013 | 0/0 | 4296 | 4 | 3 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0010c0040 | 0/0 | 4296 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0011c0011 | 0/0 | 4296 | 5 | 5 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0012c0018 | 1/0 | 4296 | 3 | 0 | 0 | 2 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0013c0020 | 0/0 | 4296 | 3 | 1 | 2 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0014c0022 | 0/0 | 4296 | 3 | 3 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0015c0025 | 0/0 | 4296 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0015c0054 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0016c0019 | 0/0 | 4296 | 3 | 3 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0017c0021 | 0/0 | 4296 | 3 | 0 | 0 | 3 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0018c0026 | 0/0 | 4296 | 2 | 0 | 2 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0019c0027 | 0/0 | 4296 | 2 | 0 | 0 | 2 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0020c0024 | 0/0 | 4296 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0021c0041 | 0/0 | 4296 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0022c0042 | 0/0 | 4296 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0023c0038 | 0/0 | 4296 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0024c0049 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0025c0045 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0026c0043 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0027c0053 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0028c0062 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0029c0065 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0030c0066 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0031c0056 | 0/0 | 4296 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0032c0030 | 0/0 | 4296 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0033c0048 | 0/0 | 4296 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0034c0032 | 0/0 | 4296 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0035c0055 | 0/0 | 4296 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0036c0064 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0037c0058 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0038c0052 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0039c0039 | 0/0 | 4296 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0040c0037 | 0/0 | 4296 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0041c0050 | 0/0 | 4296 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0042c0035 | 0/0 | 4296 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0043c0057 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0044c0061 | 0/0 | 4296 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0045c0051 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 | ||
a0046c0034 | 0/1 | 4296 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | ATGCA others(4291): Show |
chr19 | 16714847 | 16822953 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7764 | 13 | 3 | 6 | 3 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0001c0001t0002 | 0/0 | 7764 | 3 | 2 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0001c0001t0003 | 0/0 | 7764 | 12 | 0 | 9 | 2 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0001c0001t0004 | 0/0 | 7764 | 8 | 1 | 7 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0001c0001t0005 | 0/0 | 7764 | 7 | 0 | 1 | 5 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0001c0001t0014 | 0/0 | 7765 | 2 | 0 | 1 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7760): Show |
chr19 | 16714847 | 16822953 |
a0001c0001t0020 | 0/0 | 7763 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0001c0001t0021 | 0/0 | 7765 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7760): Show |
chr19 | 16714847 | 16822953 |
a0001c0001t0024 | 0/0 | 7765 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7760): Show |
chr19 | 16714847 | 16822953 |
a0001c0001t0031 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0001c0001t0033 | 0/0 | 7735 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7730): Show |
chr19 | 16714847 | 16822953 |
a0001c0007t0001 | 0/0 | 7764 | 5 | 0 | 2 | 1 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0001c0007t0002 | 0/0 | 7764 | 4 | 0 | 1 | 3 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0001c0007t0049 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0001c0046t0001 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0001c0047t0001 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0002c0002t0001 | 0/0 | 7764 | 23 | 0 | 0 | 18 | 4 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0002c0002t0002 | 0/0 | 7764 | 6 | 0 | 0 | 6 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0002c0002t0003 | 0/0 | 7764 | 5 | 0 | 3 | 1 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0002c0002t0004 | 0/0 | 7764 | 3 | 0 | 1 | 2 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0002c0002t0005 | 0/0 | 7764 | 3 | 0 | 2 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0002c0002t0007 | 0/0 | 7764 | 2 | 0 | 1 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0002c0002t0011 | 0/0 | 7763 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0002c0002t0012 | 0/0 | 7764 | 4 | 0 | 0 | 4 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0002c0002t0020 | 0/0 | 7763 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0002c0008t0001 | 0/0 | 7764 | 6 | 0 | 2 | 4 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0002c0008t0002 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0002c0008t0027 | 0/0 | 7763 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0002c0023t0001 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0002c0023t0002 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0002c0031t0001 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0002c0033t0002 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0002c0036t0002 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0003c0003t0001 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0003c0003t0002 | 0/0 | 7764 | 12 | 1 | 3 | 5 | 1 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0003c0003t0003 | 0/0 | 7764 | 2 | 0 | 0 | 0 | 1 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0003c0003t0004 | 0/0 | 7764 | 6 | 0 | 0 | 4 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0003c0003t0005 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0003c0003t0007 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0003c0003t0024 | 0/0 | 7765 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7760): Show |
chr19 | 16714847 | 16822953 |
a0003c0003t0044 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0003c0003t0046 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0003c0006t0001 | 0/0 | 7764 | 3 | 0 | 1 | 0 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0003c0006t0002 | 0/0 | 7764 | 9 | 0 | 4 | 1 | 1 | 3 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0003c0006t0038 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0003c0059t0015 | 0/0 | 7765 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7760): Show |
chr19 | 16714847 | 16822953 |
a0003c0063t0002 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0004c0005t0001 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0004c0005t0006 | 0/0 | 7764 | 7 | 7 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0004c0005t0018 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0004c0005t0022 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7757): Show |
chr19 | 16714847 | 16822953 |
a0004c0005t0023 | 0/0 | 7764 | 2 | 0 | 0 | 0 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0004c0005t0029 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7757): Show |
chr19 | 16714847 | 16822953 |
a0004c0005t0039 | 0/0 | 7763 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0004c0005t0048 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0004c0009t0005 | 0/0 | 7764 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0004c0009t0008 | 0/0 | 7763 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0004c0009t0009 | 0/0 | 7763 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0004c0009t0013 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0004c0009t0036 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0004c0017t0001 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0004c0017t0002 | 0/0 | 7764 | 3 | 3 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0004c0060t0002 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0005c0004t0001 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0005c0004t0002 | 0/0 | 7764 | 7 | 0 | 1 | 6 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0005c0004t0003 | 0/0 | 7764 | 6 | 0 | 2 | 0 | 2 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0005c0004t0004 | 0/0 | 7764 | 2 | 0 | 1 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0005c0004t0021 | 0/0 | 7765 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7760): Show |
chr19 | 16714847 | 16822953 |
a0005c0016t0002 | 0/0 | 7764 | 4 | 0 | 1 | 1 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0006c0014t0002 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0006c0014t0008 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0006c0014t0009 | 0/0 | 7763 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0006c0015t0006 | 0/0 | 7764 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0006c0015t0028 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0006c0015t0041 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0006c0044t0001 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0007c0028t0002 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0007c0028t0034 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0007c0029t0002 | 0/0 | 7764 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0007c0068t0040 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0007c0069t0043 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0008c0012t0001 | 0/0 | 7764 | 3 | 3 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0008c0012t0019 | 0/0 | 7764 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0008c0067t0003 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0009c0010t0002 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0009c0010t0010 | 0/0 | 7764 | 4 | 4 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0009c0010t0047 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0010c0013t0008 | 0/0 | 7763 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0010c0013t0009 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0010c0013t0013 | 0/0 | 7764 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0010c0040t0001 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0011c0011t0001 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0011c0011t0002 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0011c0011t0011 | 0/0 | 7763 | 3 | 3 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0012c0018t0005 | 1/0 | 7764 | 2 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0012c0018t0014 | 0/0 | 7765 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7760): Show |
chr19 | 16714847 | 16822953 |
a0013c0020t0008 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0013c0020t0016 | 0/0 | 7763 | 2 | 0 | 2 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0014c0022t0001 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0014c0022t0002 | 0/0 | 7764 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0015c0025t0002 | 0/0 | 7764 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0015c0054t0025 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0016c0019t0017 | 0/0 | 7762 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7757): Show |
chr19 | 16714847 | 16822953 |
a0016c0019t0022 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7757): Show |
chr19 | 16714847 | 16822953 |
a0017c0021t0005 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0017c0021t0007 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0017c0021t0045 | 0/0 | 7763 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0018c0026t0002 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0018c0026t0015 | 0/0 | 7765 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7760): Show |
chr19 | 16714847 | 16822953 |
a0019c0027t0007 | 0/0 | 7764 | 2 | 0 | 0 | 2 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0020c0024t0001 | 0/0 | 7764 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0021c0041t0002 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0022c0042t0001 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0023c0038t0001 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0024c0049t0042 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7757): Show |
chr19 | 16714847 | 16822953 |
a0025c0045t0016 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0026c0043t0009 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0027c0053t0001 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0028c0062t0030 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0029c0065t0032 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7757): Show |
chr19 | 16714847 | 16822953 |
a0030c0066t0008 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7758): Show |
chr19 | 16714847 | 16822953 |
a0031c0056t0001 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0032c0030t0001 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0033c0048t0018 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0034c0032t0001 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0035c0055t0037 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0036c0064t0002 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0037c0058t0035 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0038c0052t0001 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0039c0039t0015 | 0/0 | 7765 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7760): Show |
chr19 | 16714847 | 16822953 |
a0040c0037t0001 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0041c0050t0007 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0042c0035t0001 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0043c0057t0026 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7757): Show |
chr19 | 16714847 | 16822953 |
a0044c0061t0003 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0045c0051t0002 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
a0046c0034t0001 | 0/1 | 7764 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | AGTTG others(7759): Show |
chr19 | 16714847 | 16822953 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0014g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0014g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0020g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0021g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0024g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0031g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0001t0033g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0007t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0007t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0007t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0007t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0007t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0007t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0007t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0007t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0007t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0007t0049g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0046t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0001c0047t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0005g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0007g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0011g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0012g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0012g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0012g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0012g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0002t0020g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0008t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0008t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0008t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0008t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0008t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0008t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0008t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0008t0027g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0023t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0023t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0031t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0033t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0002c0036t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0024g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0044g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0003t0046g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0006t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0006t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0006t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0006t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0006t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0006t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0006t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0006t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0006t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0006t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0006t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0006t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0006t0038g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0059t0015g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0003c0063t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0005t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0005t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0005t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0005t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0005t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0005t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0005t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0005t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0005t0018g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0005t0022g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0005t0023g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0005t0023g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0005t0029g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0005t0039g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0005t0048g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0009t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0009t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0009t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0009t0008g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0009t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0009t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0009t0013g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0009t0036g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0017t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0017t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0017t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0017t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0004c0060t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0004t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0004t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0004t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0004t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0004t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0004t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0004t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0004t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0004t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0004t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0004t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0004t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0004t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0004t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0004t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0004t0021g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0016t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0016t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0016t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0005c0016t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0006c0014t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0006c0014t0008g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0006c0014t0009g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0006c0014t0009g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0006c0015t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0006c0015t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0006c0015t0028g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0006c0015t0041g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0006c0044t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0007c0028t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0007c0028t0034g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0007c0029t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0007c0029t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0007c0068t0040g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0007c0069t0043g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0008c0012t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0008c0012t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0008c0012t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0008c0012t0019g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0008c0012t0019g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0008c0067t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0009c0010t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0009c0010t0010g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0009c0010t0010g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0009c0010t0010g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0009c0010t0010g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0009c0010t0047g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0010c0013t0008g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0010c0013t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0010c0013t0013g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0010c0013t0013g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0010c0040t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0011c0011t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0011c0011t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0011c0011t0011g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0011c0011t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0011c0011t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0012c0018t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0012c0018t0005g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0012c0018t0014g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0013c0020t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0013c0020t0016g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0013c0020t0016g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0014c0022t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0014c0022t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0014c0022t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0015c0025t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0015c0025t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0015c0054t0025g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0016c0019t0017g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0016c0019t0017g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0016c0019t0022g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0017c0021t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0017c0021t0007g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0017c0021t0045g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0018c0026t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0018c0026t0015g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0019c0027t0007g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0019c0027t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0020c0024t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0020c0024t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0021c0041t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0022c0042t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0023c0038t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0024c0049t0042g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0025c0045t0016g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0026c0043t0009g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0027c0053t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0028c0062t0030g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0029c0065t0032g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0030c0066t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0031c0056t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0032c0030t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0033c0048t0018g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0034c0032t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0035c0055t0037g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0036c0064t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0037c0058t0035g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0038c0052t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0039c0039t0015g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0040c0037t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0041c0050t0007g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0042c0035t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0043c0057t0026g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0044c0061t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0045c0051t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
a0046c0034t0001g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0046 | t0001 | g0219 | EUR | GBR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0156 | EUR | GBR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00280 | hp1 | a0005 | c0004 | t0003 | g0248 | EUR | FIN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0153 | EUR | FIN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00323 | hp1 | a0005 | c0004 | t0003 | g0280 | EUR | FIN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0146 | EUR | FIN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00544 | hp1 | a0005 | c0004 | t0002 | g0042 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00558 | hp1 | a0001 | c0001 | t0005 | g0245 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00558 | hp2 | a0005 | c0004 | t0002 | g0103 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00597 | hp1 | a0003 | c0003 | t0046 | g0077 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00597 | hp2 | a0001 | c0001 | t0021 | g0150 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00609 | hp1 | a0003 | c0003 | t0004 | g0061 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00639 | hp1 | a0001 | c0007 | t0001 | g0221 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00639 | hp2 | a0005 | c0004 | t0003 | g0272 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00642 | hp1 | a0003 | c0006 | t0002 | g0072 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00642 | hp2 | a0010 | c0040 | t0001 | g0161 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00733 | hp1 | a0003 | c0006 | t0002 | g0086 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00733 | hp2 | a0005 | c0004 | t0021 | g0277 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0109 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00735 | hp2 | a0010 | c0013 | t0008 | g0188 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00738 | hp1 | a0002 | c0008 | t0001 | g0270 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG00738 | hp2 | a0003 | c0006 | t0002 | g0096 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01070 | hp1 | a0013 | c0020 | t0016 | g0004 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0112 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01071 | hp1 | a0001 | c0001 | t0024 | g0108 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01071 | hp2 | a0013 | c0020 | t0016 | g0003 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01074 | hp1 | a0005 | c0016 | t0002 | g0101 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01081 | hp1 | a0004 | c0005 | t0039 | g0084 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0107 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01099 | hp1 | a0003 | c0006 | t0001 | g0128 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01099 | hp2 | a0002 | c0002 | t0020 | g0249 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01109 | hp2 | a0006 | c0014 | t0002 | g0015 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01167 | hp2 | a0005 | c0004 | t0002 | g0039 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01175 | hp1 | a0003 | c0059 | t0015 | g0037 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01175 | hp2 | a0002 | c0002 | t0003 | g0267 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0111 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01192 | hp2 | a0003 | c0003 | t0044 | g0070 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01256 | hp1 | a0001 | c0007 | t0002 | g0110 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01256 | hp2 | a0002 | c0002 | t0003 | g0144 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01257 | hp1 | a0005 | c0004 | t0004 | g0097 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01257 | hp2 | a0001 | c0001 | t0033 | g0216 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0220 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0113 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0162 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01346 | hp2 | a0002 | c0002 | t0005 | g0287 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0184 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01358 | hp2 | a0002 | c0008 | t0001 | g0168 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01361 | hp1 | a0021 | c0041 | t0002 | g0036 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01361 | hp2 | a0018 | c0026 | t0015 | g0078 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01433 | hp1 | a0003 | c0003 | t0002 | g0060 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01433 | hp2 | a0001 | c0001 | t0014 | g0238 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01496 | hp1 | a0022 | c0042 | t0001 | g0152 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01496 | hp2 | a0005 | c0004 | t0003 | g0266 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01516 | hp1 | a0003 | c0003 | t0002 | g0091 | EUR | IBS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01516 | hp2 | a0002 | c0002 | t0003 | g0163 | EUR | IBS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01884 | hp1 | a0006 | c0015 | t0028 | g0204 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01884 | hp2 | a0014 | c0022 | t0001 | g0231 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01891 | hp1 | a0002 | c0036 | t0002 | g0020 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01891 | hp2 | a0007 | c0029 | t0002 | g0298 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01934 | hp1 | a0002 | c0002 | t0003 | g0200 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0236 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01975 | hp1 | a0002 | c0002 | t0007 | g0041 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0035 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01978 | hp1 | a0003 | c0003 | t0002 | g0085 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01981 | hp2 | a0003 | c0006 | t0002 | g0100 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02004 | hp1 | a0002 | c0002 | t0004 | g0011 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02015 | hp1 | a0002 | c0002 | t0011 | g0105 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02015 | hp2 | a0003 | c0003 | t0004 | g0079 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02027 | hp1 | a0023 | c0038 | t0001 | g0223 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02027 | hp2 | a0001 | c0001 | t0014 | g0187 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02040 | hp2 | a0012 | c0018 | t0014 | g0149 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02055 | hp1 | a0024 | c0049 | t0042 | g0054 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02055 | hp2 | a0004 | c0005 | t0048 | g0002 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02056 | hp2 | a0003 | c0003 | t0002 | g0067 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02071 | hp2 | a0019 | c0027 | t0007 | g0068 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02074 | hp2 | a0003 | c0003 | t0007 | g0064 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02080 | hp2 | a0003 | c0003 | t0002 | g0066 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02083 | hp1 | a0019 | c0027 | t0007 | g0080 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02083 | hp2 | a0002 | c0002 | t0004 | g0009 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02129 | hp1 | a0003 | c0003 | t0004 | g0073 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02132 | hp2 | a0001 | c0007 | t0002 | g0122 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02145 | hp1 | a0011 | c0011 | t0002 | g0022 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02145 | hp2 | a0026 | c0043 | t0009 | g0023 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02148 | hp2 | a0003 | c0006 | t0038 | g0106 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02155 | hp1 | a0002 | c0002 | t0004 | g0033 | EAS | CDX | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02155 | hp2 | a0001 | c0001 | t0005 | g0154 | EAS | CDX | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | CDX | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02165 | hp2 | a0005 | c0004 | t0002 | g0074 | EAS | CDX | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02257 | hp1 | a0004 | c0017 | t0001 | g0212 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02257 | hp2 | a0007 | c0029 | t0002 | g0297 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02258 | hp1 | a0004 | c0005 | t0018 | g0256 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02258 | hp2 | a0004 | c0005 | t0022 | g0050 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02273 | hp2 | a0001 | c0001 | t0004 | g0032 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02280 | hp1 | a0004 | c0017 | t0002 | g0038 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02280 | hp2 | a0015 | c0025 | t0002 | g0048 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02293 | hp1 | a0018 | c0026 | t0002 | g0083 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02293 | hp2 | a0002 | c0002 | t0005 | g0195 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0183 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02451 | hp1 | a0008 | c0012 | t0001 | g0234 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02451 | hp2 | a0027 | c0053 | t0001 | g0252 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02572 | hp1 | a0004 | c0005 | t0006 | g0227 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02572 | hp2 | a0007 | c0028 | t0034 | g0258 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0215 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02602 | hp2 | a0003 | c0063 | t0002 | g0098 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02615 | hp1 | a0004 | c0005 | t0006 | g0229 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02615 | hp2 | a0028 | c0062 | t0030 | g0250 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02622 | hp1 | a0006 | c0015 | t0041 | g0053 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02622 | hp2 | a0020 | c0024 | t0001 | g0259 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02630 | hp2 | a0004 | c0005 | t0006 | g0226 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02647 | hp1 | a0009 | c0010 | t0010 | g0283 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02647 | hp2 | a0006 | c0015 | t0006 | g0290 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02698 | hp1 | a0003 | c0006 | t0001 | g0281 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02698 | hp2 | a0003 | c0003 | t0004 | g0026 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02723 | hp1 | a0006 | c0015 | t0006 | g0293 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02723 | hp2 | a0014 | c0022 | t0002 | g0051 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02735 | hp1 | a0005 | c0016 | t0002 | g0056 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02735 | hp2 | a0005 | c0004 | t0003 | g0284 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02809 | hp1 | a0010 | c0013 | t0013 | g0173 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02809 | hp2 | a0009 | c0010 | t0010 | g0276 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02818 | hp1 | a0029 | c0065 | t0032 | g0166 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02886 | hp1 | a0004 | c0060 | t0002 | g0125 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02886 | hp2 | a0004 | c0009 | t0008 | g0286 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02895 | hp1 | a0004 | c0005 | t0006 | g0230 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02895 | hp2 | a0003 | c0003 | t0002 | g0117 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02896 | hp1 | a0007 | c0068 | t0040 | g0116 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02896 | hp2 | a0004 | c0017 | t0002 | g0018 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02897 | hp1 | a0004 | c0005 | t0006 | g0228 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02897 | hp2 | a0004 | c0017 | t0002 | g0019 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02922 | hp1 | a0030 | c0066 | t0008 | g0264 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02922 | hp2 | a0008 | c0012 | t0001 | g0232 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02965 | hp1 | a0007 | c0028 | t0002 | g0115 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02965 | hp2 | a0006 | c0014 | t0008 | g0253 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03041 | hp1 | a0004 | c0009 | t0005 | g0140 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03098 | hp1 | a0016 | c0019 | t0017 | g0295 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03098 | hp2 | a0004 | c0009 | t0008 | g0205 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03130 | hp1 | a0004 | c0009 | t0009 | g0052 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03130 | hp2 | a0009 | c0010 | t0010 | g0131 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03139 | hp1 | a0008 | c0012 | t0001 | g0235 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03139 | hp2 | a0004 | c0005 | t0006 | g0225 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03195 | hp1 | a0011 | c0011 | t0011 | g0024 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03195 | hp2 | a0009 | c0010 | t0047 | g0005 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03209 | hp1 | a0015 | c0054 | t0025 | g0118 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03209 | hp2 | a0010 | c0013 | t0013 | g0172 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03225 | hp1 | a0008 | c0012 | t0019 | g0292 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03225 | hp2 | a0006 | c0014 | t0009 | g0016 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03239 | hp1 | a0031 | c0056 | t0001 | g0279 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03239 | hp2 | a0005 | c0004 | t0001 | g0278 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03453 | hp1 | a0004 | c0009 | t0005 | g0224 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03453 | hp2 | a0020 | c0024 | t0001 | g0251 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03486 | hp1 | a0008 | c0012 | t0019 | g0233 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03490 | hp1 | a0032 | c0030 | t0001 | g0157 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03490 | hp2 | a0004 | c0005 | t0023 | g0095 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03491 | hp1 | a0003 | c0006 | t0002 | g0062 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03491 | hp2 | a0001 | c0007 | t0001 | g0213 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03492 | hp1 | a0004 | c0005 | t0023 | g0094 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03492 | hp2 | a0001 | c0007 | t0001 | g0217 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03516 | hp1 | a0014 | c0022 | t0002 | g0046 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03516 | hp2 | a0008 | c0067 | t0003 | g0275 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03540 | hp1 | a0007 | c0069 | t0043 | g0299 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03540 | hp2 | a0004 | c0009 | t0036 | g0126 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03579 | hp1 | a0004 | c0005 | t0001 | g0296 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03579 | hp2 | a0004 | c0009 | t0013 | g0206 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03654 | hp1 | a0003 | c0003 | t0004 | g0075 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03654 | hp2 | a0003 | c0006 | t0001 | g0282 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03688 | hp1 | a0002 | c0031 | t0001 | g0155 | SAS | STU | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0169 | SAS | STU | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03710 | hp1 | a0003 | c0006 | t0002 | g0082 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03710 | hp2 | a0005 | c0004 | t0003 | g0273 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03834 | hp1 | a0033 | c0048 | t0018 | g0129 | SAS | BEB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03834 | hp2 | a0001 | c0001 | t0020 | g0289 | SAS | BEB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03927 | hp1 | a0034 | c0032 | t0001 | g0269 | SAS | BEB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG04115 | hp1 | a0003 | c0006 | t0002 | g0092 | SAS | STU | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG04115 | hp2 | a0001 | c0001 | t0031 | g0214 | SAS | STU | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG04184 | hp1 | a0003 | c0003 | t0003 | g0288 | SAS | BEB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG04184 | hp2 | a0003 | c0003 | t0002 | g0065 | SAS | BEB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG04199 | hp1 | a0035 | c0055 | t0037 | g0088 | SAS | STU | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0170 | SAS | STU | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG04228 | hp1 | a0005 | c0016 | t0002 | g0058 | SAS | STU | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG04228 | hp2 | a0003 | c0003 | t0002 | g0069 | SAS | STU | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18522 | hp1 | a0013 | c0020 | t0008 | g0257 | AFR | YRI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18522 | hp2 | a0003 | c0003 | t0001 | g0210 | AFR | YRI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18747 | hp1 | a0002 | c0002 | t0005 | g0130 | EAS | CHB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18747 | hp2 | a0001 | c0007 | t0049 | g0132 | EAS | CHB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18906 | hp1 | a0037 | c0058 | t0035 | g0167 | AFR | YRI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18906 | hp2 | a0038 | c0052 | t0001 | g0254 | AFR | YRI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18945 | hp1 | a0002 | c0002 | t0012 | g0189 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18945 | hp2 | a0003 | c0003 | t0002 | g0076 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18946 | hp1 | a0002 | c0002 | t0012 | g0203 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18946 | hp2 | a0017 | c0021 | t0005 | g0222 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18951 | hp1 | a0017 | c0021 | t0045 | g0121 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18952 | hp1 | a0002 | c0002 | t0012 | g0180 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18954 | hp1 | a0012 | c0018 | t0005 | g0240 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18954 | hp2 | a0003 | c0003 | t0002 | g0089 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18960 | hp1 | a0001 | c0007 | t0001 | g0239 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18960 | hp2 | a0001 | c0001 | t0005 | g0241 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18962 | hp1 | a0003 | c0003 | t0005 | g0141 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18962 | hp2 | a0002 | c0033 | t0002 | g0012 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18966 | hp1 | a0003 | c0003 | t0024 | g0087 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18968 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18968 | hp2 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18973 | hp1 | a0003 | c0006 | t0002 | g0071 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18975 | hp1 | a0005 | c0004 | t0002 | g0093 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18980 | hp1 | a0002 | c0008 | t0001 | g0134 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18980 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18982 | hp1 | a0005 | c0004 | t0002 | g0059 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18982 | hp2 | a0002 | c0008 | t0027 | g0137 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18993 | hp1 | a0002 | c0023 | t0002 | g0102 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA18993 | hp2 | a0039 | c0039 | t0015 | g0055 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19003 | hp1 | a0002 | c0002 | t0012 | g0198 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19003 | hp2 | a0003 | c0003 | t0004 | g0099 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19005 | hp1 | a0002 | c0008 | t0001 | g0145 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19005 | hp2 | a0005 | c0004 | t0004 | g0090 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19007 | hp1 | a0002 | c0008 | t0001 | g0135 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19009 | hp1 | a0002 | c0023 | t0001 | g0151 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19011 | hp1 | a0002 | c0008 | t0002 | g0044 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19030 | hp1 | a0015 | c0025 | t0002 | g0049 | AFR | LWK | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19030 | hp2 | a0010 | c0013 | t0009 | g0045 | AFR | LWK | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19043 | hp1 | a0006 | c0044 | t0001 | g0255 | AFR | LWK | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19043 | hp2 | a0004 | c0005 | t0029 | g0265 | AFR | LWK | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19060 | hp1 | a0040 | c0037 | t0001 | g0209 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19066 | hp1 | a0041 | c0050 | t0007 | g0104 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19066 | hp2 | a0005 | c0004 | t0002 | g0120 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19068 | hp2 | a0001 | c0047 | t0001 | g0138 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19070 | hp1 | a0001 | c0007 | t0002 | g0057 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19070 | hp2 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19074 | hp2 | a0002 | c0002 | t0007 | g0030 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19077 | hp1 | a0001 | c0007 | t0002 | g0007 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19077 | hp2 | a0017 | c0021 | t0007 | g0119 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19080 | hp1 | a0005 | c0016 | t0002 | g0081 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19080 | hp2 | a0002 | c0002 | t0003 | g0186 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19085 | hp2 | a0002 | c0008 | t0001 | g0139 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19087 | hp1 | a0042 | c0035 | t0001 | g0133 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19240 | hp1 | a0006 | c0014 | t0009 | g0014 | AFR | YRI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | YRI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA20129 | hp1 | a0009 | c0010 | t0002 | g0114 | AFR | ASW | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA20129 | hp2 | a0009 | c0010 | t0010 | g0274 | AFR | ASW | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA20752 | hp1 | a0003 | c0006 | t0002 | g0027 | EUR | TSI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA20752 | hp2 | a0044 | c0061 | t0003 | g0285 | EUR | TSI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA20805 | hp1 | a0003 | c0003 | t0003 | g0143 | EUR | TSI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0165 | EUR | TSI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01123 | hp1 | a0001 | c0007 | t0001 | g0040 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG01123 | hp2 | a0003 | c0003 | t0002 | g0127 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02109 | hp1 | a0011 | c0011 | t0011 | g0017 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02109 | hp2 | a0025 | c0045 | t0016 | g0001 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02559 | hp1 | a0011 | c0011 | t0011 | g0025 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG02559 | hp2 | a0004 | c0005 | t0006 | g0211 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03471 | hp1 | a0016 | c0019 | t0017 | g0294 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG03471 | hp2 | a0004 | c0009 | t0009 | g0047 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG06807 | hp1 | a0036 | c0064 | t0002 | g0300 | AFR | USA | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | USA | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA20300 | hp1 | a0016 | c0019 | t0022 | g0124 | AFR | USA | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA20300 | hp2 | a0043 | c0057 | t0026 | g0202 | AFR | USA | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA21309 | hp1 | a0045 | c0051 | t0002 | g0028 | AFR | LWK | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
NA21309 | hp2 | a0011 | c0011 | t0001 | g0247 | AFR | LWK | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
homoSapiens | chm13v2 | a0046 | c0034 | t0001 | g0159 | REF | REF | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
homoSapiens | grch38p0 | a0012 | c0018 | t0005 | g0243 | REF | REF | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:16731241 | G | T | 20 | a0003 a0004 a0005 others(17): Show |
130 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(127): Show |
missense_variant | MODERATE | c.44G>T | p.Cys15Phe | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/19 | 595/7764 | 44/4299 | 15/1432 | chr19 | 16731241 | |||
chr19:16736665 | T | C | 1 | a0035 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.113T>C | p.Ile38Thr | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/19 | 664/7764 | 113/4299 | 38/1432 | chr19 | 16736665 | |||
chr19:16744429 | C | G | 2 | a0007 a0015 |
9 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
missense_variant | MODERATE | c.207C>G | p.Ile69Met | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/19 | 758/7764 | 207/4299 | 69/1432 | chr19 | 16744429 | |||
chr19:16744454 | A | G | 27 | a0001 a0003 a0004 others(24): Show |
187 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(184): Show |
missense_variant | MODERATE | c.232A>G | p.Ile78Val | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/19 | 783/7764 | 232/4299 | 78/1432 | chr19 | 16744454 | |||
chr19:16744622 | G | T | 2 | a0007 a0015 |
9 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
stop_gained | HIGH | c.400G>T | p.Glu134* | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/19 | 951/7764 | 400/4299 | 134/1432 | chr19 | 16744622 | |||
chr19:16744646 | C | T | 2 | a0008 a0027 |
7 | HG02451.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
missense_variant | MODERATE | c.424C>T | p.Arg142Cys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/19 | 975/7764 | 424/4299 | 142/1432 | chr19 | 16744646 | |||
chr19:16744655 | G | A | 1 | a0032 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.433G>A | p.Ala145Thr | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/19 | 984/7764 | 433/4299 | 145/1432 | chr19 | 16744655 | |||
chr19:16744661 | G | A | 1 | a0016 | 3 | HG03098.hp1 HG03471.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.439G>A | p.Glu147Lys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/19 | 990/7764 | 439/4299 | 147/1432 | chr19 | 16744661 | |||
chr19:16749159 | C | T | 1 | a0026 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.517C>T | p.Arg173Trp | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1068/7764 | 517/4299 | 173/1432 | chr19 | 16749159 | |||
chr19:16749190 | A | T | 2 | a0009 a0038 |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
missense_variant | MODERATE | c.548A>T | p.Gln183Leu | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1099/7764 | 548/4299 | 183/1432 | chr19 | 16749190 | |||
chr19:16749273 | C | T | 10 | a0007 a0009 a0020 others(7): Show |
20 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(17): Show |
missense_variant | MODERATE | c.631C>T | p.Leu211Phe | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1182/7764 | 631/4299 | 211/1432 | chr19 | 16749273 | |||
chr19:16749276 | G | A | 2 | a0009 a0038 |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
missense_variant | MODERATE | c.634G>A | p.Ala212Thr | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1185/7764 | 634/4299 | 212/1432 | chr19 | 16749276 | |||
chr19:16749280 | A | T | 1 | a0015 | 2 | HG02280.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.638A>T | p.Asp213Val | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1189/7764 | 638/4299 | 213/1432 | chr19 | 16749280 | |||
chr19:16749294 | G | A | 41 | a0001 a0002 a0003 others(38): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
missense_variant | MODERATE | c.652G>A | p.Ala218Thr | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1203/7764 | 652/4299 | 218/1432 | chr19 | 16749294 | |||
chr19:16749616 | A | G | 1 | a0039 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.974A>G | p.Gln325Arg | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1525/7764 | 974/4299 | 325/1432 | chr19 | 16749616 | |||
chr19:16749747 | G | A | 10 | a0007 a0009 a0020 others(7): Show |
20 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(17): Show |
missense_variant | MODERATE | c.1105G>A | p.Val369Ile | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1656/7764 | 1105/4299 | 369/1432 | chr19 | 16749747 | |||
chr19:16749865 | A | G | 1 | a0023 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.1223A>G | p.Asp408Gly | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1774/7764 | 1223/4299 | 408/1432 | chr19 | 16749865 | |||
chr19:16749874 | C | T | 2 | a0009 a0038 |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
missense_variant | MODERATE | c.1232C>T | p.Thr411Ile | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1783/7764 | 1232/4299 | 411/1432 | chr19 | 16749874 | |||
chr19:16749979 | G | A | 1 | a0033 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1337G>A | p.Arg446His | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1888/7764 | 1337/4299 | 446/1432 | chr19 | 16749979 | |||
chr19:16750071 | G | A | 1 | a0018 | 2 | HG01361.hp2 HG02293.hp1 |
missense_variant | MODERATE | c.1429G>A | p.Asp477Asn | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1980/7764 | 1429/4299 | 477/1432 | chr19 | 16750071 | |||
chr19:16750084 | G | A | 3 | a0029 a0030 a0043 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.1442G>A | p.Arg481Gln | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1993/7764 | 1442/4299 | 481/1432 | chr19 | 16750084 | |||
chr19:16750273 | G | A | 1 | a0029 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.1631G>A | p.Arg544Gln | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 2182/7764 | 1631/4299 | 544/1432 | chr19 | 16750273 | |||
chr19:16750396 | A | G | 1 | a0019 | 2 | HG02071.hp2 HG02083.hp1 |
missense_variant | MODERATE | c.1754A>G | p.Tyr585Cys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 2305/7764 | 1754/4299 | 585/1432 | chr19 | 16750396 | |||
chr19:16759232 | C | G | 1 | a0024 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.1777C>G | p.Leu593Val | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/19 | 2328/7764 | 1777/4299 | 593/1432 | chr19 | 16759232 | |||
chr19:16759236 | C | T | 1 | a0040 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.1781C>T | p.Ser594Leu | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/19 | 2332/7764 | 1781/4299 | 594/1432 | chr19 | 16759236 | |||
chr19:16761998 | C | T | 1 | a0042 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.1993C>T | p.Arg665Cys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/19 | 2544/7764 | 1993/4299 | 665/1432 | chr19 | 16761998 | |||
chr19:16763861 | G | T | 1 | a0014 | 3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.2167G>T | p.Val723Phe | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/19 | 2718/7764 | 2167/4299 | 723/1432 | chr19 | 16763861 | |||
chr19:16779432 | C | G | 17 | a0004 a0006 a0007 others(14): Show |
67 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(64): Show |
missense_variant | MODERATE | c.2698C>G | p.Gln900Glu | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/19 | 3249/7764 | 2698/4299 | 900/1432 | chr19 | 16779432 | |||
chr19:16789053 | C | A | 1 | a0004 | 4 | HG02257.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
missense_variant | MODERATE | c.2803C>A | p.His935Asn | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/19 | 3354/7764 | 2803/4299 | 935/1432 | chr19 | 16789053 | |||
chr19:16789054 | A | G | 20 | a0004 a0006 a0007 others(17): Show |
75 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(72): Show |
missense_variant | MODERATE | c.2804A>G | p.His935Arg | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/19 | 3355/7764 | 2804/4299 | 935/1432 | chr19 | 16789054 | |||
chr19:16799964 | G | A | 1 | a0014 | 3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.3538G>A | p.Gly1180Ser | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/19 | 4089/7764 | 3538/4299 | 1180/1432 | chr19 | 16799964 | |||
chr19:16800060 | C | G | 3 | a0007 a0020 a0036 |
5 | HG01891.hp2 HG02257.hp2 HG02622.hp2 others(2): Show |
missense_variant | MODERATE | c.3634C>G | p.Leu1212Val | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/19 | 4185/7764 | 3634/4299 | 1212/1432 | chr19 | 16800060 | |||
chr19:16800142 | C | T | 1 | a0034 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.3716C>T | p.Thr1239Ile | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/19 | 4267/7764 | 3716/4299 | 1239/1432 | chr19 | 16800142 | |||
chr19:16807648 | C | T | 1 | a0021 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.3799C>T | p.Arg1267Cys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4350/7764 | 3799/4299 | 1267/1432 | chr19 | 16807648 | |||
chr19:16807733 | C | A | 1 | a0037 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.3884C>A | p.Pro1295His | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4435/7764 | 3884/4299 | 1295/1432 | chr19 | 16807733 | |||
chr19:16807738 | G | A | 2 | a0029 a0043 |
2 | HG02818.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.3889G>A | p.Glu1297Lys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4440/7764 | 3889/4299 | 1297/1432 | chr19 | 16807738 | |||
chr19:16807782 | G | T | 1 | a0031 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.3933G>T | p.Glu1311Asp | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4484/7764 | 3933/4299 | 1311/1432 | chr19 | 16807782 | |||
chr19:16807957 | G | T | 1 | a0044 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.4108G>T | p.Asp1370Tyr | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4659/7764 | 4108/4299 | 1370/1432 | chr19 | 16807957 | |||
chr19:16808107 | C | T | 2 | a0029 a0043 |
2 | HG02818.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.4258C>T | p.Arg1420Cys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4809/7764 | 4258/4299 | 1420/1432 | chr19 | 16808107 | |||
chr19:16817953 | A | C | 2 | a0004 a0006 |
11 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(8): Show |
splice_region_variant | LOW | c.*2914A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | chr19 | 16817953 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:16749372 | C | T | 3 | a0029c0065 a0030c0066 a0043c0057 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.730C>T | p.Leu244Leu | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1281/7764 | 730/4299 | 244/1432 | chr19 | 16749372 | |||
chr19:16749383 | C | T | 1 | a0043c0057 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.741C>T | p.Ser247Ser | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1292/7764 | 741/4299 | 247/1432 | chr19 | 16749383 | |||
chr19:16749581 | C | T | 10 | a0004c0005 a0004c0017 a0006c0015 others(7): Show |
32 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(29): Show |
synonymous_variant | LOW | c.939C>T | p.Cys313Cys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1490/7764 | 939/4299 | 313/1432 | chr19 | 16749581 | |||
chr19:16749737 | G | A | 5 | a0004c0009 a0006c0014 a0010c0013 others(2): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
synonymous_variant | LOW | c.1095G>A | p.Lys365Lys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1646/7764 | 1095/4299 | 365/1432 | chr19 | 16749737 | |||
chr19:16749791 | T | C | 12 | a0007c0028 a0007c0029 a0007c0069 others(9): Show |
20 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(17): Show |
synonymous_variant | LOW | c.1149T>C | p.Arg383Arg | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1700/7764 | 1149/4299 | 383/1432 | chr19 | 16749791 | |||
chr19:16750130 | C | T | 1 | a0001c0047 | 1 | NA19068.hp2 | synonymous_variant | LOW | c.1488C>T | p.Ser496Ser | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 2039/7764 | 1488/4299 | 496/1432 | chr19 | 16750130 | |||
chr19:16759333 | C | T | 2 | a0002c0036 a0008c0012 |
6 | HG01891.hp1 HG02451.hp1 HG02922.hp2 others(3): Show |
synonymous_variant | LOW | c.1878C>T | p.Phe626Phe | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/19 | 2429/7764 | 1878/4299 | 626/1432 | chr19 | 16759333 | |||
chr19:16761983 | C | T | 2 | a0001c0046 a0003c0063 |
2 | HG00099.hp1 HG02602.hp2 |
synonymous_variant | LOW | c.1978C>T | p.Leu660Leu | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/19 | 2529/7764 | 1978/4299 | 660/1432 | chr19 | 16761983 | |||
chr19:16762129 | G | A | 44 | a0001c0007 a0001c0046 a0001c0047 others(41): Show |
117 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(114): Show |
synonymous_variant | LOW | c.2124G>A | p.Leu708Leu | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/19 | 2675/7764 | 2124/4299 | 708/1432 | chr19 | 16762129 | |||
chr19:16765183 | C | A | 1 | a0037c0058 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.2401C>A | p.Arg801Arg | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/19 | 2952/7764 | 2401/4299 | 801/1432 | chr19 | 16765183 | |||
chr19:16789118 | C | T | 2 | a0002c0023 a0014c0022 |
5 | HG01884.hp2 HG02723.hp2 HG03516.hp1 others(2): Show |
synonymous_variant | LOW | c.2868C>T | p.Pro956Pro | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/19 | 3419/7764 | 2868/4299 | 956/1432 | chr19 | 16789118 | |||
chr19:16797862 | G | A | 1 | a0002c0031 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.3435G>A | p.Thr1145Thr | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/19 | 3986/7764 | 3435/4299 | 1145/1432 | chr19 | 16797862 | |||
chr19:16807674 | G | A | 1 | a0003c0059 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.3825G>A | p.Val1275Val | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4376/7764 | 3825/4299 | 1275/1432 | chr19 | 16807674 | |||
chr19:16807734 | T | C | 1 | a0037c0058 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.3885T>C | p.Pro1295Pro | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4436/7764 | 3885/4299 | 1295/1432 | chr19 | 16807734 | |||
chr19:16807851 | G | A | 1 | a0002c0033 | 1 | NA18962.hp2 | synonymous_variant | LOW | c.4002G>A | p.Pro1334Pro | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4553/7764 | 4002/4299 | 1334/1432 | chr19 | 16807851 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:16719935 | C | T | 1 | a0001c0007t0049 | 1 | NA18747.hp2 | 5_prime_UTR_variant | MODIFIER | c.-463C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/19 | 11263 | chr19 | 16719935 | ||||||
chr19:16719936 | G | A | 1 | a0015c0054t0025 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-462G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/19 | 11262 | chr19 | 16719936 | ||||||
chr19:16719993 | C | T | 4 | a0004c0005t0048 a0009c0010t0047 a0013c0020t0016 others(1): Show |
5 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-405C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/19 | chr19 | 16719993 | |||||||
chr19:16720033 | C | T | 1 | a0002c0002t0012 | 4 | NA18945.hp1 NA18946.hp1 NA18952.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-365C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/19 | 11165 | chr19 | 16720033 | ||||||
chr19:16720144 | G | A | 4 | a0004c0005t0048 a0009c0010t0047 a0013c0020t0016 others(1): Show |
5 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-254G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/19 | 11054 | chr19 | 16720144 | ||||||
chr19:16720249 | C | T | 60 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0024 others(57): Show |
125 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(122): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-149C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/19 | chr19 | 16720249 | |||||||
chr19:16720250 | G | A | 1 | a0043c0057t0026 | 1 | NA20300.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-148G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/19 | chr19 | 16720250 | |||||||
chr19:16815101 | C | T | 1 | a0037c0058t0035 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*62C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 62 | chr19 | 16815101 | ||||||
chr19:16815256 | A | T | 17 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0021 others(14): Show |
53 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*217A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 217 | chr19 | 16815256 | ||||||
chr19:16815530 | C | A | 1 | a0037c0058t0035 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*491C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 491 | chr19 | 16815530 | ||||||
chr19:16815636 | C | T | 2 | a0029c0065t0032 a0043c0057t0026 |
2 | HG02818.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*597C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 597 | chr19 | 16815636 | ||||||
chr19:16815856 | G | A | 121 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(118): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*817G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 817 | chr19 | 16815856 | ||||||
chr19:16815930 | G | A | 1 | a0004c0009t0036 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*891G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 891 | chr19 | 16815930 | ||||||
chr19:16815936 | T | G | 3 | a0004c0005t0022 a0016c0019t0017 a0016c0019t0022 |
4 | HG02258.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*897T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 897 | chr19 | 16815936 | ||||||
chr19:16815946 | G | A | 1 | a0035c0055t0037 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*907G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 907 | chr19 | 16815946 | ||||||
chr19:16815947 | G | T | 3 | a0001c0001t0020 a0002c0002t0020 a0003c0003t0044 |
3 | HG01099.hp2 HG01192.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*908G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 908 | chr19 | 16815947 | ||||||
chr19:16815974 | C | T | 2 | a0007c0069t0043 a0009c0010t0010 |
5 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*935C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 935 | chr19 | 16815974 | ||||||
chr19:16816217 | C | T | 1 | a0007c0028t0034 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1178C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 1178 | chr19 | 16816217 | ||||||
chr19:16816407 | CA | C | 15 | a0004c0009t0008 a0004c0009t0009 a0004c0009t0013 others(12): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1369delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 1369 | chr19 | 16816407 | ||||||
chr19:16816620 | T | C | 1 | a0003c0006t0038 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1581T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 1581 | chr19 | 16816620 | ||||||
chr19:16816663 | T | C | 1 | a0037c0058t0035 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1624T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 1624 | chr19 | 16816663 | ||||||
chr19:16816684 | TC | T | 4 | a0004c0005t0029 a0024c0049t0042 a0029c0065t0032 others(1): Show |
4 | HG02055.hp1 HG02818.hp1 NA19043.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1646delC | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 1646 | chr19 | 16816684 | ||||||
chr19:16816720 | G | A | 4 | a0004c0005t0018 a0004c0005t0023 a0004c0005t0039 others(1): Show |
5 | HG01081.hp1 HG02258.hp1 HG03490.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1681G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 1681 | chr19 | 16816720 | ||||||
chr19:16816945 | A | G | 1 | a0003c0003t0046 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1906A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 1906 | chr19 | 16816945 | ||||||
chr19:16816984 | C | T | 15 | a0004c0009t0008 a0004c0009t0009 a0004c0009t0013 others(12): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1945C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 1945 | chr19 | 16816984 | ||||||
chr19:16817299 | CATA | C | 3 | a0004c0005t0022 a0016c0019t0017 a0016c0019t0022 |
4 | HG02258.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2275_*2277delAAT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2275 | INFO_REALIGN_3_PRIME | chr19 | 16817299 | |||||
chr19:16817329 | G | A | 3 | a0004c0005t0022 a0016c0019t0017 a0016c0019t0022 |
4 | HG02258.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2290G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2290 | chr19 | 16817329 | ||||||
chr19:16817334 | C | T | 1 | a0006c0015t0028 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2295C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2295 | chr19 | 16817334 | ||||||
chr19:16817341 | CTGTAATC others(22): Show |
C | 1 | a0001c0001t0033 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2303_*2331delTGTA others(25): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2303 | chr19 | 16817341 | ||||||
chr19:16817376 | G | A | 2 | a0007c0068t0040 a0015c0054t0025 |
2 | HG02896.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2337G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2337 | chr19 | 16817376 | ||||||
chr19:16817417 | A | G | 1 | a0028c0062t0030 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2378A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2378 | chr19 | 16817417 | ||||||
chr19:16817569 | T | C | 1 | a0001c0001t0031 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2530T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2530 | chr19 | 16817569 | ||||||
chr19:16817598 | C | CA | 14 | a0001c0001t0014 a0001c0001t0021 a0001c0001t0024 others(11): Show |
17 | HG00597.hp2 HG00733.hp2 HG01071.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2579dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2580 | INFO_REALIGN_3_PRIME | chr19 | 16817598 | |||||
chr19:16817598 | CA | C | 11 | a0001c0001t0020 a0002c0002t0011 a0002c0002t0020 others(8): Show |
13 | HG01081.hp1 HG01099.hp2 HG02015.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2579delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2579 | INFO_REALIGN_3_PRIME | chr19 | 16817598 | |||||
chr19:16817701 | G | T | 1 | a0008c0012t0019 | 2 | HG03225.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2662G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2662 | chr19 | 16817701 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:16720318 | AT | A | 5 | a0004c0005t0048g0002 a0009c0010t0047g0005 a0013c0020t0016g0003 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-105+26delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720318 | |||||||
chr19:16720324 | C | T | 5 | a0004c0005t0048g0002 a0009c0010t0047g0005 a0013c0020t0016g0003 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-105+31C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720324 | |||||||
chr19:16720444 | A | C | 5 | a0004c0005t0048g0002 a0009c0010t0047g0005 a0013c0020t0016g0003 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-105+151A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720444 | |||||||
chr19:16720490 | A | G | 4 | a0007c0029t0002g0297 a0007c0029t0002g0298 a0007c0069t0043g0299 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-105+197A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720490 | |||||||
chr19:16720567 | T | A | 126 | a0001c0001t0002g0021 a0001c0001t0002g0029 a0001c0001t0002g0043 others(123): Show |
126 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.-105+274T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720567 | |||||||
chr19:16720703 | C | T | 4 | a0003c0003t0002g0127 a0004c0009t0036g0126 a0004c0060t0002g0125 others(1): Show |
4 | HG01123.hp2 HG02886.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-105+410C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720703 | |||||||
chr19:16720734 | T | C | 1 | a0003c0006t0001g0128 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-105+441T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720734 | |||||||
chr19:16720845 | A | G | 136 | a0001c0001t0002g0021 a0001c0001t0002g0029 a0001c0001t0002g0043 others(133): Show |
136 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.-105+552A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720845 | |||||||
chr19:16720848 | T | C | 136 | a0001c0001t0002g0021 a0001c0001t0002g0029 a0001c0001t0002g0043 others(133): Show |
136 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.-105+555T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720848 | |||||||
chr19:16720878 | C | G | 1 | a0002c0002t0002g0123 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-105+585C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720878 | |||||||
chr19:16720903 | C | T | 1 | a0002c0002t0001g0291 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-105+610C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720903 | |||||||
chr19:16720904 | G | A | 1 | a0033c0048t0018g0129 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-105+611G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720904 | |||||||
chr19:16720914 | G | C | 1 | a0002c0002t0005g0130 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-105+621G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720914 | |||||||
chr19:16721069 | C | T | 87 | a0001c0001t0002g0043 a0001c0001t0004g0107 a0001c0001t0004g0109 others(84): Show |
87 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.-105+776C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16721069 | |||||||
chr19:16721094 | C | G | 4 | a0001c0007t0002g0122 a0005c0004t0002g0120 a0017c0021t0007g0119 others(1): Show |
4 | HG02132.hp2 NA18951.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.-105+801C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16721094 | |||||||
chr19:16721395 | C | G | 177 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(174): Show |
177 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(174): Show |
intron_variant | MODIFIER | c.-105+1102C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16721395 | |||||||
chr19:16721414 | C | T | 1 | a0006c0015t0006g0290 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-105+1121C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16721414 | |||||||
chr19:16721480 | G | C | 11 | a0004c0005t0022g0050 a0004c0009t0009g0047 a0004c0009t0009g0052 others(8): Show |
11 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-105+1187G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16721480 | |||||||
chr19:16721673 | G | C | 291 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0001c0001t0001g0158 others(288): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.-105+1380G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16721673 | |||||||
chr19:16721892 | C | T | 1 | a0002c0002t0007g0041 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-105+1599C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16721892 | |||||||
chr19:16721915 | A | G | 1 | a0009c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-105+1622A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16721915 | |||||||
chr19:16722114 | T | C | 132 | a0001c0001t0002g0021 a0001c0001t0002g0029 a0001c0001t0004g0032 others(129): Show |
132 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-105+1821T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722114 | |||||||
chr19:16722115 | GAAA | G | 132 | a0001c0001t0002g0021 a0001c0001t0002g0029 a0001c0001t0004g0032 others(129): Show |
132 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-105+1827_-105+182 others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr19 | 16722115 | ||||||
chr19:16722120 | A | C | 3 | a0001c0001t0003g0237 a0001c0001t0014g0238 a0001c0001t0020g0289 |
3 | HG01433.hp2 HG02148.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-105+1827A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722120 | |||||||
chr19:16722123 | C | A | 17 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(14): Show |
17 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.-105+1830C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722123 | |||||||
chr19:16722170 | T | C | 1 | a0010c0013t0009g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-105+1877T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722170 | |||||||
chr19:16722205 | G | A | 11 | a0004c0005t0022g0050 a0004c0009t0009g0047 a0004c0009t0009g0052 others(8): Show |
11 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-105+1912G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722205 | |||||||
chr19:16722251 | A | G | 4 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(1): Show |
4 | HG01167.hp1 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-105+1958A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722251 | |||||||
chr19:16722255 | T | C | 4 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(1): Show |
4 | HG01167.hp1 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-105+1962T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722255 | |||||||
chr19:16722256 | G | A | 4 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(1): Show |
4 | HG01167.hp1 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-105+1963G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722256 | |||||||
chr19:16722260 | C | T | 8 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
8 | HG01167.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-105+1967C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722260 | |||||||
chr19:16722271 | C | G | 1 | a0001c0001t0003g0236 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-105+1978C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722271 | |||||||
chr19:16722310 | A | G | 4 | a0003c0003t0002g0117 a0007c0028t0002g0115 a0007c0068t0040g0116 others(1): Show |
4 | HG02895.hp2 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-105+2017A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722310 | |||||||
chr19:16722490 | T | C | 58 | a0001c0007t0002g0057 a0001c0007t0002g0122 a0002c0002t0002g0063 others(55): Show |
58 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-104-1876T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722490 | |||||||
chr19:16722531 | C | T | 1 | a0004c0005t0048g0002 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-104-1835C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722531 | |||||||
chr19:16722591 | C | T | 1 | a0010c0013t0009g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-104-1775C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722591 | |||||||
chr19:16722647 | A | G | 1 | a0007c0069t0043g0299 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-104-1719A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722647 | |||||||
chr19:16722935 | G | C | 1 | a0001c0001t0001g0263 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-104-1431G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722935 | |||||||
chr19:16723128 | C | T | 1 | a0003c0059t0015g0037 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-104-1238C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723128 | |||||||
chr19:16723129 | G | A | 12 | a0003c0003t0002g0117 a0004c0005t0022g0050 a0004c0009t0009g0047 others(9): Show |
12 | HG02258.hp2 HG02280.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-104-1237G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723129 | |||||||
chr19:16723181 | G | A | 1 | a0039c0039t0015g0055 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-104-1185G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723181 | |||||||
chr19:16723230 | G | A | 1 | a0006c0015t0006g0290 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-104-1136G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723230 | |||||||
chr19:16723261 | C | T | 1 | a0004c0060t0002g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-104-1105C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723261 | |||||||
chr19:16723423 | C | A | 1 | a0005c0016t0002g0056 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-104-943C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723423 | |||||||
chr19:16723423 | C | G | 3 | a0004c0005t0001g0296 a0004c0017t0002g0038 a0016c0019t0022g0124 |
3 | HG02280.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-104-943C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723423 | |||||||
chr19:16723521 | C | T | 8 | a0004c0005t0022g0050 a0004c0009t0009g0047 a0004c0009t0009g0052 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-104-845C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723521 | |||||||
chr19:16723626 | A | C | 125 | a0001c0001t0001g0263 a0001c0001t0002g0021 a0001c0001t0002g0029 others(122): Show |
125 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.-104-740A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723626 | |||||||
chr19:16723676 | C | CTGTTT | 17 | a0001c0001t0005g0246 a0001c0001t0014g0238 a0003c0003t0002g0127 others(14): Show |
17 | HG01109.hp2 HG01123.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.-104-652_-104-648d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr19 | 16723676 | ||||||
chr19:16723676 | C | CTGTTTTG others(3): Show |
1 | a0021c0041t0002g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-104-657_-104-648d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr19 | 16723676 | ||||||
chr19:16723676 | CTGTTT | C | 97 | a0001c0001t0001g0136 a0001c0001t0001g0263 a0001c0001t0002g0021 others(94): Show |
97 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.-104-652_-104-648d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr19 | 16723676 | ||||||
chr19:16723676 | CTGTTTTG others(3): Show |
C | 19 | a0003c0003t0002g0117 a0004c0005t0001g0296 a0004c0005t0022g0050 others(16): Show |
19 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(16): Show |
intron_variant | MODIFIER | c.-104-657_-104-648d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr19 | 16723676 | ||||||
chr19:16723676 | CTGTTTTG others(8): Show |
C | 2 | a0004c0017t0002g0038 a0015c0054t0025g0118 |
2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-104-662_-104-648d others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr19 | 16723676 | ||||||
chr19:16723730 | C | T | 8 | a0004c0005t0006g0225 a0004c0005t0006g0226 a0004c0005t0006g0227 others(5): Show |
8 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-104-636C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723730 | |||||||
chr19:16723913 | C | G | 2 | a0002c0002t0005g0130 a0023c0038t0001g0223 |
2 | HG02027.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-104-453C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723913 | |||||||
chr19:16723943 | G | A | 59 | a0001c0007t0002g0057 a0001c0007t0002g0122 a0002c0002t0002g0063 others(56): Show |
59 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-104-423G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723943 | |||||||
chr19:16724089 | T | C | 1 | a0002c0002t0001g0142 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-104-277T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16724089 | |||||||
chr19:16724470 | G | A | 1 | a0012c0018t0005g0240 | 1 | NA18954.hp1 | splice_region_variant&intron_variant | LOW | c.-7+7G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16724470 | |||||||
chr19:16724660 | T | A | 2 | a0004c0005t0029g0265 a0030c0066t0008g0264 |
2 | HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-7+197T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16724660 | |||||||
chr19:16724751 | T | C | 8 | a0004c0005t0022g0050 a0004c0009t0009g0047 a0004c0009t0009g0052 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7+288T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16724751 | |||||||
chr19:16724880 | G | T | 1 | a0007c0028t0034g0258 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7+417G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16724880 | |||||||
chr19:16725007 | TA | T | 94 | a0001c0001t0001g0263 a0001c0001t0004g0032 a0001c0001t0004g0034 others(91): Show |
94 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.-7+545delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725007 | |||||||
chr19:16725008 | AT | A | 27 | a0001c0001t0002g0021 a0001c0001t0002g0029 a0002c0002t0020g0249 others(24): Show |
27 | HG00280.hp1 HG01099.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.-7+551delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16725008 | ||||||
chr19:16725050 | C | T | 1 | a0001c0007t0001g0221 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-7+587C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725050 | |||||||
chr19:16725133 | C | T | 1 | a0001c0001t0003g0220 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-7+670C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725133 | |||||||
chr19:16725158 | C | T | 1 | a0001c0046t0001g0219 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-7+695C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725158 | |||||||
chr19:16725326 | T | A | 1 | a0005c0016t0002g0058 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-7+863T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725326 | |||||||
chr19:16725386 | G | A | 1 | a0003c0003t0003g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-7+923G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725386 | |||||||
chr19:16725536 | A | G | 2 | a0003c0003t0002g0127 a0004c0009t0036g0126 |
2 | HG01123.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-7+1073A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725536 | |||||||
chr19:16725577 | G | A | 5 | a0004c0009t0009g0047 a0004c0009t0009g0052 a0014c0022t0002g0046 others(2): Show |
5 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+1114G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725577 | |||||||
chr19:16725651 | C | G | 1 | a0002c0002t0005g0130 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-7+1188C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725651 | |||||||
chr19:16725656 | G | A | 4 | a0003c0003t0002g0117 a0007c0028t0002g0115 a0007c0068t0040g0116 others(1): Show |
4 | HG02895.hp2 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+1193G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725656 | |||||||
chr19:16725755 | G | T | 21 | a0001c0001t0002g0021 a0001c0001t0002g0029 a0002c0002t0020g0249 others(18): Show |
21 | HG00280.hp1 HG01099.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+1292G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725755 | |||||||
chr19:16725834 | C | T | 21 | a0001c0001t0001g0263 a0001c0001t0004g0032 a0001c0001t0004g0034 others(18): Show |
21 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+1371C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725834 | |||||||
chr19:16725919 | A | T | 1 | a0001c0001t0002g0029 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-7+1456A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725919 | |||||||
chr19:16725945 | GT | G | 113 | a0001c0001t0001g0263 a0001c0001t0002g0021 a0001c0001t0002g0029 others(110): Show |
113 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.-7+1492delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16725945 | ||||||
chr19:16725960 | G | GT | 7 | a0001c0001t0003g0215 a0001c0001t0031g0214 a0001c0001t0033g0216 others(4): Show |
7 | HG01257.hp2 HG02056.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+1506dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16725960 | ||||||
chr19:16725961 | T | G | 1 | a0010c0013t0009g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-7+1498T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725961 | |||||||
chr19:16725964 | T | G | 8 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
8 | HG01109.hp2 HG01167.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+1501T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725964 | |||||||
chr19:16725970 | G | T | 1 | a0004c0017t0002g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-7+1507G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725970 | |||||||
chr19:16725971 | C | G | 1 | a0004c0017t0002g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-7+1508C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725971 | |||||||
chr19:16725971 | CT | C | 90 | a0001c0001t0004g0032 a0001c0001t0004g0034 a0001c0001t0004g0035 others(87): Show |
90 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.-7+1517delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16725971 | ||||||
chr19:16725972 | T | C | 1 | a0004c0017t0002g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-7+1509T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725972 | |||||||
chr19:16726050 | C | T | 3 | a0006c0014t0008g0253 a0006c0044t0001g0255 a0038c0052t0001g0254 |
3 | HG02965.hp2 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-7+1587C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16726050 | |||||||
chr19:16726081 | G | A | 3 | a0004c0005t0018g0256 a0007c0028t0034g0258 a0025c0045t0016g0001 |
3 | HG02109.hp2 HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-7+1618G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16726081 | |||||||
chr19:16726086 | C | T | 1 | a0015c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7+1623C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16726086 | |||||||
chr19:16726326 | G | A | 1 | a0005c0004t0002g0059 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-7+1863G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16726326 | |||||||
chr19:16726518 | C | T | 4 | a0007c0029t0002g0297 a0007c0029t0002g0298 a0007c0069t0043g0299 others(1): Show |
4 | HG01361.hp1 HG01891.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+2055C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16726518 | |||||||
chr19:16726522 | C | T | 1 | a0011c0011t0011g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-7+2059C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16726522 | |||||||
chr19:16726588 | C | T | 58 | a0001c0007t0002g0122 a0002c0002t0002g0063 a0002c0002t0002g0123 others(55): Show |
58 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-7+2125C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16726588 | |||||||
chr19:16726691 | G | C | 1 | a0015c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7+2228G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16726691 | |||||||
chr19:16727008 | T | C | 4 | a0003c0003t0002g0117 a0007c0028t0002g0115 a0007c0068t0040g0116 others(1): Show |
4 | HG02895.hp2 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+2545T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727008 | |||||||
chr19:16727016 | G | A | 1 | a0002c0036t0002g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-7+2553G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727016 | |||||||
chr19:16727078 | A | G | 3 | a0004c0005t0001g0296 a0004c0017t0002g0038 a0016c0019t0022g0124 |
3 | HG02280.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-7+2615A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727078 | |||||||
chr19:16727112 | C | T | 3 | a0003c0003t0001g0210 a0004c0005t0006g0211 a0004c0017t0001g0212 |
3 | HG02257.hp1 HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-7+2649C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727112 | |||||||
chr19:16727132 | A | G | 58 | a0001c0007t0002g0122 a0002c0002t0002g0063 a0002c0002t0002g0123 others(55): Show |
58 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-7+2669A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727132 | |||||||
chr19:16727240 | G | A | 1 | a0003c0003t0002g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-7+2777G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727240 | |||||||
chr19:16727252 | G | C | 4 | a0003c0003t0002g0117 a0007c0028t0002g0115 a0007c0068t0040g0116 others(1): Show |
4 | HG02895.hp2 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+2789G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727252 | |||||||
chr19:16727441 | G | A | 5 | a0004c0009t0009g0047 a0004c0009t0009g0052 a0014c0022t0002g0046 others(2): Show |
5 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+2978G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727441 | |||||||
chr19:16727526 | G | T | 20 | a0001c0001t0004g0032 a0001c0001t0004g0034 a0001c0001t0004g0035 others(17): Show |
20 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-7+3063G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727526 | |||||||
chr19:16727551 | C | T | 1 | a0040c0037t0001g0209 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-7+3088C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727551 | |||||||
chr19:16727562 | G | A | 1 | a0001c0001t0002g0029 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-7+3099G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727562 | |||||||
chr19:16727592 | C | G | 5 | a0004c0009t0009g0047 a0004c0009t0009g0052 a0014c0022t0002g0046 others(2): Show |
5 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+3129C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727592 | |||||||
chr19:16727649 | A | G | 2 | a0002c0002t0001g0207 a0002c0002t0001g0208 |
2 | HG00673.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.-7+3186A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727649 | |||||||
chr19:16727681 | G | T | 3 | a0003c0003t0002g0117 a0007c0028t0002g0115 a0007c0068t0040g0116 |
3 | HG02895.hp2 HG02896.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-7+3218G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727681 | |||||||
chr19:16727689 | T | G | 1 | a0005c0004t0003g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-7+3226T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727689 | |||||||
chr19:16727698 | G | A | 8 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
8 | HG01109.hp2 HG01167.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+3235G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727698 | |||||||
chr19:16727776 | G | A | 29 | a0001c0001t0001g0147 a0001c0001t0001g0158 a0001c0001t0001g0160 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.-7+3313G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727776 | |||||||
chr19:16727789 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-7+3326T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727789 | |||||||
chr19:16727831 | C | T | 20 | a0001c0001t0004g0032 a0001c0001t0004g0034 a0001c0001t0004g0035 others(17): Show |
20 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-6-3361C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727831 | |||||||
chr19:16727951 | A | G | 1 | a0002c0002t0001g0165 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-6-3241A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727951 | |||||||
chr19:16727994 | G | A | 4 | a0004c0017t0002g0018 a0004c0017t0002g0019 a0029c0065t0032g0166 others(1): Show |
4 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-3198G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727994 | |||||||
chr19:16728106 | T | C | 12 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(9): Show |
12 | HG01109.hp2 HG01167.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6-3086T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728106 | |||||||
chr19:16728219 | C | T | 1 | a0024c0049t0042g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-6-2973C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728219 | |||||||
chr19:16728220 | G | A | 1 | a0015c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-6-2972G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728220 | |||||||
chr19:16728281 | C | CT | 75 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(72): Show |
75 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.-6-2892dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16728281 | ||||||
chr19:16728281 | CT | C | 80 | a0001c0001t0002g0021 a0001c0001t0002g0029 a0001c0007t0001g0213 others(77): Show |
80 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-6-2892delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16728281 | ||||||
chr19:16728324 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-6-2868G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728324 | |||||||
chr19:16728631 | C | T | 6 | a0004c0009t0009g0047 a0004c0009t0009g0052 a0009c0010t0002g0114 others(3): Show |
6 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-2561C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728631 | |||||||
chr19:16728710 | C | T | 1 | a0009c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-6-2482C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728710 | |||||||
chr19:16728719 | C | A | 1 | a0002c0008t0001g0168 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-6-2473C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728719 | |||||||
chr19:16728726 | C | T | 3 | a0013c0020t0008g0257 a0013c0020t0016g0003 a0013c0020t0016g0004 |
3 | HG01070.hp1 HG01071.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-6-2466C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728726 | |||||||
chr19:16728747 | A | C | 1 | a0002c0002t0001g0201 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-6-2445A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728747 | |||||||
chr19:16728817 | G | A | 4 | a0004c0005t0022g0050 a0015c0025t0002g0048 a0015c0025t0002g0049 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-2375G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728817 | |||||||
chr19:16728851 | A | G | 2 | a0002c0002t0001g0199 a0002c0002t0003g0200 |
2 | HG01934.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-6-2341A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728851 | |||||||
chr19:16728931 | A | G | 1 | a0003c0006t0002g0096 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-6-2261A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728931 | |||||||
chr19:16728943 | CA | C | 69 | a0001c0001t0004g0034 a0001c0001t0004g0035 a0001c0001t0004g0112 others(66): Show |
69 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.-6-2228delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16728943 | ||||||
chr19:16728943 | CAA | C | 92 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(89): Show |
92 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.-6-2229_-6-2228del others(2): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16728943 | ||||||
chr19:16728943 | CAAA | C | 8 | a0004c0005t0022g0050 a0004c0005t0023g0094 a0004c0005t0023g0095 others(5): Show |
8 | HG01074.hp1 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6-2230_-6-2228del others(3): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16728943 | ||||||
chr19:16728960 | A | T | 21 | a0001c0001t0001g0263 a0001c0001t0002g0021 a0001c0001t0002g0029 others(18): Show |
21 | HG01099.hp2 HG01175.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6-2232A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728960 | |||||||
chr19:16728961 | A | T | 2 | a0009c0010t0047g0005 a0015c0054t0025g0118 |
2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-6-2231A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728961 | |||||||
chr19:16728963 | AAT | A | 6 | a0004c0005t0006g0225 a0004c0009t0009g0047 a0014c0022t0002g0046 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-2227_-6-2226del others(2): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16728963 | ||||||
chr19:16728965 | T | A | 1 | a0002c0002t0002g0008 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-6-2227T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728965 | |||||||
chr19:16729405 | C | G | 1 | a0002c0002t0005g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-6-1787C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16729405 | |||||||
chr19:16729545 | G | A | 2 | a0004c0060t0002g0125 a0009c0010t0047g0005 |
2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-6-1647G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16729545 | |||||||
chr19:16729577 | T | TAAAAAAA others(6): Show |
3 | a0006c0015t0006g0293 a0016c0019t0017g0294 a0016c0019t0017g0295 |
3 | HG02723.hp1 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-6-1611_-6-1599dup others(13): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16729577 | ||||||
chr19:16729577 | T | TAAAAAAA others(7): Show |
8 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
8 | HG01167.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6-1612_-6-1599dup others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16729577 | ||||||
chr19:16729577 | T | TAAAAAAA others(8): Show |
7 | a0006c0014t0002g0015 a0006c0014t0009g0014 a0006c0015t0006g0290 others(4): Show |
7 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-1613_-6-1599dup others(15): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16729577 | ||||||
chr19:16729577 | TA | T | 11 | a0002c0002t0012g0198 a0002c0002t0012g0203 a0004c0005t0006g0225 others(8): Show |
11 | HG02615.hp2 HG02723.hp2 HG03130.hp2 others(8): Show |
intron_variant | MODIFIER | c.-6-1599delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16729577 | ||||||
chr19:16729627 | C | T | 1 | a0005c0004t0002g0093 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-6-1565C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16729627 | |||||||
chr19:16729644 | G | A | 1 | a0002c0002t0001g0199 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-6-1548G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16729644 | |||||||
chr19:16729790 | A | G | 1 | a0002c0002t0002g0013 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-6-1402A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16729790 | |||||||
chr19:16729905 | A | AGAAG | 23 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(20): Show |
23 | HG01109.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-6-1263_-6-1260dup others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16729905 | ||||||
chr19:16729905 | AGAAG | A | 10 | a0002c0002t0020g0249 a0006c0014t0008g0253 a0006c0044t0001g0255 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.-6-1263_-6-1260del others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16729905 | ||||||
chr19:16729959 | C | T | 1 | a0003c0003t0003g0288 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-6-1233C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16729959 | |||||||
chr19:16730040 | T | C | 3 | a0007c0029t0002g0297 a0007c0029t0002g0298 a0007c0069t0043g0299 |
3 | HG01891.hp2 HG02257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-6-1152T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730040 | |||||||
chr19:16730045 | C | T | 1 | a0004c0005t0048g0002 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-6-1147C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730045 | |||||||
chr19:16730050 | G | A | 1 | a0001c0001t0005g0169 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-6-1142G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730050 | |||||||
chr19:16730061 | C | T | 1 | a0004c0005t0048g0002 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-6-1131C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730061 | |||||||
chr19:16730138 | A | G | 2 | a0004c0005t0018g0256 a0004c0009t0008g0286 |
2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-6-1054A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730138 | |||||||
chr19:16730253 | C | A | 1 | a0004c0005t0048g0002 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-6-939C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730253 | |||||||
chr19:16730254 | A | G | 61 | a0002c0002t0020g0249 a0003c0003t0001g0210 a0003c0003t0002g0127 others(58): Show |
61 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.-6-938A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730254 | |||||||
chr19:16730305 | A | C | 1 | a0002c0002t0004g0033 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-6-887A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730305 | |||||||
chr19:16730461 | C | T | 2 | a0004c0060t0002g0125 a0009c0010t0047g0005 |
2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-6-731C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730461 | |||||||
chr19:16730515 | G | A | 26 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(23): Show |
26 | HG01109.hp2 HG01167.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.-6-677G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730515 | |||||||
chr19:16730568 | A | G | 157 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(154): Show |
157 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.-6-624A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730568 | |||||||
chr19:16730674 | ACCACTGC | A | 5 | a0002c0036t0002g0020 a0011c0011t0002g0022 a0011c0011t0011g0024 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-515_-6-509delAC others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16730674 | ||||||
chr19:16730732 | T | A | 1 | a0045c0051t0002g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-6-460T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730732 | |||||||
chr19:16730733 | A | T | 61 | a0003c0003t0002g0006 a0003c0003t0002g0060 a0003c0003t0002g0065 others(58): Show |
61 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.-6-459A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730733 | |||||||
chr19:16730911 | C | CT | 125 | a0001c0001t0004g0032 a0001c0001t0004g0034 a0001c0001t0004g0035 others(122): Show |
125 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.-6-264dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16730911 | ||||||
chr19:16730911 | CT | C | 16 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(13): Show |
16 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-6-264delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16730911 | ||||||
chr19:16730914 | T | TC | 3 | a0004c0005t0006g0225 a0009c0010t0010g0131 a0028c0062t0030g0250 |
3 | HG02615.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-6-278_-6-277insC | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730914 | |||||||
chr19:16730981 | C | T | 2 | a0003c0006t0002g0092 a0005c0016t0002g0058 |
2 | HG04115.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-6-211C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730981 | |||||||
chr19:16731020 | A | G | 68 | a0003c0003t0001g0210 a0003c0003t0002g0117 a0003c0003t0002g0127 others(65): Show |
68 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.-6-172A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16731020 | |||||||
chr19:16731296 | C | T | 1 | a0016c0019t0022g0124 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.81+18C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731296 | |||||||
chr19:16731299 | G | C | 7 | a0004c0005t0006g0225 a0004c0009t0009g0047 a0009c0010t0010g0131 others(4): Show |
7 | HG02615.hp2 HG02723.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+21G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731299 | |||||||
chr19:16731314 | T | A | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.81+36T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731314 | |||||||
chr19:16731410 | G | A | 26 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(23): Show |
26 | HG01099.hp2 HG01109.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.81+132G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731410 | |||||||
chr19:16731414 | C | T | 1 | a0044c0061t0003g0285 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.81+136C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731414 | |||||||
chr19:16731440 | G | A | 61 | a0003c0003t0002g0006 a0003c0003t0002g0060 a0003c0003t0002g0065 others(58): Show |
61 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.81+162G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731440 | |||||||
chr19:16731451 | C | T | 130 | a0003c0003t0001g0210 a0003c0003t0002g0006 a0003c0003t0002g0060 others(127): Show |
130 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.81+173C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731451 | |||||||
chr19:16731556 | C | T | 61 | a0003c0003t0002g0006 a0003c0003t0002g0060 a0003c0003t0002g0065 others(58): Show |
61 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.81+278C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731556 | |||||||
chr19:16731568 | A | G | 130 | a0003c0003t0001g0210 a0003c0003t0002g0006 a0003c0003t0002g0060 others(127): Show |
130 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.81+290A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731568 | |||||||
chr19:16731601 | A | G | 131 | a0003c0003t0001g0210 a0003c0003t0002g0006 a0003c0003t0002g0060 others(128): Show |
131 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.81+323A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731601 | |||||||
chr19:16731610 | C | CTT | 63 | a0003c0003t0002g0006 a0003c0003t0002g0060 a0003c0003t0002g0065 others(60): Show |
63 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.81+343_81+344dupTT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16731610 | ||||||
chr19:16731610 | C | CTTT | 60 | a0003c0003t0001g0210 a0003c0003t0002g0127 a0003c0003t0003g0143 others(57): Show |
60 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.81+342_81+344dupTT others(1): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16731610 | ||||||
chr19:16731610 | C | CTTTT | 7 | a0003c0003t0002g0117 a0007c0028t0002g0115 a0007c0028t0034g0258 others(4): Show |
7 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+341_81+344dupTT others(2): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16731610 | ||||||
chr19:16731636 | G | A | 1 | a0045c0051t0002g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.81+358G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731636 | |||||||
chr19:16731666 | G | A | 16 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(13): Show |
16 | HG01109.hp2 HG01167.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+388G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731666 | |||||||
chr19:16731689 | T | C | 131 | a0003c0003t0001g0210 a0003c0003t0002g0006 a0003c0003t0002g0060 others(128): Show |
131 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.81+411T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731689 | |||||||
chr19:16731715 | T | C | 130 | a0003c0003t0001g0210 a0003c0003t0002g0006 a0003c0003t0002g0060 others(127): Show |
130 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.81+437T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731715 | |||||||
chr19:16731717 | G | A | 1 | a0021c0041t0002g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.81+439G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731717 | |||||||
chr19:16731754 | G | A | 130 | a0003c0003t0001g0210 a0003c0003t0002g0006 a0003c0003t0002g0060 others(127): Show |
130 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.81+476G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731754 | |||||||
chr19:16731767 | T | G | 130 | a0003c0003t0001g0210 a0003c0003t0002g0006 a0003c0003t0002g0060 others(127): Show |
130 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.81+489T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731767 | |||||||
chr19:16731854 | C | T | 130 | a0003c0003t0001g0210 a0003c0003t0002g0006 a0003c0003t0002g0060 others(127): Show |
130 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.81+576C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731854 | |||||||
chr19:16731929 | A | G | 60 | a0003c0003t0002g0006 a0003c0003t0002g0060 a0003c0003t0002g0065 others(57): Show |
60 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.81+651A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731929 | |||||||
chr19:16732078 | G | A | 2 | a0001c0007t0002g0007 a0001c0007t0002g0057 |
2 | NA19070.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.81+800G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732078 | |||||||
chr19:16732100 | C | G | 1 | a0002c0002t0002g0031 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.81+822C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732100 | |||||||
chr19:16732216 | C | CA | 6 | a0001c0001t0001g0171 a0001c0001t0002g0043 a0001c0001t0005g0241 others(3): Show |
6 | HG01175.hp2 HG01361.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+956dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732216 | ||||||
chr19:16732216 | CAA | C | 78 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(75): Show |
78 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.81+955_81+956delAA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732216 | ||||||
chr19:16732216 | CAAA | C | 68 | a0003c0003t0001g0210 a0003c0003t0002g0117 a0003c0003t0002g0127 others(65): Show |
68 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.81+954_81+956delAA others(1): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732216 | ||||||
chr19:16732351 | G | C | 2 | a0006c0015t0028g0204 a0045c0051t0002g0028 |
2 | HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.81+1073G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732351 | |||||||
chr19:16732397 | G | C | 1 | a0002c0002t0001g0146 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.81+1119G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732397 | |||||||
chr19:16732433 | C | T | 151 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(148): Show |
151 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.81+1155C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732433 | |||||||
chr19:16732438 | T | C | 1 | a0011c0011t0002g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.81+1160T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732438 | |||||||
chr19:16732516 | G | A | 2 | a0004c0060t0002g0125 a0009c0010t0047g0005 |
2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.81+1238G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732516 | |||||||
chr19:16732568 | C | G | 143 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.81+1290C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732568 | |||||||
chr19:16732598 | A | ATTTT | 13 | a0001c0001t0001g0260 a0003c0003t0003g0143 a0003c0003t0007g0064 others(10): Show |
13 | HG01884.hp2 HG02055.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.81+1320_81+1321ins others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732598 | |||||||
chr19:16732598 | A | ATTTTT | 94 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0004g0032 others(91): Show |
94 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.81+1320_81+1321ins others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732598 | |||||||
chr19:16732598 | A | ATTTTTT | 32 | a0003c0003t0002g0089 a0003c0003t0002g0091 a0003c0003t0002g0127 others(29): Show |
32 | HG01123.hp2 HG01175.hp1 HG01516.hp1 others(29): Show |
intron_variant | MODIFIER | c.81+1320_81+1321ins others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732598 | |||||||
chr19:16732598 | A | ATTTTTTT | 4 | a0004c0005t0006g0230 a0004c0005t0018g0256 a0004c0009t0009g0047 others(1): Show |
4 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+1320_81+1321ins others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732598 | |||||||
chr19:16732599 | A | AT | 10 | a0001c0001t0004g0111 a0002c0002t0001g0201 a0003c0003t0002g0117 others(7): Show |
10 | HG01192.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+1336dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732599 | ||||||
chr19:16732599 | A | T | 143 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.81+1321A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732599 | |||||||
chr19:16732654 | C | CAAAAA | 8 | a0003c0003t0002g0085 a0003c0003t0004g0026 a0003c0003t0024g0087 others(5): Show |
8 | HG00733.hp1 HG01099.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+1387_81+1391dup others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | ||||||
chr19:16732654 | C | CAAAAAA | 46 | a0001c0001t0004g0032 a0001c0001t0004g0034 a0001c0001t0004g0035 others(43): Show |
46 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.81+1386_81+1391dup others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | ||||||
chr19:16732654 | C | CAAAAAAA | 24 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(21): Show |
24 | HG00323.hp1 HG01167.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+1385_81+1391dup others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | ||||||
chr19:16732654 | C | CAAAAAAA others(1): Show |
40 | a0003c0003t0003g0143 a0003c0006t0001g0281 a0003c0006t0001g0282 others(37): Show |
40 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.81+1384_81+1391dup others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | ||||||
chr19:16732654 | C | CAAAAAAA others(2): Show |
12 | a0003c0003t0003g0288 a0004c0005t0006g0226 a0004c0005t0006g0227 others(9): Show |
12 | HG00280.hp1 HG00639.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+1383_81+1391dup others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | ||||||
chr19:16732654 | C | CAAAAAAA others(3): Show |
2 | a0003c0003t0001g0210 a0003c0003t0002g0127 |
2 | HG01123.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.81+1382_81+1391dup others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | ||||||
chr19:16732654 | C | CAAAAAAA others(5): Show |
1 | a0028c0062t0030g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81+1380_81+1391dup others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | ||||||
chr19:16732654 | C | CAAAAAAA others(6): Show |
3 | a0004c0005t0006g0225 a0014c0022t0002g0051 a0036c0064t0002g0300 |
3 | HG02723.hp2 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.81+1379_81+1391dup others(13): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | ||||||
chr19:16732654 | C | CAAAAAAA others(7): Show |
2 | a0004c0009t0009g0047 a0009c0010t0010g0131 |
2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.81+1378_81+1391dup others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | ||||||
chr19:16732654 | C | CAAAAAAA others(8): Show |
1 | a0014c0022t0002g0046 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.81+1377_81+1391dup others(15): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | ||||||
chr19:16732658 | A | AAAAAAAA others(6): Show |
3 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0006c0015t0028g0204 |
3 | HG01099.hp2 HG01884.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.81+1391_81+1392ins others(13): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732658 | ||||||
chr19:16732658 | A | AAAAAAAA others(5): Show |
13 | a0003c0003t0002g0117 a0006c0014t0008g0253 a0006c0044t0001g0255 others(10): Show |
13 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.81+1386_81+1397dup others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732658 | ||||||
chr19:16732658 | A | AAAAAAAA others(4): Show |
1 | a0027c0053t0001g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.81+1390_81+1391ins others(11): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732658 | ||||||
chr19:16732670 | G | A | 143 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.81+1392G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732670 | |||||||
chr19:16732673 | A | AAAAAAAA others(6): Show |
1 | a0004c0005t0001g0296 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.81+1397_81+1398ins others(13): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732673 | ||||||
chr19:16732676 | G | A | 60 | a0003c0003t0001g0210 a0003c0003t0002g0127 a0003c0003t0003g0143 others(57): Show |
60 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.81+1398G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732676 | |||||||
chr19:16732677 | T | A | 143 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.81+1399T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732677 | |||||||
chr19:16732716 | C | A | 2 | a0010c0013t0013g0172 a0010c0013t0013g0173 |
2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.81+1438C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732716 | |||||||
chr19:16732722 | G | C | 150 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(147): Show |
150 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.81+1444G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732722 | |||||||
chr19:16732743 | T | C | 2 | a0004c0060t0002g0125 a0009c0010t0047g0005 |
2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.81+1465T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732743 | |||||||
chr19:16732787 | G | A | 1 | a0003c0003t0044g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.81+1509G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732787 | |||||||
chr19:16732847 | C | T | 10 | a0001c0001t0001g0263 a0001c0001t0002g0021 a0001c0001t0002g0029 others(7): Show |
10 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.81+1569C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732847 | |||||||
chr19:16732876 | G | C | 160 | a0001c0001t0001g0147 a0001c0001t0001g0260 a0001c0001t0001g0261 others(157): Show |
160 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.81+1598G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732876 | |||||||
chr19:16732890 | G | A | 143 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(140): Show |
143 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.81+1612G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732890 | |||||||
chr19:16732902 | GA | G | 7 | a0003c0003t0002g0117 a0007c0028t0002g0115 a0007c0028t0034g0258 others(4): Show |
7 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+1625delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732902 | |||||||
chr19:16733002 | G | A | 4 | a0003c0003t0002g0065 a0003c0003t0005g0141 a0003c0003t0007g0064 others(1): Show |
4 | HG02074.hp2 HG04184.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+1724G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733002 | |||||||
chr19:16733026 | G | A | 141 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(138): Show |
141 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.81+1748G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733026 | |||||||
chr19:16733046 | A | G | 53 | a0003c0003t0001g0210 a0003c0003t0002g0127 a0003c0003t0003g0143 others(50): Show |
53 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.81+1768A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733046 | |||||||
chr19:16733051 | G | A | 64 | a0001c0001t0004g0032 a0001c0001t0004g0034 a0001c0001t0004g0035 others(61): Show |
64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.81+1773G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733051 | |||||||
chr19:16733146 | A | C | 53 | a0003c0003t0001g0210 a0003c0003t0002g0127 a0003c0003t0003g0143 others(50): Show |
53 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.81+1868A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733146 | |||||||
chr19:16733156 | G | A | 60 | a0003c0003t0001g0210 a0003c0003t0002g0127 a0003c0003t0003g0143 others(57): Show |
60 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.81+1878G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733156 | |||||||
chr19:16733191 | A | C | 144 | a0001c0001t0001g0164 a0001c0001t0001g0260 a0001c0001t0001g0261 others(141): Show |
144 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.81+1913A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733191 | |||||||
chr19:16733192 | G | A | 144 | a0001c0001t0001g0164 a0001c0001t0001g0260 a0001c0001t0001g0261 others(141): Show |
144 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.81+1914G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733192 | |||||||
chr19:16733280 | G | A | 53 | a0003c0003t0001g0210 a0003c0003t0002g0127 a0003c0003t0003g0143 others(50): Show |
53 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.81+2002G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733280 | |||||||
chr19:16733291 | C | T | 151 | a0001c0001t0001g0164 a0001c0001t0001g0260 a0001c0001t0001g0261 others(148): Show |
151 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.81+2013C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733291 | |||||||
chr19:16733326 | G | C | 2 | a0004c0009t0005g0140 a0004c0009t0005g0224 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.81+2048G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733326 | |||||||
chr19:16733463 | G | A | 1 | a0002c0002t0002g0013 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.81+2185G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733463 | |||||||
chr19:16733520 | C | CA | 93 | a0001c0001t0001g0164 a0001c0001t0001g0260 a0001c0001t0001g0261 others(90): Show |
93 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.81+2258dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16733520 | ||||||
chr19:16733520 | CA | C | 142 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0197 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.81+2258delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16733520 | ||||||
chr19:16733749 | C | G | 9 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0006c0014t0008g0253 others(6): Show |
9 | HG01099.hp2 HG02300.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+2471C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733749 | |||||||
chr19:16733752 | C | G | 9 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0006c0014t0008g0253 others(6): Show |
9 | HG01099.hp2 HG02300.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+2474C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733752 | |||||||
chr19:16733792 | C | T | 14 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(11): Show |
14 | HG01109.hp2 HG01167.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+2514C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733792 | |||||||
chr19:16733802 | CG | C | 68 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0003c0003t0001g0210 others(65): Show |
68 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.81+2526delG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16733802 | ||||||
chr19:16733921 | G | C | 9 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0006c0014t0008g0253 others(6): Show |
9 | HG01099.hp2 HG02300.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+2643G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733921 | |||||||
chr19:16733931 | A | G | 70 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0003c0003t0001g0210 others(67): Show |
70 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.81+2653A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733931 | |||||||
chr19:16733962 | C | G | 2 | a0006c0014t0008g0253 a0006c0044t0001g0255 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.82-2672C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733962 | |||||||
chr19:16734033 | A | G | 73 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0003c0003t0001g0210 others(70): Show |
73 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.82-2601A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734033 | |||||||
chr19:16734049 | C | T | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.82-2585C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734049 | |||||||
chr19:16734140 | G | A | 1 | a0003c0003t0007g0064 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.82-2494G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734140 | |||||||
chr19:16734522 | A | C | 60 | a0001c0001t0001g0164 a0001c0001t0001g0197 a0001c0001t0003g0162 others(57): Show |
60 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.82-2112A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734522 | |||||||
chr19:16734534 | CA | C | 79 | a0001c0001t0001g0164 a0001c0001t0001g0197 a0001c0001t0003g0162 others(76): Show |
79 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.82-2086delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16734534 | ||||||
chr19:16734549 | G | T | 2 | a0004c0060t0002g0125 a0009c0010t0047g0005 |
2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.82-2085G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734549 | |||||||
chr19:16734559 | C | CT | 63 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0003c0003t0001g0210 others(60): Show |
63 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.82-2064dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16734559 | ||||||
chr19:16734608 | G | A | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.82-2026G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734608 | |||||||
chr19:16734612 | T | C | 63 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0003c0003t0001g0210 others(60): Show |
63 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.82-2022T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734612 | |||||||
chr19:16734652 | C | A | 1 | a0003c0003t0003g0288 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.82-1982C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734652 | |||||||
chr19:16734734 | C | CTATT | 18 | a0001c0001t0001g0147 a0002c0002t0001g0196 a0002c0002t0001g0218 others(15): Show |
18 | HG00280.hp1 HG01081.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.82-1871_82-1868dup others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16734734 | ||||||
chr19:16734734 | C | CTATTTAT others(1): Show |
38 | a0003c0003t0002g0127 a0003c0003t0003g0143 a0003c0003t0003g0288 others(35): Show |
38 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.82-1875_82-1868dup others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16734734 | ||||||
chr19:16734734 | C | CTATTTAT others(5): Show |
12 | a0004c0005t0006g0226 a0004c0005t0006g0227 a0004c0005t0006g0228 others(9): Show |
12 | HG02258.hp2 HG02451.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-1879_82-1868dup others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16734734 | ||||||
chr19:16734734 | CTATTTAT others(1): Show |
C | 15 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(12): Show |
15 | HG01109.hp2 HG01167.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.82-1875_82-1868del others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16734734 | ||||||
chr19:16734734 | CTATTTAT others(5): Show |
C | 1 | a0001c0007t0049g0132 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.82-1879_82-1868del others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16734734 | ||||||
chr19:16734892 | C | T | 2 | a0004c0005t0018g0256 a0004c0009t0008g0286 |
2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.82-1742C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734892 | |||||||
chr19:16734929 | C | A | 8 | a0001c0001t0014g0187 a0001c0047t0001g0138 a0002c0002t0001g0268 others(5): Show |
8 | HG00738.hp1 HG01175.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-1705C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734929 | |||||||
chr19:16735114 | G | A | 1 | a0013c0020t0008g0257 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.82-1520G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735114 | |||||||
chr19:16735164 | G | A | 74 | a0001c0001t0001g0164 a0001c0001t0001g0197 a0001c0001t0003g0162 others(71): Show |
74 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.82-1470G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735164 | |||||||
chr19:16735256 | C | T | 3 | a0005c0004t0002g0039 a0005c0004t0003g0273 a0031c0056t0001g0279 |
3 | HG01167.hp2 HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.82-1378C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735256 | |||||||
chr19:16735367 | G | A | 9 | a0004c0005t0006g0225 a0004c0009t0009g0047 a0004c0060t0002g0125 others(6): Show |
9 | HG02615.hp2 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-1267G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735367 | |||||||
chr19:16735388 | C | A | 1 | a0003c0006t0002g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.82-1246C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735388 | |||||||
chr19:16735399 | G | A | 2 | a0003c0006t0001g0281 a0003c0006t0001g0282 |
2 | HG02698.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.82-1235G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735399 | |||||||
chr19:16735403 | G | T | 1 | a0001c0001t0005g0169 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.82-1231G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735403 | |||||||
chr19:16735520 | A | G | 4 | a0006c0015t0006g0293 a0016c0019t0017g0294 a0016c0019t0017g0295 others(1): Show |
4 | HG02723.hp1 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-1114A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735520 | |||||||
chr19:16735557 | A | C | 1 | a0003c0003t0003g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.82-1077A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735557 | |||||||
chr19:16735792 | TGGAAGGA others(1): Show |
T | 72 | a0001c0001t0001g0164 a0001c0001t0001g0197 a0001c0001t0003g0162 others(69): Show |
72 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-813_82-806delGG others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735792 | ||||||
chr19:16735795 | AAGGAAGG others(64): Show |
A | 38 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(35): Show |
38 | HG01123.hp2 HG01167.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.82-806_82-736delAA others(69): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735795 | ||||||
chr19:16735803 | AAGGAAGG others(56): Show |
A | 1 | a0004c0009t0013g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.82-805_82-743delAG others(61): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735803 | ||||||
chr19:16735807 | AAGGAAGG others(52): Show |
A | 1 | a0045c0051t0002g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-805_82-747delAG others(57): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735807 | ||||||
chr19:16735811 | AAGGAAGG others(48): Show |
A | 9 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0039g0084 others(6): Show |
9 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-805_82-751delAG others(53): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735811 | ||||||
chr19:16735815 | AAGGAAGG others(44): Show |
A | 16 | a0003c0003t0003g0288 a0003c0006t0001g0281 a0003c0006t0001g0282 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.82-805_82-755delAG others(49): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735815 | ||||||
chr19:16735819 | AAGGAAGG others(40): Show |
A | 1 | a0005c0004t0001g0278 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.82-805_82-759delAG others(45): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735819 | ||||||
chr19:16735821 | G | A | 3 | a0003c0003t0002g0069 a0003c0006t0002g0062 a0015c0054t0025g0118 |
3 | HG03209.hp1 HG03491.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.82-813G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735821 | |||||||
chr19:16735829 | A | AGAAG | 4 | a0001c0001t0005g0241 a0001c0007t0001g0239 a0002c0002t0001g0199 others(1): Show |
4 | NA18951.hp1 NA18960.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-770_82-767dupAG others(2): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735829 | ||||||
chr19:16735829 | A | G | 22 | a0003c0003t0002g0069 a0003c0006t0002g0062 a0004c0005t0006g0225 others(19): Show |
22 | HG01109.hp2 HG01361.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.82-805A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735829 | |||||||
chr19:16735829 | AGAAG | A | 17 | a0001c0001t0001g0136 a0001c0001t0002g0043 a0001c0001t0003g0193 others(14): Show |
17 | HG00735.hp1 HG00735.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.82-770_82-767delAG others(2): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735829 | ||||||
chr19:16735833 | G | A | 10 | a0006c0014t0002g0015 a0006c0014t0009g0014 a0006c0014t0009g0016 others(7): Show |
10 | HG01109.hp2 HG01361.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.82-801G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735833 | |||||||
chr19:16735837 | G | A | 3 | a0004c0005t0006g0225 a0004c0060t0002g0125 a0036c0064t0002g0300 |
3 | HG02886.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.82-797G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735837 | |||||||
chr19:16735841 | G | A | 6 | a0004c0009t0009g0047 a0009c0010t0010g0131 a0009c0010t0047g0005 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-793G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735841 | |||||||
chr19:16735843 | AAGGAAGG others(16): Show |
A | 1 | a0004c0005t0006g0225 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.82-766_82-744delGG others(21): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735843 | ||||||
chr19:16735847 | AAGGAAGG others(12): Show |
A | 2 | a0009c0010t0010g0131 a0028c0062t0030g0250 |
2 | HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.82-766_82-748delGG others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735847 | ||||||
chr19:16735850 | GAAGGA | G | 3 | a0003c0003t0002g0069 a0003c0006t0002g0062 a0015c0054t0025g0118 |
3 | HG03209.hp1 HG03491.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.82-782_82-778delAG others(3): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735850 | ||||||
chr19:16735854 | GAAGGA | G | 7 | a0004c0005t0048g0002 a0007c0029t0002g0297 a0007c0029t0002g0298 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-778_82-774delAG others(3): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735854 | ||||||
chr19:16735858 | GA | G | 63 | a0001c0001t0001g0164 a0001c0001t0001g0197 a0001c0001t0003g0162 others(60): Show |
63 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.82-774delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735858 | ||||||
chr19:16735858 | GAAGGAAG others(5): Show |
G | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.82-774_82-763delAG others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735858 | ||||||
chr19:16735863 | AAGG | A | 74 | a0001c0001t0001g0164 a0001c0001t0001g0197 a0001c0001t0003g0162 others(71): Show |
74 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.82-766_82-764delGG others(1): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735863 | ||||||
chr19:16735864 | A | G | 1 | a0005c0004t0002g0103 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.82-770A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735864 | |||||||
chr19:16735866 | G | A | 1 | a0005c0004t0002g0103 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.82-768G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735866 | |||||||
chr19:16735866 | G | GA | 4 | a0001c0001t0005g0169 a0004c0060t0002g0125 a0009c0010t0047g0005 others(1): Show |
4 | HG02723.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-767dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735866 | ||||||
chr19:16735866 | GAGGA | G | 5 | a0004c0005t0001g0296 a0006c0015t0006g0290 a0006c0015t0041g0053 others(2): Show |
5 | HG02055.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-739_82-736delAG others(2): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735866 | ||||||
chr19:16735868 | G | A | 7 | a0006c0014t0002g0015 a0006c0014t0009g0014 a0006c0014t0009g0016 others(4): Show |
7 | HG01109.hp2 HG02109.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-766G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735868 | |||||||
chr19:16735870 | A | G | 7 | a0006c0014t0002g0015 a0006c0014t0009g0014 a0006c0014t0009g0016 others(4): Show |
7 | HG01109.hp2 HG02109.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-764A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735870 | |||||||
chr19:16735960 | A | T | 20 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0006g0225 others(17): Show |
20 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(17): Show |
intron_variant | MODIFIER | c.82-674A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735960 | |||||||
chr19:16735963 | C | CA | 27 | a0001c0001t0001g0147 a0001c0001t0001g0242 a0002c0002t0020g0249 others(24): Show |
27 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.82-656dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735963 | ||||||
chr19:16735963 | C | CAA | 62 | a0001c0001t0001g0164 a0001c0001t0001g0197 a0001c0001t0003g0162 others(59): Show |
62 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.82-657_82-656dupAA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735963 | ||||||
chr19:16735963 | CA | C | 11 | a0001c0001t0001g0260 a0002c0008t0027g0137 a0004c0005t0006g0226 others(8): Show |
11 | HG02027.hp1 HG02258.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.82-656delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735963 | ||||||
chr19:16736082 | C | T | 6 | a0004c0009t0009g0047 a0004c0060t0002g0125 a0009c0010t0047g0005 others(3): Show |
6 | HG02723.hp2 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-552C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736082 | |||||||
chr19:16736189 | C | CTTCGTTC others(21): Show |
3 | a0004c0005t0006g0225 a0009c0010t0010g0131 a0028c0062t0030g0250 |
3 | HG02615.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.82-442_82-441insGT others(26): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736189 | ||||||
chr19:16736193 | T | C | 4 | a0002c0008t0001g0139 a0004c0005t0006g0225 a0009c0010t0010g0131 others(1): Show |
4 | HG02615.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-441T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736193 | |||||||
chr19:16736193 | T | TTTCCTTC others(29): Show |
1 | a0009c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.82-434_82-433insTT others(34): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | ||||||
chr19:16736193 | T | TTTCCTTC others(33): Show |
2 | a0014c0022t0002g0051 a0036c0064t0002g0300 |
2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.82-434_82-433insTT others(38): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | ||||||
chr19:16736193 | T | TTTCCTTC others(37): Show |
1 | a0004c0060t0002g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.82-434_82-433insTT others(42): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | ||||||
chr19:16736193 | T | TTTCCTTC others(41): Show |
2 | a0004c0009t0009g0047 a0014c0022t0002g0046 |
2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.82-434_82-433insTT others(46): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | ||||||
chr19:16736193 | T | TTTCCTTC others(13): Show |
1 | a0045c0051t0002g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-434_82-433insTT others(18): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | ||||||
chr19:16736193 | T | TTTCCTTC others(21): Show |
3 | a0018c0026t0002g0083 a0020c0024t0001g0251 a0038c0052t0001g0254 |
3 | HG02293.hp1 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.82-434_82-433insTT others(26): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | ||||||
chr19:16736193 | T | TTTCCTTC others(25): Show |
5 | a0002c0002t0020g0249 a0006c0014t0008g0253 a0006c0044t0001g0255 others(2): Show |
5 | HG01099.hp2 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-434_82-433insTT others(30): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | ||||||
chr19:16736193 | T | TTTCCTTC others(29): Show |
1 | a0004c0005t0039g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.82-434_82-433insTT others(34): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | ||||||
chr19:16736193 | T | TTTCCTTC others(33): Show |
1 | a0001c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.82-434_82-433insTT others(38): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | ||||||
chr19:16736209 | T | C | 21 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0002c0008t0001g0139 others(18): Show |
21 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(18): Show |
intron_variant | MODIFIER | c.82-425T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736209 | |||||||
chr19:16736209 | T | TTTCCTTC others(9): Show |
3 | a0001c0001t0001g0160 a0001c0007t0001g0221 a0006c0015t0028g0204 |
3 | HG00639.hp1 HG01109.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.82-423_82-408dupTC others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | ||||||
chr19:16736209 | T | TTTCCTTC others(13): Show |
4 | a0006c0014t0002g0015 a0006c0014t0009g0014 a0006c0014t0009g0016 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-408_82-407insTC others(18): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | ||||||
chr19:16736209 | T | TTTCCTTC others(17): Show |
10 | a0004c0005t0006g0226 a0004c0005t0006g0227 a0004c0005t0006g0228 others(7): Show |
10 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.82-408_82-407insTC others(22): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | ||||||
chr19:16736209 | T | TTTCCTTC others(21): Show |
56 | a0001c0001t0001g0164 a0001c0001t0001g0260 a0001c0001t0001g0261 others(53): Show |
56 | HG00609.hp1 HG00642.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.82-408_82-407insTC others(26): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | ||||||
chr19:16736209 | T | TTTCCTTC others(25): Show |
39 | a0001c0001t0001g0197 a0001c0001t0004g0032 a0001c0001t0004g0034 others(36): Show |
39 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.82-408_82-407insTC others(30): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | ||||||
chr19:16736209 | T | TTTCCTTC others(29): Show |
23 | a0003c0003t0002g0091 a0003c0003t0003g0288 a0003c0003t0007g0064 others(20): Show |
23 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.82-408_82-407insTC others(34): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | ||||||
chr19:16736209 | T | TTTCCTTC others(33): Show |
5 | a0003c0003t0002g0065 a0004c0009t0008g0286 a0005c0016t0002g0056 others(2): Show |
5 | HG02735.hp1 HG02886.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-408_82-407insTC others(38): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | ||||||
chr19:16736209 | T | TTTCCTTC others(37): Show |
2 | a0004c0005t0048g0002 a0005c0004t0002g0039 |
2 | HG01167.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.82-408_82-407insTC others(42): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | ||||||
chr19:16736209 | T | TTTCCTTC others(41): Show |
1 | a0003c0006t0001g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.82-408_82-407insTC others(46): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | ||||||
chr19:16736209 | T | TTTCCTTC others(45): Show |
1 | a0003c0006t0001g0282 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.82-408_82-407insTC others(50): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | ||||||
chr19:16736227 | A | T | 20 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0006g0225 others(17): Show |
20 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(17): Show |
intron_variant | MODIFIER | c.82-407A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736227 | |||||||
chr19:16736267 | C | G | 1 | a0008c0012t0001g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.82-367C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736267 | |||||||
chr19:16736364 | G | T | 10 | a0003c0003t0002g0117 a0007c0028t0002g0115 a0007c0028t0034g0258 others(7): Show |
10 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-270G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736364 | |||||||
chr19:16736376 | C | A | 1 | a0011c0011t0001g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.82-258C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736376 | |||||||
chr19:16736431 | C | G | 4 | a0001c0001t0001g0158 a0001c0001t0020g0289 a0001c0007t0001g0040 others(1): Show |
4 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-203C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736431 | |||||||
chr19:16736495 | C | A | 9 | a0004c0005t0006g0225 a0004c0009t0009g0047 a0004c0060t0002g0125 others(6): Show |
9 | HG02615.hp2 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-139C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736495 | |||||||
chr19:16736955 | G | A | 1 | a0021c0041t0002g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.198+205G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16736955 | |||||||
chr19:16737054 | T | G | 4 | a0004c0017t0002g0018 a0004c0017t0002g0019 a0029c0065t0032g0166 others(1): Show |
4 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+304T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737054 | |||||||
chr19:16737176 | C | T | 3 | a0003c0003t0004g0079 a0005c0004t0002g0074 a0005c0004t0002g0103 |
3 | HG00558.hp2 HG02015.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.198+426C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737176 | |||||||
chr19:16737566 | G | GT | 14 | a0001c0001t0005g0246 a0002c0002t0020g0249 a0004c0005t0039g0084 others(11): Show |
14 | HG01081.hp1 HG01099.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+831dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737566 | ||||||
chr19:16737567 | T | G | 6 | a0004c0009t0009g0047 a0004c0060t0002g0125 a0009c0010t0047g0005 others(3): Show |
6 | HG02723.hp2 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+817T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737567 | |||||||
chr19:16737568 | T | G | 3 | a0004c0005t0006g0225 a0009c0010t0010g0131 a0028c0062t0030g0250 |
3 | HG02615.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.198+818T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737568 | |||||||
chr19:16737577 | T | C | 3 | a0004c0005t0006g0225 a0009c0010t0010g0131 a0028c0062t0030g0250 |
3 | HG02615.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.198+827T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737577 | |||||||
chr19:16737635 | C | T | 1 | a0043c0057t0026g0202 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.198+885C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737635 | |||||||
chr19:16737699 | C | T | 2 | a0004c0060t0002g0125 a0009c0010t0047g0005 |
2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.198+949C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737699 | |||||||
chr19:16737817 | T | C | 2 | a0001c0007t0002g0122 a0041c0050t0007g0104 |
2 | HG02132.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.198+1067T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737817 | |||||||
chr19:16737943 | C | T | 6 | a0004c0005t0006g0226 a0004c0005t0006g0227 a0004c0005t0006g0228 others(3): Show |
6 | HG02258.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+1193C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737943 | |||||||
chr19:16737954 | G | A | 2 | a0004c0060t0002g0125 a0009c0010t0047g0005 |
2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.198+1204G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737954 | |||||||
chr19:16737964 | C | CAAAA | 3 | a0001c0001t0001g0147 a0004c0005t0039g0084 a0018c0026t0002g0083 |
3 | HG01081.hp1 HG02293.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.198+1214_198+1215i others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737964 | |||||||
chr19:16737964 | C | CAAAAGAA others(132): Show |
1 | a0020c0024t0001g0251 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.198+1214_198+1215i others(141): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737964 | |||||||
chr19:16737964 | C | CAAAAGAA others(157): Show |
1 | a0020c0024t0001g0259 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.198+1214_198+1215i others(166): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737964 | |||||||
chr19:16737964 | C | CAAAAGAA others(162): Show |
1 | a0006c0044t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.198+1214_198+1215i others(171): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737964 | |||||||
chr19:16737964 | C | CAAAAGAA others(172): Show |
1 | a0038c0052t0001g0254 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.198+1214_198+1215i others(181): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737964 | |||||||
chr19:16737964 | C | CAAAAGAA others(182): Show |
1 | a0006c0014t0008g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.198+1214_198+1215i others(191): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737964 | |||||||
chr19:16737964 | C | CAAAAGAA others(187): Show |
1 | a0002c0002t0020g0249 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.198+1214_198+1215i others(196): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737964 | |||||||
chr19:16737964 | C | CAAAAGAA others(142): Show |
1 | a0027c0053t0001g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.198+1214_198+1215i others(151): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737964 | |||||||
chr19:16737964 | C | CGAAAA | 88 | a0001c0001t0001g0160 a0001c0001t0001g0164 a0001c0001t0001g0171 others(85): Show |
88 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.198+1259_198+1263d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | ||||||
chr19:16737964 | C | CGAAAAGA others(3): Show |
52 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(49): Show |
52 | HG00544.hp1 HG00642.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.198+1254_198+1263d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | ||||||
chr19:16737964 | C | CGAAAAGA others(8): Show |
7 | a0003c0003t0002g0006 a0003c0003t0002g0066 a0003c0003t0002g0067 others(4): Show |
7 | HG01361.hp1 HG02056.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+1249_198+1263d others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | ||||||
chr19:16737964 | C | CGAAAAGA others(13): Show |
6 | a0004c0005t0029g0265 a0004c0060t0002g0125 a0014c0022t0002g0051 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+1244_198+1263d others(22): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | ||||||
chr19:16737964 | C | CGAAAAGA others(18): Show |
2 | a0009c0010t0010g0131 a0045c0051t0002g0028 |
2 | HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.198+1239_198+1263d others(27): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | ||||||
chr19:16737964 | C | CGAAAAGA others(23): Show |
1 | a0009c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.198+1234_198+1263d others(32): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | ||||||
chr19:16737964 | CGAAAA | C | 9 | a0006c0014t0002g0015 a0006c0014t0009g0014 a0006c0014t0009g0016 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.198+1259_198+1263d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | ||||||
chr19:16737964 | CGAAAAGA others(3): Show |
C | 3 | a0002c0002t0001g0194 a0002c0002t0005g0195 a0040c0037t0001g0209 |
3 | HG02293.hp2 NA19060.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.198+1254_198+1263d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | ||||||
chr19:16737964 | CGAAAAGA others(13): Show |
C | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.198+1244_198+1263d others(22): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | ||||||
chr19:16738003 | A | AAG | 7 | a0002c0002t0020g0249 a0006c0014t0008g0253 a0006c0044t0001g0255 others(4): Show |
7 | HG01099.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+1255_198+1256d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738003 | ||||||
chr19:16738003 | A | AAGAAAAG others(98): Show |
1 | a0018c0026t0002g0083 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.198+1263_198+1264i others(107): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738003 | ||||||
chr19:16738003 | A | AAGAAAAG others(122): Show |
1 | a0004c0005t0039g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.198+1263_198+1264i others(131): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738003 | ||||||
chr19:16738003 | A | AAGAAAAG others(123): Show |
1 | a0001c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.198+1263_198+1264i others(132): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738003 | ||||||
chr19:16738178 | C | A | 3 | a0004c0005t0006g0225 a0009c0010t0010g0131 a0028c0062t0030g0250 |
3 | HG02615.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.198+1428C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738178 | |||||||
chr19:16738216 | C | T | 1 | a0002c0002t0001g0291 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.198+1466C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738216 | |||||||
chr19:16738391 | AAACCCCA others(472): Show |
A | 1 | a0045c0051t0002g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.198+1644_198+2122d others(2): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738391 | ||||||
chr19:16738396 | C | G | 2 | a0013c0020t0016g0003 a0013c0020t0016g0004 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.198+1646C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738396 | |||||||
chr19:16738429 | C | T | 8 | a0004c0005t0001g0296 a0006c0015t0006g0290 a0006c0015t0006g0293 others(5): Show |
8 | HG02055.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.198+1679C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738429 | |||||||
chr19:16738448 | G | A | 161 | a0001c0001t0001g0147 a0001c0001t0001g0164 a0001c0001t0001g0197 others(158): Show |
161 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.198+1698G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738448 | |||||||
chr19:16738555 | G | A | 1 | a0042c0035t0001g0133 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.198+1805G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738555 | |||||||
chr19:16738566 | C | CA | 23 | a0001c0001t0001g0147 a0001c0001t0003g0179 a0001c0001t0004g0111 others(20): Show |
23 | HG00609.hp1 HG01081.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.198+1834dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738566 | ||||||
chr19:16738566 | C | CAA | 14 | a0004c0005t0006g0225 a0004c0009t0009g0047 a0004c0060t0002g0125 others(11): Show |
14 | HG02451.hp2 HG02615.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+1833_198+1834d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738566 | ||||||
chr19:16738566 | CA | C | 56 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(53): Show |
56 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.198+1834delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738566 | ||||||
chr19:16738627 | TA | T | 19 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0006g0225 others(16): Show |
19 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+1878delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738627 | |||||||
chr19:16738629 | T | G | 19 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0006g0225 others(16): Show |
19 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+1879T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738629 | |||||||
chr19:16738630 | T | C | 19 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0006g0225 others(16): Show |
19 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+1880T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738630 | |||||||
chr19:16738730 | C | A | 19 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0006g0225 others(16): Show |
19 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+1980C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738730 | |||||||
chr19:16738748 | T | A | 1 | a0002c0002t0002g0013 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.198+1998T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738748 | |||||||
chr19:16738748 | TTA | T | 6 | a0004c0009t0009g0047 a0004c0060t0002g0125 a0009c0010t0047g0005 others(3): Show |
6 | HG02723.hp2 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+2009_198+2010d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738748 | ||||||
chr19:16738749 | T | A | 3 | a0004c0005t0006g0225 a0009c0010t0010g0131 a0028c0062t0030g0250 |
3 | HG02615.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.198+1999T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738749 | |||||||
chr19:16738750 | A | ATATATAT others(2): Show |
3 | a0004c0005t0006g0225 a0009c0010t0010g0131 a0028c0062t0030g0250 |
3 | HG02615.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.198+2001_198+2009d others(11): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738750 | ||||||
chr19:16738768 | G | A | 1 | a0003c0003t0004g0079 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.198+2018G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738768 | |||||||
chr19:16738768 | G | T | 1 | a0007c0029t0002g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198+2018G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738768 | |||||||
chr19:16738768 | GATATATA | G | 10 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0039g0084 others(7): Show |
10 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+2036_198+2042d others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738768 | ||||||
chr19:16738768 | GATATATA others(7): Show |
G | 72 | a0001c0001t0001g0160 a0001c0001t0001g0164 a0001c0001t0001g0197 others(69): Show |
72 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.198+2029_198+2042d others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738768 | ||||||
chr19:16738782 | A | ATATTATA others(16): Show |
1 | a0007c0029t0002g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198+2032_198+2033i others(25): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738782 | |||||||
chr19:16738782 | A | G | 1 | a0003c0003t0004g0079 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.198+2032A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738782 | |||||||
chr19:16738802 | ATAC | A | 10 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0039g0084 others(7): Show |
10 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+2055_198+2057d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738802 | ||||||
chr19:16738805 | C | T | 7 | a0004c0005t0006g0225 a0004c0009t0009g0047 a0004c0060t0002g0125 others(4): Show |
7 | HG02723.hp2 HG02886.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+2055C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738805 | |||||||
chr19:16738822 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.198+2072T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738822 | |||||||
chr19:16738829 | T | TATACATT others(277): Show |
1 | a0001c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.198+2092_198+2093i others(286): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738829 | ||||||
chr19:16738829 | T | TATACATT others(77): Show |
4 | a0004c0009t0009g0047 a0014c0022t0002g0046 a0014c0022t0002g0051 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+2092_198+2093i others(86): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738829 | ||||||
chr19:16738829 | T | TATACATT others(119): Show |
2 | a0004c0060t0002g0125 a0009c0010t0047g0005 |
2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.198+2092_198+2093i others(128): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738829 | ||||||
chr19:16738829 | T | TATACATT others(319): Show |
3 | a0006c0014t0008g0253 a0006c0044t0001g0255 a0027c0053t0001g0252 |
3 | HG02451.hp2 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.198+2106_198+2107i others(328): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738829 | ||||||
chr19:16738829 | T | TATACATT others(298): Show |
5 | a0004c0005t0039g0084 a0018c0026t0002g0083 a0020c0024t0001g0251 others(2): Show |
5 | HG01081.hp1 HG02293.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+2106_198+2107i others(307): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738829 | ||||||
chr19:16738829 | T | TATACATT others(340): Show |
1 | a0002c0002t0020g0249 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.198+2106_198+2107i others(349): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738829 | ||||||
chr19:16738843 | T | A | 7 | a0004c0005t0006g0225 a0004c0009t0009g0047 a0009c0010t0010g0131 others(4): Show |
7 | HG02615.hp2 HG02723.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+2093T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738843 | |||||||
chr19:16738847 | T | G | 12 | a0004c0005t0001g0296 a0006c0014t0002g0015 a0006c0014t0009g0014 others(9): Show |
12 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.198+2097T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738847 | |||||||
chr19:16738860 | C | A | 19 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0006g0225 others(16): Show |
19 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+2110C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738860 | |||||||
chr19:16738886 | A | ATATATAA others(56): Show |
3 | a0004c0005t0006g0225 a0009c0010t0010g0131 a0028c0062t0030g0250 |
3 | HG02615.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.198+2142_198+2143i others(65): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738886 | ||||||
chr19:16738913 | C | T | 20 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0006g0225 others(17): Show |
20 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(17): Show |
intron_variant | MODIFIER | c.198+2163C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738913 | |||||||
chr19:16739189 | A | G | 9 | a0001c0001t0003g0193 a0001c0001t0004g0107 a0001c0001t0004g0109 others(6): Show |
9 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.198+2439A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739189 | |||||||
chr19:16739190 | G | GA | 162 | a0001c0001t0001g0147 a0001c0001t0001g0160 a0001c0001t0001g0164 others(159): Show |
162 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.198+2451dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16739190 | ||||||
chr19:16739242 | C | T | 1 | a0005c0016t0002g0081 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.198+2492C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739242 | |||||||
chr19:16739272 | A | T | 2 | a0009c0010t0010g0274 a0009c0010t0010g0283 |
2 | HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.198+2522A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739272 | |||||||
chr19:16739284 | G | A | 11 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0039g0084 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.198+2534G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739284 | |||||||
chr19:16739329 | C | CA | 24 | a0001c0001t0001g0171 a0001c0001t0001g0178 a0001c0001t0003g0179 others(21): Show |
24 | HG00735.hp2 HG01175.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.198+2605dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16739329 | ||||||
chr19:16739329 | CA | C | 33 | a0001c0001t0003g0193 a0001c0001t0004g0107 a0001c0001t0004g0109 others(30): Show |
33 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.198+2605delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16739329 | ||||||
chr19:16739329 | CAA | C | 70 | a0001c0001t0001g0160 a0001c0001t0001g0197 a0001c0001t0003g0162 others(67): Show |
70 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.198+2604_198+2605d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16739329 | ||||||
chr19:16739329 | CAAA | C | 51 | a0001c0001t0001g0164 a0001c0001t0001g0260 a0001c0001t0001g0261 others(48): Show |
51 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.198+2603_198+2605d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16739329 | ||||||
chr19:16739329 | CAAAA | C | 13 | a0004c0005t0001g0296 a0004c0005t0018g0256 a0005c0004t0002g0039 others(10): Show |
13 | HG01109.hp2 HG01167.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.198+2602_198+2605d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16739329 | ||||||
chr19:16739355 | A | T | 5 | a0004c0009t0009g0047 a0014c0022t0002g0046 a0014c0022t0002g0051 others(2): Show |
5 | HG02723.hp2 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+2605A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739355 | |||||||
chr19:16739377 | G | A | 1 | a0002c0002t0002g0008 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.198+2627G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739377 | |||||||
chr19:16739388 | G | A | 1 | a0003c0003t0002g0085 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.198+2638G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739388 | |||||||
chr19:16739486 | G | A | 1 | a0011c0011t0011g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.198+2736G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739486 | |||||||
chr19:16739705 | T | C | 1 | a0007c0069t0043g0299 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.198+2955T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739705 | |||||||
chr19:16739724 | T | C | 11 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0039g0084 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.198+2974T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739724 | |||||||
chr19:16739922 | A | G | 162 | a0001c0001t0001g0147 a0001c0001t0001g0160 a0001c0001t0001g0164 others(159): Show |
162 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.198+3172A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739922 | |||||||
chr19:16739949 | G | A | 1 | a0031c0056t0001g0279 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.198+3199G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739949 | |||||||
chr19:16740026 | T | G | 17 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0039g0084 others(14): Show |
17 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(14): Show |
intron_variant | MODIFIER | c.198+3276T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16740026 | |||||||
chr19:16740193 | G | A | 17 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0039g0084 others(14): Show |
17 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(14): Show |
intron_variant | MODIFIER | c.198+3443G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16740193 | |||||||
chr19:16740220 | G | A | 2 | a0003c0006t0001g0281 a0003c0006t0001g0282 |
2 | HG02698.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.198+3470G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16740220 | |||||||
chr19:16740398 | A | C | 108 | a0001c0001t0001g0147 a0001c0001t0001g0160 a0001c0001t0001g0164 others(105): Show |
108 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.198+3648A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16740398 | |||||||
chr19:16740642 | A | AT | 13 | a0001c0001t0002g0029 a0001c0001t0003g0162 a0001c0001t0003g0176 others(10): Show |
13 | HG00609.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.199-3757dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16740642 | ||||||
chr19:16740642 | A | ATTTTTTT | 6 | a0004c0009t0009g0047 a0004c0060t0002g0125 a0009c0010t0047g0005 others(3): Show |
6 | HG02723.hp2 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-3763_199-3757d others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16740642 | ||||||
chr19:16740642 | ATTTTTT | A | 11 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0039g0084 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.199-3762_199-3757d others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16740642 | ||||||
chr19:16740680 | C | A | 1 | a0015c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-3741C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16740680 | |||||||
chr19:16740934 | G | A | 3 | a0002c0002t0002g0031 a0002c0002t0007g0030 a0002c0002t0011g0105 |
3 | HG02015.hp1 NA18951.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.199-3487G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16740934 | |||||||
chr19:16741037 | A | G | 11 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0039g0084 others(8): Show |
11 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.199-3384A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16741037 | |||||||
chr19:16741104 | G | A | 10 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0039g0084 others(7): Show |
10 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-3317G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16741104 | |||||||
chr19:16741123 | A | G | 15 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0039g0084 others(12): Show |
15 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-3298A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16741123 | |||||||
chr19:16741301 | T | G | 1 | a0014c0022t0002g0051 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.199-3120T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16741301 | |||||||
chr19:16741366 | G | GTGT | 10 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0039g0084 others(7): Show |
10 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-3053_199-3051d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16741366 | ||||||
chr19:16741368 | G | GT | 12 | a0001c0001t0003g0193 a0001c0007t0001g0040 a0001c0007t0001g0213 others(9): Show |
12 | HG01123.hp1 HG01943.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.199-3036dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16741368 | ||||||
chr19:16741368 | GT | G | 84 | a0001c0001t0001g0164 a0001c0001t0001g0197 a0001c0001t0001g0260 others(81): Show |
84 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.199-3036delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16741368 | ||||||
chr19:16741436 | G | A | 4 | a0004c0009t0009g0047 a0014c0022t0002g0046 a0014c0022t0002g0051 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-2985G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16741436 | |||||||
chr19:16741439 | C | T | 1 | a0025c0045t0016g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.199-2982C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16741439 | |||||||
chr19:16741478 | T | TCCTCAGC others(2315): Show |
1 | a0009c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.199-1500_199-1499i others(2324): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16741478 | ||||||
chr19:16741565 | C | T | 4 | a0006c0014t0002g0015 a0006c0014t0009g0014 a0006c0014t0009g0016 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2856C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16741565 | |||||||
chr19:16741968 | G | A | 1 | a0003c0003t0002g0117 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.199-2453G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16741968 | |||||||
chr19:16742046 | G | T | 12 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0039g0084 others(9): Show |
12 | HG01081.hp1 HG01099.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.199-2375G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742046 | |||||||
chr19:16742227 | T | A | 2 | a0007c0029t0002g0297 a0007c0029t0002g0298 |
2 | HG01891.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.199-2194T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742227 | |||||||
chr19:16742272 | G | A | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.199-2149G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742272 | |||||||
chr19:16742353 | C | T | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.199-2068C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742353 | |||||||
chr19:16742393 | A | C | 1 | a0003c0003t0002g0006 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.199-2028A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742393 | |||||||
chr19:16742452 | C | T | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.199-1969C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742452 | |||||||
chr19:16742511 | C | T | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.199-1910C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742511 | |||||||
chr19:16742568 | AG | A | 6 | a0001c0001t0001g0147 a0002c0002t0020g0249 a0004c0005t0039g0084 others(3): Show |
6 | HG01081.hp1 HG01099.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-1850delG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16742568 | ||||||
chr19:16742635 | C | A | 4 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(1): Show |
4 | HG01167.hp1 HG01884.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-1786C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742635 | |||||||
chr19:16742707 | G | A | 9 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(6): Show |
9 | HG01167.hp1 HG01884.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-1714G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742707 | |||||||
chr19:16742730 | G | A | 1 | a0003c0003t0003g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.199-1691G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742730 | |||||||
chr19:16742731 | C | T | 5 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(2): Show |
5 | HG01167.hp1 HG01884.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-1690C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742731 | |||||||
chr19:16742847 | A | T | 4 | a0004c0009t0009g0047 a0014c0022t0002g0046 a0014c0022t0002g0051 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-1574A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742847 | |||||||
chr19:16742848 | A | T | 6 | a0004c0009t0009g0047 a0004c0060t0002g0125 a0014c0022t0002g0046 others(3): Show |
6 | HG02723.hp2 HG02886.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-1573A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742848 | |||||||
chr19:16742881 | C | CTAT | 44 | a0001c0001t0003g0193 a0001c0001t0004g0107 a0001c0001t0004g0109 others(41): Show |
44 | HG00642.hp2 HG00735.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.199-1499_199-1497d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16742881 | ||||||
chr19:16742881 | C | CTATTAT | 3 | a0001c0001t0004g0034 a0001c0001t0005g0169 a0014c0022t0001g0231 |
3 | HG01884.hp2 HG03688.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.199-1502_199-1497d others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16742881 | ||||||
chr19:16742881 | CTAT | C | 84 | a0001c0001t0001g0158 a0001c0001t0001g0261 a0001c0001t0001g0262 others(81): Show |
84 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.199-1499_199-1497d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16742881 | ||||||
chr19:16742881 | CTATTAT | C | 23 | a0001c0001t0001g0147 a0001c0001t0001g0164 a0001c0001t0014g0238 others(20): Show |
23 | HG00099.hp2 HG00609.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-1502_199-1497d others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16742881 | ||||||
chr19:16742881 | CTATTATT others(2): Show |
C | 4 | a0001c0001t0001g0260 a0009c0010t0010g0274 a0009c0010t0010g0276 others(1): Show |
4 | HG02647.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-1505_199-1497d others(11): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16742881 | ||||||
chr19:16742881 | CTATTATT others(5): Show |
C | 1 | a0001c0001t0001g0160 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.199-1508_199-1497d others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16742881 | ||||||
chr19:16742881 | CTATTATT others(8): Show |
C | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.199-1511_199-1497d others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16742881 | ||||||
chr19:16743057 | T | C | 4 | a0006c0014t0008g0253 a0006c0044t0001g0255 a0011c0011t0011g0017 others(1): Show |
4 | HG02109.hp1 HG02965.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-1364T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743057 | |||||||
chr19:16743071 | C | T | 1 | a0004c0060t0002g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.199-1350C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743071 | |||||||
chr19:16743109 | T | C | 12 | a0001c0001t0001g0147 a0002c0036t0002g0020 a0004c0005t0039g0084 others(9): Show |
12 | HG01081.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.199-1312T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743109 | |||||||
chr19:16743195 | G | A | 1 | a0004c0005t0018g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.199-1226G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743195 | |||||||
chr19:16743273 | C | T | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | HG01167.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.199-1148C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743273 | |||||||
chr19:16743296 | G | A | 1 | a0002c0002t0020g0249 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.199-1125G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743296 | |||||||
chr19:16743478 | G | C | 7 | a0010c0013t0008g0188 a0010c0013t0009g0045 a0010c0013t0013g0172 others(4): Show |
7 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-943G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743478 | |||||||
chr19:16743648 | C | CCATA | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | HG01167.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.199-768_199-765dup others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16743648 | ||||||
chr19:16743668 | A | G | 10 | a0004c0005t0001g0296 a0007c0028t0002g0115 a0007c0028t0034g0258 others(7): Show |
10 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.199-753A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743668 | |||||||
chr19:16743672 | A | G | 16 | a0004c0005t0001g0296 a0004c0009t0008g0286 a0004c0009t0013g0206 others(13): Show |
16 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.199-749A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743672 | |||||||
chr19:16743675 | A | T | 188 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0001c0001t0001g0158 others(185): Show |
188 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(185): Show |
intron_variant | MODIFIER | c.199-746A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743675 | |||||||
chr19:16743676 | G | A | 1 | a0003c0003t0002g0085 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.199-745G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743676 | |||||||
chr19:16743680 | G | A | 10 | a0004c0005t0001g0296 a0007c0028t0002g0115 a0007c0028t0034g0258 others(7): Show |
10 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.199-741G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743680 | |||||||
chr19:16743680 | G | GTTTGTTT others(1): Show |
44 | a0001c0001t0001g0147 a0004c0005t0006g0211 a0004c0005t0006g0225 others(41): Show |
44 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.199-738_199-737ins others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16743680 | ||||||
chr19:16743775 | C | T | 75 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0164 others(72): Show |
75 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.199-646C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743775 | |||||||
chr19:16743792 | C | T | 1 | a0003c0003t0002g0006 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.199-629C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743792 | |||||||
chr19:16743839 | C | T | 1 | a0003c0003t0003g0288 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.199-582C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743839 | |||||||
chr19:16743881 | C | T | 5 | a0001c0001t0001g0147 a0004c0005t0039g0084 a0004c0017t0002g0038 others(2): Show |
5 | HG01081.hp1 HG02280.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-540C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743881 | |||||||
chr19:16743929 | C | T | 54 | a0001c0001t0001g0147 a0004c0005t0001g0296 a0004c0005t0006g0211 others(51): Show |
54 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(51): Show |
intron_variant | MODIFIER | c.199-492C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743929 | |||||||
chr19:16743945 | A | T | 5 | a0004c0005t0018g0256 a0004c0005t0029g0265 a0004c0009t0008g0205 others(2): Show |
5 | HG02258.hp1 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-476A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743945 | |||||||
chr19:16744050 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.199-371A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16744050 | |||||||
chr19:16744089 | G | C | 55 | a0001c0001t0001g0147 a0004c0005t0001g0296 a0004c0005t0006g0211 others(52): Show |
55 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(52): Show |
intron_variant | MODIFIER | c.199-332G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16744089 | |||||||
chr19:16744130 | A | T | 54 | a0001c0001t0001g0147 a0004c0005t0001g0296 a0004c0005t0006g0211 others(51): Show |
54 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(51): Show |
intron_variant | MODIFIER | c.199-291A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16744130 | |||||||
chr19:16744138 | C | A | 1 | a0005c0004t0003g0272 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.199-283C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16744138 | |||||||
chr19:16744316 | G | T | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | HG01167.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.199-105G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16744316 | |||||||
chr19:16744780 | C | T | 1 | a0007c0029t0002g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.496+62C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16744780 | |||||||
chr19:16744983 | C | A | 1 | a0038c0052t0001g0254 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.496+265C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16744983 | |||||||
chr19:16745067 | A | G | 1 | a0007c0028t0034g0258 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.496+349A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745067 | |||||||
chr19:16745179 | A | G | 74 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0003g0162 others(71): Show |
74 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.496+461A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745179 | |||||||
chr19:16745204 | T | C | 126 | a0001c0001t0001g0158 a0001c0001t0001g0164 a0001c0001t0001g0197 others(123): Show |
126 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.496+486T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745204 | |||||||
chr19:16745225 | A | G | 21 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(18): Show |
21 | HG01109.hp2 HG01167.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.496+507A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745225 | |||||||
chr19:16745294 | G | A | 1 | a0002c0031t0001g0155 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.496+576G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745294 | |||||||
chr19:16745342 | C | T | 1 | a0001c0007t0002g0110 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.496+624C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745342 | |||||||
chr19:16745358 | G | C | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.496+640G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745358 | |||||||
chr19:16745375 | C | T | 60 | a0001c0001t0003g0162 a0001c0001t0003g0191 a0001c0001t0003g0193 others(57): Show |
60 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.496+657C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745375 | |||||||
chr19:16745481 | A | C | 200 | a0001c0001t0001g0136 a0001c0001t0001g0171 a0001c0001t0001g0260 others(197): Show |
200 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.496+763A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745481 | |||||||
chr19:16745485 | T | G | 9 | a0002c0036t0002g0020 a0004c0005t0006g0226 a0007c0068t0040g0116 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.496+767T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745485 | |||||||
chr19:16745508 | C | T | 18 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(15): Show |
18 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.496+790C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745508 | |||||||
chr19:16745565 | C | CA | 16 | a0001c0001t0001g0147 a0001c0001t0014g0187 a0001c0001t0014g0238 others(13): Show |
16 | HG01433.hp2 HG01516.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.496+862dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16745565 | ||||||
chr19:16745573 | A | T | 8 | a0007c0028t0002g0115 a0007c0028t0034g0258 a0007c0029t0002g0297 others(5): Show |
8 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+855A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745573 | |||||||
chr19:16745679 | G | A | 8 | a0007c0028t0002g0115 a0007c0028t0034g0258 a0007c0029t0002g0297 others(5): Show |
8 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+961G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745679 | |||||||
chr19:16745776 | G | A | 1 | a0001c0001t0003g0220 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.496+1058G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745776 | |||||||
chr19:16745904 | G | A | 29 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(26): Show |
29 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+1186G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745904 | |||||||
chr19:16745909 | C | T | 1 | a0006c0044t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.496+1191C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745909 | |||||||
chr19:16745930 | T | A | 2 | a0006c0015t0028g0204 a0015c0054t0025g0118 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.496+1212T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745930 | |||||||
chr19:16746036 | C | G | 1 | a0008c0067t0003g0275 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.496+1318C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746036 | |||||||
chr19:16746043 | A | G | 2 | a0003c0003t0004g0073 a0003c0003t0004g0079 |
2 | HG02015.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.496+1325A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746043 | |||||||
chr19:16746053 | C | T | 41 | a0003c0006t0002g0100 a0004c0005t0029g0265 a0004c0005t0048g0002 others(38): Show |
41 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.496+1335C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746053 | |||||||
chr19:16746145 | C | T | 87 | a0001c0001t0003g0191 a0001c0001t0003g0193 a0001c0001t0003g0237 others(84): Show |
87 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.496+1427C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746145 | |||||||
chr19:16746154 | G | T | 2 | a0008c0012t0001g0234 a0008c0012t0001g0235 |
2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.496+1436G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746154 | |||||||
chr19:16746189 | AT | A | 19 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(16): Show |
19 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.496+1474delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16746189 | ||||||
chr19:16746192 | TA | T | 22 | a0001c0001t0003g0193 a0001c0001t0005g0246 a0001c0007t0002g0057 others(19): Show |
22 | HG01496.hp1 HG01516.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.496+1486delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16746192 | ||||||
chr19:16746263 | C | G | 8 | a0003c0006t0002g0100 a0009c0010t0002g0114 a0009c0010t0010g0131 others(5): Show |
8 | HG01981.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+1545C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746263 | |||||||
chr19:16746264 | G | A | 1 | a0001c0007t0001g0239 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.496+1546G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746264 | |||||||
chr19:16746278 | T | C | 6 | a0004c0005t0001g0296 a0006c0044t0001g0255 a0014c0022t0001g0231 others(3): Show |
6 | HG01884.hp2 HG02723.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+1560T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746278 | |||||||
chr19:16746296 | A | G | 8 | a0003c0006t0002g0100 a0009c0010t0002g0114 a0009c0010t0010g0131 others(5): Show |
8 | HG01981.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+1578A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746296 | |||||||
chr19:16746449 | C | T | 8 | a0003c0006t0002g0100 a0009c0010t0002g0114 a0009c0010t0010g0131 others(5): Show |
8 | HG01981.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+1731C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746449 | |||||||
chr19:16746548 | C | T | 1 | a0002c0002t0001g0177 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.496+1830C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746548 | |||||||
chr19:16746565 | C | T | 62 | a0001c0001t0003g0191 a0001c0001t0003g0193 a0001c0001t0003g0237 others(59): Show |
62 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.496+1847C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746565 | |||||||
chr19:16746576 | G | A | 2 | a0002c0002t0007g0030 a0002c0002t0011g0105 |
2 | HG02015.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.496+1858G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746576 | |||||||
chr19:16746614 | A | G | 29 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(26): Show |
29 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+1896A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746614 | |||||||
chr19:16746627 | C | T | 29 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(26): Show |
29 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+1909C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746627 | |||||||
chr19:16746675 | AC | A | 29 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(26): Show |
29 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+1958delC | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746675 | |||||||
chr19:16746676 | C | A | 8 | a0003c0006t0002g0100 a0009c0010t0002g0114 a0009c0010t0010g0131 others(5): Show |
8 | HG01981.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+1958C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746676 | |||||||
chr19:16746690 | C | CAAA | 10 | a0007c0028t0002g0115 a0007c0028t0034g0258 a0007c0029t0002g0297 others(7): Show |
10 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+1974_496+1975i others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16746690 | ||||||
chr19:16746692 | A | AAAC | 19 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(16): Show |
19 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.496+1974_496+1975i others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746692 | |||||||
chr19:16746692 | AC | A | 101 | a0001c0001t0003g0191 a0001c0001t0003g0193 a0001c0001t0003g0237 others(98): Show |
101 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.496+1975delC | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746692 | |||||||
chr19:16746693 | C | A | 39 | a0001c0001t0004g0109 a0001c0001t0004g0111 a0002c0036t0002g0020 others(36): Show |
39 | HG00735.hp1 HG00735.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.496+1975C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746693 | |||||||
chr19:16746835 | A | G | 1 | a0002c0008t0001g0145 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.496+2117A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746835 | |||||||
chr19:16747039 | C | CT | 95 | a0001c0001t0001g0147 a0001c0001t0003g0191 a0001c0001t0003g0193 others(92): Show |
95 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.497-2085dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16747039 | ||||||
chr19:16747039 | CT | C | 14 | a0001c0001t0005g0246 a0002c0023t0002g0102 a0003c0003t0002g0117 others(11): Show |
14 | HG02647.hp1 HG02809.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-2085delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16747039 | ||||||
chr19:16747186 | G | A | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.497-1953G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747186 | |||||||
chr19:16747243 | C | G | 1 | a0021c0041t0002g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.497-1896C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747243 | |||||||
chr19:16747252 | G | A | 10 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(7): Show |
10 | HG02647.hp1 HG02809.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-1887G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747252 | |||||||
chr19:16747279 | C | A | 6 | a0002c0036t0002g0020 a0011c0011t0001g0247 a0011c0011t0002g0022 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-1860C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747279 | |||||||
chr19:16747282 | G | A | 3 | a0014c0022t0001g0231 a0014c0022t0002g0046 a0014c0022t0002g0051 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.497-1857G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747282 | |||||||
chr19:16747333 | C | T | 10 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(7): Show |
10 | HG02647.hp1 HG02809.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-1806C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747333 | |||||||
chr19:16747345 | T | TTTTA | 32 | a0001c0001t0001g0164 a0001c0001t0001g0178 a0001c0001t0001g0242 others(29): Show |
32 | HG00280.hp1 HG00597.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.497-1757_497-1754d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16747345 | ||||||
chr19:16747345 | T | TTTTATTT others(5): Show |
1 | a0038c0052t0001g0254 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.497-1765_497-1754d others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16747345 | ||||||
chr19:16747345 | TTTTA | T | 57 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(54): Show |
57 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.497-1757_497-1754d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16747345 | ||||||
chr19:16747345 | TTTTATTT others(1): Show |
T | 71 | a0002c0036t0002g0020 a0003c0006t0002g0086 a0004c0005t0001g0296 others(68): Show |
71 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.497-1761_497-1754d others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16747345 | ||||||
chr19:16747345 | TTTTATTT others(5): Show |
T | 1 | a0032c0030t0001g0157 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.497-1765_497-1754d others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16747345 | ||||||
chr19:16747386 | A | T | 2 | a0029c0065t0032g0166 a0043c0057t0026g0202 |
2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.497-1753A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747386 | |||||||
chr19:16747447 | G | A | 10 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(7): Show |
10 | HG02647.hp1 HG02809.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-1692G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747447 | |||||||
chr19:16747448 | C | T | 32 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(29): Show |
32 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.497-1691C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747448 | |||||||
chr19:16747739 | C | A | 31 | a0002c0002t0001g0201 a0004c0009t0005g0140 a0004c0009t0005g0224 others(28): Show |
31 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.497-1400C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747739 | |||||||
chr19:16747793 | T | C | 1 | a0004c0005t0022g0050 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.497-1346T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747793 | |||||||
chr19:16747872 | T | C | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.497-1267T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747872 | |||||||
chr19:16747910 | A | G | 1 | a0003c0003t0003g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.497-1229A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747910 | |||||||
chr19:16748006 | T | C | 41 | a0002c0002t0001g0201 a0004c0009t0005g0140 a0004c0009t0005g0224 others(38): Show |
41 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.497-1133T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748006 | |||||||
chr19:16748127 | G | A | 10 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(7): Show |
10 | HG02647.hp1 HG02809.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-1012G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748127 | |||||||
chr19:16748141 | G | A | 11 | a0004c0005t0006g0211 a0004c0005t0006g0225 a0004c0005t0006g0227 others(8): Show |
11 | HG02055.hp1 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.497-998G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748141 | |||||||
chr19:16748173 | A | G | 41 | a0002c0002t0001g0201 a0004c0009t0005g0140 a0004c0009t0005g0224 others(38): Show |
41 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.497-966A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748173 | |||||||
chr19:16748176 | G | A | 1 | a0003c0003t0044g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.497-963G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748176 | |||||||
chr19:16748264 | A | G | 41 | a0002c0002t0001g0201 a0004c0009t0005g0140 a0004c0009t0005g0224 others(38): Show |
41 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.497-875A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748264 | |||||||
chr19:16748272 | C | T | 2 | a0010c0013t0008g0188 a0010c0013t0009g0045 |
2 | HG00735.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.497-867C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748272 | |||||||
chr19:16748566 | C | T | 1 | a0004c0005t0006g0225 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.497-573C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748566 | |||||||
chr19:16748716 | C | T | 2 | a0004c0009t0005g0140 a0004c0009t0005g0224 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.497-423C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748716 | |||||||
chr19:16748823 | C | CAAT | 11 | a0001c0001t0001g0171 a0001c0001t0005g0241 a0001c0001t0005g0244 others(8): Show |
11 | HG01433.hp1 HG01433.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-301_497-299dup others(3): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16748823 | ||||||
chr19:16748838 | T | G | 29 | a0001c0001t0024g0108 a0001c0046t0001g0219 a0002c0002t0001g0142 others(26): Show |
29 | HG00099.hp1 HG01071.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.497-301T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748838 | |||||||
chr19:16748838 | TAAG | T | 30 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(27): Show |
30 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.497-292_497-290del others(3): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16748838 | ||||||
chr19:16748841 | G | T | 16 | a0002c0002t0001g0177 a0002c0008t0001g0135 a0002c0008t0001g0139 others(13): Show |
16 | HG01192.hp2 HG02055.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.497-298G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748841 | |||||||
chr19:16748844 | G | T | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.497-295G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748844 | |||||||
chr19:16748904 | C | G | 1 | a0033c0048t0018g0129 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.497-235C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748904 | |||||||
chr19:16748930 | C | T | 2 | a0004c0009t0013g0206 a0006c0014t0002g0015 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.497-209C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748930 | |||||||
chr19:16749008 | A | G | 41 | a0002c0002t0001g0201 a0004c0009t0005g0140 a0004c0009t0005g0224 others(38): Show |
41 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.497-131A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16749008 | |||||||
chr19:16749046 | T | C | 2 | a0016c0019t0017g0294 a0016c0019t0017g0295 |
2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.497-93T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16749046 | |||||||
chr19:16749110 | C | T | 10 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(7): Show |
10 | HG02647.hp1 HG02809.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-29C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16749110 | |||||||
chr19:16750564 | C | G | 3 | a0029c0065t0032g0166 a0030c0066t0008g0264 a0043c0057t0026g0202 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1769+153C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16750564 | |||||||
chr19:16750736 | A | G | 1 | a0003c0003t0002g0069 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1769+325A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16750736 | |||||||
chr19:16750834 | C | G | 1 | a0002c0002t0002g0123 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1769+423C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16750834 | |||||||
chr19:16750865 | T | C | 1 | a0045c0051t0002g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1769+454T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16750865 | |||||||
chr19:16750910 | AG | A | 13 | a0007c0028t0002g0115 a0007c0028t0034g0258 a0007c0029t0002g0297 others(10): Show |
13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1769+500delG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16750910 | |||||||
chr19:16750952 | T | C | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1769+541T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16750952 | |||||||
chr19:16751093 | G | A | 32 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(29): Show |
32 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.1769+682G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16751093 | |||||||
chr19:16751181 | G | A | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1769+770G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16751181 | |||||||
chr19:16751224 | CA | C | 74 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(71): Show |
74 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.1769+830delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16751224 | ||||||
chr19:16751224 | CAA | C | 34 | a0001c0007t0002g0007 a0001c0007t0002g0057 a0004c0005t0001g0296 others(31): Show |
34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.1769+829_1769+830d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16751224 | ||||||
chr19:16751241 | AT | A | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1769+831delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16751241 | |||||||
chr19:16751246 | A | G | 20 | a0007c0028t0002g0115 a0007c0028t0034g0258 a0007c0029t0002g0297 others(17): Show |
20 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1769+835A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16751246 | |||||||
chr19:16751432 | AAAGG | A | 3 | a0029c0065t0032g0166 a0030c0066t0008g0264 a0043c0057t0026g0202 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1769+1035_1769+103 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16751432 | ||||||
chr19:16751481 | AAAGG | A | 9 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(6): Show |
9 | HG02280.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1769+1087_1769+109 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16751481 | ||||||
chr19:16751540 | C | T | 1 | a0005c0016t0002g0101 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1769+1129C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16751540 | |||||||
chr19:16751658 | C | T | 55 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(52): Show |
55 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1769+1247C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16751658 | |||||||
chr19:16751779 | C | T | 3 | a0001c0001t0005g0154 a0001c0001t0005g0245 a0001c0001t0014g0187 |
3 | HG00558.hp1 HG02027.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1769+1368C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16751779 | |||||||
chr19:16751817 | AGAAG | A | 16 | a0002c0002t0001g0142 a0002c0002t0001g0190 a0007c0028t0002g0115 others(13): Show |
16 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1769+1427_1769+143 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16751817 | ||||||
chr19:16751860 | AAAG | A | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1769+1453_1769+145 others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16751860 | ||||||
chr19:16751982 | AAAGG | A | 11 | a0001c0001t0001g0263 a0001c0001t0002g0021 a0001c0001t0002g0029 others(8): Show |
11 | HG02630.hp1 HG02647.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1769+1591_1769+159 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16751982 | ||||||
chr19:16752215 | G | GT | 21 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(18): Show |
21 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1769+1806dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16752215 | ||||||
chr19:16752215 | G | T | 13 | a0007c0028t0002g0115 a0007c0028t0034g0258 a0007c0029t0002g0297 others(10): Show |
13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1769+1804G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752215 | |||||||
chr19:16752217 | TG | T | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1769+1807delG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752217 | |||||||
chr19:16752218 | G | T | 34 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(31): Show |
34 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1769+1807G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752218 | |||||||
chr19:16752252 | C | T | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1769+1841C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752252 | |||||||
chr19:16752259 | C | T | 13 | a0007c0028t0002g0115 a0007c0028t0034g0258 a0007c0029t0002g0297 others(10): Show |
13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1769+1848C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752259 | |||||||
chr19:16752270 | A | G | 6 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(3): Show |
6 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1769+1859A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752270 | |||||||
chr19:16752458 | C | G | 1 | a0004c0009t0008g0286 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1769+2047C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752458 | |||||||
chr19:16752526 | T | TGCATGCC others(10): Show |
74 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(71): Show |
74 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.1769+2117_1769+211 others(21): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16752526 | ||||||
chr19:16752590 | A | G | 1 | a0003c0006t0002g0086 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1769+2179A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752590 | |||||||
chr19:16752714 | C | A | 1 | a0005c0004t0002g0074 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1769+2303C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752714 | |||||||
chr19:16752739 | G | A | 2 | a0002c0008t0001g0168 a0043c0057t0026g0202 |
2 | HG01358.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1769+2328G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752739 | |||||||
chr19:16752783 | G | C | 1 | a0001c0001t0001g0242 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1769+2372G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752783 | |||||||
chr19:16752798 | A | C | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1769+2387A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752798 | |||||||
chr19:16752876 | G | C | 1 | a0003c0006t0002g0100 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1769+2465G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752876 | |||||||
chr19:16752892 | G | A | 22 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(19): Show |
22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1769+2481G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752892 | |||||||
chr19:16752951 | T | C | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1769+2540T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752951 | |||||||
chr19:16753120 | C | T | 22 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(19): Show |
22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1769+2709C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16753120 | |||||||
chr19:16753205 | A | G | 4 | a0004c0017t0001g0212 a0004c0017t0002g0018 a0004c0017t0002g0019 others(1): Show |
4 | HG02257.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1769+2794A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16753205 | |||||||
chr19:16753553 | C | T | 22 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(19): Show |
22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1769+3142C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16753553 | |||||||
chr19:16753571 | C | A | 2 | a0002c0002t0001g0142 a0002c0002t0001g0190 |
2 | NA18963.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1769+3160C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16753571 | |||||||
chr19:16753610 | G | T | 1 | a0002c0002t0020g0249 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1769+3199G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16753610 | |||||||
chr19:16753829 | T | TCATC | 93 | a0001c0001t0001g0136 a0001c0001t0004g0032 a0001c0001t0004g0034 others(90): Show |
93 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.1769+3454_1769+345 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16753829 | ||||||
chr19:16753829 | T | TCATCCAT others(5): Show |
1 | a0003c0003t0044g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1769+3446_1769+345 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16753829 | ||||||
chr19:16753829 | TCATC | T | 15 | a0003c0003t0002g0091 a0007c0028t0002g0115 a0007c0028t0034g0258 others(12): Show |
15 | HG00642.hp2 HG01496.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1769+3454_1769+345 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16753829 | ||||||
chr19:16753829 | TCATCCAT others(13): Show |
T | 1 | a0001c0001t0001g0197 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1769+3438_1769+345 others(24): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16753829 | ||||||
chr19:16753876 | T | C | 140 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(137): Show |
140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1769+3465T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16753876 | |||||||
chr19:16754026 | TATCC | T | 66 | a0001c0001t0002g0021 a0002c0002t0001g0170 a0002c0002t0005g0287 others(63): Show |
66 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.1769+3641_1769+364 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16754026 | ||||||
chr19:16754303 | G | A | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1769+3892G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16754303 | |||||||
chr19:16754462 | T | TTCCA | 28 | a0001c0001t0001g0263 a0001c0001t0002g0029 a0001c0001t0003g0220 others(25): Show |
28 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.1769+4094_1769+409 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16754462 | ||||||
chr19:16754462 | T | TTCCATCC others(1): Show |
3 | a0001c0001t0003g0162 a0002c0002t0004g0009 a0037c0058t0035g0167 |
3 | HG01346.hp1 HG02083.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1769+4090_1769+409 others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16754462 | ||||||
chr19:16754462 | TTCCA | T | 88 | a0001c0001t0002g0043 a0001c0001t0005g0154 a0001c0001t0005g0245 others(85): Show |
88 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.1769+4094_1769+409 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16754462 | ||||||
chr19:16754462 | TTCCATCC others(1): Show |
T | 32 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(29): Show |
32 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.1769+4090_1769+409 others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16754462 | ||||||
chr19:16754462 | TTCCATCC others(5): Show |
T | 1 | a0005c0004t0001g0278 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1769+4086_1769+409 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16754462 | ||||||
chr19:16754506 | A | G | 32 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(29): Show |
32 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.1769+4095A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16754506 | |||||||
chr19:16754513 | C | G | 2 | a0003c0003t0004g0099 a0003c0003t0024g0087 |
2 | NA18966.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1769+4102C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16754513 | |||||||
chr19:16754790 | T | TCATC | 43 | a0002c0002t0001g0291 a0004c0005t0001g0296 a0004c0005t0006g0211 others(40): Show |
43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.1769+4406_1770-440 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16754790 | ||||||
chr19:16754790 | T | TCATCCAT others(1): Show |
29 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(26): Show |
29 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1769+4402_1770-440 others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16754790 | ||||||
chr19:16754800 | A | G | 6 | a0007c0029t0002g0297 a0007c0029t0002g0298 a0007c0069t0043g0299 others(3): Show |
6 | HG01891.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1769+4389A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16754800 | |||||||
chr19:16754921 | A | G | 1 | a0004c0060t0002g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1770-4304A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16754921 | |||||||
chr19:16755124 | T | C | 14 | a0002c0002t0001g0201 a0007c0028t0002g0115 a0007c0028t0034g0258 others(11): Show |
14 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1770-4101T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755124 | |||||||
chr19:16755228 | G | T | 11 | a0002c0002t0004g0033 a0002c0033t0002g0012 a0003c0003t0004g0061 others(8): Show |
11 | HG00609.hp1 HG02155.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1770-3997G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755228 | |||||||
chr19:16755230 | G | A | 2 | a0014c0022t0001g0231 a0014c0022t0002g0046 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1770-3995G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755230 | |||||||
chr19:16755251 | C | G | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1770-3974C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755251 | |||||||
chr19:16755292 | C | T | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1770-3933C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755292 | |||||||
chr19:16755293 | G | A | 3 | a0014c0022t0001g0231 a0014c0022t0002g0046 a0014c0022t0002g0051 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1770-3932G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755293 | |||||||
chr19:16755314 | C | T | 6 | a0001c0007t0001g0239 a0001c0007t0002g0007 a0001c0007t0002g0057 others(3): Show |
6 | NA18747.hp2 NA18960.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1770-3911C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755314 | |||||||
chr19:16755523 | G | A | 1 | a0004c0005t0006g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1770-3702G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755523 | |||||||
chr19:16755663 | C | T | 22 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(19): Show |
22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1770-3562C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755663 | |||||||
chr19:16755687 | C | CTTAT | 6 | a0001c0001t0003g0179 a0001c0001t0003g0191 a0005c0004t0002g0042 others(3): Show |
6 | HG00544.hp1 HG02004.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1770-3510_1770-350 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16755687 | ||||||
chr19:16755687 | C | CTTATTTA others(5): Show |
69 | a0001c0001t0001g0178 a0001c0001t0001g0260 a0001c0001t0001g0261 others(66): Show |
69 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1770-3518_1770-350 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16755687 | ||||||
chr19:16755687 | C | CTTATTTA others(9): Show |
10 | a0001c0001t0001g0136 a0001c0001t0001g0164 a0001c0001t0001g0197 others(7): Show |
10 | HG00544.hp2 HG01934.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.1770-3522_1770-350 others(20): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16755687 | ||||||
chr19:16755687 | C | CTTATTTA others(13): Show |
1 | a0001c0001t0001g0158 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1770-3526_1770-350 others(24): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16755687 | ||||||
chr19:16755687 | CTTAT | C | 123 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(120): Show |
123 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.1770-3510_1770-350 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16755687 | ||||||
chr19:16755687 | CTTATTTA others(9): Show |
C | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1770-3522_1770-350 others(20): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16755687 | ||||||
chr19:16755726 | T | TG | 13 | a0007c0028t0002g0115 a0007c0028t0034g0258 a0007c0029t0002g0297 others(10): Show |
13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1770-3495dupG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16755726 | ||||||
chr19:16755971 | G | C | 28 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(25): Show |
28 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.1770-3254G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755971 | |||||||
chr19:16756014 | T | C | 3 | a0016c0019t0017g0294 a0016c0019t0017g0295 a0016c0019t0022g0124 |
3 | HG03098.hp1 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1770-3211T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756014 | |||||||
chr19:16756031 | A | G | 3 | a0001c0001t0021g0150 a0002c0002t0003g0186 a0005c0004t0004g0090 |
3 | HG00597.hp2 NA19005.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1770-3194A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756031 | |||||||
chr19:16756145 | T | A | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770-3080T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756145 | |||||||
chr19:16756251 | C | A | 1 | a0004c0005t0018g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1770-2974C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756251 | |||||||
chr19:16756346 | T | C | 1 | a0004c0060t0002g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1770-2879T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756346 | |||||||
chr19:16756721 | C | CAGTACCC others(12): Show |
1 | a0001c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1770-2498_1770-249 others(23): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16756721 | ||||||
chr19:16756831 | C | A | 1 | a0002c0002t0020g0249 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1770-2394C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756831 | |||||||
chr19:16756853 | C | T | 21 | a0001c0001t0024g0108 a0004c0009t0005g0140 a0004c0009t0005g0224 others(18): Show |
21 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1770-2372C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756853 | |||||||
chr19:16756862 | C | G | 1 | a0003c0003t0044g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1770-2363C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756862 | |||||||
chr19:16756992 | C | A | 2 | a0002c0002t0001g0291 a0039c0039t0015g0055 |
2 | NA18993.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1770-2233C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756992 | |||||||
chr19:16757162 | T | C | 134 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(131): Show |
134 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(131): Show |
intron_variant | MODIFIER | c.1770-2063T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757162 | |||||||
chr19:16757279 | C | A | 1 | a0005c0004t0002g0059 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1770-1946C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757279 | |||||||
chr19:16757360 | G | A | 21 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(18): Show |
21 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1770-1865G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757360 | |||||||
chr19:16757447 | A | G | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770-1778A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757447 | |||||||
chr19:16757612 | G | A | 13 | a0007c0028t0002g0115 a0007c0028t0034g0258 a0007c0029t0002g0297 others(10): Show |
13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1770-1613G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757612 | |||||||
chr19:16757632 | A | G | 14 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(11): Show |
14 | HG02055.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1770-1593A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757632 | |||||||
chr19:16757671 | A | T | 32 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(29): Show |
32 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.1770-1554A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757671 | |||||||
chr19:16757744 | G | C | 134 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(131): Show |
134 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(131): Show |
intron_variant | MODIFIER | c.1770-1481G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757744 | |||||||
chr19:16757917 | T | A | 1 | a0001c0007t0002g0110 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1770-1308T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757917 | |||||||
chr19:16757918 | G | C | 1 | a0001c0007t0002g0110 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1770-1307G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757918 | |||||||
chr19:16757933 | T | C | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770-1292T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757933 | |||||||
chr19:16758051 | C | CA | 95 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(92): Show |
95 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.1770-1161dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16758051 | ||||||
chr19:16758051 | C | CAA | 8 | a0004c0060t0002g0125 a0009c0010t0002g0114 a0009c0010t0010g0131 others(5): Show |
8 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1770-1162_1770-116 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16758051 | ||||||
chr19:16758051 | CA | C | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770-1161delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16758051 | ||||||
chr19:16758073 | G | C | 136 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(133): Show |
136 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(133): Show |
intron_variant | MODIFIER | c.1770-1152G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758073 | |||||||
chr19:16758152 | T | C | 136 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(133): Show |
136 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(133): Show |
intron_variant | MODIFIER | c.1770-1073T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758152 | |||||||
chr19:16758344 | A | G | 13 | a0007c0028t0002g0115 a0007c0028t0034g0258 a0007c0029t0002g0297 others(10): Show |
13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1770-881A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758344 | |||||||
chr19:16758449 | A | G | 101 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(98): Show |
101 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.1770-776A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758449 | |||||||
chr19:16758510 | C | T | 5 | a0007c0029t0002g0297 a0007c0029t0002g0298 a0020c0024t0001g0251 others(2): Show |
5 | HG01891.hp2 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770-715C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758510 | |||||||
chr19:16758628 | A | G | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770-597A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758628 | |||||||
chr19:16758655 | C | T | 51 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(48): Show |
51 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1770-570C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758655 | |||||||
chr19:16758849 | A | G | 33 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(30): Show |
33 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.1770-376A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758849 | |||||||
chr19:16758868 | C | G | 18 | a0001c0001t0001g0147 a0001c0001t0001g0160 a0002c0002t0001g0142 others(15): Show |
18 | HG00673.hp1 HG01109.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.1770-357C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758868 | |||||||
chr19:16758948 | G | T | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770-277G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758948 | |||||||
chr19:16758965 | C | T | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1770-260C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758965 | |||||||
chr19:16759003 | C | CA | 39 | a0001c0001t0001g0147 a0001c0001t0001g0160 a0001c0001t0003g0176 others(36): Show |
39 | HG00597.hp2 HG00673.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1770-194dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | ||||||
chr19:16759003 | C | CAA | 8 | a0001c0001t0005g0245 a0001c0001t0031g0214 a0002c0002t0001g0207 others(5): Show |
8 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.1770-195_1770-194d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | ||||||
chr19:16759003 | CA | C | 51 | a0001c0001t0001g0158 a0001c0001t0001g0164 a0001c0001t0001g0178 others(48): Show |
51 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1770-194delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | ||||||
chr19:16759003 | CAAA | C | 13 | a0004c0060t0002g0125 a0009c0010t0002g0114 a0009c0010t0010g0131 others(10): Show |
13 | HG01361.hp1 HG02559.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1770-196_1770-194d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | ||||||
chr19:16759003 | CAAAA | C | 14 | a0003c0006t0002g0092 a0004c0005t0006g0211 a0004c0005t0006g0226 others(11): Show |
14 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1770-197_1770-194d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | ||||||
chr19:16759003 | CAAAAA | C | 27 | a0002c0008t0001g0168 a0002c0036t0002g0020 a0004c0005t0001g0296 others(24): Show |
27 | HG00642.hp2 HG01081.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.1770-198_1770-194d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | ||||||
chr19:16759003 | CAAAAAA | C | 46 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(43): Show |
46 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1770-199_1770-194d others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | ||||||
chr19:16759003 | CAAAAAAA others(3): Show |
C | 19 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(16): Show |
19 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1770-203_1770-194d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | ||||||
chr19:16759003 | CAAAAAAA others(4): Show |
C | 1 | a0006c0014t0008g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1770-204_1770-194d others(13): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | ||||||
chr19:16759003 | CAAAAAAA others(5): Show |
C | 1 | a0015c0025t0002g0048 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1770-205_1770-194d others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | ||||||
chr19:16759003 | CAAAAAAA others(6): Show |
C | 1 | a0015c0025t0002g0049 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1770-206_1770-194d others(15): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | ||||||
chr19:16759072 | C | G | 11 | a0007c0028t0002g0115 a0007c0028t0034g0258 a0007c0029t0002g0297 others(8): Show |
11 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1770-153C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16759072 | |||||||
chr19:16759115 | T | C | 33 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(30): Show |
33 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.1770-110T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16759115 | |||||||
chr19:16759155 | T | C | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770-70T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16759155 | |||||||
chr19:16759758 | G | T | 4 | a0006c0044t0001g0255 a0014c0022t0001g0231 a0014c0022t0002g0046 others(1): Show |
4 | HG01884.hp2 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1973+330G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16759758 | |||||||
chr19:16759759 | C | T | 4 | a0006c0044t0001g0255 a0014c0022t0001g0231 a0014c0022t0002g0046 others(1): Show |
4 | HG01884.hp2 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1973+331C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16759759 | |||||||
chr19:16759856 | C | T | 1 | a0037c0058t0035g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1973+428C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16759856 | |||||||
chr19:16759858 | G | A | 2 | a0018c0026t0002g0083 a0018c0026t0015g0078 |
2 | HG01361.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1973+430G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16759858 | |||||||
chr19:16759976 | G | C | 7 | a0004c0009t0008g0205 a0004c0009t0008g0286 a0004c0009t0013g0206 others(4): Show |
7 | HG01109.hp2 HG02886.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1973+548G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16759976 | |||||||
chr19:16760037 | C | G | 6 | a0002c0002t0002g0010 a0002c0002t0002g0013 a0002c0002t0003g0200 others(3): Show |
6 | HG00597.hp1 HG00609.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1973+609C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760037 | |||||||
chr19:16760110 | G | A | 6 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(3): Show |
6 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1973+682G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760110 | |||||||
chr19:16760128 | C | T | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1973+700C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760128 | |||||||
chr19:16760171 | G | GACTAA | 19 | a0004c0005t0023g0094 a0004c0005t0023g0095 a0004c0005t0029g0265 others(16): Show |
19 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1973+768_1973+772d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760171 | ||||||
chr19:16760171 | G | GACTAAAC others(3): Show |
16 | a0001c0001t0004g0109 a0004c0005t0001g0296 a0004c0005t0006g0211 others(13): Show |
16 | HG00735.hp1 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1973+763_1973+772d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760171 | ||||||
chr19:16760171 | GACTAA | G | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1973+768_1973+772d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760171 | ||||||
chr19:16760229 | C | CATTTT | 43 | a0001c0001t0001g0158 a0001c0001t0005g0169 a0001c0001t0014g0187 others(40): Show |
43 | HG00544.hp1 HG00597.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.1973+844_1973+848d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | ||||||
chr19:16760229 | C | CATTTTAT others(3): Show |
21 | a0001c0001t0004g0032 a0001c0001t0004g0034 a0001c0001t0004g0035 others(18): Show |
21 | HG00280.hp1 HG01192.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1973+839_1973+848d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | ||||||
chr19:16760229 | C | CATTTTAT others(8): Show |
39 | a0001c0001t0001g0171 a0001c0001t0003g0176 a0001c0001t0003g0179 others(36): Show |
39 | HG00323.hp1 HG00558.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1973+834_1973+848d others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | ||||||
chr19:16760229 | C | CATTTTAT others(13): Show |
16 | a0001c0001t0005g0184 a0001c0001t0005g0241 a0001c0001t0005g0244 others(13): Show |
16 | HG01358.hp1 HG01433.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1973+829_1973+848d others(22): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | ||||||
chr19:16760229 | C | CATTTTAT others(18): Show |
4 | a0002c0002t0005g0195 a0002c0002t0007g0041 a0007c0029t0002g0297 others(1): Show |
4 | HG01975.hp1 HG02257.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1973+824_1973+848d others(27): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | ||||||
chr19:16760229 | CATTTT | C | 71 | a0001c0001t0001g0147 a0001c0001t0001g0164 a0001c0001t0001g0178 others(68): Show |
71 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.1973+844_1973+848d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | ||||||
chr19:16760229 | CATTTTAT others(3): Show |
C | 2 | a0014c0022t0001g0231 a0014c0022t0002g0046 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1973+839_1973+848d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | ||||||
chr19:16760229 | CATTTTAT others(8): Show |
C | 68 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(65): Show |
68 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.1973+834_1973+848d others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | ||||||
chr19:16760229 | CATTTTAT others(13): Show |
C | 1 | a0001c0001t0002g0029 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1973+829_1973+848d others(22): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | ||||||
chr19:16760569 | CATTTT | C | 4 | a0006c0044t0001g0255 a0014c0022t0001g0231 a0014c0022t0002g0046 others(1): Show |
4 | HG01884.hp2 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1973+1151_1973+115 others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760569 | ||||||
chr19:16760682 | C | A | 1 | a0029c0065t0032g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1973+1254C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760682 | |||||||
chr19:16760694 | G | T | 1 | a0026c0043t0009g0023 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1973+1266G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760694 | |||||||
chr19:16760820 | C | A | 1 | a0002c0002t0001g0170 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1974-1159C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760820 | |||||||
chr19:16760827 | T | A | 1 | a0002c0002t0005g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1974-1152T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760827 | |||||||
chr19:16760894 | T | C | 51 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(48): Show |
51 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1974-1085T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760894 | |||||||
chr19:16760896 | T | C | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1974-1083T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760896 | |||||||
chr19:16760911 | G | A | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1974-1068G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760911 | |||||||
chr19:16761135 | C | T | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1974-844C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761135 | |||||||
chr19:16761174 | A | C | 14 | a0007c0028t0002g0115 a0007c0028t0034g0258 a0007c0029t0002g0297 others(11): Show |
14 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1974-805A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761174 | |||||||
chr19:16761312 | T | C | 3 | a0029c0065t0032g0166 a0030c0066t0008g0264 a0043c0057t0026g0202 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1974-667T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761312 | |||||||
chr19:16761348 | T | C | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1974-631T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761348 | |||||||
chr19:16761350 | C | CTCTT | 28 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(25): Show |
28 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.1974-614_1974-611d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761350 | ||||||
chr19:16761358 | T | TTCTTTCT others(24): Show |
2 | a0006c0014t0002g0015 a0010c0013t0009g0045 |
2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1974-611_1974-610i others(33): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761358 | ||||||
chr19:16761358 | T | TTCTTTCT others(28): Show |
7 | a0004c0009t0008g0205 a0004c0009t0008g0286 a0004c0009t0013g0206 others(4): Show |
7 | HG00735.hp2 HG02886.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1974-611_1974-610i others(37): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761358 | ||||||
chr19:16761358 | T | TTCTTTCT others(32): Show |
2 | a0004c0009t0005g0140 a0004c0009t0005g0224 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1974-611_1974-610i others(41): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761358 | ||||||
chr19:16761358 | T | TTCTTTCT others(36): Show |
2 | a0004c0009t0009g0047 a0006c0014t0008g0253 |
2 | HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1974-611_1974-610i others(45): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761358 | ||||||
chr19:16761358 | T | TTCTTTCT others(40): Show |
3 | a0010c0013t0013g0172 a0010c0013t0013g0173 a0026c0043t0009g0023 |
3 | HG02145.hp2 HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1974-611_1974-610i others(49): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761358 | ||||||
chr19:16761358 | T | TTCTTTCT others(44): Show |
2 | a0013c0020t0016g0003 a0013c0020t0016g0004 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1974-611_1974-610i others(53): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761358 | ||||||
chr19:16761358 | T | TTCTTTCT others(48): Show |
1 | a0004c0009t0009g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1974-611_1974-610i others(57): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761358 | ||||||
chr19:16761358 | T | TTCTTTCT others(52): Show |
1 | a0013c0020t0008g0257 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1974-611_1974-610i others(61): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761358 | ||||||
chr19:16761440 | C | T | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1974-539C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761440 | |||||||
chr19:16761475 | T | A | 5 | a0001c0001t0004g0032 a0001c0001t0004g0034 a0001c0001t0004g0035 others(2): Show |
5 | HG01975.hp2 HG02273.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1974-504T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761475 | |||||||
chr19:16761514 | G | A | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1974-465G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761514 | |||||||
chr19:16761534 | C | CT | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1974-437dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761534 | ||||||
chr19:16761610 | G | A | 55 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(52): Show |
55 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1974-369G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761610 | |||||||
chr19:16761685 | C | T | 3 | a0003c0006t0002g0092 a0015c0025t0002g0048 a0015c0025t0002g0049 |
3 | HG02280.hp2 HG04115.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1974-294C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761685 | |||||||
chr19:16761701 | G | A | 51 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(48): Show |
51 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1974-278G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761701 | |||||||
chr19:16761804 | GA | G | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1974-165delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761804 | ||||||
chr19:16761947 | C | G | 1 | a0001c0001t0005g0169 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1974-32C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761947 | |||||||
chr19:16762195 | C | G | 1 | a0002c0002t0001g0199 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2133+57C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762195 | |||||||
chr19:16762287 | C | T | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2133+149C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762287 | |||||||
chr19:16762292 | C | A | 1 | a0003c0006t0002g0096 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2133+154C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762292 | |||||||
chr19:16762297 | C | CT | 9 | a0001c0001t0001g0136 a0002c0002t0003g0267 a0004c0005t0006g0228 others(6): Show |
9 | HG01175.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2133+176dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16762297 | ||||||
chr19:16762297 | C | CTT | 35 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(32): Show |
35 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.2133+175_2133+176d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16762297 | ||||||
chr19:16762297 | C | CTTT | 6 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(3): Show |
6 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2133+174_2133+176d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16762297 | ||||||
chr19:16762297 | C | CTTTT | 7 | a0002c0008t0001g0139 a0002c0008t0027g0137 a0002c0023t0001g0151 others(4): Show |
7 | HG01496.hp1 HG02886.hp1 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.2133+173_2133+176d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16762297 | ||||||
chr19:16762297 | C | CTTTTT | 48 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(45): Show |
48 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.2133+172_2133+176d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16762297 | ||||||
chr19:16762297 | CT | C | 11 | a0004c0009t0008g0205 a0004c0009t0008g0286 a0004c0009t0013g0206 others(8): Show |
11 | HG01109.hp2 HG02040.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2133+176delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16762297 | ||||||
chr19:16762298 | T | TTTTC | 9 | a0007c0028t0002g0115 a0007c0028t0034g0258 a0007c0029t0002g0297 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2133+163_2133+164i others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16762298 | ||||||
chr19:16762335 | C | T | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2133+197C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762335 | |||||||
chr19:16762336 | G | A | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2133+198G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762336 | |||||||
chr19:16762357 | C | T | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2133+219C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762357 | |||||||
chr19:16762361 | A | G | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2133+223A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762361 | |||||||
chr19:16762442 | A | G | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2133+304A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762442 | |||||||
chr19:16762555 | A | AAAAC | 33 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(30): Show |
33 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.2133+433_2133+436d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16762555 | ||||||
chr19:16762594 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2133+456T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762594 | |||||||
chr19:16762774 | C | T | 1 | a0004c0009t0008g0286 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2133+636C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762774 | |||||||
chr19:16762798 | C | T | 3 | a0001c0001t0005g0154 a0001c0001t0005g0245 a0001c0001t0014g0187 |
3 | HG00558.hp1 HG02027.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.2133+660C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762798 | |||||||
chr19:16762917 | G | C | 1 | a0002c0002t0011g0105 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2133+779G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762917 | |||||||
chr19:16762925 | A | G | 33 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(30): Show |
33 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.2133+787A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762925 | |||||||
chr19:16763165 | G | A | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2134-663G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763165 | |||||||
chr19:16763183 | C | T | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2134-645C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763183 | |||||||
chr19:16763231 | C | G | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2134-597C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763231 | |||||||
chr19:16763320 | C | T | 51 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(48): Show |
51 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.2134-508C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763320 | |||||||
chr19:16763491 | A | G | 3 | a0029c0065t0032g0166 a0030c0066t0008g0264 a0043c0057t0026g0202 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2134-337A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763491 | |||||||
chr19:16763694 | G | A | 11 | a0001c0001t0001g0136 a0002c0002t0001g0148 a0002c0002t0001g0174 others(8): Show |
11 | HG00544.hp2 HG02027.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2134-134G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763694 | |||||||
chr19:16763697 | G | T | 1 | a0001c0001t0005g0246 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2134-131G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763697 | |||||||
chr19:16763699 | A | C | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2134-129A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763699 | |||||||
chr19:16763713 | T | C | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2134-115T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763713 | |||||||
chr19:16763977 | G | A | 1 | a0003c0003t0002g0091 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2251+32G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16763977 | |||||||
chr19:16763994 | C | T | 2 | a0008c0012t0001g0234 a0008c0012t0001g0235 |
2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2251+49C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16763994 | |||||||
chr19:16763995 | G | A | 1 | a0001c0007t0002g0122 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2251+50G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16763995 | |||||||
chr19:16764047 | C | G | 2 | a0013c0020t0016g0003 a0013c0020t0016g0004 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2251+102C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764047 | |||||||
chr19:16764199 | A | G | 1 | a0010c0013t0008g0188 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2251+254A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764199 | |||||||
chr19:16764265 | C | A | 1 | a0001c0001t0003g0237 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2251+320C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764265 | |||||||
chr19:16764278 | A | C | 1 | a0002c0002t0001g0156 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2251+333A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764278 | |||||||
chr19:16764304 | C | T | 1 | a0015c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2251+359C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764304 | |||||||
chr19:16764324 | C | T | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2251+379C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764324 | |||||||
chr19:16764349 | C | T | 1 | a0004c0005t0018g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2251+404C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764349 | |||||||
chr19:16764360 | T | TGTCC | 17 | a0004c0009t0008g0205 a0004c0009t0008g0286 a0004c0009t0009g0047 others(14): Show |
17 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.2251+416_2251+419d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764360 | ||||||
chr19:16764361 | G | GTCCA | 57 | a0001c0001t0001g0147 a0001c0001t0001g0160 a0001c0001t0001g0164 others(54): Show |
57 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.2251+455_2251+458d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764361 | ||||||
chr19:16764361 | G | GTCCATCC others(1): Show |
4 | a0002c0002t0001g0194 a0002c0002t0012g0198 a0003c0003t0002g0076 others(1): Show |
4 | HG00558.hp2 NA18945.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.2251+451_2251+458d others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764361 | ||||||
chr19:16764361 | GTCCA | G | 71 | a0001c0001t0003g0176 a0001c0001t0020g0289 a0001c0007t0001g0040 others(68): Show |
71 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.2251+455_2251+458d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764361 | ||||||
chr19:16764361 | GTCCATCC others(1): Show |
G | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2251+451_2251+458d others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764361 | ||||||
chr19:16764361 | GTCCATCC others(5): Show |
G | 3 | a0029c0065t0032g0166 a0030c0066t0008g0264 a0043c0057t0026g0202 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2251+447_2251+458d others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764361 | ||||||
chr19:16764361 | GTCCATCC others(13): Show |
G | 34 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(31): Show |
34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.2251+439_2251+458d others(22): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764361 | ||||||
chr19:16764365 | A | G | 11 | a0001c0007t0002g0122 a0002c0008t0001g0134 a0002c0008t0001g0135 others(8): Show |
11 | HG02132.hp2 HG02965.hp2 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.2251+420A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764365 | |||||||
chr19:16764369 | A | G | 67 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(64): Show |
67 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.2251+424A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764369 | |||||||
chr19:16764373 | A | G | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2251+428A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764373 | |||||||
chr19:16764377 | A | G | 3 | a0029c0065t0032g0166 a0030c0066t0008g0264 a0043c0057t0026g0202 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2251+432A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764377 | |||||||
chr19:16764385 | A | G | 34 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(31): Show |
34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.2251+440A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764385 | |||||||
chr19:16764392 | CATCCATC others(5): Show |
C | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2251+449_2251+460d others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764392 | ||||||
chr19:16764415 | T | C | 18 | a0001c0001t0004g0032 a0001c0001t0004g0034 a0001c0001t0004g0035 others(15): Show |
18 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.2251+470T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764415 | |||||||
chr19:16764466 | A | ACCAT | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2252-544_2252-541d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764466 | ||||||
chr19:16764777 | C | T | 72 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(69): Show |
72 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.2252-257C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764777 | |||||||
chr19:16765288 | T | C | 254 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0001c0001t0001g0158 others(251): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.2410+96T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765288 | |||||||
chr19:16765293 | A | G | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2410+101A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765293 | |||||||
chr19:16765305 | T | C | 1 | a0009c0010t0010g0276 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2410+113T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765305 | |||||||
chr19:16765401 | G | A | 2 | a0004c0005t0006g0228 a0004c0005t0006g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2410+209G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765401 | |||||||
chr19:16765415 | C | T | 1 | a0002c0002t0001g0201 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2410+223C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765415 | |||||||
chr19:16765550 | T | C | 51 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(48): Show |
51 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.2410+358T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765550 | |||||||
chr19:16765592 | C | T | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2410+400C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765592 | |||||||
chr19:16765690 | G | A | 34 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(31): Show |
34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.2410+498G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765690 | |||||||
chr19:16765704 | G | A | 69 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(66): Show |
69 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.2410+512G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765704 | |||||||
chr19:16765745 | G | A | 1 | a0009c0010t0010g0276 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2410+553G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765745 | |||||||
chr19:16765966 | G | A | 4 | a0006c0044t0001g0255 a0014c0022t0001g0231 a0014c0022t0002g0046 others(1): Show |
4 | HG01884.hp2 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2410+774G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765966 | |||||||
chr19:16765972 | G | A | 1 | a0022c0042t0001g0152 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2410+780G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765972 | |||||||
chr19:16766016 | C | CA | 18 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0002g0021 others(15): Show |
18 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.2410+843dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16766016 | ||||||
chr19:16766016 | CA | C | 76 | a0001c0001t0001g0171 a0001c0001t0004g0035 a0001c0001t0004g0112 others(73): Show |
76 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.2410+843delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16766016 | ||||||
chr19:16766032 | A | G | 69 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(66): Show |
69 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.2410+840A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16766032 | |||||||
chr19:16766036 | G | A | 1 | a0015c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2410+844G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16766036 | |||||||
chr19:16766161 | TATA | T | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2410+977_2410+979d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16766161 | ||||||
chr19:16766172 | C | T | 1 | a0018c0026t0015g0078 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2410+980C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16766172 | |||||||
chr19:16766277 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0020g0289 |
2 | HG01074.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2410+1085C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16766277 | |||||||
chr19:16766522 | T | C | 69 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(66): Show |
69 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.2410+1330T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16766522 | |||||||
chr19:16766553 | GGTTTT | G | 69 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(66): Show |
69 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.2410+1367_2410+137 others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16766553 | ||||||
chr19:16766554 | G | A | 1 | a0002c0002t0004g0033 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2410+1362G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16766554 | |||||||
chr19:16766591 | AT | A | 159 | a0001c0001t0001g0158 a0001c0001t0001g0164 a0001c0001t0003g0162 others(156): Show |
159 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.2410+1411delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16766591 | ||||||
chr19:16767014 | C | G | 1 | a0002c0002t0001g0170 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2410+1822C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767014 | |||||||
chr19:16767024 | A | G | 1 | a0027c0053t0001g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2410+1832A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767024 | |||||||
chr19:16767100 | C | T | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2410+1908C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767100 | |||||||
chr19:16767164 | C | T | 3 | a0029c0065t0032g0166 a0030c0066t0008g0264 a0043c0057t0026g0202 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2410+1972C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767164 | |||||||
chr19:16767167 | C | CT | 18 | a0001c0001t0001g0171 a0001c0001t0003g0176 a0001c0001t0004g0107 others(15): Show |
18 | HG00597.hp2 HG01081.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.2410+2002dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767167 | ||||||
chr19:16767167 | CT | C | 100 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0001c0001t0001g0158 others(97): Show |
100 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.2410+2002delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767167 | ||||||
chr19:16767167 | CTT | C | 50 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(47): Show |
50 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.2410+2001_2410+200 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767167 | ||||||
chr19:16767167 | CTTT | C | 12 | a0009c0010t0010g0131 a0009c0010t0010g0276 a0009c0010t0010g0283 others(9): Show |
12 | HG02109.hp1 HG02293.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2410+2000_2410+200 others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767167 | ||||||
chr19:16767167 | CTTTTTT | C | 50 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(47): Show |
50 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.2410+1997_2410+200 others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767167 | ||||||
chr19:16767167 | CTTTTTTT others(5): Show |
C | 9 | a0007c0028t0002g0115 a0007c0028t0034g0258 a0007c0029t0002g0297 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2410+1991_2410+200 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767167 | ||||||
chr19:16767167 | CTTTTTTT others(6): Show |
C | 4 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0022c0042t0001g0152 others(1): Show |
4 | HG01496.hp1 NA18993.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2410+1990_2410+200 others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767167 | ||||||
chr19:16767219 | G | A | 8 | a0004c0005t0048g0002 a0009c0010t0002g0114 a0009c0010t0010g0131 others(5): Show |
8 | HG02055.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.2410+2027G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767219 | |||||||
chr19:16767294 | C | A | 5 | a0002c0002t0004g0009 a0002c0002t0004g0033 a0002c0033t0002g0012 others(2): Show |
5 | HG00597.hp1 HG00609.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.2410+2102C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767294 | |||||||
chr19:16767364 | C | T | 2 | a0005c0004t0003g0248 a0005c0004t0004g0097 |
2 | HG00280.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.2410+2172C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767364 | |||||||
chr19:16767476 | G | A | 1 | a0005c0004t0002g0042 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2410+2284G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767476 | |||||||
chr19:16767543 | C | T | 69 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(66): Show |
69 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.2410+2351C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767543 | |||||||
chr19:16767561 | C | G | 138 | a0001c0001t0001g0160 a0001c0007t0001g0040 a0001c0007t0001g0213 others(135): Show |
138 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.2410+2369C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767561 | |||||||
chr19:16767593 | G | A | 9 | a0007c0028t0002g0115 a0007c0028t0034g0258 a0007c0029t0002g0297 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2410+2401G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767593 | |||||||
chr19:16767650 | C | T | 69 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(66): Show |
69 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.2410+2458C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767650 | |||||||
chr19:16767713 | C | T | 1 | a0002c0002t0001g0175 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2410+2521C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767713 | |||||||
chr19:16767771 | A | T | 3 | a0029c0065t0032g0166 a0030c0066t0008g0264 a0043c0057t0026g0202 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2410+2579A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767771 | |||||||
chr19:16767797 | C | A | 2 | a0002c0002t0001g0196 a0002c0002t0001g0218 |
2 | HG02056.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.2410+2605C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767797 | |||||||
chr19:16767816 | T | A | 1 | a0002c0002t0001g0177 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2410+2624T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767816 | |||||||
chr19:16767894 | G | A | 15 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(12): Show |
15 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2410+2702G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767894 | |||||||
chr19:16767982 | C | CT | 52 | a0001c0001t0001g0164 a0001c0001t0001g0171 a0001c0001t0001g0242 others(49): Show |
52 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.2410+2815dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767982 | ||||||
chr19:16767982 | CT | C | 77 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(74): Show |
77 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.2410+2815delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767982 | ||||||
chr19:16767982 | CTT | C | 6 | a0001c0007t0001g0239 a0002c0002t0002g0008 a0008c0012t0001g0232 others(3): Show |
6 | HG02818.hp1 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2410+2814_2410+281 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767982 | ||||||
chr19:16767982 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0136 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2410+2803_2410+281 others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767982 | ||||||
chr19:16768068 | C | T | 140 | a0001c0001t0001g0160 a0001c0007t0001g0040 a0001c0007t0001g0213 others(137): Show |
140 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(137): Show |
intron_variant | MODIFIER | c.2410+2876C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768068 | |||||||
chr19:16768135 | C | T | 13 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0007c0028t0002g0115 others(10): Show |
13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2410+2943C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768135 | |||||||
chr19:16768149 | C | A | 2 | a0005c0004t0003g0248 a0005c0004t0004g0097 |
2 | HG00280.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.2410+2957C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768149 | |||||||
chr19:16768216 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2410+3024G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768216 | |||||||
chr19:16768232 | G | A | 1 | a0035c0055t0037g0088 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2410+3040G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768232 | |||||||
chr19:16768291 | TGGCTAAG others(18): Show |
T | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2410+3122_2410+314 others(29): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16768291 | ||||||
chr19:16768333 | C | T | 1 | a0003c0003t0044g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2410+3141C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768333 | |||||||
chr19:16768389 | G | A | 13 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0007c0028t0002g0115 others(10): Show |
13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2410+3197G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768389 | |||||||
chr19:16768406 | C | T | 1 | a0009c0010t0010g0276 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2410+3214C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768406 | |||||||
chr19:16768450 | T | C | 1 | a0001c0001t0005g0246 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2410+3258T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768450 | |||||||
chr19:16768453 | A | C | 1 | a0001c0001t0001g0263 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2410+3261A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768453 | |||||||
chr19:16768462 | A | C | 138 | a0001c0001t0001g0160 a0001c0007t0001g0040 a0001c0007t0001g0213 others(135): Show |
138 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.2410+3270A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768462 | |||||||
chr19:16768569 | C | G | 1 | a0013c0020t0008g0257 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2410+3377C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768569 | |||||||
chr19:16768700 | G | A | 1 | a0007c0028t0002g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2410+3508G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768700 | |||||||
chr19:16768720 | A | C | 1 | a0001c0001t0005g0246 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2410+3528A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768720 | |||||||
chr19:16768740 | C | G | 138 | a0001c0001t0001g0160 a0001c0007t0001g0040 a0001c0007t0001g0213 others(135): Show |
138 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.2410+3548C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768740 | |||||||
chr19:16768795 | G | A | 10 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(7): Show |
10 | HG02647.hp1 HG02809.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2410+3603G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768795 | |||||||
chr19:16768858 | C | T | 13 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0007c0028t0002g0115 others(10): Show |
13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2410+3666C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768858 | |||||||
chr19:16768895 | A | G | 138 | a0001c0001t0001g0160 a0001c0007t0001g0040 a0001c0007t0001g0213 others(135): Show |
138 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.2410+3703A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768895 | |||||||
chr19:16768991 | T | C | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2410+3799T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768991 | |||||||
chr19:16769332 | C | T | 1 | a0004c0005t0006g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2411-3794C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16769332 | |||||||
chr19:16769459 | T | TA | 49 | a0001c0007t0002g0007 a0002c0023t0001g0151 a0002c0023t0002g0102 others(46): Show |
49 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(46): Show |
intron_variant | MODIFIER | c.2411-3655dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16769459 | ||||||
chr19:16769459 | T | TAA | 69 | a0001c0001t0001g0160 a0001c0007t0001g0040 a0001c0007t0001g0213 others(66): Show |
69 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.2411-3656_2411-365 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16769459 | ||||||
chr19:16769459 | TA | T | 70 | a0001c0001t0001g0136 a0001c0001t0001g0158 a0001c0001t0001g0164 others(67): Show |
70 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.2411-3655delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16769459 | ||||||
chr19:16769515 | G | T | 1 | a0002c0023t0001g0151 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2411-3611G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16769515 | |||||||
chr19:16769653 | G | T | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2411-3473G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16769653 | |||||||
chr19:16769673 | C | T | 56 | a0001c0001t0001g0160 a0001c0007t0001g0040 a0001c0007t0001g0213 others(53): Show |
56 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.2411-3453C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16769673 | |||||||
chr19:16769698 | ACTTTGGA others(47): Show |
A | 1 | a0003c0003t0024g0087 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2411-3427_2411-337 others(58): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16769698 | |||||||
chr19:16769734 | G | A | 4 | a0004c0017t0001g0212 a0004c0017t0002g0018 a0004c0017t0002g0019 others(1): Show |
4 | HG02257.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2411-3392G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16769734 | |||||||
chr19:16769770 | T | C | 1 | a0001c0007t0002g0057 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2411-3356T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16769770 | |||||||
chr19:16769969 | C | G | 4 | a0004c0017t0001g0212 a0004c0017t0002g0018 a0004c0017t0002g0019 others(1): Show |
4 | HG02257.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2411-3157C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16769969 | |||||||
chr19:16770027 | C | A | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2411-3099C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770027 | |||||||
chr19:16770090 | G | A | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2411-3036G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770090 | |||||||
chr19:16770144 | T | C | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2411-2982T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770144 | |||||||
chr19:16770162 | G | A | 71 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(68): Show |
71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2411-2964G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770162 | |||||||
chr19:16770354 | C | T | 8 | a0001c0001t0003g0176 a0001c0001t0003g0183 a0001c0001t0003g0185 others(5): Show |
8 | HG01081.hp2 HG01257.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.2411-2772C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770354 | |||||||
chr19:16770498 | G | A | 49 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(46): Show |
49 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.2411-2628G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770498 | |||||||
chr19:16770553 | C | G | 138 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(135): Show |
138 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.2411-2573C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770553 | |||||||
chr19:16770568 | G | A | 1 | a0021c0041t0002g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2411-2558G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770568 | |||||||
chr19:16770839 | T | C | 1 | a0002c0031t0001g0155 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2411-2287T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770839 | |||||||
chr19:16771021 | C | T | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2411-2105C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771021 | |||||||
chr19:16771054 | C | A | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2411-2072C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771054 | |||||||
chr19:16771083 | A | G | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2411-2043A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771083 | |||||||
chr19:16771189 | C | T | 1 | a0011c0011t0011g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2411-1937C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771189 | |||||||
chr19:16771232 | G | T | 1 | a0004c0005t0018g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2411-1894G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771232 | |||||||
chr19:16771321 | A | G | 54 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(51): Show |
54 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.2411-1805A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771321 | |||||||
chr19:16771359 | A | C | 1 | a0010c0013t0009g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2411-1767A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771359 | |||||||
chr19:16771610 | T | G | 71 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(68): Show |
71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2411-1516T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771610 | |||||||
chr19:16771618 | A | G | 1 | a0009c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2411-1508A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771618 | |||||||
chr19:16771746 | C | T | 19 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(16): Show |
19 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.2411-1380C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771746 | |||||||
chr19:16771831 | C | CT | 62 | a0001c0001t0001g0242 a0001c0001t0003g0176 a0001c0001t0004g0032 others(59): Show |
62 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.2411-1277dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16771831 | ||||||
chr19:16771831 | C | CTT | 6 | a0004c0005t0023g0094 a0004c0005t0023g0095 a0004c0005t0029g0265 others(3): Show |
6 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2411-1278_2411-127 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16771831 | ||||||
chr19:16771831 | CT | C | 9 | a0001c0001t0001g0261 a0002c0002t0005g0195 a0004c0009t0005g0140 others(6): Show |
9 | HG01167.hp1 HG01167.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2411-1277delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16771831 | ||||||
chr19:16771858 | G | GCCTCGCT others(5): Show |
1 | a0002c0002t0011g0105 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2411-1267_2411-125 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16771858 | ||||||
chr19:16771949 | C | A | 3 | a0016c0019t0017g0294 a0016c0019t0017g0295 a0016c0019t0022g0124 |
3 | HG03098.hp1 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2411-1177C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771949 | |||||||
chr19:16771959 | G | A | 1 | a0002c0002t0001g0194 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2411-1167G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771959 | |||||||
chr19:16772054 | C | T | 1 | a0010c0040t0001g0161 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2411-1072C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16772054 | |||||||
chr19:16772140 | A | T | 71 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(68): Show |
71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2411-986A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16772140 | |||||||
chr19:16772377 | T | C | 1 | a0037c0058t0035g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2411-749T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16772377 | |||||||
chr19:16772507 | C | G | 71 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(68): Show |
71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2411-619C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16772507 | |||||||
chr19:16772575 | G | C | 1 | a0030c0066t0008g0264 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2411-551G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16772575 | |||||||
chr19:16772585 | G | T | 1 | a0027c0053t0001g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2411-541G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16772585 | |||||||
chr19:16772686 | T | C | 1 | a0001c0007t0049g0132 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2411-440T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16772686 | |||||||
chr19:16773101 | C | T | 71 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(68): Show |
71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2411-25C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16773101 | |||||||
chr19:16773455 | C | T | 1 | a0001c0001t0003g0162 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2608+132C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16773455 | |||||||
chr19:16773809 | CA | C | 13 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0007c0028t0002g0115 others(10): Show |
13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2608+487delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16773809 | |||||||
chr19:16773923 | C | T | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2608+600C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16773923 | |||||||
chr19:16773939 | T | TATCC | 28 | a0001c0001t0003g0176 a0001c0001t0003g0179 a0001c0001t0003g0182 others(25): Show |
28 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.2608+651_2608+654d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16773939 | ||||||
chr19:16773939 | TATCC | T | 67 | a0001c0001t0001g0147 a0001c0007t0001g0040 a0001c0007t0001g0213 others(64): Show |
67 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.2608+651_2608+654d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16773939 | ||||||
chr19:16773939 | TATCCATC others(9): Show |
T | 71 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(68): Show |
71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2608+639_2608+654d others(18): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16773939 | ||||||
chr19:16773976 | A | ATTAATTC others(8): Show |
1 | a0003c0003t0004g0075 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2608+654_2608+668d others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16773976 | ||||||
chr19:16774050 | C | G | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2608+727C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774050 | |||||||
chr19:16774082 | C | T | 1 | a0004c0005t0006g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2608+759C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774082 | |||||||
chr19:16774083 | T | C | 1 | a0004c0005t0006g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2608+760T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774083 | |||||||
chr19:16774284 | C | T | 1 | a0012c0018t0005g0240 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2608+961C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774284 | |||||||
chr19:16774299 | T | C | 1 | a0001c0001t0020g0289 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2608+976T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774299 | |||||||
chr19:16774306 | A | G | 12 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(9): Show |
12 | HG02280.hp2 HG02647.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.2608+983A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774306 | |||||||
chr19:16774326 | C | CTCCA | 68 | a0003c0003t0002g0065 a0004c0005t0001g0296 a0004c0005t0006g0211 others(65): Show |
68 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.2608+1023_2608+102 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16774326 | ||||||
chr19:16774358 | A | T | 1 | a0004c0005t0006g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2608+1035A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774358 | |||||||
chr19:16774466 | TCCATCCA others(1): Show |
T | 18 | a0001c0001t0003g0176 a0001c0001t0003g0179 a0001c0001t0003g0182 others(15): Show |
18 | HG00597.hp2 HG01081.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.2608+1159_2608+116 others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16774466 | ||||||
chr19:16774509 | T | C | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2608+1186T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774509 | |||||||
chr19:16774511 | C | T | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2608+1188C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774511 | |||||||
chr19:16774554 | C | T | 1 | a0030c0066t0008g0264 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2608+1231C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774554 | |||||||
chr19:16774659 | C | T | 2 | a0002c0002t0005g0195 a0002c0002t0007g0041 |
2 | HG01975.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2608+1336C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774659 | |||||||
chr19:16774730 | A | G | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2608+1407A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774730 | |||||||
chr19:16774735 | T | C | 3 | a0016c0019t0017g0294 a0016c0019t0017g0295 a0016c0019t0022g0124 |
3 | HG03098.hp1 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2608+1412T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774735 | |||||||
chr19:16774760 | C | T | 1 | a0003c0003t0003g0288 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2608+1437C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774760 | |||||||
chr19:16774769 | C | A | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2608+1446C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774769 | |||||||
chr19:16775035 | C | A | 1 | a0008c0067t0003g0275 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2608+1712C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775035 | |||||||
chr19:16775180 | A | T | 1 | a0003c0003t0004g0026 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2608+1857A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775180 | |||||||
chr19:16775210 | G | A | 13 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0007c0028t0002g0115 others(10): Show |
13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2608+1887G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775210 | |||||||
chr19:16775264 | G | T | 3 | a0003c0006t0002g0072 a0005c0016t0002g0056 a0034c0032t0001g0269 |
3 | HG00642.hp1 HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2608+1941G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775264 | |||||||
chr19:16775300 | T | TA | 22 | a0003c0003t0044g0070 a0004c0009t0009g0047 a0009c0010t0002g0114 others(19): Show |
22 | HG01192.hp2 HG02040.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2608+1986dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16775300 | ||||||
chr19:16775300 | T | TAA | 47 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(44): Show |
47 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.2608+1985_2608+198 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16775300 | ||||||
chr19:16775389 | G | A | 71 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(68): Show |
71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2608+2066G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775389 | |||||||
chr19:16775434 | C | CT | 71 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(68): Show |
71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2608+2111_2608+211 others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775434 | |||||||
chr19:16775442 | C | T | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2608+2119C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775442 | |||||||
chr19:16775455 | G | GGGCTGTC others(15): Show |
1 | a0019c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2608+2133_2608+215 others(26): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16775455 | ||||||
chr19:16775466 | G | A | 17 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(14): Show |
17 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2608+2143G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775466 | |||||||
chr19:16775700 | T | C | 71 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(68): Show |
71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2608+2377T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775700 | |||||||
chr19:16775730 | G | A | 21 | a0003c0003t0044g0070 a0004c0009t0005g0140 a0004c0009t0005g0224 others(18): Show |
21 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.2608+2407G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775730 | |||||||
chr19:16775865 | A | G | 4 | a0002c0002t0001g0142 a0002c0002t0001g0190 a0002c0002t0001g0201 others(1): Show |
4 | NA18963.hp1 NA18963.hp2 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.2608+2542A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775865 | |||||||
chr19:16776203 | G | A | 71 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(68): Show |
71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2608+2880G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776203 | |||||||
chr19:16776276 | T | A | 138 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0217 others(135): Show |
138 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.2608+2953T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776276 | |||||||
chr19:16776322 | C | T | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2608+2999C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776322 | |||||||
chr19:16776330 | G | A | 13 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0007c0028t0002g0115 others(10): Show |
13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2608+3007G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776330 | |||||||
chr19:16776424 | C | CG | 3 | a0001c0007t0002g0007 a0002c0023t0002g0102 a0014c0022t0002g0046 |
3 | HG03516.hp1 NA18993.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2609-2916dupG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16776424 | ||||||
chr19:16776424 | C | T | 34 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(31): Show |
34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.2609-2919C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776424 | |||||||
chr19:16776484 | C | T | 3 | a0002c0002t0001g0142 a0002c0002t0001g0201 a0042c0035t0001g0133 |
3 | NA18963.hp2 NA19087.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2609-2859C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776484 | |||||||
chr19:16776546 | C | T | 1 | a0001c0001t0003g0236 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2609-2797C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776546 | |||||||
chr19:16776569 | C | CA | 48 | a0001c0001t0001g0136 a0001c0001t0003g0215 a0001c0001t0033g0216 others(45): Show |
48 | HG00642.hp2 HG01081.hp1 HG01257.hp2 others(45): Show |
intron_variant | MODIFIER | c.2609-2760dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16776569 | ||||||
chr19:16776569 | CA | C | 6 | a0001c0001t0003g0183 a0002c0002t0007g0030 a0004c0017t0001g0212 others(3): Show |
6 | HG01109.hp2 HG02040.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2609-2760delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16776569 | ||||||
chr19:16776584 | T | A | 1 | a0001c0007t0002g0007 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2759T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776584 | |||||||
chr19:16776611 | G | T | 1 | a0010c0013t0009g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2609-2732G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776611 | |||||||
chr19:16776612 | T | C | 1 | a0010c0013t0009g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2609-2731T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776612 | |||||||
chr19:16776634 | A | G | 94 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0001c0001t0001g0158 others(91): Show |
94 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.2609-2709A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776634 | |||||||
chr19:16776718 | G | A | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2609-2625G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776718 | |||||||
chr19:16776773 | T | TA | 44 | a0001c0001t0003g0191 a0001c0001t0003g0215 a0001c0001t0003g0220 others(41): Show |
44 | HG00642.hp1 HG00642.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.2609-2548dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16776773 | ||||||
chr19:16776773 | TA | T | 51 | a0001c0001t0001g0197 a0001c0001t0003g0193 a0001c0001t0003g0236 others(48): Show |
51 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.2609-2548delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16776773 | ||||||
chr19:16776875 | G | A | 36 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(33): Show |
36 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(33): Show |
intron_variant | MODIFIER | c.2609-2468G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776875 | |||||||
chr19:16776941 | GA | G | 72 | a0002c0008t0002g0044 a0004c0005t0001g0296 a0004c0005t0006g0211 others(69): Show |
72 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(69): Show |
intron_variant | MODIFIER | c.2609-2391delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16776941 | ||||||
chr19:16776984 | AG | A | 3 | a0002c0002t0012g0203 a0019c0027t0007g0080 a0040c0037t0001g0209 |
3 | HG02083.hp1 NA18946.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2609-2355delG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16776984 | ||||||
chr19:16776985 | G | GGGGAAGG others(57): Show |
1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2325_2609-232 others(68): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16776985 | ||||||
chr19:16777108 | A | G | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2235A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777108 | |||||||
chr19:16777137 | G | A | 1 | a0001c0007t0002g0007 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2206G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777137 | |||||||
chr19:16777140 | A | G | 1 | a0001c0007t0002g0007 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2203A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777140 | |||||||
chr19:16777141 | G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2202G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777141 | |||||||
chr19:16777150 | AGGGAAGG others(12): Show |
A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2190_2609-217 others(23): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777150 | ||||||
chr19:16777152 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2609-2191G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777152 | |||||||
chr19:16777159 | G | A | 1 | a0001c0007t0002g0007 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2184G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777159 | |||||||
chr19:16777161 | AGGGAAAG others(20): Show |
A | 4 | a0003c0003t0004g0079 a0014c0022t0001g0231 a0014c0022t0002g0046 others(1): Show |
4 | HG01884.hp2 HG02015.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2609-2145_2609-211 others(31): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777161 | ||||||
chr19:16777162 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2609-2181G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777162 | |||||||
chr19:16777162 | G | GGGGAGGA others(5): Show |
1 | a0001c0007t0002g0007 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2179_2609-217 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777162 | ||||||
chr19:16777165 | A | G | 1 | a0001c0007t0002g0007 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2178A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777165 | |||||||
chr19:16777181 | A | C | 1 | a0002c0002t0012g0203 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2609-2162A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777181 | |||||||
chr19:16777188 | G | A | 2 | a0001c0007t0002g0007 a0011c0011t0011g0025 |
2 | HG02559.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2609-2155G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777188 | |||||||
chr19:16777194 | A | G | 1 | a0001c0007t0002g0007 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2149A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777194 | |||||||
chr19:16777205 | G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2138G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777205 | |||||||
chr19:16777215 | G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2128G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777215 | |||||||
chr19:16777215 | G | GGGGAAAG others(35): Show |
1 | a0002c0002t0002g0123 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2609-2118_2609-207 others(46): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777215 | ||||||
chr19:16777219 | A | G | 1 | a0015c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2609-2124A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777219 | |||||||
chr19:16777220 | AAGGGAAG others(8): Show |
A | 68 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(65): Show |
68 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.2609-2108_2609-209 others(19): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777220 | ||||||
chr19:16777221 | AGGGAAGG others(7): Show |
A | 1 | a0015c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2609-2121_2609-210 others(18): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777221 | |||||||
chr19:16777225 | A | G | 1 | a0001c0001t0005g0245 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2609-2118A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777225 | |||||||
chr19:16777230 | G | A | 2 | a0001c0001t0005g0245 a0001c0007t0002g0007 |
2 | HG00558.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2609-2113G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777230 | |||||||
chr19:16777232 | G | A | 1 | a0010c0013t0009g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2609-2111G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777232 | |||||||
chr19:16777235 | G | A | 2 | a0001c0001t0005g0245 a0011c0011t0011g0025 |
2 | HG00558.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2609-2108G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777235 | |||||||
chr19:16777240 | A | G | 1 | a0001c0001t0005g0245 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2609-2103A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777240 | |||||||
chr19:16777250 | A | G | 1 | a0001c0007t0002g0007 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2093A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777250 | |||||||
chr19:16777262 | A | G | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2081A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777262 | |||||||
chr19:16777264 | G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2079G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777264 | |||||||
chr19:16777267 | G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2076G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777267 | |||||||
chr19:16777272 | A | G | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2071A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777272 | |||||||
chr19:16777274 | G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2069G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777274 | |||||||
chr19:16777274 | G | T | 4 | a0006c0044t0001g0255 a0014c0022t0001g0231 a0014c0022t0002g0046 others(1): Show |
4 | HG01884.hp2 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2609-2069G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777274 | |||||||
chr19:16777279 | G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2064G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777279 | |||||||
chr19:16777283 | A | G | 1 | a0015c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2609-2060A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777283 | |||||||
chr19:16777284 | G | A | 1 | a0001c0007t0002g0007 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2059G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777284 | |||||||
chr19:16777287 | A | G | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2056A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777287 | |||||||
chr19:16777291 | G | A | 1 | a0004c0005t0006g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2609-2052G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777291 | |||||||
chr19:16777294 | G | A | 1 | a0001c0007t0002g0007 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2049G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777294 | |||||||
chr19:16777296 | G | A | 1 | a0004c0005t0006g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2609-2047G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777296 | |||||||
chr19:16777318 | A | G | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2025A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777318 | |||||||
chr19:16777319 | G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2024G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777319 | |||||||
chr19:16777325 | A | T | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2018A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777325 | |||||||
chr19:16777345 | A | G | 1 | a0017c0021t0005g0222 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2609-1998A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777345 | |||||||
chr19:16777361 | AAGGGG | A | 16 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(13): Show |
16 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.2609-1970_2609-196 others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777361 | ||||||
chr19:16777379 | G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-1964G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777379 | |||||||
chr19:16777404 | G | T | 1 | a0040c0037t0001g0209 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2609-1939G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777404 | |||||||
chr19:16777425 | G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-1918G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777425 | |||||||
chr19:16777450 | G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-1893G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777450 | |||||||
chr19:16777453 | A | G | 1 | a0003c0006t0002g0071 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2609-1890A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777453 | |||||||
chr19:16777455 | T | A | 1 | a0003c0006t0002g0071 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2609-1888T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777455 | |||||||
chr19:16777463 | G | A | 1 | a0004c0005t0018g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2609-1880G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777463 | |||||||
chr19:16777475 | G | T | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-1868G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777475 | |||||||
chr19:16777541 | A | T | 2 | a0002c0002t0007g0030 a0002c0002t0011g0105 |
2 | HG02015.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2609-1802A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777541 | |||||||
chr19:16777555 | G | T | 1 | a0002c0002t0001g0177 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2609-1788G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777555 | |||||||
chr19:16777580 | GGGAGGGG others(10): Show |
G | 16 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(13): Show |
16 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.2609-1746_2609-173 others(21): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777580 | ||||||
chr19:16777604 | G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-1739G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777604 | |||||||
chr19:16777635 | G | T | 1 | a0007c0028t0034g0258 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2609-1708G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777635 | |||||||
chr19:16777644 | A | G | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-1699A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777644 | |||||||
chr19:16777656 | A | AG | 12 | a0001c0001t0005g0244 a0001c0007t0001g0239 a0002c0002t0002g0063 others(9): Show |
12 | HG00280.hp1 HG00642.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2609-1683dupG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777656 | ||||||
chr19:16777663 | A | G | 1 | a0019c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1680A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777663 | |||||||
chr19:16777664 | G | A | 1 | a0019c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1679G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777664 | |||||||
chr19:16777665 | C | G | 1 | a0019c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1678C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777665 | |||||||
chr19:16777668 | G | A | 1 | a0019c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1675G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777668 | |||||||
chr19:16777671 | A | G | 1 | a0019c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1672A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777671 | |||||||
chr19:16777671 | A | T | 1 | a0002c0002t0001g0142 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2609-1672A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777671 | |||||||
chr19:16777684 | G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-1659G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777684 | |||||||
chr19:16777690 | A | T | 1 | a0019c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1653A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777690 | |||||||
chr19:16777694 | GAGGGA | G | 4 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2609-1634_2609-163 others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777694 | ||||||
chr19:16777741 | G | A | 4 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2609-1602G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777741 | |||||||
chr19:16777741 | G | T | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-1602G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777741 | |||||||
chr19:16777755 | A | T | 1 | a0019c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1588A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777755 | |||||||
chr19:16777756 | T | G | 1 | a0019c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1587T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777756 | |||||||
chr19:16777806 | A | T | 1 | a0002c0002t0012g0203 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2609-1537A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777806 | |||||||
chr19:16777807 | A | C | 1 | a0002c0002t0012g0203 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2609-1536A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777807 | |||||||
chr19:16777903 | AAG | A | 9 | a0007c0028t0002g0115 a0007c0028t0034g0258 a0007c0029t0002g0297 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2609-1439_2609-143 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777903 | |||||||
chr19:16777910 | G | GGGGAAGG others(23): Show |
8 | a0002c0002t0001g0207 a0009c0010t0002g0114 a0009c0010t0010g0131 others(5): Show |
8 | HG00673.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.2609-1392_2609-136 others(34): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777910 | ||||||
chr19:16777910 | GGGGAAGG others(23): Show |
G | 2 | a0004c0009t0005g0140 a0004c0009t0005g0224 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2609-1392_2609-136 others(34): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777910 | ||||||
chr19:16778005 | A | G | 1 | a0002c0002t0012g0203 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2609-1338A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778005 | |||||||
chr19:16778045 | G | T | 1 | a0001c0001t0005g0241 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2609-1298G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778045 | |||||||
chr19:16778057 | A | G | 1 | a0040c0037t0001g0209 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2609-1286A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778057 | |||||||
chr19:16778062 | A | G | 4 | a0019c0027t0007g0080 a0029c0065t0032g0166 a0030c0066t0008g0264 others(1): Show |
4 | HG02083.hp1 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2609-1281A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778062 | |||||||
chr19:16778074 | A | T | 1 | a0040c0037t0001g0209 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2609-1269A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778074 | |||||||
chr19:16778076 | C | A | 1 | a0019c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1267C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778076 | |||||||
chr19:16778078 | C | T | 1 | a0019c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1265C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778078 | |||||||
chr19:16778094 | G | C | 10 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(7): Show |
10 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2609-1249G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778094 | |||||||
chr19:16778100 | G | T | 2 | a0001c0001t0005g0241 a0002c0002t0005g0130 |
2 | NA18747.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.2609-1243G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778100 | |||||||
chr19:16778153 | C | A | 1 | a0019c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1190C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778153 | |||||||
chr19:16778198 | C | T | 1 | a0019c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1145C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778198 | |||||||
chr19:16778199 | C | T | 1 | a0010c0013t0013g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2609-1144C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778199 | |||||||
chr19:16778210 | C | T | 1 | a0019c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1133C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778210 | |||||||
chr19:16778253 | G | A | 12 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(9): Show |
12 | HG02280.hp2 HG02647.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.2609-1090G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778253 | |||||||
chr19:16778491 | CTTCT | C | 6 | a0002c0002t0001g0153 a0002c0002t0001g0156 a0002c0002t0001g0165 others(3): Show |
6 | HG00099.hp2 HG00280.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.2609-849_2609-846d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16778491 | ||||||
chr19:16778494 | C | CTTCTTTT others(5): Show |
1 | a0004c0005t0039g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2609-847_2609-846i others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16778494 | ||||||
chr19:16778494 | C | CTTCTTTT others(6): Show |
3 | a0004c0005t0023g0094 a0004c0005t0023g0095 a0033c0048t0018g0129 |
3 | HG03490.hp2 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2609-847_2609-846i others(15): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16778494 | ||||||
chr19:16778494 | C | CTTCTTTT others(7): Show |
17 | a0004c0005t0006g0211 a0004c0005t0006g0225 a0004c0005t0006g0228 others(14): Show |
17 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2609-847_2609-846i others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16778494 | ||||||
chr19:16778494 | C | CTTCTTTT others(8): Show |
10 | a0004c0005t0001g0296 a0004c0005t0006g0226 a0004c0017t0001g0212 others(7): Show |
10 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2609-847_2609-846i others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16778494 | ||||||
chr19:16778494 | C | CTTCTTTT others(9): Show |
2 | a0004c0005t0006g0227 a0015c0054t0025g0118 |
2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2609-847_2609-846i others(18): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16778494 | ||||||
chr19:16778494 | CT | C | 183 | a0001c0001t0001g0147 a0001c0001t0001g0158 a0001c0001t0001g0160 others(180): Show |
183 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.2609-835delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16778494 | ||||||
chr19:16778497 | T | C | 9 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(6): Show |
9 | HG02647.hp1 HG02809.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.2609-846T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778497 | |||||||
chr19:16778500 | T | C | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2609-843T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778500 | |||||||
chr19:16778506 | T | G | 63 | a0001c0001t0003g0176 a0001c0001t0003g0183 a0001c0001t0003g0185 others(60): Show |
63 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.2609-837T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778506 | |||||||
chr19:16778506 | TTTG | T | 16 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(13): Show |
16 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.2609-818_2609-816d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16778506 | ||||||
chr19:16778508 | TG | T | 6 | a0001c0001t0004g0109 a0001c0001t0020g0289 a0006c0044t0001g0255 others(3): Show |
6 | HG00735.hp1 HG01884.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2609-834delG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778508 | |||||||
chr19:16778508 | TGTTG | T | 9 | a0004c0009t0009g0052 a0006c0014t0008g0253 a0009c0010t0002g0114 others(6): Show |
9 | HG02647.hp1 HG02809.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.2609-834_2609-831d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778508 | |||||||
chr19:16778509 | G | T | 44 | a0002c0002t0001g0165 a0004c0005t0001g0296 a0004c0005t0006g0211 others(41): Show |
44 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.2609-834G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778509 | |||||||
chr19:16778512 | G | T | 28 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(25): Show |
28 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.2609-831G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778512 | |||||||
chr19:16778560 | G | C | 1 | a0002c0002t0001g0190 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2609-783G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778560 | |||||||
chr19:16778800 | A | G | 1 | a0043c0057t0026g0202 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2609-543A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778800 | |||||||
chr19:16778801 | C | A | 66 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(63): Show |
66 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.2609-542C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778801 | |||||||
chr19:16778818 | A | G | 1 | a0005c0004t0003g0272 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2609-525A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778818 | |||||||
chr19:16778915 | T | C | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2609-428T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778915 | |||||||
chr19:16778916 | G | A | 7 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2609-427G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778916 | |||||||
chr19:16779031 | C | T | 3 | a0029c0065t0032g0166 a0030c0066t0008g0264 a0043c0057t0026g0202 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2609-312C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16779031 | |||||||
chr19:16779063 | G | A | 1 | a0021c0041t0002g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2609-280G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16779063 | |||||||
chr19:16779092 | C | G | 3 | a0002c0002t0001g0271 a0003c0003t0002g0066 a0003c0003t0002g0067 |
3 | HG02056.hp2 HG02080.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.2609-251C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16779092 | |||||||
chr19:16779340 | C | T | 1 | a0006c0044t0001g0255 | 1 | NA19043.hp1 | splice_region_variant&intron_variant | LOW | c.2609-3C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16779340 | |||||||
chr19:16779500 | C | G | 33 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(30): Show |
33 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.2731+35C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16779500 | |||||||
chr19:16779510 | A | G | 33 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(30): Show |
33 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.2731+45A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16779510 | |||||||
chr19:16779648 | T | C | 12 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0007c0028t0002g0115 others(9): Show |
12 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2731+183T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16779648 | |||||||
chr19:16779764 | G | A | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2731+299G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16779764 | |||||||
chr19:16779777 | C | T | 20 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2731+312C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16779777 | |||||||
chr19:16779780 | G | A | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2731+315G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16779780 | |||||||
chr19:16779835 | T | C | 2 | a0002c0002t0003g0186 a0005c0004t0004g0090 |
2 | NA19005.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2731+370T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16779835 | |||||||
chr19:16779946 | C | T | 34 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(31): Show |
34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.2731+481C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16779946 | |||||||
chr19:16780099 | C | T | 1 | a0003c0006t0002g0092 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2731+634C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16780099 | |||||||
chr19:16780158 | C | CT | 11 | a0001c0001t0003g0215 a0001c0001t0014g0238 a0001c0001t0033g0216 others(8): Show |
11 | HG01257.hp2 HG01433.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.2731+708dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16780158 | ||||||
chr19:16780158 | C | CTT | 9 | a0001c0001t0005g0184 a0004c0060t0002g0125 a0006c0044t0001g0255 others(6): Show |
9 | HG01358.hp1 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2731+707_2731+708d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16780158 | ||||||
chr19:16780172 | T | A | 2 | a0002c0002t0001g0208 a0005c0004t0002g0059 |
2 | HG02129.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.2731+707T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16780172 | |||||||
chr19:16780357 | C | T | 12 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0007c0028t0002g0115 others(9): Show |
12 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2731+892C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16780357 | |||||||
chr19:16780378 | A | G | 1 | a0003c0059t0015g0037 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2731+913A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16780378 | |||||||
chr19:16780529 | T | TCACATTC others(1): Show |
5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2731+1067_2731+107 others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16780529 | ||||||
chr19:16780662 | C | T | 84 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0004c0005t0001g0296 others(81): Show |
84 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(81): Show |
intron_variant | MODIFIER | c.2731+1197C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16780662 | |||||||
chr19:16781012 | G | A | 12 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0007c0028t0002g0115 others(9): Show |
12 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2731+1547G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16781012 | |||||||
chr19:16781178 | T | C | 34 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(31): Show |
34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.2731+1713T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16781178 | |||||||
chr19:16781189 | C | T | 34 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(31): Show |
34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.2731+1724C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16781189 | |||||||
chr19:16781190 | G | A | 33 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(30): Show |
33 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.2731+1725G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16781190 | |||||||
chr19:16781351 | G | A | 34 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(31): Show |
34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.2731+1886G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16781351 | |||||||
chr19:16781547 | T | C | 1 | a0003c0003t0004g0075 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2731+2082T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16781547 | |||||||
chr19:16781955 | G | C | 1 | a0001c0001t0031g0214 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2731+2490G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16781955 | |||||||
chr19:16782084 | A | G | 1 | a0009c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2731+2619A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782084 | |||||||
chr19:16782093 | C | CA | 8 | a0001c0001t0001g0242 a0001c0001t0003g0236 a0002c0002t0001g0192 others(5): Show |
8 | HG00673.hp1 HG01943.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2731+2642dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782093 | ||||||
chr19:16782100 | A | T | 12 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0007c0028t0002g0115 others(9): Show |
12 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2731+2635A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782100 | |||||||
chr19:16782108 | G | A | 1 | a0001c0001t0003g0215 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2731+2643G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782108 | |||||||
chr19:16782108 | GA | G | 15 | a0002c0002t0002g0010 a0002c0023t0001g0151 a0002c0023t0002g0102 others(12): Show |
15 | HG00642.hp1 HG01496.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2731+2654delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782108 | ||||||
chr19:16782284 | T | TA | 35 | a0001c0001t0002g0029 a0001c0001t0003g0183 a0002c0002t0001g0291 others(32): Show |
35 | HG00642.hp1 HG00735.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2731+2841dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782284 | ||||||
chr19:16782284 | T | TAA | 15 | a0004c0005t0023g0094 a0004c0005t0023g0095 a0004c0005t0039g0084 others(12): Show |
15 | HG00642.hp2 HG01081.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2731+2840_2731+284 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782284 | ||||||
chr19:16782284 | T | TAAA | 6 | a0004c0017t0002g0038 a0009c0010t0047g0005 a0021c0041t0002g0036 others(3): Show |
6 | HG01361.hp1 HG02280.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2731+2839_2731+284 others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782284 | ||||||
chr19:16782284 | TA | T | 18 | a0001c0001t0003g0162 a0001c0001t0031g0214 a0002c0002t0001g0192 others(15): Show |
18 | HG00323.hp1 HG00673.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.2731+2841delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782284 | ||||||
chr19:16782333 | G | A | 8 | a0006c0044t0001g0255 a0009c0010t0002g0114 a0009c0010t0010g0131 others(5): Show |
8 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.2731+2868G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782333 | |||||||
chr19:16782497 | G | A | 4 | a0002c0002t0001g0199 a0002c0002t0001g0268 a0002c0002t0012g0189 others(1): Show |
4 | HG02071.hp1 NA18945.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.2731+3032G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782497 | |||||||
chr19:16782526 | A | G | 1 | a0037c0058t0035g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2731+3061A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782526 | |||||||
chr19:16782558 | TA | T | 3 | a0001c0001t0001g0260 a0001c0001t0003g0193 a0004c0005t0023g0095 |
3 | HG01943.hp1 HG03041.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.2731+3099delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782558 | ||||||
chr19:16782861 | C | CTT | 66 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(63): Show |
66 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.2731+3397_2731+339 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782861 | ||||||
chr19:16782861 | CTTCT | C | 97 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0001c0001t0001g0158 others(94): Show |
97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.2731+3417_2731+342 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782861 | ||||||
chr19:16782865 | T | C | 66 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(63): Show |
66 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.2731+3400T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782865 | |||||||
chr19:16782869 | T | C | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2731+3404T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782869 | |||||||
chr19:16782898 | ATCCTTCC others(18): Show |
A | 67 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(64): Show |
67 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.2731+3448_2731+347 others(29): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782898 | ||||||
chr19:16782912 | CTTTCCTT others(9): Show |
C | 1 | a0015c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2731+3448_2731+346 others(20): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782912 | |||||||
chr19:16783009 | T | C | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2731+3544T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783009 | |||||||
chr19:16783009 | T | TTTCTTTC others(1): Show |
45 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(42): Show |
45 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.2731+3552_2731+355 others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16783009 | ||||||
chr19:16783041 | CT | C | 51 | a0001c0001t0004g0112 a0004c0005t0001g0296 a0004c0005t0006g0211 others(48): Show |
51 | HG00642.hp2 HG01070.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.2731+3588delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16783041 | ||||||
chr19:16783234 | C | T | 22 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(19): Show |
22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2731+3769C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783234 | |||||||
chr19:16783279 | C | G | 3 | a0029c0065t0032g0166 a0030c0066t0008g0264 a0043c0057t0026g0202 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2731+3814C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783279 | |||||||
chr19:16783360 | A | C | 70 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(67): Show |
70 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.2731+3895A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783360 | |||||||
chr19:16783469 | T | C | 2 | a0016c0019t0017g0294 a0016c0019t0017g0295 |
2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2731+4004T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783469 | |||||||
chr19:16783539 | C | A | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2731+4074C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783539 | |||||||
chr19:16783563 | G | A | 1 | a0017c0021t0007g0119 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2731+4098G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783563 | |||||||
chr19:16783590 | C | T | 43 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(40): Show |
43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.2731+4125C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783590 | |||||||
chr19:16783591 | G | T | 11 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0007c0028t0002g0115 others(8): Show |
11 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2731+4126G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783591 | |||||||
chr19:16783641 | T | TA | 70 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(67): Show |
70 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.2731+4181dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16783641 | ||||||
chr19:16783643 | A | G | 1 | a0002c0008t0001g0145 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2731+4178A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783643 | |||||||
chr19:16783969 | C | T | 4 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0022c0042t0001g0152 others(1): Show |
4 | HG01496.hp1 NA18993.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2731+4504C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783969 | |||||||
chr19:16783970 | G | A | 27 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(24): Show |
27 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.2731+4505G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783970 | |||||||
chr19:16783977 | C | T | 1 | a0001c0001t0003g0191 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2731+4512C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783977 | |||||||
chr19:16783979 | C | T | 23 | a0002c0002t0007g0030 a0004c0009t0005g0140 a0004c0009t0005g0224 others(20): Show |
23 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.2731+4514C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783979 | |||||||
chr19:16784120 | A | C | 1 | a0001c0007t0002g0057 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2731+4655A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16784120 | |||||||
chr19:16784208 | G | GA | 6 | a0001c0001t0001g0242 a0001c0001t0004g0113 a0001c0047t0001g0138 others(3): Show |
6 | HG00673.hp1 HG01261.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2731+4756dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16784208 | ||||||
chr19:16784358 | C | T | 70 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(67): Show |
70 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.2732-4624C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16784358 | |||||||
chr19:16784360 | G | A | 1 | a0002c0036t0002g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2732-4622G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16784360 | |||||||
chr19:16784449 | G | A | 27 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(24): Show |
27 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.2732-4533G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16784449 | |||||||
chr19:16784536 | G | A | 2 | a0007c0028t0034g0258 a0008c0067t0003g0275 |
2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2732-4446G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16784536 | |||||||
chr19:16784668 | C | T | 1 | a0003c0006t0002g0072 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2732-4314C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16784668 | |||||||
chr19:16784856 | G | C | 9 | a0001c0001t0001g0242 a0001c0001t0002g0043 a0002c0002t0001g0190 others(6): Show |
9 | HG00673.hp1 NA18954.hp2 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.2732-4126G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16784856 | |||||||
chr19:16784861 | GGAGGTTG others(9): Show |
G | 22 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(19): Show |
22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2732-4117_2732-410 others(20): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16784861 | ||||||
chr19:16785015 | C | T | 2 | a0004c0005t0023g0094 a0004c0005t0023g0095 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2732-3967C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785015 | |||||||
chr19:16785127 | G | T | 1 | a0002c0002t0001g0208 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2732-3855G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785127 | |||||||
chr19:16785259 | C | A | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2732-3723C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785259 | |||||||
chr19:16785261 | T | C | 139 | a0001c0001t0001g0160 a0001c0001t0003g0176 a0001c0001t0003g0183 others(136): Show |
139 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(136): Show |
intron_variant | MODIFIER | c.2732-3721T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785261 | |||||||
chr19:16785282 | C | CG | 3 | a0002c0008t0001g0168 a0003c0059t0015g0037 a0010c0013t0009g0045 |
3 | HG01175.hp1 HG01358.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2732-3697dupG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16785282 | ||||||
chr19:16785317 | G | A | 22 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(19): Show |
22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2732-3665G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785317 | |||||||
chr19:16785448 | T | G | 1 | a0013c0020t0016g0004 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2732-3534T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785448 | |||||||
chr19:16785513 | AAAAAT | A | 5 | a0015c0025t0002g0048 a0015c0025t0002g0049 a0029c0065t0032g0166 others(2): Show |
5 | HG02280.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2732-3445_2732-344 others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16785513 | ||||||
chr19:16785584 | ATGAC | A | 43 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(40): Show |
43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.2732-3395_2732-339 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16785584 | ||||||
chr19:16785638 | A | T | 1 | a0001c0001t0005g0154 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2732-3344A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785638 | |||||||
chr19:16785769 | AAC | A | 11 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0007c0028t0002g0115 others(8): Show |
11 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2732-3211_2732-321 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16785769 | ||||||
chr19:16785801 | C | CTA | 22 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(19): Show |
22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2732-3171_2732-317 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16785801 | ||||||
chr19:16785867 | A | T | 4 | a0004c0017t0001g0212 a0004c0017t0002g0018 a0004c0017t0002g0019 others(1): Show |
4 | HG02257.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2732-3115A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785867 | |||||||
chr19:16785988 | C | T | 2 | a0002c0002t0005g0195 a0002c0002t0007g0041 |
2 | HG01975.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2732-2994C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785988 | |||||||
chr19:16786084 | C | T | 11 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0007c0028t0002g0115 others(8): Show |
11 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2732-2898C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786084 | |||||||
chr19:16786131 | T | C | 70 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(67): Show |
70 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.2732-2851T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786131 | |||||||
chr19:16786181 | CT | C | 70 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(67): Show |
70 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.2732-2791delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16786181 | ||||||
chr19:16786202 | A | T | 75 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(72): Show |
75 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.2732-2780A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786202 | |||||||
chr19:16786217 | C | T | 22 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(19): Show |
22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2732-2765C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786217 | |||||||
chr19:16786228 | G | A | 4 | a0002c0008t0001g0135 a0002c0008t0001g0139 a0002c0008t0002g0044 others(1): Show |
4 | NA18982.hp2 NA19007.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.2732-2754G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786228 | |||||||
chr19:16786266 | T | C | 70 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(67): Show |
70 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.2732-2716T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786266 | |||||||
chr19:16786267 | G | A | 1 | a0001c0001t0031g0214 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2732-2715G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786267 | |||||||
chr19:16786553 | C | CT | 69 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(66): Show |
69 | HG00642.hp2 HG00735.hp2 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.2732-2418dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16786553 | ||||||
chr19:16786635 | T | C | 43 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(40): Show |
43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.2732-2347T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786635 | |||||||
chr19:16786692 | G | A | 22 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(19): Show |
22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2732-2290G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786692 | |||||||
chr19:16786747 | T | G | 1 | a0004c0005t0039g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2732-2235T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786747 | |||||||
chr19:16786774 | A | T | 1 | a0002c0002t0001g0192 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2732-2208A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786774 | |||||||
chr19:16786854 | G | A | 43 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(40): Show |
43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.2732-2128G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786854 | |||||||
chr19:16786894 | G | A | 43 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(40): Show |
43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.2732-2088G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786894 | |||||||
chr19:16787093 | G | A | 3 | a0029c0065t0032g0166 a0030c0066t0008g0264 a0043c0057t0026g0202 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2732-1889G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787093 | |||||||
chr19:16787368 | G | A | 1 | a0011c0011t0002g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2732-1614G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787368 | |||||||
chr19:16787626 | G | A | 4 | a0007c0069t0043g0299 a0029c0065t0032g0166 a0030c0066t0008g0264 others(1): Show |
4 | HG02818.hp1 HG02922.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2732-1356G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787626 | |||||||
chr19:16787870 | TAATAAC | T | 7 | a0001c0001t0001g0171 a0001c0001t0005g0184 a0001c0001t0005g0241 others(4): Show |
7 | HG01358.hp1 HG01433.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.2732-1106_2732-110 others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787870 | ||||||
chr19:16787876 | C | A | 34 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(31): Show |
34 | HG00642.hp2 HG01081.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.2732-1106C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787876 | |||||||
chr19:16787876 | C | T | 11 | a0002c0002t0005g0195 a0002c0002t0007g0041 a0004c0005t0029g0265 others(8): Show |
11 | HG01361.hp1 HG01975.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.2732-1106C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787876 | |||||||
chr19:16787876 | CAAT | C | 39 | a0001c0001t0001g0160 a0001c0001t0003g0176 a0001c0001t0003g0183 others(36): Show |
39 | HG00099.hp1 HG00597.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.2732-1078_2732-107 others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787876 | ||||||
chr19:16787876 | CAATAAT | C | 6 | a0001c0001t0003g0236 a0002c0008t0002g0044 a0003c0003t0004g0079 others(3): Show |
6 | HG01884.hp2 HG01943.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.2732-1081_2732-107 others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787876 | ||||||
chr19:16787898 | AATAATAA others(14): Show |
A | 2 | a0004c0005t0022g0050 a0038c0052t0001g0254 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2732-1081_2732-106 others(25): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787898 | ||||||
chr19:16787898 | AATAATAA others(17): Show |
A | 1 | a0009c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2732-1081_2732-105 others(28): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787898 | ||||||
chr19:16787901 | A | C | 5 | a0001c0001t0001g0160 a0001c0001t0003g0176 a0001c0001t0005g0241 others(2): Show |
5 | HG01109.hp1 HG01361.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.2732-1081A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787901 | |||||||
chr19:16787901 | AATAATC | A | 7 | a0002c0008t0001g0134 a0002c0008t0001g0135 a0002c0008t0001g0139 others(4): Show |
7 | HG02129.hp1 HG02572.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.2732-1078_2732-107 others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787901 | ||||||
chr19:16787901 | AATAATCA others(2): Show |
A | 4 | a0002c0002t0005g0195 a0002c0002t0020g0249 a0027c0053t0001g0252 others(1): Show |
4 | HG01099.hp2 HG02293.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2732-1078_2732-107 others(13): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787901 | ||||||
chr19:16787901 | AATAATCA others(5): Show |
A | 1 | a0004c0005t0006g0226 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2732-1078_2732-106 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787901 | ||||||
chr19:16787901 | AATAATCA others(17): Show |
A | 1 | a0009c0010t0002g0114 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2732-1078_2732-105 others(28): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787901 | ||||||
chr19:16787904 | A | C | 21 | a0001c0001t0001g0160 a0001c0001t0003g0176 a0001c0001t0003g0183 others(18): Show |
21 | HG00099.hp1 HG00738.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2732-1078A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787904 | |||||||
chr19:16787904 | AATC | A | 76 | a0001c0001t0001g0242 a0001c0001t0001g0260 a0001c0001t0001g0261 others(73): Show |
76 | HG00280.hp1 HG00597.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.2732-1039_2732-103 others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787904 | ||||||
chr19:16787904 | AATCATC | A | 65 | a0001c0001t0001g0136 a0001c0001t0001g0158 a0001c0001t0001g0164 others(62): Show |
65 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.2732-1042_2732-103 others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787904 | ||||||
chr19:16787904 | AATCATCA others(2): Show |
A | 33 | a0001c0001t0001g0147 a0002c0002t0001g0146 a0002c0002t0001g0153 others(30): Show |
33 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.2732-1045_2732-103 others(13): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787904 | ||||||
chr19:16787904 | AATCATCA others(5): Show |
A | 4 | a0004c0005t0018g0256 a0007c0068t0040g0116 a0007c0069t0043g0299 others(1): Show |
4 | HG02258.hp1 HG02896.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2732-1048_2732-103 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787904 | ||||||
chr19:16787904 | AATCATCA others(8): Show |
A | 11 | a0004c0005t0006g0211 a0004c0005t0006g0227 a0004c0005t0006g0228 others(8): Show |
11 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2732-1051_2732-103 others(19): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787904 | ||||||
chr19:16787904 | AATCATCA others(11): Show |
A | 4 | a0009c0010t0010g0131 a0009c0010t0010g0274 a0009c0010t0010g0276 others(1): Show |
4 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2732-1054_2732-103 others(22): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787904 | ||||||
chr19:16787904 | AATCATCA others(14): Show |
A | 2 | a0004c0060t0002g0125 a0021c0041t0002g0036 |
2 | HG01361.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2732-1057_2732-103 others(25): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787904 | ||||||
chr19:16787904 | AATCATCA others(17): Show |
A | 2 | a0004c0005t0029g0265 a0006c0044t0001g0255 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2732-1060_2732-103 others(28): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787904 | ||||||
chr19:16787907 | C | A | 25 | a0001c0001t0001g0171 a0001c0001t0003g0237 a0001c0001t0005g0184 others(22): Show |
25 | HG00323.hp1 HG00558.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.2732-1075C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787907 | |||||||
chr19:16787910 | C | A | 64 | a0001c0001t0001g0242 a0001c0001t0001g0261 a0001c0001t0003g0162 others(61): Show |
64 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.2732-1072C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787910 | |||||||
chr19:16787913 | C | A | 87 | a0001c0001t0001g0158 a0001c0001t0001g0164 a0001c0001t0001g0178 others(84): Show |
87 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.2732-1069C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787913 | |||||||
chr19:16787916 | C | A | 82 | a0001c0001t0001g0147 a0001c0001t0001g0158 a0001c0001t0001g0164 others(79): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.2732-1066C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787916 | |||||||
chr19:16787919 | C | A | 43 | a0001c0001t0001g0147 a0001c0001t0001g0164 a0001c0001t0001g0178 others(40): Show |
43 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.2732-1063C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787919 | |||||||
chr19:16787922 | C | A | 16 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0002c0002t0001g0190 others(13): Show |
16 | HG00642.hp2 HG00673.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.2732-1060C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787922 | |||||||
chr19:16787925 | C | A | 8 | a0001c0001t0001g0178 a0002c0002t0001g0192 a0002c0002t0001g0194 others(5): Show |
8 | HG00642.hp2 HG00673.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2732-1057C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787925 | |||||||
chr19:16787928 | C | A | 3 | a0004c0005t0023g0094 a0004c0005t0023g0095 a0004c0060t0002g0125 |
3 | HG02886.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2732-1054C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787928 | |||||||
chr19:16787995 | G | A | 1 | a0007c0069t0043g0299 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2732-987G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787995 | |||||||
chr19:16788186 | C | T | 22 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(19): Show |
22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2732-796C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16788186 | |||||||
chr19:16788232 | A | AAAT | 5 | a0001c0001t0001g0262 a0002c0002t0001g0196 a0002c0002t0001g0207 others(2): Show |
5 | HG00673.hp2 HG02083.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.2732-699_2732-697d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788232 | ||||||
chr19:16788232 | AAAT | A | 106 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0001c0001t0001g0158 others(103): Show |
106 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.2732-699_2732-697d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788232 | ||||||
chr19:16788232 | AAATAAT | A | 50 | a0001c0001t0001g0164 a0001c0001t0001g0178 a0001c0001t0003g0179 others(47): Show |
50 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.2732-702_2732-697d others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788232 | ||||||
chr19:16788232 | AAATAATA others(2): Show |
A | 39 | a0002c0002t0001g0291 a0002c0023t0001g0151 a0003c0003t0003g0288 others(36): Show |
39 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.2732-705_2732-697d others(11): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788232 | ||||||
chr19:16788232 | AAATAATA others(5): Show |
A | 7 | a0004c0005t0018g0256 a0004c0017t0001g0212 a0004c0017t0002g0018 others(4): Show |
7 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2732-708_2732-697d others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788232 | ||||||
chr19:16788232 | AAATAATA others(8): Show |
A | 12 | a0004c0005t0001g0296 a0004c0060t0002g0125 a0007c0028t0002g0115 others(9): Show |
12 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2732-711_2732-697d others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788232 | ||||||
chr19:16788232 | AAATAATA others(11): Show |
A | 1 | a0002c0023t0002g0102 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2732-714_2732-697d others(20): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788232 | ||||||
chr19:16788232 | AAATAATA others(14): Show |
A | 4 | a0011c0011t0002g0022 a0011c0011t0011g0017 a0011c0011t0011g0024 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2732-717_2732-697d others(23): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788232 | ||||||
chr19:16788270 | A | T | 22 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(19): Show |
22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2732-712A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16788270 | |||||||
chr19:16788284 | A | G | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2732-698A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16788284 | |||||||
chr19:16788396 | C | T | 1 | a0004c0017t0001g0212 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2732-586C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16788396 | |||||||
chr19:16788467 | G | C | 3 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0022c0042t0001g0152 |
3 | HG01496.hp1 NA18993.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.2732-515G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16788467 | |||||||
chr19:16788533 | C | G | 1 | a0003c0006t0002g0100 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2732-449C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16788533 | |||||||
chr19:16788564 | C | CA | 65 | a0002c0002t0001g0156 a0002c0002t0001g0271 a0002c0002t0020g0249 others(62): Show |
65 | HG00099.hp2 HG00642.hp2 HG01081.hp1 others(62): Show |
intron_variant | MODIFIER | c.2732-399dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788564 | ||||||
chr19:16788564 | CA | C | 16 | a0001c0001t0003g0185 a0001c0001t0003g0215 a0001c0001t0003g0236 others(13): Show |
16 | HG01070.hp2 HG01256.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.2732-399delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788564 | ||||||
chr19:16788920 | A | G | 86 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0004c0005t0001g0296 others(83): Show |
86 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.2732-62A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16788920 | |||||||
chr19:16789368 | C | T | 3 | a0002c0008t0001g0270 a0003c0006t0002g0086 a0003c0006t0002g0096 |
3 | HG00733.hp1 HG00738.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.2940+178C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16789368 | |||||||
chr19:16789716 | C | CT | 62 | a0001c0001t0001g0160 a0001c0001t0014g0187 a0001c0007t0001g0040 others(59): Show |
62 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.2940+545dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16789716 | ||||||
chr19:16789716 | C | CTT | 28 | a0001c0047t0001g0138 a0004c0005t0001g0296 a0004c0005t0006g0211 others(25): Show |
28 | HG00642.hp2 HG01081.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.2940+544_2940+545d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16789716 | ||||||
chr19:16789716 | CT | C | 10 | a0001c0001t0004g0107 a0002c0002t0002g0010 a0002c0002t0012g0198 others(7): Show |
10 | HG01081.hp2 HG02040.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2940+545delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16789716 | ||||||
chr19:16789757 | G | A | 3 | a0029c0065t0032g0166 a0030c0066t0008g0264 a0043c0057t0026g0202 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2940+567G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16789757 | |||||||
chr19:16789855 | C | T | 1 | a0009c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2940+665C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16789855 | |||||||
chr19:16790009 | T | C | 11 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0007c0028t0002g0115 others(8): Show |
11 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2940+819T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790009 | |||||||
chr19:16790067 | G | A | 129 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0221 others(126): Show |
129 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(126): Show |
intron_variant | MODIFIER | c.2940+877G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790067 | |||||||
chr19:16790356 | G | A | 1 | a0045c0051t0002g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2941-994G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790356 | |||||||
chr19:16790372 | G | A | 1 | a0009c0010t0002g0114 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2941-978G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790372 | |||||||
chr19:16790469 | T | C | 1 | a0010c0013t0008g0188 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2941-881T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790469 | |||||||
chr19:16790471 | G | A | 1 | a0001c0001t0020g0289 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2941-879G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790471 | |||||||
chr19:16790472 | G | C | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2941-878G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790472 | |||||||
chr19:16790491 | C | A | 1 | a0003c0003t0002g0127 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2941-859C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790491 | |||||||
chr19:16790636 | AAAAAATA others(3): Show |
A | 43 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(40): Show |
43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.2941-710_2941-701d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16790636 | ||||||
chr19:16790638 | A | AAATAATA others(2): Show |
5 | a0015c0025t0002g0048 a0015c0025t0002g0049 a0029c0065t0032g0166 others(2): Show |
5 | HG02280.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2941-710_2941-709i others(11): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16790638 | ||||||
chr19:16790639 | A | AAAAT | 145 | a0001c0001t0001g0147 a0001c0001t0001g0158 a0001c0001t0001g0160 others(142): Show |
145 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.2941-709_2941-708i others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16790639 | ||||||
chr19:16790639 | A | ATAAT | 6 | a0001c0007t0049g0132 a0003c0006t0002g0071 a0003c0006t0002g0100 others(3): Show |
6 | HG01884.hp2 HG01981.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.2941-711_2941-710i others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790639 | |||||||
chr19:16790640 | A | T | 21 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(18): Show |
21 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.2941-710A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790640 | |||||||
chr19:16790641 | AT | A | 7 | a0001c0001t0004g0035 a0003c0003t0003g0143 a0003c0003t0004g0026 others(4): Show |
7 | HG00280.hp1 HG01257.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.2941-708delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790641 | |||||||
chr19:16790642 | T | A | 42 | a0001c0001t0001g0197 a0001c0001t0001g0242 a0001c0001t0002g0043 others(39): Show |
42 | HG00639.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.2941-708T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790642 | |||||||
chr19:16790643 | A | T | 34 | a0001c0001t0001g0197 a0001c0001t0001g0242 a0001c0001t0002g0043 others(31): Show |
34 | HG00639.hp1 HG00673.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.2941-707A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790643 | |||||||
chr19:16790646 | T | A | 9 | a0001c0001t0004g0032 a0001c0001t0004g0034 a0001c0001t0004g0035 others(6): Show |
9 | HG00280.hp1 HG01257.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.2941-704T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790646 | |||||||
chr19:16790652 | AAT | A | 43 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(40): Show |
43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.2941-696_2941-695d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16790652 | ||||||
chr19:16790655 | A | T | 43 | a0004c0005t0001g0296 a0004c0005t0006g0211 a0004c0005t0006g0225 others(40): Show |
43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.2941-695A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790655 | |||||||
chr19:16790743 | C | T | 22 | a0004c0009t0005g0140 a0004c0009t0005g0224 a0004c0009t0008g0205 others(19): Show |
22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2941-607C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790743 | |||||||
chr19:16790794 | G | T | 3 | a0029c0065t0032g0166 a0030c0066t0008g0264 a0043c0057t0026g0202 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2941-556G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790794 | |||||||
chr19:16790950 | G | A | 1 | a0006c0014t0002g0015 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2941-400G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790950 | |||||||
chr19:16790999 | A | G | 2 | a0001c0007t0001g0217 a0003c0006t0002g0062 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2941-351A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790999 | |||||||
chr19:16791813 | A | G | 11 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0007c0028t0002g0115 others(8): Show |
11 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3213+191A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16791813 | |||||||
chr19:16791954 | T | C | 3 | a0029c0065t0032g0166 a0030c0066t0008g0264 a0043c0057t0026g0202 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3213+332T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16791954 | |||||||
chr19:16792276 | C | A | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3213+654C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792276 | |||||||
chr19:16792299 | G | A | 2 | a0013c0020t0016g0003 a0013c0020t0016g0004 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.3213+677G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792299 | |||||||
chr19:16792360 | G | A | 3 | a0029c0065t0032g0166 a0030c0066t0008g0264 a0043c0057t0026g0202 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3213+738G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792360 | |||||||
chr19:16792443 | G | A | 11 | a0003c0003t0003g0143 a0003c0003t0004g0026 a0003c0003t0004g0075 others(8): Show |
11 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.3213+821G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792443 | |||||||
chr19:16792479 | C | G | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3213+857C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792479 | |||||||
chr19:16792526 | C | T | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3213+904C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792526 | |||||||
chr19:16792539 | G | A | 1 | a0004c0017t0001g0212 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3213+917G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792539 | |||||||
chr19:16792635 | T | C | 3 | a0001c0001t0003g0162 a0002c0002t0003g0144 a0002c0002t0003g0163 |
3 | HG01256.hp2 HG01346.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.3213+1013T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792635 | |||||||
chr19:16792734 | G | A | 1 | a0003c0003t0002g0127 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3213+1112G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792734 | |||||||
chr19:16792791 | C | A | 1 | a0003c0006t0002g0072 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3213+1169C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792791 | |||||||
chr19:16792876 | C | CA | 31 | a0001c0001t0003g0176 a0002c0002t0001g0199 a0002c0008t0001g0145 others(28): Show |
31 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.3213+1273dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16792876 | ||||||
chr19:16792876 | CA | C | 27 | a0001c0001t0003g0185 a0001c0001t0004g0035 a0001c0001t0005g0245 others(24): Show |
27 | HG00558.hp1 HG01074.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.3213+1273delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16792876 | ||||||
chr19:16793060 | TA | T | 173 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0001c0001t0001g0158 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.3214-1392delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16793060 | ||||||
chr19:16793176 | C | T | 3 | a0001c0001t0005g0154 a0001c0001t0005g0245 a0001c0001t0014g0187 |
3 | HG00558.hp1 HG02027.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.3214-1287C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16793176 | |||||||
chr19:16793250 | T | C | 1 | a0001c0001t0002g0021 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3214-1213T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16793250 | |||||||
chr19:16793583 | GT | G | 198 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0001c0001t0001g0158 others(195): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.3214-869delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16793583 | ||||||
chr19:16793738 | G | A | 20 | a0004c0009t0008g0205 a0004c0009t0008g0286 a0004c0009t0009g0047 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.3214-725G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16793738 | |||||||
chr19:16793806 | A | G | 2 | a0001c0001t0005g0154 a0001c0001t0014g0187 |
2 | HG02027.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.3214-657A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16793806 | |||||||
chr19:16793813 | G | A | 1 | a0001c0007t0002g0057 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3214-650G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16793813 | |||||||
chr19:16793975 | T | C | 3 | a0029c0065t0032g0166 a0030c0066t0008g0264 a0043c0057t0026g0202 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3214-488T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16793975 | |||||||
chr19:16794049 | A | G | 40 | a0001c0001t0001g0160 a0001c0007t0001g0040 a0001c0007t0001g0213 others(37): Show |
40 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.3214-414A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16794049 | |||||||
chr19:16794120 | C | T | 2 | a0002c0002t0003g0186 a0005c0004t0004g0090 |
2 | NA19005.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.3214-343C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16794120 | |||||||
chr19:16794183 | T | C | 1 | a0014c0022t0001g0231 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3214-280T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16794183 | |||||||
chr19:16794290 | C | T | 32 | a0004c0005t0001g0296 a0004c0005t0018g0256 a0004c0005t0023g0094 others(29): Show |
32 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.3214-173C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16794290 | |||||||
chr19:16794412 | G | A | 1 | a0037c0058t0035g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3214-51G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16794412 | |||||||
chr19:16794644 | A | C | 41 | a0001c0001t0001g0136 a0001c0001t0001g0164 a0001c0001t0001g0178 others(38): Show |
41 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.3304+91A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16794644 | |||||||
chr19:16794714 | C | T | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3304+161C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16794714 | |||||||
chr19:16794716 | A | T | 81 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0004c0005t0001g0296 others(78): Show |
81 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.3304+163A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16794716 | |||||||
chr19:16794800 | T | G | 125 | a0001c0007t0001g0040 a0001c0007t0001g0213 a0001c0007t0001g0221 others(122): Show |
125 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(122): Show |
intron_variant | MODIFIER | c.3304+247T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16794800 | |||||||
chr19:16794896 | G | A | 1 | a0003c0059t0015g0037 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3304+343G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16794896 | |||||||
chr19:16794931 | A | G | 1 | a0003c0003t0007g0064 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3304+378A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16794931 | |||||||
chr19:16795076 | G | A | 2 | a0001c0001t0001g0197 a0004c0060t0002g0125 |
2 | HG02886.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.3304+523G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16795076 | |||||||
chr19:16795217 | G | A | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3304+664G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16795217 | |||||||
chr19:16795318 | G | A | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3304+765G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16795318 | |||||||
chr19:16795395 | T | A | 4 | a0009c0010t0010g0131 a0009c0010t0010g0274 a0009c0010t0010g0276 others(1): Show |
4 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3304+842T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16795395 | |||||||
chr19:16795415 | C | CT | 36 | a0001c0001t0001g0147 a0001c0001t0001g0171 a0001c0001t0003g0220 others(33): Show |
36 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.3304+881dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr19 | 16795415 | ||||||
chr19:16795415 | CT | C | 18 | a0001c0001t0005g0241 a0001c0001t0033g0216 a0001c0046t0001g0219 others(15): Show |
18 | HG00099.hp1 HG01074.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.3304+881delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr19 | 16795415 | ||||||
chr19:16795415 | CTTTT | C | 8 | a0009c0010t0002g0114 a0009c0010t0010g0131 a0009c0010t0010g0274 others(5): Show |
8 | HG01361.hp1 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.3304+878_3304+881d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr19 | 16795415 | ||||||
chr19:16795519 | C | T | 1 | a0001c0001t0033g0216 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3304+966C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16795519 | |||||||
chr19:16795573 | C | T | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3304+1020C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16795573 | |||||||
chr19:16795579 | G | A | 1 | a0009c0010t0010g0283 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3304+1026G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16795579 | |||||||
chr19:16796560 | T | C | 25 | a0004c0005t0001g0296 a0004c0005t0018g0256 a0004c0005t0023g0094 others(22): Show |
25 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.3305-1172T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16796560 | |||||||
chr19:16796570 | T | C | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3305-1162T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16796570 | |||||||
chr19:16796588 | T | C | 30 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0004c0005t0006g0211 others(27): Show |
30 | HG01496.hp1 HG01884.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.3305-1144T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16796588 | |||||||
chr19:16796605 | G | A | 21 | a0004c0009t0008g0205 a0004c0009t0008g0286 a0004c0009t0009g0047 others(18): Show |
21 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.3305-1127G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16796605 | |||||||
chr19:16796677 | C | T | 45 | a0001c0001t0003g0176 a0001c0001t0003g0183 a0001c0001t0003g0185 others(42): Show |
45 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.3305-1055C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16796677 | |||||||
chr19:16796696 | C | CTTT | 25 | a0004c0005t0001g0296 a0004c0005t0018g0256 a0004c0005t0023g0094 others(22): Show |
25 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.3305-1034_3305-103 others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr19 | 16796696 | ||||||
chr19:16796765 | G | A | 14 | a0002c0023t0001g0151 a0002c0023t0002g0102 a0005c0004t0001g0278 others(11): Show |
14 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.3305-967G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16796765 | |||||||
chr19:16797125 | A | G | 2 | a0004c0009t0008g0205 a0004c0009t0036g0126 |
2 | HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.3305-607A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16797125 | |||||||
chr19:16797194 | AT | A | 5 | a0004c0005t0023g0094 a0004c0005t0023g0095 a0004c0005t0039g0084 others(2): Show |
5 | HG00642.hp2 HG01081.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.3305-536delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr19 | 16797194 | ||||||
chr19:16797197 | G | C | 3 | a0014c0022t0001g0231 a0014c0022t0002g0046 a0014c0022t0002g0051 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3305-535G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16797197 | |||||||
chr19:16797290 | C | G | 1 | a0045c0051t0002g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3305-442C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16797290 | |||||||
chr19:16797324 | ATC | A | 20 | a0004c0009t0008g0205 a0004c0009t0008g0286 a0004c0009t0009g0047 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.3305-404_3305-403d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr19 | 16797324 | ||||||
chr19:16797328 | C | CT | 34 | a0001c0001t0003g0183 a0001c0001t0031g0214 a0001c0007t0002g0007 others(31): Show |
34 | HG00609.hp1 HG01175.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.3305-384dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr19 | 16797328 | ||||||
chr19:16797372 | C | A | 1 | a0040c0037t0001g0209 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3305-360C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16797372 | |||||||
chr19:16797555 | C | T | 7 | a0002c0002t0001g0146 a0002c0002t0001g0153 a0002c0002t0001g0156 others(4): Show |
7 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.3305-177C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16797555 | |||||||
chr19:16798156 | T | G | 2 | a0004c0009t0013g0206 a0006c0014t0002g0015 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3459+270T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798156 | |||||||
chr19:16798268 | CT | C | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3459+389delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr19 | 16798268 | ||||||
chr19:16798364 | C | T | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3459+478C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798364 | |||||||
chr19:16798431 | A | G | 27 | a0004c0005t0001g0296 a0004c0005t0018g0256 a0004c0005t0023g0094 others(24): Show |
27 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.3459+545A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798431 | |||||||
chr19:16798467 | C | G | 1 | a0002c0002t0002g0008 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3459+581C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798467 | |||||||
chr19:16798479 | C | T | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3459+593C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798479 | |||||||
chr19:16798708 | C | T | 2 | a0008c0012t0001g0234 a0008c0012t0001g0235 |
2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3459+822C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798708 | |||||||
chr19:16798903 | G | A | 3 | a0014c0022t0001g0231 a0014c0022t0002g0046 a0014c0022t0002g0051 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3460-983G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798903 | |||||||
chr19:16798939 | T | TA | 78 | a0002c0002t0002g0013 a0002c0023t0001g0151 a0002c0023t0002g0102 others(75): Show |
78 | HG00609.hp1 HG00609.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.3460-934dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr19 | 16798939 | ||||||
chr19:16798940 | A | T | 1 | a0003c0006t0038g0106 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3460-946A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798940 | |||||||
chr19:16798950 | A | AC | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3460-936_3460-935i others(3): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798950 | |||||||
chr19:16799256 | C | T | 1 | a0019c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3460-630C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799256 | |||||||
chr19:16799528 | C | T | 31 | a0002c0002t0002g0013 a0002c0023t0001g0151 a0002c0023t0002g0102 others(28): Show |
31 | HG00609.hp2 HG01496.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.3460-358C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799528 | |||||||
chr19:16799663 | A | C | 27 | a0004c0005t0001g0296 a0004c0005t0018g0256 a0004c0005t0023g0094 others(24): Show |
27 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.3460-223A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799663 | |||||||
chr19:16799664 | G | A | 25 | a0004c0005t0001g0296 a0004c0005t0018g0256 a0004c0005t0023g0094 others(22): Show |
25 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.3460-222G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799664 | |||||||
chr19:16799667 | T | C | 25 | a0004c0005t0001g0296 a0004c0005t0018g0256 a0004c0005t0023g0094 others(22): Show |
25 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.3460-219T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799667 | |||||||
chr19:16799668 | G | A | 25 | a0004c0005t0001g0296 a0004c0005t0018g0256 a0004c0005t0023g0094 others(22): Show |
25 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.3460-218G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799668 | |||||||
chr19:16799669 | G | A | 25 | a0004c0005t0001g0296 a0004c0005t0018g0256 a0004c0005t0023g0094 others(22): Show |
25 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.3460-217G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799669 | |||||||
chr19:16799675 | T | A | 25 | a0004c0005t0001g0296 a0004c0005t0018g0256 a0004c0005t0023g0094 others(22): Show |
25 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.3460-211T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799675 | |||||||
chr19:16799727 | C | T | 1 | a0022c0042t0001g0152 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3460-159C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799727 | |||||||
chr19:16799734 | C | A | 1 | a0002c0002t0005g0195 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3460-152C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799734 | |||||||
chr19:16800178 | G | A | 4 | a0007c0069t0043g0299 a0016c0019t0017g0294 a0016c0019t0017g0295 others(1): Show |
4 | HG03098.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.3736+16G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16800178 | |||||||
chr19:16800390 | C | T | 1 | a0002c0002t0002g0008 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3736+228C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16800390 | |||||||
chr19:16800426 | T | C | 1 | a0002c0002t0002g0063 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.3736+264T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16800426 | |||||||
chr19:16800439 | C | CAGG | 209 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0001c0001t0001g0158 others(206): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.3736+279_3736+280i others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16800439 | ||||||
chr19:16800479 | C | T | 3 | a0001c0001t0001g0178 a0002c0002t0001g0271 a0003c0003t0002g0067 |
3 | HG02056.hp2 HG02080.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.3736+317C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16800479 | |||||||
chr19:16800500 | C | T | 21 | a0004c0009t0008g0205 a0004c0009t0008g0286 a0004c0009t0009g0047 others(18): Show |
21 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.3736+338C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16800500 | |||||||
chr19:16800505 | T | G | 1 | a0003c0003t0002g0065 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3736+343T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16800505 | |||||||
chr19:16800863 | G | T | 2 | a0006c0014t0009g0014 a0006c0014t0009g0016 |
2 | HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3736+701G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16800863 | |||||||
chr19:16800901 | G | A | 3 | a0001c0001t0001g0260 a0001c0001t0001g0262 a0005c0004t0002g0039 |
3 | HG01167.hp2 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3736+739G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16800901 | |||||||
chr19:16801067 | C | T | 2 | a0001c0001t0001g0261 a0031c0056t0001g0279 |
2 | HG01167.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3736+905C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16801067 | |||||||
chr19:16801589 | A | G | 84 | a0002c0002t0002g0013 a0002c0023t0001g0151 a0002c0023t0002g0102 others(81): Show |
84 | HG00609.hp2 HG00642.hp2 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.3736+1427A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16801589 | |||||||
chr19:16801862 | A | T | 136 | a0001c0001t0001g0136 a0001c0001t0001g0160 a0001c0007t0001g0040 others(133): Show |
136 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.3736+1700A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16801862 | |||||||
chr19:16801879 | C | T | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3736+1717C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16801879 | |||||||
chr19:16801904 | C | T | 15 | a0002c0002t0002g0013 a0002c0023t0001g0151 a0002c0023t0002g0102 others(12): Show |
15 | HG00609.hp2 HG01496.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.3736+1742C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16801904 | |||||||
chr19:16802234 | T | C | 4 | a0007c0069t0043g0299 a0016c0019t0017g0294 a0016c0019t0017g0295 others(1): Show |
4 | HG03098.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.3736+2072T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16802234 | |||||||
chr19:16802286 | T | TAAATAAA others(5): Show |
49 | a0001c0001t0001g0136 a0001c0001t0001g0160 a0001c0007t0001g0040 others(46): Show |
49 | HG00099.hp1 HG00544.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.3736+2137_3736+214 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16802286 | ||||||
chr19:16802323 | G | A | 21 | a0004c0009t0008g0205 a0004c0009t0008g0286 a0004c0009t0009g0047 others(18): Show |
21 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.3736+2161G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16802323 | |||||||
chr19:16802374 | C | T | 65 | a0001c0001t0001g0147 a0001c0001t0001g0158 a0001c0001t0001g0164 others(62): Show |
65 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.3736+2212C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16802374 | |||||||
chr19:16802410 | T | C | 42 | a0001c0001t0001g0164 a0001c0001t0001g0171 a0001c0001t0001g0178 others(39): Show |
42 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.3736+2248T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16802410 | |||||||
chr19:16802451 | C | A | 31 | a0002c0002t0002g0013 a0002c0023t0001g0151 a0002c0023t0002g0102 others(28): Show |
31 | HG00609.hp2 HG01496.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.3736+2289C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16802451 | |||||||
chr19:16802463 | TA | T | 93 | a0001c0001t0001g0160 a0001c0001t0003g0193 a0001c0001t0004g0112 others(90): Show |
93 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.3736+2323delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16802463 | ||||||
chr19:16802463 | TAA | T | 18 | a0001c0007t0002g0110 a0001c0046t0001g0219 a0002c0002t0002g0013 others(15): Show |
18 | HG00099.hp1 HG00609.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.3736+2322_3736+232 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16802463 | ||||||
chr19:16802547 | C | T | 6 | a0001c0046t0001g0219 a0003c0006t0001g0128 a0003c0059t0015g0037 others(3): Show |
6 | HG00099.hp1 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.3736+2385C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16802547 | |||||||
chr19:16802605 | T | G | 1 | a0004c0005t0006g0226 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3736+2443T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16802605 | |||||||
chr19:16802943 | G | A | 1 | a0003c0006t0002g0071 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3736+2781G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16802943 | |||||||
chr19:16802947 | C | CA | 10 | a0001c0001t0003g0183 a0002c0002t0001g0271 a0002c0002t0020g0249 others(7): Show |
10 | HG01099.hp2 HG02080.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.3736+2803dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16802947 | ||||||
chr19:16802947 | C | CAA | 21 | a0004c0005t0006g0211 a0004c0005t0006g0225 a0004c0005t0006g0226 others(18): Show |
21 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.3736+2802_3736+280 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16802947 | ||||||
chr19:16802947 | C | CAAA | 15 | a0002c0002t0002g0013 a0002c0023t0001g0151 a0002c0023t0002g0102 others(12): Show |
15 | HG00609.hp2 HG01496.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.3736+2801_3736+280 others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16802947 | ||||||
chr19:16803076 | T | C | 1 | a0003c0003t0002g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3736+2914T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16803076 | |||||||
chr19:16803105 | G | A | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3736+2943G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16803105 | |||||||
chr19:16803109 | G | A | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3736+2947G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16803109 | |||||||
chr19:16803151 | G | A | 65 | a0001c0001t0001g0147 a0001c0001t0001g0158 a0001c0001t0001g0164 others(62): Show |
65 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.3736+2989G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16803151 | |||||||
chr19:16803336 | A | G | 1 | a0020c0024t0001g0251 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3736+3174A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16803336 | |||||||
chr19:16803623 | C | G | 31 | a0002c0002t0002g0013 a0002c0023t0001g0151 a0002c0023t0002g0102 others(28): Show |
31 | HG00609.hp2 HG01496.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.3736+3461C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16803623 | |||||||
chr19:16803639 | A | G | 33 | a0002c0002t0002g0013 a0002c0023t0001g0151 a0002c0023t0002g0102 others(30): Show |
33 | HG00609.hp2 HG01496.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.3736+3477A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16803639 | |||||||
chr19:16803692 | G | A | 1 | a0002c0002t0002g0031 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3736+3530G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16803692 | |||||||
chr19:16803755 | T | TA | 14 | a0001c0001t0004g0113 a0002c0002t0002g0008 a0002c0031t0001g0155 others(11): Show |
14 | HG01261.hp2 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.3736+3613dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16803755 | ||||||
chr19:16803755 | TA | T | 26 | a0001c0001t0001g0178 a0001c0001t0002g0029 a0001c0001t0004g0032 others(23): Show |
26 | HG00280.hp2 HG01099.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.3736+3613delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16803755 | ||||||
chr19:16803927 | G | GA | 6 | a0002c0002t0002g0013 a0002c0023t0001g0151 a0002c0023t0002g0102 others(3): Show |
6 | HG00609.hp2 HG01496.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.3737-3649dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16803927 | ||||||
chr19:16804019 | G | A | 2 | a0004c0009t0013g0206 a0006c0014t0002g0015 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3737-3567G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804019 | |||||||
chr19:16804141 | C | T | 46 | a0004c0005t0001g0296 a0004c0005t0018g0256 a0004c0005t0023g0094 others(43): Show |
46 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.3737-3445C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804141 | |||||||
chr19:16804182 | C | A | 1 | a0040c0037t0001g0209 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3737-3404C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804182 | |||||||
chr19:16804370 | C | G | 17 | a0001c0001t0003g0176 a0001c0001t0003g0179 a0001c0001t0003g0182 others(14): Show |
17 | HG00597.hp2 HG01081.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3737-3216C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804370 | |||||||
chr19:16804518 | C | T | 19 | a0002c0002t0002g0013 a0002c0023t0001g0151 a0002c0023t0002g0102 others(16): Show |
19 | HG00609.hp2 HG01496.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.3737-3068C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804518 | |||||||
chr19:16804554 | C | T | 46 | a0004c0005t0001g0296 a0004c0005t0018g0256 a0004c0005t0023g0094 others(43): Show |
46 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.3737-3032C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804554 | |||||||
chr19:16804575 | A | G | 3 | a0002c0031t0001g0155 a0003c0006t0001g0281 a0003c0006t0001g0282 |
3 | HG02698.hp1 HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.3737-3011A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804575 | |||||||
chr19:16804594 | G | GTTTTT | 18 | a0002c0002t0002g0013 a0002c0023t0001g0151 a0002c0023t0002g0102 others(15): Show |
18 | HG00609.hp2 HG01496.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.3737-2985_3737-298 others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16804594 | ||||||
chr19:16804605 | T | A | 1 | a0004c0005t0022g0050 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3737-2981T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804605 | |||||||
chr19:16804649 | G | A | 2 | a0015c0025t0002g0048 a0015c0025t0002g0049 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3737-2937G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804649 | |||||||
chr19:16804754 | G | A | 1 | a0001c0001t0002g0043 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3737-2832G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804754 | |||||||
chr19:16804816 | CT | C | 72 | a0002c0002t0002g0013 a0002c0023t0001g0151 a0002c0023t0002g0102 others(69): Show |
72 | HG00609.hp2 HG00642.hp2 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.3737-2762delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16804816 | ||||||
chr19:16804894 | G | A | 1 | a0003c0006t0002g0071 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3737-2692G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804894 | |||||||
chr19:16804981 | C | T | 5 | a0011c0011t0001g0247 a0011c0011t0002g0022 a0011c0011t0011g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3737-2605C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804981 | |||||||
chr19:16805020 | T | C | 1 | a0009c0010t0002g0114 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3737-2566T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16805020 | |||||||
chr19:16805328 | G | A | 19 | a0002c0002t0002g0013 a0002c0023t0001g0151 a0002c0023t0002g0102 others(16): Show |
19 | HG00609.hp2 HG01496.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.3737-2258G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16805328 | |||||||
chr19:16805330 | A | G | 9 | a0006c0044t0001g0255 a0009c0010t0002g0114 a0009c0010t0010g0131 others(6): Show |
9 | HG01361.hp1 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.3737-2256A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16805330 | |||||||
chr19:16805667 | A | G | 1 | a0004c0009t0009g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3737-1919A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16805667 | |||||||
chr19:16805873 | C | CT | 6 | a0004c0005t0023g0094 a0004c0005t0023g0095 a0004c0005t0039g0084 others(3): Show |
6 | HG00642.hp2 HG01081.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3737-1711dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16805873 | ||||||
chr19:16805876 | C | T | 53 | a0004c0005t0001g0296 a0004c0005t0018g0256 a0004c0005t0023g0094 others(50): Show |
53 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.3737-1710C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16805876 | |||||||
chr19:16805901 | A | G | 9 | a0001c0001t0003g0176 a0001c0001t0003g0183 a0001c0001t0003g0185 others(6): Show |
9 | HG01081.hp2 HG01257.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.3737-1685A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16805901 | |||||||
chr19:16806084 | A | G | 67 | a0002c0002t0002g0013 a0002c0023t0001g0151 a0002c0023t0002g0102 others(64): Show |
67 | HG00609.hp2 HG00642.hp2 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.3737-1502A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16806084 | |||||||
chr19:16806311 | C | T | 3 | a0016c0019t0017g0294 a0016c0019t0017g0295 a0016c0019t0022g0124 |
3 | HG03098.hp1 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3737-1275C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16806311 | |||||||
chr19:16806646 | G | A | 3 | a0006c0015t0028g0204 a0029c0065t0032g0166 a0043c0057t0026g0202 |
3 | HG01884.hp1 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3737-940G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16806646 | |||||||
chr19:16806740 | C | T | 2 | a0003c0006t0038g0106 a0037c0058t0035g0167 |
2 | HG02148.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3737-846C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16806740 | |||||||
chr19:16806879 | T | C | 1 | a0004c0005t0006g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3737-707T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16806879 | |||||||
chr19:16807137 | T | C | 1 | a0001c0001t0002g0043 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3737-449T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16807137 | |||||||
chr19:16807145 | G | A | 1 | a0004c0060t0002g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3737-441G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16807145 | |||||||
chr19:16807170 | CA | C | 48 | a0001c0007t0002g0007 a0002c0008t0001g0270 a0003c0003t0046g0077 others(45): Show |
48 | HG00597.hp1 HG00642.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.3737-399delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16807170 | ||||||
chr19:16807170 | CAA | C | 16 | a0002c0002t0002g0013 a0002c0023t0001g0151 a0002c0023t0002g0102 others(13): Show |
16 | HG00609.hp2 HG01496.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.3737-400_3737-399d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16807170 | ||||||
chr19:16807285 | G | A | 12 | a0001c0001t0001g0136 a0002c0002t0001g0148 a0002c0002t0001g0174 others(9): Show |
12 | HG00544.hp2 HG00673.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.3737-301G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16807285 | |||||||
chr19:16807325 | C | A | 5 | a0002c0002t0001g0199 a0002c0002t0001g0268 a0002c0002t0012g0189 others(2): Show |
5 | HG02071.hp1 HG02080.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.3737-261C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16807325 | |||||||
chr19:16807512 | A | G | 1 | a0003c0059t0015g0037 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3737-74A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16807512 | |||||||
chr19:16807516 | A | C | 7 | a0004c0009t0009g0047 a0010c0013t0013g0172 a0010c0013t0013g0173 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.3737-70A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16807516 | |||||||
chr19:16808230 | G | A | 1 | a0002c0002t0002g0013 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4287+94G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16808230 | |||||||
chr19:16808232 | C | T | 1 | a0009c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4287+96C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16808232 | |||||||
chr19:16808237 | A | G | 1 | a0002c0002t0002g0123 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.4287+101A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16808237 | |||||||
chr19:16808378 | C | T | 1 | a0003c0003t0002g0069 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4287+242C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16808378 | |||||||
chr19:16808549 | A | AAAAAG | 7 | a0004c0005t0029g0265 a0006c0015t0028g0204 a0012c0018t0014g0149 others(4): Show |
7 | HG01884.hp1 HG02040.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.4287+434_4287+438d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr19 | 16808549 | ||||||
chr19:16808614 | A | T | 2 | a0004c0005t0023g0094 a0004c0005t0023g0095 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4287+478A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16808614 | |||||||
chr19:16808645 | G | A | 1 | a0009c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4287+509G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16808645 | |||||||
chr19:16808720 | G | A | 1 | a0003c0006t0002g0096 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4287+584G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16808720 | |||||||
chr19:16808827 | C | T | 20 | a0004c0009t0008g0205 a0004c0009t0008g0286 a0004c0009t0009g0047 others(17): Show |
20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.4287+691C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16808827 | |||||||
chr19:16809095 | A | AT | 17 | a0001c0001t0003g0176 a0001c0001t0003g0179 a0001c0001t0003g0182 others(14): Show |
17 | HG01081.hp2 HG01257.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.4287+971dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr19 | 16809095 | ||||||
chr19:16809195 | C | T | 42 | a0001c0001t0020g0289 a0002c0002t0020g0249 a0003c0003t0044g0070 others(39): Show |
42 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.4287+1059C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809195 | |||||||
chr19:16809200 | C | T | 1 | a0037c0058t0035g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4287+1064C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809200 | |||||||
chr19:16809541 | T | C | 2 | a0001c0001t0003g0179 a0001c0001t0003g0182 |
2 | NA18952.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.4287+1405T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809541 | |||||||
chr19:16809553 | CTTTTTCT others(5): Show |
C | 17 | a0004c0005t0006g0211 a0004c0005t0006g0225 a0004c0005t0006g0226 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.4287+1423_4287+143 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr19 | 16809553 | ||||||
chr19:16809559 | C | CT | 9 | a0004c0005t0029g0265 a0006c0015t0028g0204 a0011c0011t0002g0022 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.4287+1436dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr19 | 16809559 | ||||||
chr19:16809559 | CTTTTTT | C | 33 | a0001c0001t0020g0289 a0002c0002t0020g0249 a0003c0003t0044g0070 others(30): Show |
33 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.4287+1431_4287+143 others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr19 | 16809559 | ||||||
chr19:16809585 | T | C | 42 | a0001c0001t0020g0289 a0002c0002t0020g0249 a0003c0003t0044g0070 others(39): Show |
42 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.4287+1449T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809585 | |||||||
chr19:16809647 | C | T | 5 | a0004c0005t0029g0265 a0006c0015t0028g0204 a0024c0049t0042g0054 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4287+1511C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809647 | |||||||
chr19:16809703 | C | T | 2 | a0029c0065t0032g0166 a0043c0057t0026g0202 |
2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4287+1567C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809703 | |||||||
chr19:16809711 | C | T | 3 | a0004c0005t0001g0296 a0007c0068t0040g0116 a0015c0054t0025g0118 |
3 | HG02896.hp1 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4287+1575C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809711 | |||||||
chr19:16809835 | T | G | 1 | a0001c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4287+1699T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809835 | |||||||
chr19:16809836 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4287+1700C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809836 | |||||||
chr19:16809837 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4287+1701A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809837 | |||||||
chr19:16809838 | T | C | 4 | a0011c0011t0002g0022 a0011c0011t0011g0017 a0011c0011t0011g0024 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4287+1702T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809838 | |||||||
chr19:16809861 | C | T | 4 | a0011c0011t0002g0022 a0011c0011t0011g0017 a0011c0011t0011g0024 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4287+1725C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809861 | |||||||
chr19:16809903 | T | A | 3 | a0001c0001t0020g0289 a0002c0002t0020g0249 a0003c0003t0044g0070 |
3 | HG01099.hp2 HG01192.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.4287+1767T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809903 | |||||||
chr19:16810049 | G | T | 124 | a0001c0001t0001g0147 a0001c0001t0001g0158 a0001c0001t0001g0164 others(121): Show |
124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.4287+1913G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810049 | |||||||
chr19:16810332 | G | C | 5 | a0004c0005t0029g0265 a0006c0015t0028g0204 a0024c0049t0042g0054 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4287+2196G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810332 | |||||||
chr19:16810386 | C | T | 6 | a0002c0002t0001g0146 a0002c0002t0001g0156 a0002c0002t0001g0165 others(3): Show |
6 | HG00099.hp2 HG00323.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.4287+2250C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810386 | |||||||
chr19:16810395 | G | A | 21 | a0004c0009t0008g0205 a0004c0009t0008g0286 a0004c0009t0009g0047 others(18): Show |
21 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.4287+2259G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810395 | |||||||
chr19:16810437 | C | CA | 50 | a0001c0001t0001g0263 a0001c0001t0002g0043 a0001c0001t0003g0162 others(47): Show |
50 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.4287+2321dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr19 | 16810437 | ||||||
chr19:16810437 | C | CAA | 45 | a0002c0002t0002g0013 a0002c0023t0001g0151 a0002c0023t0002g0102 others(42): Show |
45 | HG00609.hp2 HG00735.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.4287+2320_4287+232 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr19 | 16810437 | ||||||
chr19:16810454 | A | G | 12 | a0004c0005t0006g0211 a0004c0005t0006g0225 a0004c0005t0006g0226 others(9): Show |
12 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.4287+2318A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810454 | |||||||
chr19:16810651 | T | C | 1 | a0002c0002t0001g0181 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4287+2515T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810651 | |||||||
chr19:16810652 | A | T | 1 | a0002c0002t0001g0181 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4287+2516A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810652 | |||||||
chr19:16810719 | C | T | 9 | a0004c0005t0029g0265 a0006c0015t0028g0204 a0011c0011t0002g0022 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.4287+2583C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810719 | |||||||
chr19:16810745 | G | T | 3 | a0001c0001t0005g0154 a0001c0001t0005g0245 a0001c0001t0014g0187 |
3 | HG00558.hp1 HG02027.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.4287+2609G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810745 | |||||||
chr19:16810774 | T | C | 1 | a0003c0006t0002g0096 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4287+2638T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810774 | |||||||
chr19:16810951 | C | T | 40 | a0001c0001t0001g0164 a0001c0001t0001g0171 a0001c0001t0001g0178 others(37): Show |
40 | HG00280.hp2 HG00558.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.4287+2815C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810951 | |||||||
chr19:16811252 | A | T | 3 | a0001c0001t0020g0289 a0002c0002t0020g0249 a0003c0003t0044g0070 |
3 | HG01099.hp2 HG01192.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.4287+3116A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16811252 | |||||||
chr19:16811323 | C | T | 30 | a0004c0005t0001g0296 a0004c0005t0018g0256 a0004c0005t0023g0094 others(27): Show |
30 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.4287+3187C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16811323 | |||||||
chr19:16811441 | G | A | 17 | a0001c0001t0001g0160 a0002c0002t0002g0013 a0002c0023t0001g0151 others(14): Show |
17 | HG00609.hp2 HG01109.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.4287+3305G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16811441 | |||||||
chr19:16811447 | G | C | 1 | a0009c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4287+3311G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16811447 | |||||||
chr19:16811485 | G | T | 2 | a0002c0002t0007g0030 a0017c0021t0045g0121 |
2 | NA18951.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.4287+3349G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16811485 | |||||||
chr19:16811586 | GA | G | 10 | a0001c0001t0004g0112 a0001c0001t0005g0154 a0001c0001t0014g0187 others(7): Show |
10 | HG01070.hp2 HG01257.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.4288-3428delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr19 | 16811586 | ||||||
chr19:16812104 | T | A | 1 | a0003c0003t0002g0069 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4288-2924T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16812104 | |||||||
chr19:16812360 | A | T | 4 | a0011c0011t0002g0022 a0011c0011t0011g0017 a0011c0011t0011g0024 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4288-2668A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16812360 | |||||||
chr19:16812378 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4288-2650T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16812378 | |||||||
chr19:16812402 | C | T | 1 | a0004c0017t0001g0212 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4288-2626C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16812402 | |||||||
chr19:16812538 | T | C | 6 | a0001c0001t0001g0242 a0001c0001t0002g0043 a0002c0002t0001g0291 others(3): Show |
6 | NA18954.hp2 NA18968.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.4288-2490T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16812538 | |||||||
chr19:16812683 | C | G | 146 | a0001c0001t0001g0136 a0001c0001t0001g0160 a0001c0001t0003g0176 others(143): Show |
146 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.4288-2345C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16812683 | |||||||
chr19:16812954 | C | G | 1 | a0003c0006t0002g0086 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.4288-2074C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16812954 | |||||||
chr19:16812967 | C | T | 1 | a0002c0002t0001g0177 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.4288-2061C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16812967 | |||||||
chr19:16813038 | C | T | 1 | a0002c0002t0001g0199 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4288-1990C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813038 | |||||||
chr19:16813055 | G | A | 1 | a0009c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4288-1973G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813055 | |||||||
chr19:16813177 | G | C | 1 | a0005c0004t0003g0266 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4288-1851G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813177 | |||||||
chr19:16813444 | G | C | 1 | a0001c0001t0033g0216 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4288-1584G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813444 | |||||||
chr19:16813445 | C | G | 1 | a0001c0001t0033g0216 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4288-1583C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813445 | |||||||
chr19:16813447 | T | C | 1 | a0001c0001t0033g0216 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4288-1581T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813447 | |||||||
chr19:16813618 | G | A | 1 | a0002c0033t0002g0012 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.4288-1410G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813618 | |||||||
chr19:16813714 | T | C | 5 | a0004c0005t0029g0265 a0006c0015t0028g0204 a0024c0049t0042g0054 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4288-1314T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813714 | |||||||
chr19:16813740 | G | T | 1 | a0001c0001t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.4288-1288G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813740 | |||||||
chr19:16814030 | T | C | 9 | a0004c0005t0029g0265 a0006c0015t0028g0204 a0011c0011t0002g0022 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.4288-998T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16814030 | |||||||
chr19:16814118 | C | A | 9 | a0004c0005t0029g0265 a0006c0015t0028g0204 a0011c0011t0002g0022 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.4288-910C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16814118 | |||||||
chr19:16814141 | C | A | 4 | a0004c0017t0001g0212 a0004c0017t0002g0018 a0004c0017t0002g0019 others(1): Show |
4 | HG02257.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4288-887C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16814141 | |||||||
chr19:16814381 | C | T | 2 | a0007c0068t0040g0116 a0015c0054t0025g0118 |
2 | HG02896.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.4288-647C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16814381 | |||||||
chr19:16814584 | A | G | 1 | a0029c0065t0032g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4288-444A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16814584 | |||||||
chr19:16814781 | C | G | 1 | a0003c0003t0002g0076 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.4288-247C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16814781 | |||||||
chr19:16814862 | A | G | 9 | a0004c0005t0029g0265 a0006c0015t0028g0204 a0011c0011t0002g0022 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.4288-166A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16814862 |