Item | Value |
---|---|
geneid | 51199 |
ensemblid | ENSG00000100503.27 |
hgncid | 14906 |
symbol | NIN |
name | ninein |
refseq_nuc | NM_020921.4 |
refseq_prot | NP_065972.4 |
ensembl_nuc | ENST00000530997.7 |
ensembl_prot | ENSP00000436092.2 |
mane_status | MANE Select |
chr | chr14 |
start | 50719763 |
end | 50831162 |
strand | - |
ver | v1.2 |
region | chr14:50719763-50831162 |
region5000 | chr14:50714763-50836162 |
regionname0 | NIN_chr14_50719763_50831162 |
regionname5000 | NIN_chr14_50714763_50836162 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 2133 | 96 | 59 | 23 | 2 | 4 | 7 | 2 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0002 | 1/0 | 2133 | 64 | 9 | 10 | 26 | 4 | 14 | 20 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0003 | 0/0 | 2133 | 55 | 2 | 20 | 24 | 2 | 7 | 19 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0004 | 0/0 | 2133 | 25 | 2 | 8 | 13 | 0 | 2 | 10 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0005 | 0/0 | 2133 | 10 | 0 | 0 | 10 | 0 | 0 | 9 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0006 | 0/0 | 2133 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0007 | 0/0 | 2133 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0008 | 0/0 | 2133 | 5 | 2 | 3 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0009 | 0/0 | 2133 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0010 | 0/0 | 2133 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0011 | 0/0 | 2133 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0012 | 0/0 | 2133 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0013 | 0/0 | 2133 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0014 | 0/0 | 2133 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0015 | 0/0 | 2133 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0016 | 0/0 | 2133 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0017 | 0/0 | 2133 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0018 | 0/0 | 2133 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0019 | 0/0 | 2133 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0020 | 0/0 | 2133 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0021 | 0/0 | 2133 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0022 | 0/0 | 2133 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0023 | 0/0 | 2133 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0024 | 0/0 | 2133 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0025 | 0/0 | 2133 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
a0026 | 0/0 | 2133 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | MDEVE others(2128): Show |
chr14 | 50714763 | 50836162 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 6399 | 46 | 32 | 10 | 0 | 3 | 1 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0001c0005 | 0/0 | 6399 | 13 | 5 | 4 | 2 | 1 | 1 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0001c0006 | 0/1 | 6399 | 10 | 2 | 6 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0001c0011 | 0/0 | 6399 | 5 | 5 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0001c0012 | 0/0 | 6399 | 3 | 2 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0001c0017 | 0/0 | 6399 | 2 | 0 | 0 | 0 | 0 | 2 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0001c0018 | 0/0 | 6399 | 2 | 0 | 2 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0001c0025 | 0/0 | 6399 | 2 | 2 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0001c0027 | 0/0 | 6399 | 2 | 2 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0001c0028 | 0/0 | 6399 | 2 | 2 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0001c0029 | 0/0 | 6399 | 2 | 2 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0001c0030 | 0/0 | 6399 | 2 | 0 | 0 | 0 | 0 | 2 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0001c0047 | 0/0 | 6399 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0001c0052 | 0/0 | 6399 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0001c0054 | 0/0 | 6399 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0001c0056 | 0/0 | 6399 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0001c0060 | 0/0 | 6399 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0002c0001 | 0/0 | 6399 | 53 | 4 | 8 | 26 | 4 | 11 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0002c0013 | 0/0 | 6399 | 3 | 3 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0002c0015 | 0/0 | 6399 | 3 | 1 | 0 | 0 | 0 | 2 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0002c0043 | 0/0 | 6399 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0002c0051 | 0/0 | 6399 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0002c0058 | 0/0 | 6399 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0002c0059 | 1/0 | 6399 | 1 | 0 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0002c0061 | 0/0 | 6399 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0003c0003 | 0/0 | 6399 | 41 | 0 | 14 | 19 | 2 | 6 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0003c0008 | 0/0 | 6399 | 9 | 2 | 1 | 5 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0003c0016 | 0/0 | 6399 | 3 | 0 | 3 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0003c0022 | 0/0 | 6399 | 2 | 0 | 2 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0004c0004 | 0/0 | 6399 | 21 | 1 | 7 | 11 | 0 | 2 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0004c0026 | 0/0 | 6399 | 2 | 1 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0004c0039 | 0/0 | 6399 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0004c0048 | 0/0 | 6399 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0005c0007 | 0/0 | 6399 | 9 | 0 | 0 | 9 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0005c0031 | 0/0 | 6399 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0006c0010 | 0/0 | 6399 | 5 | 5 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0006c0062 | 0/0 | 6399 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0007c0009 | 0/0 | 6399 | 5 | 5 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0007c0055 | 0/0 | 6399 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0008c0020 | 0/0 | 6399 | 2 | 1 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0008c0021 | 0/0 | 6399 | 2 | 1 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0008c0036 | 0/0 | 6399 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0009c0014 | 0/0 | 6399 | 3 | 2 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0009c0053 | 0/0 | 6399 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0010c0023 | 0/0 | 6399 | 2 | 0 | 1 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0010c0035 | 0/0 | 6399 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0011c0024 | 0/0 | 6399 | 2 | 2 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0012c0019 | 0/0 | 6399 | 2 | 0 | 0 | 0 | 0 | 2 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0013c0044 | 0/0 | 6399 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0014c0040 | 0/0 | 6399 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0015c0057 | 0/0 | 6399 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0016c0049 | 0/0 | 6399 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0017c0037 | 0/0 | 6399 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0018c0034 | 0/0 | 6399 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0019c0042 | 0/0 | 6399 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0020c0033 | 0/0 | 6399 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0021c0032 | 0/0 | 6399 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0022c0046 | 0/0 | 6399 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0023c0050 | 0/0 | 6399 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0024c0041 | 0/0 | 6399 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0025c0045 | 0/0 | 6399 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 | ||
a0026c0038 | 0/0 | 6399 | 1 | 0 | 0 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | ATGGA others(6394): Show |
chr14 | 50714763 | 50836162 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 10334 | 3 | 3 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0001c0002t0002 | 0/0 | 10333 | 4 | 0 | 2 | 0 | 2 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0001c0002t0003 | 0/0 | 10337 | 28 | 19 | 8 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0002t0005 | 0/0 | 10337 | 6 | 6 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0002t0008 | 0/0 | 10337 | 2 | 2 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0002t0020 | 0/0 | 10337 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0002t0021 | 0/0 | 10337 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0002t0023 | 0/0 | 10337 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0005t0001 | 0/0 | 10334 | 12 | 5 | 3 | 2 | 1 | 1 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0001c0005t0004 | 0/0 | 10337 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0006t0003 | 0/1 | 10337 | 9 | 2 | 5 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0006t0013 | 0/0 | 10337 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0011t0001 | 0/0 | 10334 | 3 | 3 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0001c0011t0006 | 0/0 | 10337 | 2 | 2 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0012t0001 | 0/0 | 10334 | 3 | 2 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0001c0017t0002 | 0/0 | 10333 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0001c0017t0003 | 0/0 | 10337 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0018t0001 | 0/0 | 10334 | 2 | 0 | 2 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0001c0025t0010 | 0/0 | 10337 | 2 | 2 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0027t0012 | 0/0 | 10337 | 2 | 2 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0028t0003 | 0/0 | 10337 | 2 | 2 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0029t0001 | 0/0 | 10334 | 2 | 2 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0001c0030t0004 | 0/0 | 10337 | 2 | 0 | 0 | 0 | 0 | 2 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0047t0003 | 0/0 | 10337 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0052t0005 | 0/0 | 10337 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0054t0006 | 0/0 | 10337 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0001c0056t0001 | 0/0 | 10334 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0001c0060t0003 | 0/0 | 10337 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0002c0001t0002 | 0/0 | 10333 | 48 | 4 | 5 | 26 | 2 | 11 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0002c0001t0007 | 0/0 | 10333 | 2 | 0 | 2 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0002c0001t0014 | 0/0 | 10333 | 1 | 0 | 0 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0002c0001t0016 | 0/0 | 10333 | 1 | 0 | 0 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0002c0001t0017 | 0/0 | 10333 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0002c0013t0004 | 0/0 | 10337 | 3 | 3 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0002c0015t0002 | 0/0 | 10333 | 3 | 1 | 0 | 0 | 0 | 2 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0002c0043t0002 | 0/0 | 10333 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0002c0051t0002 | 0/0 | 10333 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0002c0058t0002 | 0/0 | 10333 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0002c0059t0001 | 1/0 | 10334 | 1 | 0 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0002c0061t0002 | 0/0 | 10333 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0003c0003t0001 | 0/0 | 10334 | 37 | 0 | 12 | 17 | 2 | 6 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0003c0003t0009 | 0/0 | 10334 | 2 | 0 | 2 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0003c0003t0011 | 0/0 | 10334 | 2 | 0 | 0 | 2 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0003c0008t0002 | 0/0 | 10333 | 6 | 0 | 0 | 5 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0003c0008t0004 | 0/0 | 10337 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0003c0008t0007 | 0/0 | 10333 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0003c0008t0015 | 0/0 | 10333 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0003c0016t0001 | 0/0 | 10334 | 3 | 0 | 3 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0003c0022t0001 | 0/0 | 10334 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0003c0022t0009 | 0/0 | 10334 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0004c0004t0001 | 0/0 | 10334 | 20 | 1 | 7 | 10 | 0 | 2 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0004c0004t0019 | 0/0 | 10334 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0004c0026t0001 | 0/0 | 10334 | 2 | 1 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0004c0039t0001 | 0/0 | 10334 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0004c0048t0001 | 0/0 | 10334 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0005c0007t0001 | 0/0 | 10334 | 9 | 0 | 0 | 9 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0005c0031t0001 | 0/0 | 10334 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0006c0010t0002 | 0/0 | 10333 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0006c0010t0006 | 0/0 | 10337 | 3 | 3 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0006c0010t0008 | 0/0 | 10337 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0006c0062t0006 | 0/0 | 10337 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0007c0009t0004 | 0/0 | 10337 | 5 | 5 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0007c0055t0004 | 0/0 | 10337 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0008c0020t0003 | 0/0 | 10337 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0008c0020t0004 | 0/0 | 10337 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0008c0021t0001 | 0/0 | 10334 | 2 | 1 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0008c0036t0004 | 0/0 | 10337 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0009c0014t0005 | 0/0 | 10337 | 2 | 2 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0009c0014t0022 | 0/0 | 10337 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0009c0053t0005 | 0/0 | 10337 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0010c0023t0002 | 0/0 | 10333 | 2 | 0 | 1 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0010c0035t0002 | 0/0 | 10333 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0011c0024t0003 | 0/0 | 10337 | 2 | 2 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0012c0019t0001 | 0/0 | 10334 | 2 | 0 | 0 | 0 | 0 | 2 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0013c0044t0002 | 0/0 | 10333 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0014c0040t0003 | 0/0 | 10337 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0015c0057t0018 | 0/0 | 10334 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0016c0049t0001 | 0/0 | 10334 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0017c0037t0001 | 0/0 | 10334 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0018c0034t0024 | 0/0 | 10334 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0019c0042t0001 | 0/0 | 10334 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0020c0033t0010 | 0/0 | 10337 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0021c0032t0006 | 0/0 | 10337 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10332): Show |
chr14 | 50714763 | 50836162 |
a0022c0046t0001 | 0/0 | 10334 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10329): Show |
chr14 | 50714763 | 50836162 |
a0023c0050t0002 | 0/0 | 10333 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0024c0041t0002 | 0/0 | 10333 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0025c0045t0002 | 0/0 | 10333 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
a0026c0038t0002 | 0/0 | 10333 | 1 | 0 | 0 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | GGCCC others(10328): Show |
chr14 | 50714763 | 50836162 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0005g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0020g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0021g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0002t0023g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0005t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0005t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0005t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0005t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0005t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0005t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0005t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0005t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0005t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0005t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0005t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0005t0004g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0006t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0006t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0006t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0006t0003g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0006t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0006t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0006t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0006t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0006t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0006t0013g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0011t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0011t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0011t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0011t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0011t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0012t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0012t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0012t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0017t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0017t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0018t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0018t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0025t0010g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0025t0010g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0027t0012g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0027t0012g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0028t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0028t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0029t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0029t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0030t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0030t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0047t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0052t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0054t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0056t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0001c0060t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0007g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0007g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0014g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0016g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0001t0017g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0013t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0013t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0013t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0015t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0015t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0015t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0043t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0051t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0058t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0059t0001g0020 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0002c0061t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0009g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0009g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0011g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0003t0011g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0008t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0008t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0008t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0008t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0008t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0008t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0008t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0008t0007g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0008t0015g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0016t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0016t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0022t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0003c0022t0009g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0004t0019g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0026t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0026t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0039t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0004c0048t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0005c0007t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0005c0007t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0005c0007t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0005c0007t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0005c0007t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0005c0007t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0005c0007t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0005c0007t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0005c0007t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0005c0031t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0006c0010t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0006c0010t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0006c0010t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0006c0010t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0006c0010t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0006c0062t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0007c0009t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0007c0009t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0007c0009t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0007c0009t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0007c0009t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0007c0055t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0008c0020t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0008c0020t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0008c0021t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0008c0021t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0008c0036t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0009c0014t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0009c0014t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0009c0014t0022g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0009c0053t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0010c0023t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0010c0023t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0010c0035t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0011c0024t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0012c0019t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0012c0019t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0013c0044t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0014c0040t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0015c0057t0018g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0016c0049t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0017c0037t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0018c0034t0024g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0019c0042t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0020c0033t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0021c0032t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0022c0046t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0023c0050t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0024c0041t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0025c0045t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
a0026c0038t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0002 | g0215 | EUR | GBR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00099 | hp2 | a0001 | c0002 | t0002 | g0204 | EUR | GBR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0064 | EUR | GBR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00140 | hp2 | a0003 | c0003 | t0001 | g0151 | EUR | GBR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00280 | hp1 | a0002 | c0001 | t0002 | g0181 | EUR | FIN | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00280 | hp2 | a0001 | c0002 | t0003 | g0212 | EUR | FIN | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00408 | hp1 | a0003 | c0003 | t0001 | g0251 | EAS | CHS | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00408 | hp2 | a0002 | c0001 | t0002 | g0028 | EAS | CHS | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00438 | hp1 | a0004 | c0004 | t0001 | g0152 | EAS | CHS | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00438 | hp2 | a0013 | c0044 | t0002 | g0159 | EAS | CHS | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00621 | hp1 | a0002 | c0001 | t0002 | g0240 | EAS | CHS | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00621 | hp2 | a0004 | c0026 | t0001 | g0107 | EAS | CHS | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00639 | hp1 | a0001 | c0006 | t0003 | g0219 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00639 | hp2 | a0003 | c0003 | t0001 | g0096 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00642 | hp1 | a0001 | c0006 | t0003 | g0187 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00642 | hp2 | a0004 | c0004 | t0001 | g0050 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00733 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00733 | hp2 | a0001 | c0006 | t0003 | g0188 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00735 | hp1 | a0001 | c0006 | t0003 | g0060 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00735 | hp2 | a0003 | c0022 | t0001 | g0211 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00738 | hp1 | a0010 | c0023 | t0002 | g0253 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00738 | hp2 | a0003 | c0003 | t0001 | g0148 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00741 | hp1 | a0004 | c0039 | t0001 | g0146 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG00741 | hp2 | a0003 | c0003 | t0009 | g0259 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01069 | hp1 | a0003 | c0016 | t0001 | g0003 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01069 | hp2 | a0001 | c0002 | t0003 | g0184 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01070 | hp1 | a0002 | c0001 | t0002 | g0191 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01070 | hp2 | a0003 | c0003 | t0001 | g0047 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01071 | hp1 | a0003 | c0016 | t0001 | g0003 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01071 | hp2 | a0003 | c0003 | t0001 | g0048 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01074 | hp1 | a0004 | c0004 | t0001 | g0042 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01074 | hp2 | a0001 | c0002 | t0003 | g0172 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01099 | hp1 | a0003 | c0008 | t0007 | g0267 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01099 | hp2 | a0001 | c0005 | t0001 | g0252 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01106 | hp1 | a0010 | c0035 | t0002 | g0026 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01106 | hp2 | a0003 | c0003 | t0001 | g0208 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01109 | hp1 | a0014 | c0040 | t0003 | g0275 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01109 | hp2 | a0002 | c0001 | t0002 | g0202 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01167 | hp1 | a0003 | c0003 | t0001 | g0207 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01167 | hp2 | a0001 | c0002 | t0003 | g0063 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01168 | hp1 | a0002 | c0001 | t0007 | g0277 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01168 | hp2 | a0001 | c0018 | t0001 | g0230 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01169 | hp1 | a0002 | c0001 | t0007 | g0268 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01169 | hp2 | a0001 | c0002 | t0003 | g0062 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01192 | hp1 | a0002 | c0001 | t0002 | g0258 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01192 | hp2 | a0003 | c0016 | t0001 | g0130 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01243 | hp1 | a0003 | c0003 | t0001 | g0257 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01243 | hp2 | a0004 | c0004 | t0001 | g0179 | AMR | PUR | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0203 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01255 | hp2 | a0003 | c0003 | t0001 | g0223 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01256 | hp1 | a0003 | c0003 | t0001 | g0206 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01256 | hp2 | a0001 | c0002 | t0003 | g0102 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01257 | hp1 | a0001 | c0005 | t0001 | g0040 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01257 | hp2 | a0002 | c0061 | t0002 | g0121 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01258 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01258 | hp2 | a0001 | c0005 | t0001 | g0041 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01261 | hp1 | a0008 | c0036 | t0004 | g0069 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01261 | hp2 | a0001 | c0006 | t0013 | g0006 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01346 | hp1 | a0001 | c0002 | t0003 | g0171 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01346 | hp2 | a0001 | c0005 | t0004 | g0263 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01358 | hp1 | a0015 | c0057 | t0018 | g0030 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01358 | hp2 | a0008 | c0021 | t0001 | g0019 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01361 | hp1 | a0001 | c0012 | t0001 | g0061 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01361 | hp2 | a0002 | c0001 | t0017 | g0031 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01433 | hp1 | a0001 | c0018 | t0001 | g0027 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01433 | hp2 | a0009 | c0014 | t0022 | g0013 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01496 | hp1 | a0003 | c0003 | t0001 | g0222 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01496 | hp2 | a0008 | c0020 | t0004 | g0105 | AMR | CLM | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01515 | hp1 | a0002 | c0001 | t0014 | g0264 | EUR | IBS | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01515 | hp2 | a0010 | c0023 | t0002 | g0175 | EUR | IBS | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01884 | hp1 | a0011 | c0024 | t0003 | g0001 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01884 | hp2 | a0001 | c0011 | t0001 | g0008 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01891 | hp1 | a0009 | c0014 | t0005 | g0014 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01891 | hp2 | a0006 | c0062 | t0006 | g0100 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01943 | hp1 | a0004 | c0004 | t0001 | g0224 | AMR | PEL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01943 | hp2 | a0001 | c0006 | t0003 | g0162 | AMR | PEL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01952 | hp1 | a0002 | c0001 | t0002 | g0214 | AMR | PEL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01952 | hp2 | a0004 | c0004 | t0001 | g0239 | AMR | PEL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01975 | hp1 | a0002 | c0001 | t0002 | g0218 | AMR | PEL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01975 | hp2 | a0003 | c0003 | t0009 | g0160 | AMR | PEL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01978 | hp1 | a0003 | c0003 | t0001 | g0182 | AMR | PEL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01978 | hp2 | a0004 | c0004 | t0001 | g0238 | AMR | PEL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0233 | AMR | PEL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01981 | hp2 | a0003 | c0022 | t0009 | g0127 | AMR | PEL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01993 | hp1 | a0016 | c0049 | t0001 | g0124 | AMR | PEL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG01993 | hp2 | a0002 | c0043 | t0002 | g0247 | AMR | PEL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02015 | hp1 | a0002 | c0001 | t0002 | g0168 | EAS | KHV | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02015 | hp2 | a0003 | c0008 | t0002 | g0104 | EAS | KHV | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02055 | hp1 | a0002 | c0001 | t0002 | g0163 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02055 | hp2 | a0007 | c0009 | t0004 | g0136 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02056 | hp1 | a0017 | c0037 | t0001 | g0056 | EAS | KHV | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02056 | hp2 | a0004 | c0004 | t0001 | g0071 | EAS | KHV | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02071 | hp1 | a0002 | c0001 | t0002 | g0116 | EAS | KHV | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02071 | hp2 | a0003 | c0003 | t0001 | g0256 | EAS | KHV | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02135 | hp1 | a0003 | c0003 | t0001 | g0193 | EAS | KHV | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02135 | hp2 | a0002 | c0001 | t0002 | g0088 | EAS | KHV | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02145 | hp1 | a0001 | c0005 | t0001 | g0186 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02145 | hp2 | a0001 | c0002 | t0003 | g0110 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02165 | hp1 | a0005 | c0007 | t0001 | g0098 | EAS | CDX | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02165 | hp2 | a0003 | c0003 | t0001 | g0066 | EAS | CDX | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02257 | hp1 | a0001 | c0002 | t0005 | g0004 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02257 | hp2 | a0008 | c0020 | t0003 | g0232 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02258 | hp1 | a0001 | c0028 | t0003 | g0012 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02258 | hp2 | a0004 | c0004 | t0001 | g0052 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02273 | hp1 | a0003 | c0003 | t0001 | g0054 | AMR | PEL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02273 | hp2 | a0004 | c0004 | t0001 | g0237 | AMR | PEL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02280 | hp1 | a0018 | c0034 | t0024 | g0284 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02280 | hp2 | a0001 | c0060 | t0003 | g0035 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02451 | hp1 | a0001 | c0002 | t0003 | g0070 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02451 | hp2 | a0001 | c0011 | t0006 | g0076 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02523 | hp1 | a0019 | c0042 | t0001 | g0283 | EAS | KHV | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02523 | hp2 | a0002 | c0001 | t0002 | g0117 | EAS | KHV | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02572 | hp1 | a0001 | c0005 | t0001 | g0046 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02572 | hp2 | a0001 | c0028 | t0003 | g0101 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02602 | hp1 | a0002 | c0001 | t0002 | g0213 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02602 | hp2 | a0002 | c0001 | t0002 | g0190 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02615 | hp1 | a0001 | c0002 | t0003 | g0018 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02615 | hp2 | a0002 | c0001 | t0002 | g0229 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02622 | hp1 | a0001 | c0002 | t0005 | g0084 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02622 | hp2 | a0001 | c0011 | t0006 | g0077 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02630 | hp1 | a0001 | c0002 | t0003 | g0009 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02630 | hp2 | a0001 | c0025 | t0010 | g0135 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02647 | hp1 | a0020 | c0033 | t0010 | g0049 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02647 | hp2 | a0001 | c0027 | t0012 | g0287 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02683 | hp1 | a0001 | c0017 | t0002 | g0079 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02683 | hp2 | a0003 | c0003 | t0001 | g0192 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02738 | hp1 | a0004 | c0004 | t0001 | g0043 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02738 | hp2 | a0003 | c0003 | t0001 | g0091 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02809 | hp1 | a0002 | c0013 | t0004 | g0140 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02809 | hp2 | a0001 | c0029 | t0001 | g0089 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02818 | hp1 | a0001 | c0002 | t0003 | g0236 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02818 | hp2 | a0001 | c0002 | t0020 | g0173 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02886 | hp1 | a0001 | c0005 | t0001 | g0072 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02886 | hp2 | a0001 | c0054 | t0006 | g0196 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02895 | hp1 | a0006 | c0010 | t0006 | g0093 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02895 | hp2 | a0001 | c0002 | t0005 | g0141 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02896 | hp1 | a0001 | c0012 | t0001 | g0059 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02896 | hp2 | a0007 | c0009 | t0004 | g0138 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02897 | hp1 | a0006 | c0010 | t0006 | g0092 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02897 | hp2 | a0007 | c0009 | t0004 | g0103 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02922 | hp1 | a0001 | c0011 | t0001 | g0011 | AFR | ESN | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02922 | hp2 | a0001 | c0002 | t0003 | g0099 | AFR | ESN | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02965 | hp1 | a0002 | c0013 | t0004 | g0065 | AFR | ESN | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02965 | hp2 | a0009 | c0014 | t0005 | g0015 | AFR | ESN | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02976 | hp1 | a0002 | c0001 | t0002 | g0132 | AFR | ESN | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02976 | hp2 | a0001 | c0047 | t0003 | g0007 | AFR | ESN | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03017 | hp1 | a0002 | c0001 | t0002 | g0221 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03017 | hp2 | a0001 | c0005 | t0001 | g0133 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03041 | hp1 | a0001 | c0002 | t0003 | g0034 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03041 | hp2 | a0001 | c0012 | t0001 | g0039 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03098 | hp1 | a0001 | c0002 | t0003 | g0017 | AFR | MSL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03098 | hp2 | a0021 | c0032 | t0006 | g0286 | AFR | MSL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03130 | hp1 | a0001 | c0002 | t0005 | g0142 | AFR | ESN | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03130 | hp2 | a0003 | c0008 | t0015 | g0036 | AFR | ESN | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03139 | hp1 | a0006 | c0010 | t0008 | g0139 | AFR | ESN | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03139 | hp2 | a0007 | c0055 | t0004 | g0022 | AFR | ESN | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03195 | hp1 | a0001 | c0011 | t0001 | g0227 | AFR | ESN | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03195 | hp2 | a0001 | c0002 | t0003 | g0074 | AFR | ESN | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03209 | hp1 | a0001 | c0002 | t0003 | g0131 | AFR | MSL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03209 | hp2 | a0011 | c0024 | t0003 | g0001 | AFR | MSL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03225 | hp1 | a0008 | c0021 | t0001 | g0010 | AFR | MSL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0242 | AFR | MSL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03239 | hp1 | a0002 | c0001 | t0002 | g0032 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03239 | hp2 | a0003 | c0008 | t0002 | g0261 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03453 | hp1 | a0006 | c0010 | t0006 | g0094 | AFR | MSL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03453 | hp2 | a0001 | c0002 | t0003 | g0078 | AFR | MSL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03486 | hp1 | a0009 | c0053 | t0005 | g0016 | AFR | MSL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03486 | hp2 | a0001 | c0029 | t0001 | g0197 | AFR | MSL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03490 | hp1 | a0002 | c0001 | t0002 | g0145 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03490 | hp2 | a0003 | c0003 | t0001 | g0005 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03492 | hp1 | a0003 | c0003 | t0001 | g0005 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03492 | hp2 | a0002 | c0001 | t0002 | g0144 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03516 | hp1 | a0002 | c0058 | t0002 | g0024 | AFR | ESN | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03516 | hp2 | a0001 | c0002 | t0003 | g0225 | AFR | ESN | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0226 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03540 | hp2 | a0001 | c0002 | t0003 | g0199 | AFR | GWD | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03579 | hp1 | a0001 | c0025 | t0010 | g0067 | AFR | MSL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03579 | hp2 | a0007 | c0009 | t0004 | g0025 | AFR | MSL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03669 | hp1 | a0002 | c0001 | t0002 | g0220 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03669 | hp2 | a0002 | c0001 | t0002 | g0176 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03688 | hp1 | a0001 | c0006 | t0003 | g0271 | SAS | STU | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03688 | hp2 | a0001 | c0030 | t0004 | g0111 | SAS | STU | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03704 | hp1 | a0001 | c0017 | t0003 | g0115 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03704 | hp2 | a0001 | c0002 | t0021 | g0246 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03710 | hp1 | a0002 | c0001 | t0002 | g0109 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03710 | hp2 | a0003 | c0003 | t0001 | g0200 | SAS | PJL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03927 | hp1 | a0002 | c0051 | t0002 | g0245 | SAS | BEB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03927 | hp2 | a0012 | c0019 | t0001 | g0210 | SAS | BEB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG04199 | hp1 | a0001 | c0030 | t0004 | g0274 | SAS | STU | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG04199 | hp2 | a0004 | c0004 | t0001 | g0087 | SAS | STU | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG04204 | hp1 | a0012 | c0019 | t0001 | g0269 | SAS | STU | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG04204 | hp2 | a0002 | c0015 | t0002 | g0254 | SAS | STU | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG04228 | hp1 | a0002 | c0015 | t0002 | g0174 | SAS | STU | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG04228 | hp2 | a0002 | c0001 | t0002 | g0189 | SAS | STU | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18522 | hp1 | a0007 | c0009 | t0004 | g0137 | AFR | YRI | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18522 | hp2 | a0001 | c0002 | t0003 | g0086 | AFR | YRI | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18906 | hp1 | a0001 | c0002 | t0008 | g0198 | AFR | YRI | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18906 | hp2 | a0001 | c0006 | t0003 | g0037 | AFR | YRI | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18939 | hp1 | a0003 | c0003 | t0001 | g0249 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18939 | hp2 | a0005 | c0031 | t0001 | g0157 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18943 | hp1 | a0005 | c0007 | t0001 | g0154 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18943 | hp2 | a0002 | c0001 | t0002 | g0120 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18944 | hp1 | a0004 | c0004 | t0001 | g0051 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18944 | hp2 | a0002 | c0001 | t0002 | g0106 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18945 | hp1 | a0002 | c0001 | t0002 | g0270 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18945 | hp2 | a0001 | c0005 | t0001 | g0158 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18950 | hp1 | a0003 | c0003 | t0001 | g0279 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18950 | hp2 | a0002 | c0001 | t0002 | g0166 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18951 | hp1 | a0003 | c0003 | t0001 | g0216 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18951 | hp2 | a0004 | c0004 | t0001 | g0155 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18953 | hp1 | a0002 | c0001 | t0002 | g0122 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18953 | hp2 | a0004 | c0004 | t0001 | g0273 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18957 | hp1 | a0005 | c0007 | t0001 | g0044 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18957 | hp2 | a0003 | c0003 | t0001 | g0260 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18960 | hp1 | a0002 | c0001 | t0002 | g0108 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18960 | hp2 | a0003 | c0003 | t0001 | g0029 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18963 | hp1 | a0005 | c0007 | t0001 | g0097 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18963 | hp2 | a0003 | c0003 | t0001 | g0282 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18964 | hp1 | a0004 | c0004 | t0001 | g0183 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18964 | hp2 | a0003 | c0003 | t0001 | g0255 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18965 | hp1 | a0003 | c0003 | t0011 | g0169 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18965 | hp2 | a0003 | c0008 | t0002 | g0080 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18967 | hp1 | a0005 | c0007 | t0001 | g0231 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18967 | hp2 | a0002 | c0001 | t0002 | g0165 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18977 | hp1 | a0001 | c0005 | t0001 | g0170 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18977 | hp2 | a0003 | c0008 | t0002 | g0262 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18981 | hp1 | a0004 | c0004 | t0019 | g0081 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18981 | hp2 | a0002 | c0001 | t0002 | g0209 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18988 | hp1 | a0002 | c0001 | t0002 | g0082 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18988 | hp2 | a0003 | c0003 | t0001 | g0280 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18992 | hp1 | a0022 | c0046 | t0001 | g0112 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18992 | hp2 | a0003 | c0008 | t0002 | g0266 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18998 | hp1 | a0002 | c0001 | t0002 | g0129 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18998 | hp2 | a0023 | c0050 | t0002 | g0244 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18999 | hp1 | a0002 | c0001 | t0002 | g0123 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18999 | hp2 | a0003 | c0003 | t0001 | g0038 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19000 | hp1 | a0002 | c0001 | t0002 | g0185 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19000 | hp2 | a0003 | c0003 | t0001 | g0250 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19004 | hp1 | a0002 | c0001 | t0002 | g0235 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19004 | hp2 | a0002 | c0001 | t0002 | g0278 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19011 | hp1 | a0005 | c0007 | t0001 | g0058 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19011 | hp2 | a0002 | c0001 | t0002 | g0201 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19030 | hp1 | a0002 | c0015 | t0002 | g0085 | AFR | LWK | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19030 | hp2 | a0001 | c0005 | t0001 | g0241 | AFR | LWK | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19043 | hp1 | a0001 | c0052 | t0005 | g0285 | AFR | LWK | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19043 | hp2 | a0001 | c0002 | t0003 | g0090 | AFR | LWK | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19056 | hp1 | a0024 | c0041 | t0002 | g0114 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19056 | hp2 | a0004 | c0048 | t0001 | g0083 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19060 | hp1 | a0005 | c0007 | t0001 | g0045 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19060 | hp2 | a0002 | c0001 | t0002 | g0113 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19068 | hp1 | a0004 | c0004 | t0001 | g0248 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19068 | hp2 | a0003 | c0003 | t0001 | g0164 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19074 | hp1 | a0002 | c0001 | t0002 | g0118 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19074 | hp2 | a0005 | c0007 | t0001 | g0156 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19077 | hp1 | a0025 | c0045 | t0002 | g0128 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19077 | hp2 | a0004 | c0004 | t0001 | g0055 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19078 | hp1 | a0004 | c0004 | t0001 | g0119 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19078 | hp2 | a0003 | c0003 | t0011 | g0243 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19079 | hp1 | a0002 | c0001 | t0002 | g0272 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19079 | hp2 | a0003 | c0003 | t0001 | g0281 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19080 | hp1 | a0004 | c0004 | t0001 | g0126 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19080 | hp2 | a0003 | c0008 | t0002 | g0265 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19085 | hp1 | a0002 | c0001 | t0002 | g0057 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19085 | hp2 | a0003 | c0003 | t0001 | g0217 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19240 | hp1 | a0001 | c0027 | t0012 | g0023 | AFR | YRI | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA19240 | hp2 | a0001 | c0002 | t0003 | g0073 | AFR | YRI | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA20129 | hp1 | a0002 | c0001 | t0002 | g0180 | AFR | ASW | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA20129 | hp2 | a0001 | c0002 | t0003 | g0178 | AFR | ASW | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA20752 | hp1 | a0001 | c0005 | t0001 | g0134 | EUR | TSI | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA20752 | hp2 | a0003 | c0003 | t0001 | g0149 | EUR | TSI | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA20805 | hp1 | a0026 | c0038 | t0002 | g0167 | EUR | TSI | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA20805 | hp2 | a0002 | c0001 | t0016 | g0234 | EUR | TSI | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA20905 | hp1 | a0003 | c0003 | t0001 | g0150 | SAS | GIH | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA20905 | hp2 | a0002 | c0001 | t0002 | g0205 | SAS | GIH | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02109 | hp1 | a0001 | c0006 | t0003 | g0276 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02109 | hp2 | a0002 | c0013 | t0004 | g0194 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0228 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02486 | hp2 | a0001 | c0005 | t0001 | g0147 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02559 | hp1 | a0001 | c0002 | t0005 | g0004 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG02559 | hp2 | a0001 | c0002 | t0003 | g0075 | AFR | ACB | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03471 | hp1 | a0001 | c0002 | t0005 | g0033 | AFR | MSL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG03471 | hp2 | a0001 | c0056 | t0001 | g0143 | AFR | MSL | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG06807 | hp1 | a0003 | c0008 | t0004 | g0095 | AFR | USA | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
HG06807 | hp2 | a0001 | c0002 | t0003 | g0021 | AFR | USA | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18955 | hp1 | a0005 | c0007 | t0001 | g0125 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA18955 | hp2 | a0002 | c0001 | t0002 | g0153 | EAS | JPT | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA20300 | hp1 | a0001 | c0002 | t0008 | g0195 | AFR | USA | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA20300 | hp2 | a0004 | c0026 | t0001 | g0053 | AFR | USA | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA21309 | hp1 | a0001 | c0002 | t0023 | g0068 | AFR | LWK | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
NA21309 | hp2 | a0006 | c0010 | t0002 | g0161 | AFR | LWK | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
homoSapiens | chm13v2 | a0001 | c0006 | t0003 | g0177 | REF | REF | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
homoSapiens | grch38p0 | a0002 | c0059 | t0001 | g0020 | REF | REF | NIN_chr14_50714763_50836162 | NIN | chr14 | 50714763 | 50836162 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:50729606 | G | A | 1 | a0013 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.5995C>T | p.Arg1999Cys | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/31 | 6227/10334 | 5995/6402 | 1999/2133 | chr14 | 50729606 | |||
chr14:50729698 | G | A | 1 | a0014 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.5903C>T | p.Thr1968Met | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/31 | 6135/10334 | 5903/6402 | 1968/2133 | chr14 | 50729698 | |||
chr14:50729707 | G | C | 1 | a0025 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.5894C>G | p.Ser1965Cys | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/31 | 6126/10334 | 5894/6402 | 1965/2133 | chr14 | 50729707 | |||
chr14:50735593 | G | C | 5 | a0004 a0005 a0016 others(2): Show |
38 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(35): Show |
missense_variant | MODERATE | c.5800C>G | p.Gln1934Glu | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/31 | 6032/10334 | 5800/6402 | 1934/2133 | chr14 | 50735593 | |||
chr14:50739427 | A | T | 1 | a0010 | 3 | HG00738.hp1 HG01106.hp1 HG01515.hp2 |
missense_variant | MODERATE | c.5509T>A | p.Ser1837Thr | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 26/31 | 5741/10334 | 5509/6402 | 1837/2133 | chr14 | 50739427 | |||
chr14:50744355 | C | T | 1 | a0008 | 5 | HG01261.hp1 HG01358.hp2 HG01496.hp2 others(2): Show |
missense_variant | MODERATE | c.5075G>A | p.Cys1692Tyr | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 23/31 | 5307/10334 | 5075/6402 | 1692/2133 | chr14 | 50744355 | |||
chr14:50748045 | T | C | 1 | a0007 | 6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
missense_variant | MODERATE | c.5011A>G | p.Ile1671Val | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/31 | 5243/10334 | 5011/6402 | 1671/2133 | chr14 | 50748045 | |||
chr14:50752531 | C | T | 1 | a0019 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.4937G>A | p.Arg1646His | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/31 | 5169/10334 | 4937/6402 | 1646/2133 | chr14 | 50752531 | |||
chr14:50752602 | T | G | 1 | a0009 | 4 | HG01433.hp2 HG01891.hp1 HG02965.hp2 others(1): Show |
missense_variant | MODERATE | c.4866A>C | p.Glu1622Asp | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/31 | 5098/10334 | 4866/6402 | 1622/2133 | chr14 | 50752602 | |||
chr14:50752631 | G | A | 2 | a0005 a0024 |
11 | HG02165.hp1 NA18939.hp2 NA18943.hp1 others(8): Show |
missense_variant | MODERATE | c.4837C>T | p.Arg1613Cys | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/31 | 5069/10334 | 4837/6402 | 1613/2133 | chr14 | 50752631 | |||
chr14:50754821 | C | T | 1 | a0026 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.4585G>A | p.Glu1529Lys | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 19/31 | 4817/10334 | 4585/6402 | 1529/2133 | chr14 | 50754821 | |||
chr14:50756886 | G | C | 1 | a0012 | 2 | HG03927.hp2 HG04204.hp1 |
missense_variant | MODERATE | c.4144C>G | p.His1382Asp | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/31 | 4376/10334 | 4144/6402 | 1382/2133 | chr14 | 50756886 | |||
chr14:50757071 | C | T | 19 | a0001 a0003 a0004 others(16): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
missense_variant | MODERATE | c.3959G>A | p.Gly1320Glu | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/31 | 4191/10334 | 3959/6402 | 1320/2133 | chr14 | 50757071 | |||
chr14:50757576 | C | A | 2 | a0007 a0021 |
7 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
missense_variant | MODERATE | c.3454G>T | p.Val1152Phe | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/31 | 3686/10334 | 3454/6402 | 1152/2133 | chr14 | 50757576 | |||
chr14:50757656 | T | G | 21 | a0001 a0003 a0004 others(18): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
missense_variant | MODERATE | c.3374A>C | p.Gln1125Pro | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/31 | 3606/10334 | 3374/6402 | 1125/2133 | chr14 | 50757656 | |||
chr14:50757699 | G | C | 5 | a0003 a0015 a0016 others(2): Show |
59 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(56): Show |
missense_variant | MODERATE | c.3331C>G | p.Pro1111Ala | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/31 | 3563/10334 | 3331/6402 | 1111/2133 | chr14 | 50757699 | |||
chr14:50757735 | C | T | 1 | a0017 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.3295G>A | p.Glu1099Lys | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/31 | 3527/10334 | 3295/6402 | 1099/2133 | chr14 | 50757735 | |||
chr14:50758379 | T | C | 1 | a0015 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.2651A>G | p.Lys884Arg | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/31 | 2883/10334 | 2651/6402 | 884/2133 | chr14 | 50758379 | |||
chr14:50760184 | T | C | 1 | a0011 | 2 | HG01884.hp1 HG03209.hp2 |
missense_variant | MODERATE | c.2072A>G | p.His691Arg | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 17/31 | 2304/10334 | 2072/6402 | 691/2133 | chr14 | 50760184 | |||
chr14:50760332 | C | T | 1 | a0018 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.1924G>A | p.Glu642Lys | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 17/31 | 2156/10334 | 1924/6402 | 642/2133 | chr14 | 50760332 | |||
chr14:50773089 | C | T | 1 | a0020 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.673G>A | p.Glu225Lys | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 8/31 | 905/10334 | 673/6402 | 225/2133 | chr14 | 50773089 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:50726004 | C | G | 1 | a0002c0043 | 1 | HG01993.hp2 | synonymous_variant | LOW | c.6141G>C | p.Leu2047Leu | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/31 | 6373/10334 | 6141/6402 | 2047/2133 | chr14 | 50726004 | |||
chr14:50729640 | C | T | 1 | a0003c0016 | 3 | HG01069.hp1 HG01071.hp1 HG01192.hp2 |
synonymous_variant | LOW | c.5961G>A | p.Pro1987Pro | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/31 | 6193/10334 | 5961/6402 | 1987/2133 | chr14 | 50729640 | |||
chr14:50738278 | C | T | 35 | a0001c0002 a0001c0006 a0001c0011 others(32): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
synonymous_variant | LOW | c.5637G>A | p.Gln1879Gln | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/31 | 5869/10334 | 5637/6402 | 1879/2133 | chr14 | 50738278 | |||
chr14:50739338 | G | A | 1 | a0009c0053 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.5598C>T | p.Thr1866Thr | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 26/31 | 5830/10334 | 5598/6402 | 1866/2133 | chr14 | 50739338 | |||
chr14:50752680 | A | G | 1 | a0001c0030 | 2 | HG03688.hp2 HG04199.hp1 |
synonymous_variant | LOW | c.4788T>C | p.Leu1596Leu | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/31 | 5020/10334 | 4788/6402 | 1596/2133 | chr14 | 50752680 | |||
chr14:50754623 | C | T | 1 | a0004c0039 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.4674G>A | p.Thr1558Thr | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/31 | 4906/10334 | 4674/6402 | 1558/2133 | chr14 | 50754623 | |||
chr14:50756635 | A | G | 1 | a0001c0025 | 2 | HG02630.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.4395T>C | p.Thr1465Thr | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/31 | 4627/10334 | 4395/6402 | 1465/2133 | chr14 | 50756635 | |||
chr14:50757940 | T | A | 16 | a0001c0005 a0001c0006 a0001c0054 others(13): Show |
67 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(64): Show |
synonymous_variant | LOW | c.3090A>T | p.Ser1030Ser | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/31 | 3322/10334 | 3090/6402 | 1030/2133 | chr14 | 50757940 | |||
chr14:50758042 | C | T | 1 | a0001c0027 | 2 | HG02647.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.2988G>A | p.Ala996Ala | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/31 | 3220/10334 | 2988/6402 | 996/2133 | chr14 | 50758042 | |||
chr14:50758354 | C | T | 1 | a0008c0036 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.2676G>A | p.Gln892Gln | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/31 | 2908/10334 | 2676/6402 | 892/2133 | chr14 | 50758354 | |||
chr14:50758414 | G | T | 25 | a0001c0005 a0001c0006 a0001c0011 others(22): Show |
90 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(87): Show |
synonymous_variant | LOW | c.2616C>A | p.Ala872Ala | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/31 | 2848/10334 | 2616/6402 | 872/2133 | chr14 | 50758414 | |||
chr14:50760012 | G | A | 1 | a0001c0030 | 2 | HG03688.hp2 HG04199.hp1 |
synonymous_variant | LOW | c.2244C>T | p.Ser748Ser | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 17/31 | 2476/10334 | 2244/6402 | 748/2133 | chr14 | 50760012 | |||
chr14:50760282 | A | G | 5 | a0001c0002 a0001c0054 a0010c0023 others(2): Show |
52 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(49): Show |
synonymous_variant | LOW | c.1974T>C | p.His658His | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 17/31 | 2206/10334 | 1974/6402 | 658/2133 | chr14 | 50760282 | |||
chr14:50760333 | G | A | 1 | a0002c0051 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.1923C>T | p.Asp641Asp | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 17/31 | 2155/10334 | 1923/6402 | 641/2133 | chr14 | 50760333 | |||
chr14:50763872 | C | T | 3 | a0001c0052 a0009c0014 a0009c0053 |
5 | HG01433.hp2 HG01891.hp1 HG02965.hp2 others(2): Show |
synonymous_variant | LOW | c.1728G>A | p.Pro576Pro | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/31 | 1960/10334 | 1728/6402 | 576/2133 | chr14 | 50763872 | |||
chr14:50770905 | C | T | 1 | a0005c0031 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.1206G>A | p.Ser402Ser | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 11/31 | 1438/10334 | 1206/6402 | 402/2133 | chr14 | 50770905 | |||
chr14:50770983 | A | G | 35 | a0001c0005 a0001c0006 a0001c0012 others(32): Show |
149 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(146): Show |
synonymous_variant | LOW | c.1128T>C | p.Val376Val | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 11/31 | 1360/10334 | 1128/6402 | 376/2133 | chr14 | 50770983 | |||
chr14:50772349 | C | G | 59 | a0001c0002 a0001c0005 a0001c0006 others(56): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
synonymous_variant | LOW | c.933G>C | p.Leu311Leu | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 9/31 | 1165/10334 | 933/6402 | 311/2133 | chr14 | 50772349 | |||
chr14:50772463 | G | A | 1 | a0002c0061 | 1 | HG01257.hp2 | synonymous_variant | LOW | c.819C>T | p.Phe273Phe | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 9/31 | 1051/10334 | 819/6402 | 273/2133 | chr14 | 50772463 | |||
chr14:50777003 | C | T | 1 | a0001c0012 | 3 | HG01361.hp1 HG02896.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.612G>A | p.Arg204Arg | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/31 | 844/10334 | 612/6402 | 204/2133 | chr14 | 50777003 | |||
chr14:50777015 | A | G | 2 | a0007c0009 a0021c0032 |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
synonymous_variant | LOW | c.600T>C | p.Gly200Gly | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/31 | 832/10334 | 600/6402 | 200/2133 | chr14 | 50777015 | |||
chr14:50792796 | C | T | 1 | a0005c0031 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.351G>A | p.Val117Val | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/31 | 583/10334 | 351/6402 | 117/2133 | chr14 | 50792796 | |||
chr14:50806738 | T | A | 1 | a0006c0062 | 1 | HG01891.hp2 | splice_region_variant&synonymous_variant | LOW | c.264A>T | p.Pro88Pro | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/31 | 496/10334 | 264/6402 | 88/2133 | chr14 | 50806738 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:50719895 | A | G | 1 | a0001c0027t0012 | 2 | HG02647.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3568T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 3568 | chr14 | 50719895 | ||||||
chr14:50719918 | C | A | 1 | a0015c0057t0018 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3545G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 3545 | chr14 | 50719918 | ||||||
chr14:50720409 | C | T | 1 | a0002c0001t0017 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3054G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 3054 | chr14 | 50720409 | ||||||
chr14:50720573 | G | A | 2 | a0002c0001t0007 a0003c0008t0007 |
3 | HG01099.hp1 HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2890C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 2890 | chr14 | 50720573 | ||||||
chr14:50721202 | T | A | 2 | a0003c0003t0009 a0003c0022t0009 |
3 | HG00741.hp2 HG01975.hp2 HG01981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2261A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 2261 | chr14 | 50721202 | ||||||
chr14:50721281 | T | G | 1 | a0009c0014t0022 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2182A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 2182 | chr14 | 50721281 | ||||||
chr14:50721312 | T | A | 1 | a0004c0004t0019 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2151A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 2151 | chr14 | 50721312 | ||||||
chr14:50721405 | C | T | 1 | a0002c0001t0016 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2058G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 2058 | chr14 | 50721405 | ||||||
chr14:50721406 | G | A | 12 | a0001c0002t0003 a0001c0002t0021 a0001c0002t0023 others(9): Show |
48 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2057C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 2057 | chr14 | 50721406 | ||||||
chr14:50721436 | A | G | 1 | a0003c0008t0015 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2027T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 2027 | chr14 | 50721436 | ||||||
chr14:50721513 | A | G | 2 | a0001c0025t0010 a0020c0033t0010 |
3 | HG02630.hp2 HG02647.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1950T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 1950 | chr14 | 50721513 | ||||||
chr14:50721623 | A | G | 51 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0008 others(48): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*1840T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 1840 | chr14 | 50721623 | ||||||
chr14:50721724 | A | C | 1 | a0001c0002t0021 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1739T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 1739 | chr14 | 50721724 | ||||||
chr14:50722036 | C | T | 17 | a0001c0002t0003 a0001c0002t0021 a0001c0002t0023 others(14): Show |
56 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1427G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 1427 | chr14 | 50722036 | ||||||
chr14:50722066 | C | G | 1 | a0001c0002t0020 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1397G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 1397 | chr14 | 50722066 | ||||||
chr14:50722133 | G | A | 1 | a0001c0002t0023 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1330C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 1330 | chr14 | 50722133 | ||||||
chr14:50722142 | T | TAGA | 59 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0005 others(56): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*1320_*1321insTCT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 1320 | chr14 | 50722142 | ||||||
chr14:50722157 | T | C | 1 | a0018c0034t0024 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1306A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 1306 | chr14 | 50722157 | ||||||
chr14:50722406 | C | T | 1 | a0003c0003t0011 | 2 | NA18965.hp1 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1057G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 1057 | chr14 | 50722406 | ||||||
chr14:50723063 | A | C | 2 | a0001c0002t0008 a0006c0010t0008 |
3 | HG03139.hp1 NA18906.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*400T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 400 | chr14 | 50723063 | ||||||
chr14:50723142 | TAAAA | T | 23 | a0001c0002t0002 a0001c0017t0002 a0002c0001t0002 others(20): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*317_*320delTTTT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 317 | chr14 | 50723142 | ||||||
chr14:50723152 | A | C | 10 | a0001c0002t0005 a0001c0002t0020 a0001c0027t0012 others(7): Show |
17 | HG01261.hp1 HG01433.hp2 HG01496.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*311T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 311 | chr14 | 50723152 | ||||||
chr14:50723153 | C | A | 1 | a0017c0037t0001 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*310G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 310 | chr14 | 50723153 | ||||||
chr14:50723347 | A | T | 1 | a0002c0001t0014 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*116T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 31/31 | 116 | chr14 | 50723347 | ||||||
chr14:50831115 | G | T | 1 | a0001c0006t0013 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-185C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 1/31 | 9059 | chr14 | 50831115 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:50723757 | G | A | 1 | a0001c0006t0003g0271 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.6193-85C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50723757 | |||||||
chr14:50723875 | C | A | 1 | a0003c0008t0002g0104 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.6193-203G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50723875 | |||||||
chr14:50723976 | T | C | 3 | a0001c0054t0006g0196 a0008c0021t0001g0010 a0008c0021t0001g0019 |
3 | HG01358.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.6193-304A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50723976 | |||||||
chr14:50724110 | A | G | 5 | a0003c0003t0009g0160 a0003c0003t0009g0259 a0003c0016t0001g0003 others(2): Show |
6 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.6193-438T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50724110 | |||||||
chr14:50724275 | A | G | 1 | a0002c0013t0004g0194 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.6193-603T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50724275 | |||||||
chr14:50724277 | T | C | 2 | a0001c0027t0012g0023 a0001c0027t0012g0287 |
2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.6193-605A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50724277 | |||||||
chr14:50724387 | G | A | 2 | a0003c0008t0004g0095 a0003c0008t0015g0036 |
2 | HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6193-715C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50724387 | |||||||
chr14:50724577 | T | C | 5 | a0001c0025t0010g0067 a0001c0025t0010g0135 a0001c0030t0004g0111 others(2): Show |
5 | HG02630.hp2 HG02647.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.6193-905A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50724577 | |||||||
chr14:50724634 | G | A | 11 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(8): Show |
12 | HG01433.hp2 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.6193-962C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50724634 | |||||||
chr14:50724690 | G | A | 1 | a0001c0002t0002g0204 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.6193-1018C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50724690 | |||||||
chr14:50724695 | G | T | 1 | a0001c0002t0002g0233 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.6193-1023C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50724695 | |||||||
chr14:50724785 | T | TC | 17 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(14): Show |
18 | HG01433.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.6193-1114dupG | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50724785 | |||||||
chr14:50724904 | T | C | 1 | a0002c0001t0002g0117 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.6192+1049A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50724904 | |||||||
chr14:50724958 | C | T | 174 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(171): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.6192+995G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50724958 | |||||||
chr14:50724960 | C | G | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.6192+993G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50724960 | |||||||
chr14:50724983 | T | G | 2 | a0003c0008t0004g0095 a0003c0008t0015g0036 |
2 | HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6192+970A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50724983 | |||||||
chr14:50725000 | T | C | 17 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(14): Show |
18 | HG01433.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.6192+953A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50725000 | |||||||
chr14:50725016 | C | T | 96 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.6192+937G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50725016 | |||||||
chr14:50725185 | G | A | 1 | a0001c0056t0001g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6192+768C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50725185 | |||||||
chr14:50725238 | C | T | 2 | a0001c0002t0003g0086 a0001c0028t0003g0101 |
2 | HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.6192+715G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50725238 | |||||||
chr14:50725694 | GT | G | 3 | a0001c0002t0008g0195 a0001c0002t0008g0198 a0006c0010t0008g0139 |
3 | HG03139.hp1 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6192+258delA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50725694 | |||||||
chr14:50725742 | G | A | 1 | a0001c0006t0013g0006 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6192+211C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50725742 | |||||||
chr14:50725777 | G | A | 17 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(14): Show |
18 | HG01433.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.6192+176C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50725777 | |||||||
chr14:50725789 | G | A | 1 | a0002c0001t0002g0185 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.6192+164C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50725789 | |||||||
chr14:50725815 | G | C | 2 | a0003c0003t0011g0169 a0003c0003t0011g0243 |
2 | NA18965.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.6192+138C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50725815 | |||||||
chr14:50725818 | C | A | 1 | a0001c0005t0001g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.6192+135G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50725818 | |||||||
chr14:50725853 | G | C | 20 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(17): Show |
20 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.6192+100C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50725853 | |||||||
chr14:50725941 | G | A | 78 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(75): Show |
78 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(75): Show |
intron_variant | MODIFIER | c.6192+12C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 30/30 | chr14 | 50725941 | |||||||
chr14:50726169 | C | G | 1 | a0004c0004t0001g0071 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.6079-103G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50726169 | |||||||
chr14:50726193 | C | T | 1 | a0003c0008t0015g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6079-127G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50726193 | |||||||
chr14:50726203 | G | A | 2 | a0008c0020t0004g0105 a0008c0036t0004g0069 |
2 | HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.6079-137C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50726203 | |||||||
chr14:50726216 | C | T | 1 | a0003c0003t0001g0200 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6079-150G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50726216 | |||||||
chr14:50726320 | A | C | 4 | a0009c0014t0005g0014 a0009c0014t0005g0015 a0009c0014t0022g0013 others(1): Show |
4 | HG01433.hp2 HG01891.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.6079-254T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50726320 | |||||||
chr14:50726398 | C | A | 45 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(42): Show |
46 | HG01261.hp1 HG01433.hp2 HG01496.hp2 others(43): Show |
intron_variant | MODIFIER | c.6079-332G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50726398 | |||||||
chr14:50726408 | C | G | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.6079-342G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50726408 | |||||||
chr14:50726425 | G | A | 1 | a0003c0003t0001g0192 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.6079-359C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50726425 | |||||||
chr14:50726495 | A | T | 96 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(93): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.6079-429T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50726495 | |||||||
chr14:50726568 | T | C | 3 | a0001c0012t0001g0039 a0001c0012t0001g0059 a0001c0012t0001g0061 |
3 | HG01361.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.6079-502A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50726568 | |||||||
chr14:50726674 | T | C | 1 | a0003c0003t0001g0280 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.6079-608A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50726674 | |||||||
chr14:50726697 | C | T | 1 | a0002c0001t0002g0180 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.6079-631G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50726697 | |||||||
chr14:50726706 | C | T | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.6079-640G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50726706 | |||||||
chr14:50726728 | T | A | 1 | a0002c0001t0002g0153 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.6079-662A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50726728 | |||||||
chr14:50726792 | C | T | 3 | a0002c0001t0007g0268 a0002c0001t0007g0277 a0003c0008t0007g0267 |
3 | HG01099.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.6079-726G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50726792 | |||||||
chr14:50726988 | T | C | 1 | a0002c0015t0002g0174 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.6079-922A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50726988 | |||||||
chr14:50726990 | C | T | 11 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(8): Show |
12 | HG01433.hp2 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.6079-924G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50726990 | |||||||
chr14:50727098 | T | A | 1 | a0002c0001t0002g0229 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.6079-1032A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50727098 | |||||||
chr14:50727132 | A | ATGTC | 231 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(228): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.6079-1067_6079-106 others(8): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50727132 | |||||||
chr14:50727187 | T | C | 1 | a0003c0003t0011g0169 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.6079-1121A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50727187 | |||||||
chr14:50727286 | T | C | 1 | a0012c0019t0001g0269 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6079-1220A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50727286 | |||||||
chr14:50727399 | G | C | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.6079-1333C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50727399 | |||||||
chr14:50727475 | T | C | 1 | a0005c0007t0001g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.6079-1409A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50727475 | |||||||
chr14:50727509 | CATAA | C | 3 | a0004c0004t0001g0051 a0004c0004t0001g0055 a0019c0042t0001g0283 |
3 | HG02523.hp1 NA18944.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.6079-1447_6079-144 others(8): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50727509 | |||||||
chr14:50727996 | C | T | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.6078+1527G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50727996 | |||||||
chr14:50728035 | T | C | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.6078+1488A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728035 | |||||||
chr14:50728037 | T | C | 1 | a0003c0008t0015g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6078+1486A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728037 | |||||||
chr14:50728054 | A | AT | 46 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(43): Show |
48 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.6078+1468dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728054 | |||||||
chr14:50728055 | T | C | 6 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(3): Show |
7 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.6078+1468A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728055 | |||||||
chr14:50728118 | A | AT | 13 | a0001c0011t0006g0076 a0001c0011t0006g0077 a0006c0010t0006g0092 others(10): Show |
13 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.6078+1404dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728118 | |||||||
chr14:50728154 | A | C | 1 | a0018c0034t0024g0284 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.6078+1369T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728154 | |||||||
chr14:50728158 | T | C | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.6078+1365A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728158 | |||||||
chr14:50728217 | G | A | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.6078+1306C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728217 | |||||||
chr14:50728291 | C | T | 13 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(10): Show |
13 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.6078+1232G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728291 | |||||||
chr14:50728355 | G | A | 11 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(8): Show |
12 | HG01433.hp2 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.6078+1168C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728355 | |||||||
chr14:50728465 | G | A | 2 | a0001c0002t0003g0002 a0001c0002t0003g0102 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.6078+1058C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728465 | |||||||
chr14:50728473 | A | G | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.6078+1050T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728473 | |||||||
chr14:50728534 | C | CTT | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.6078+988_6078+989i others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728534 | |||||||
chr14:50728577 | T | G | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.6078+946A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728577 | |||||||
chr14:50728599 | T | A | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.6078+924A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728599 | |||||||
chr14:50728622 | G | A | 1 | a0003c0008t0002g0261 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.6078+901C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728622 | |||||||
chr14:50728623 | C | T | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.6078+900G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728623 | |||||||
chr14:50728647 | T | C | 97 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(94): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.6078+876A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728647 | |||||||
chr14:50728672 | T | C | 92 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(89): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.6078+851A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728672 | |||||||
chr14:50728718 | G | A | 3 | a0006c0010t0006g0092 a0006c0010t0006g0093 a0006c0010t0006g0094 |
3 | HG02895.hp1 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.6078+805C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728718 | |||||||
chr14:50728729 | C | G | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.6078+794G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728729 | |||||||
chr14:50728969 | C | A | 47 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(44): Show |
49 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.6078+554G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50728969 | |||||||
chr14:50729021 | C | T | 2 | a0001c0002t0001g0226 a0001c0002t0001g0228 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6078+502G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50729021 | |||||||
chr14:50729078 | C | T | 1 | a0002c0001t0002g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6078+445G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50729078 | |||||||
chr14:50729108 | C | T | 2 | a0001c0027t0012g0023 a0001c0027t0012g0287 |
2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.6078+415G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50729108 | |||||||
chr14:50729130 | C | T | 11 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(8): Show |
12 | HG01433.hp2 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.6078+393G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50729130 | |||||||
chr14:50729188 | C | T | 3 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0186 |
3 | HG01257.hp1 HG01258.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.6078+335G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50729188 | |||||||
chr14:50729255 | G | GT | 8 | a0002c0001t0002g0032 a0002c0001t0002g0181 a0002c0001t0002g0205 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.6078+267dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50729255 | |||||||
chr14:50729255 | G | T | 1 | a0002c0051t0002g0245 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6078+268C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50729255 | |||||||
chr14:50729255 | GT | G | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.6078+267delA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50729255 | |||||||
chr14:50729269 | T | A | 50 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(47): Show |
51 | HG01261.hp1 HG01433.hp2 HG01496.hp2 others(48): Show |
intron_variant | MODIFIER | c.6078+254A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50729269 | |||||||
chr14:50729269 | T | TA | 47 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(44): Show |
49 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.6078+253dupT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50729269 | |||||||
chr14:50729424 | T | C | 276 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(273): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.6078+99A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50729424 | |||||||
chr14:50729450 | T | C | 5 | a0007c0009t0004g0103 a0007c0009t0004g0136 a0007c0009t0004g0137 others(2): Show |
5 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.6078+73A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 29/30 | chr14 | 50729450 | |||||||
chr14:50729825 | A | G | 2 | a0002c0015t0002g0085 a0002c0058t0002g0024 |
2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.5878-102T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50729825 | |||||||
chr14:50729836 | C | G | 2 | a0001c0002t0003g0021 a0001c0002t0003g0099 |
2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.5878-113G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50729836 | |||||||
chr14:50729923 | A | C | 4 | a0001c0027t0012g0023 a0001c0027t0012g0287 a0008c0020t0004g0105 others(1): Show |
4 | HG01261.hp1 HG01496.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.5878-200T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50729923 | |||||||
chr14:50729939 | T | C | 47 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(44): Show |
49 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.5878-216A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50729939 | |||||||
chr14:50729947 | T | C | 1 | a0003c0008t0002g0261 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5878-224A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50729947 | |||||||
chr14:50729993 | C | T | 97 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(94): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.5878-270G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50729993 | |||||||
chr14:50730049 | C | T | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5878-326G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50730049 | |||||||
chr14:50730067 | C | CTG | 235 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(232): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.5878-345_5878-344i others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50730067 | |||||||
chr14:50730084 | C | T | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5878-361G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50730084 | |||||||
chr14:50730308 | C | T | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.5878-585G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50730308 | |||||||
chr14:50730401 | C | T | 1 | a0003c0003t0011g0169 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.5878-678G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50730401 | |||||||
chr14:50730429 | A | G | 36 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(33): Show |
36 | HG01168.hp2 HG01261.hp1 HG01361.hp1 others(33): Show |
intron_variant | MODIFIER | c.5878-706T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50730429 | |||||||
chr14:50730453 | G | A | 1 | a0006c0010t0002g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5878-730C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50730453 | |||||||
chr14:50730491 | G | A | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5878-768C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50730491 | |||||||
chr14:50730495 | C | T | 1 | a0001c0002t0008g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5878-772G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50730495 | |||||||
chr14:50730703 | C | T | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5878-980G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50730703 | |||||||
chr14:50730708 | T | C | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5878-985A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50730708 | |||||||
chr14:50730758 | G | C | 13 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(10): Show |
13 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.5878-1035C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50730758 | |||||||
chr14:50730780 | CATATT | C | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5878-1062_5878-105 others(9): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50730780 | |||||||
chr14:50730934 | A | G | 5 | a0001c0002t0003g0086 a0001c0028t0003g0012 a0001c0028t0003g0101 others(2): Show |
5 | HG02257.hp2 HG02258.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.5878-1211T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50730934 | |||||||
chr14:50730957 | T | G | 1 | a0021c0032t0006g0286 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5878-1234A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50730957 | |||||||
chr14:50731061 | A | G | 3 | a0002c0001t0002g0176 a0002c0001t0002g0202 a0002c0001t0002g0221 |
3 | HG01109.hp2 HG03017.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.5878-1338T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731061 | |||||||
chr14:50731094 | T | C | 1 | a0008c0020t0003g0232 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5878-1371A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731094 | |||||||
chr14:50731140 | T | TC | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5878-1418_5878-141 others(5): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731140 | |||||||
chr14:50731175 | A | G | 173 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.5878-1452T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731175 | |||||||
chr14:50731345 | C | T | 2 | a0001c0002t0003g0090 a0001c0002t0003g0131 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5878-1622G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731345 | |||||||
chr14:50731346 | G | A | 1 | a0001c0002t0002g0204 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5878-1623C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731346 | |||||||
chr14:50731388 | G | A | 52 | a0001c0005t0001g0072 a0001c0005t0001g0133 a0001c0005t0001g0134 others(49): Show |
52 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.5878-1665C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731388 | |||||||
chr14:50731528 | C | CAAA | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5878-1808_5878-180 others(7): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731528 | |||||||
chr14:50731528 | CA | C | 157 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(154): Show |
158 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.5878-1806delT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731528 | |||||||
chr14:50731528 | CAA | C | 51 | a0001c0002t0002g0064 a0001c0002t0002g0204 a0001c0002t0003g0002 others(48): Show |
53 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.5878-1807_5878-180 others(6): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731528 | |||||||
chr14:50731545 | A | G | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.5878-1822T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731545 | |||||||
chr14:50731559 | C | T | 2 | a0008c0020t0004g0105 a0008c0036t0004g0069 |
2 | HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.5878-1836G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731559 | |||||||
chr14:50731560 | G | A | 1 | a0005c0007t0001g0098 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.5878-1837C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731560 | |||||||
chr14:50731575 | C | A | 1 | a0001c0005t0001g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5878-1852G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731575 | |||||||
chr14:50731578 | G | A | 1 | a0001c0005t0001g0186 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5878-1855C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731578 | |||||||
chr14:50731604 | G | A | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5878-1881C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731604 | |||||||
chr14:50731766 | C | T | 2 | a0002c0001t0002g0218 a0002c0001t0016g0234 |
2 | HG01975.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.5878-2043G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731766 | |||||||
chr14:50731767 | A | G | 1 | a0003c0008t0015g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5878-2044T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731767 | |||||||
chr14:50731823 | T | G | 2 | a0003c0003t0001g0066 a0003c0003t0001g0256 |
2 | HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.5878-2100A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731823 | |||||||
chr14:50731913 | G | A | 1 | a0003c0003t0001g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5878-2190C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731913 | |||||||
chr14:50731999 | T | C | 1 | a0002c0043t0002g0247 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.5878-2276A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50731999 | |||||||
chr14:50732046 | G | A | 19 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(16): Show |
19 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.5878-2323C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50732046 | |||||||
chr14:50732065 | C | T | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5878-2342G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50732065 | |||||||
chr14:50732070 | T | C | 7 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(4): Show |
8 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.5878-2347A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50732070 | |||||||
chr14:50732097 | T | C | 47 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(44): Show |
49 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.5878-2374A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50732097 | |||||||
chr14:50732123 | G | C | 10 | a0001c0002t0003g0034 a0001c0002t0003g0070 a0001c0002t0003g0110 others(7): Show |
10 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.5878-2400C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50732123 | |||||||
chr14:50732352 | G | A | 2 | a0001c0005t0001g0072 a0001c0056t0001g0143 |
2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.5878-2629C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50732352 | |||||||
chr14:50732517 | G | C | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.5878-2794C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50732517 | |||||||
chr14:50732671 | C | T | 1 | a0002c0058t0002g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5877+2845G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50732671 | |||||||
chr14:50732727 | G | GT | 161 | a0001c0002t0001g0242 a0001c0002t0002g0064 a0001c0002t0002g0203 others(158): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.5877+2788dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50732727 | |||||||
chr14:50732734 | G | T | 1 | a0001c0002t0003g0062 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.5877+2782C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50732734 | |||||||
chr14:50732736 | G | T | 2 | a0001c0002t0002g0233 a0002c0001t0002g0165 |
2 | HG01981.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.5877+2780C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50732736 | |||||||
chr14:50732737 | T | G | 1 | a0001c0002t0003g0062 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.5877+2779A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50732737 | |||||||
chr14:50732899 | A | G | 164 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(161): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.5877+2617T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50732899 | |||||||
chr14:50732981 | T | C | 1 | a0001c0017t0003g0115 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5877+2535A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50732981 | |||||||
chr14:50733022 | C | G | 169 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(166): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.5877+2494G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50733022 | |||||||
chr14:50733098 | AT | A | 166 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(163): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.5877+2417delA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50733098 | |||||||
chr14:50733195 | C | T | 2 | a0001c0002t0003g0021 a0001c0002t0003g0099 |
2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.5877+2321G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50733195 | |||||||
chr14:50733238 | G | A | 1 | a0001c0029t0001g0197 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5877+2278C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50733238 | |||||||
chr14:50733373 | G | T | 9 | a0001c0002t0008g0195 a0001c0002t0008g0198 a0001c0005t0001g0046 others(6): Show |
9 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.5877+2143C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50733373 | |||||||
chr14:50733473 | AT | A | 5 | a0001c0002t0003g0086 a0001c0028t0003g0012 a0001c0028t0003g0101 others(2): Show |
5 | HG02257.hp2 HG02258.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.5877+2042delA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50733473 | |||||||
chr14:50733474 | T | C | 165 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(162): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.5877+2042A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50733474 | |||||||
chr14:50733497 | C | A | 1 | a0002c0001t0002g0191 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.5877+2019G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50733497 | |||||||
chr14:50733670 | C | A | 1 | a0002c0001t0002g0191 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.5877+1846G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50733670 | |||||||
chr14:50733701 | T | C | 6 | a0001c0005t0001g0046 a0001c0012t0001g0039 a0001c0012t0001g0059 others(3): Show |
6 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.5877+1815A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50733701 | |||||||
chr14:50733883 | C | G | 2 | a0002c0015t0002g0085 a0002c0058t0002g0024 |
2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.5877+1633G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50733883 | |||||||
chr14:50734079 | CTTCT | C | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5877+1433_5877+143 others(8): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734079 | |||||||
chr14:50734086 | A | AT | 16 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(13): Show |
17 | HG01433.hp2 HG01891.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.5877+1429dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734086 | |||||||
chr14:50734086 | AT | A | 58 | a0001c0005t0004g0263 a0001c0006t0003g0037 a0001c0017t0002g0079 others(55): Show |
58 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.5877+1429delA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734086 | |||||||
chr14:50734090 | T | A | 3 | a0001c0002t0008g0195 a0001c0002t0008g0198 a0006c0010t0008g0139 |
3 | HG03139.hp1 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5877+1426A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734090 | |||||||
chr14:50734120 | G | A | 3 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 |
3 | HG02559.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5877+1396C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734120 | |||||||
chr14:50734246 | C | T | 1 | a0001c0002t0003g0172 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.5877+1270G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734246 | |||||||
chr14:50734383 | C | A | 1 | a0016c0049t0001g0124 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.5877+1133G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734383 | |||||||
chr14:50734383 | C | T | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5877+1133G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734383 | |||||||
chr14:50734390 | C | A | 1 | a0002c0001t0002g0181 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.5877+1126G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734390 | |||||||
chr14:50734541 | G | A | 1 | a0003c0003t0001g0206 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.5877+975C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734541 | |||||||
chr14:50734684 | T | C | 1 | a0018c0034t0024g0284 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.5877+832A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734684 | |||||||
chr14:50734768 | C | T | 2 | a0004c0004t0001g0050 a0004c0004t0001g0052 |
2 | HG00642.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.5877+748G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734768 | |||||||
chr14:50734824 | G | C | 3 | a0001c0025t0010g0067 a0001c0025t0010g0135 a0020c0033t0010g0049 |
3 | HG02630.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5877+692C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734824 | |||||||
chr14:50734851 | A | AT | 46 | a0001c0002t0003g0086 a0001c0028t0003g0012 a0001c0028t0003g0101 others(43): Show |
46 | HG00408.hp2 HG00621.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.5877+664dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734851 | |||||||
chr14:50734851 | A | ATT | 8 | a0003c0008t0002g0080 a0003c0008t0007g0267 a0007c0009t0004g0025 others(5): Show |
8 | HG01099.hp1 HG02055.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.5877+663_5877+664d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734851 | |||||||
chr14:50734934 | C | T | 74 | a0001c0005t0001g0170 a0001c0005t0004g0263 a0001c0017t0002g0079 others(71): Show |
74 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.5877+582G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734934 | |||||||
chr14:50734949 | A | G | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5877+567T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734949 | |||||||
chr14:50734964 | G | A | 2 | a0003c0016t0001g0003 a0003c0016t0001g0130 |
3 | HG01069.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.5877+552C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734964 | |||||||
chr14:50734990 | A | G | 1 | a0004c0004t0001g0042 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.5877+526T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734990 | |||||||
chr14:50734993 | C | T | 54 | a0001c0005t0001g0072 a0001c0005t0001g0133 a0001c0005t0001g0134 others(51): Show |
54 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.5877+523G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50734993 | |||||||
chr14:50735070 | T | C | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5877+446A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50735070 | |||||||
chr14:50735111 | G | A | 46 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(43): Show |
48 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.5877+405C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50735111 | |||||||
chr14:50735444 | C | G | 2 | a0001c0002t0005g0084 a0001c0002t0005g0142 |
2 | HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.5877+72G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 28/30 | chr14 | 50735444 | |||||||
chr14:50735638 | A | C | 2 | a0002c0001t0002g0218 a0002c0001t0016g0234 |
2 | HG01975.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.5776-21T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50735638 | |||||||
chr14:50735745 | GACAA | G | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5776-132_5776-129d others(6): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50735745 | |||||||
chr14:50735884 | T | C | 1 | a0014c0040t0003g0275 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5776-267A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50735884 | |||||||
chr14:50736131 | C | T | 1 | a0001c0002t0021g0246 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5776-514G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50736131 | |||||||
chr14:50736189 | G | C | 6 | a0001c0005t0001g0046 a0001c0012t0001g0039 a0001c0012t0001g0059 others(3): Show |
6 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.5776-572C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50736189 | |||||||
chr14:50736192 | GCA | G | 45 | a0001c0005t0001g0072 a0001c0005t0001g0133 a0001c0005t0001g0134 others(42): Show |
45 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.5776-577_5776-576d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50736192 | |||||||
chr14:50736219 | G | A | 5 | a0001c0027t0012g0023 a0001c0027t0012g0287 a0008c0020t0003g0232 others(2): Show |
5 | HG01261.hp1 HG01496.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.5776-602C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50736219 | |||||||
chr14:50736242 | C | A | 10 | a0001c0006t0003g0037 a0001c0006t0003g0060 a0001c0006t0003g0162 others(7): Show |
10 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.5776-625G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50736242 | |||||||
chr14:50736253 | T | C | 2 | a0004c0004t0001g0050 a0004c0004t0001g0052 |
2 | HG00642.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.5776-636A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50736253 | |||||||
chr14:50736281 | C | T | 12 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(9): Show |
12 | HG02258.hp1 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.5776-664G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50736281 | |||||||
chr14:50736307 | A | G | 1 | a0001c0002t0003g0017 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5776-690T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50736307 | |||||||
chr14:50736309 | A | AT | 6 | a0001c0027t0012g0023 a0001c0027t0012g0287 a0003c0003t0001g0091 others(3): Show |
6 | HG01261.hp1 HG01496.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.5776-693dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50736309 | |||||||
chr14:50736309 | AT | A | 12 | a0001c0005t0001g0046 a0001c0012t0001g0039 a0001c0012t0001g0059 others(9): Show |
12 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.5776-693delA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50736309 | |||||||
chr14:50736311 | T | A | 1 | a0003c0003t0001g0256 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.5776-694A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50736311 | |||||||
chr14:50736359 | G | A | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5776-742C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50736359 | |||||||
chr14:50736893 | G | C | 1 | a0001c0002t0021g0246 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5775+1247C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50736893 | |||||||
chr14:50737075 | A | T | 3 | a0001c0002t0008g0195 a0001c0002t0008g0198 a0006c0010t0008g0139 |
3 | HG03139.hp1 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5775+1065T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737075 | |||||||
chr14:50737146 | A | C | 3 | a0001c0002t0008g0195 a0001c0002t0008g0198 a0006c0010t0008g0139 |
3 | HG03139.hp1 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5775+994T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737146 | |||||||
chr14:50737181 | C | T | 6 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(3): Show |
7 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.5775+959G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737181 | |||||||
chr14:50737329 | T | G | 9 | a0001c0025t0010g0067 a0001c0025t0010g0135 a0007c0009t0004g0025 others(6): Show |
9 | HG02055.hp2 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5775+811A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737329 | |||||||
chr14:50737351 | G | C | 1 | a0002c0001t0002g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5775+789C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737351 | |||||||
chr14:50737399 | C | T | 72 | a0001c0017t0002g0079 a0002c0001t0002g0028 a0002c0001t0002g0032 others(69): Show |
72 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.5775+741G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737399 | |||||||
chr14:50737442 | G | T | 4 | a0004c0004t0001g0224 a0004c0004t0001g0237 a0004c0004t0001g0238 others(1): Show |
4 | HG01943.hp1 HG01952.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.5775+698C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737442 | |||||||
chr14:50737495 | C | CA | 39 | a0001c0002t0003g0063 a0001c0002t0003g0110 a0001c0002t0003g0178 others(36): Show |
39 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.5775+644dupT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737495 | |||||||
chr14:50737495 | CAA | C | 16 | a0001c0002t0008g0195 a0001c0002t0008g0198 a0001c0025t0010g0067 others(13): Show |
16 | HG01361.hp2 HG02055.hp1 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.5775+643_5775+644d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737495 | |||||||
chr14:50737495 | CAAA | C | 63 | a0001c0017t0002g0079 a0001c0054t0006g0196 a0002c0001t0002g0028 others(60): Show |
63 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.5775+642_5775+644d others(5): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737495 | |||||||
chr14:50737495 | CAAAA | C | 29 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(26): Show |
30 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.5775+641_5775+644d others(6): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737495 | |||||||
chr14:50737495 | CAAAAAAA others(3): Show |
C | 5 | a0001c0027t0012g0023 a0001c0027t0012g0287 a0008c0020t0003g0232 others(2): Show |
5 | HG01261.hp1 HG01496.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.5775+635_5775+644d others(12): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737495 | |||||||
chr14:50737535 | G | A | 1 | a0017c0037t0001g0056 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.5775+605C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737535 | |||||||
chr14:50737578 | GCTT | G | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5775+559_5775+561d others(5): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737578 | |||||||
chr14:50737593 | A | C | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5775+547T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737593 | |||||||
chr14:50737615 | T | A | 3 | a0001c0025t0010g0067 a0001c0025t0010g0135 a0020c0033t0010g0049 |
3 | HG02630.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5775+525A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737615 | |||||||
chr14:50737646 | G | GT | 10 | a0001c0005t0004g0263 a0003c0003t0001g0091 a0003c0003t0001g0164 others(7): Show |
10 | HG01192.hp2 HG01346.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.5775+493dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737646 | |||||||
chr14:50737646 | GT | G | 71 | a0001c0002t0002g0204 a0001c0017t0002g0079 a0002c0001t0002g0028 others(68): Show |
71 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.5775+493delA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737646 | |||||||
chr14:50737646 | GTT | G | 89 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(86): Show |
92 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.5775+492_5775+493d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737646 | |||||||
chr14:50737651 | T | G | 9 | a0001c0005t0001g0252 a0001c0027t0012g0023 a0001c0027t0012g0287 others(6): Show |
9 | HG01099.hp2 HG01261.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.5775+489A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737651 | |||||||
chr14:50737673 | T | A | 4 | a0009c0014t0005g0014 a0009c0014t0005g0015 a0009c0014t0022g0013 others(1): Show |
4 | HG01433.hp2 HG01891.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.5775+467A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737673 | |||||||
chr14:50737723 | C | T | 1 | a0001c0005t0001g0170 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.5775+417G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737723 | |||||||
chr14:50737847 | G | A | 229 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(226): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.5775+293C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737847 | |||||||
chr14:50737878 | T | C | 9 | a0001c0025t0010g0067 a0001c0025t0010g0135 a0007c0009t0004g0025 others(6): Show |
9 | HG02055.hp2 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5775+262A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737878 | |||||||
chr14:50737880 | G | A | 9 | a0001c0025t0010g0067 a0001c0025t0010g0135 a0007c0009t0004g0025 others(6): Show |
9 | HG02055.hp2 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5775+260C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737880 | |||||||
chr14:50737952 | T | C | 2 | a0002c0015t0002g0085 a0002c0058t0002g0024 |
2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.5775+188A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737952 | |||||||
chr14:50737973 | A | G | 7 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(4): Show |
8 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.5775+167T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50737973 | |||||||
chr14:50738102 | A | G | 2 | a0001c0002t0003g0090 a0001c0002t0003g0131 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5775+38T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50738102 | |||||||
chr14:50738116 | C | T | 5 | a0001c0027t0012g0023 a0001c0027t0012g0287 a0008c0020t0003g0232 others(2): Show |
5 | HG01261.hp1 HG01496.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.5775+24G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50738116 | |||||||
chr14:50738124 | A | G | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5775+16T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 27/30 | chr14 | 50738124 | |||||||
chr14:50738296 | A | G | 1 | a0001c0002t0003g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.5629-10T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 26/30 | chr14 | 50738296 | |||||||
chr14:50738381 | G | T | 2 | a0001c0011t0001g0011 a0001c0011t0001g0227 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5629-95C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 26/30 | chr14 | 50738381 | |||||||
chr14:50738559 | T | C | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5629-273A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 26/30 | chr14 | 50738559 | |||||||
chr14:50738755 | A | G | 2 | a0001c0005t0001g0040 a0001c0005t0001g0041 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.5629-469T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 26/30 | chr14 | 50738755 | |||||||
chr14:50738837 | T | C | 9 | a0001c0011t0001g0008 a0001c0011t0001g0011 a0001c0011t0001g0227 others(6): Show |
9 | HG01884.hp2 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.5628+471A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 26/30 | chr14 | 50738837 | |||||||
chr14:50739303 | A | G | 283 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(280): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
splice_region_variant&intron_variant | LOW | c.5628+5T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 26/30 | chr14 | 50739303 | |||||||
chr14:50739688 | G | T | 1 | a0001c0017t0003g0115 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5449-201C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50739688 | |||||||
chr14:50739735 | C | T | 209 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(206): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.5449-248G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50739735 | |||||||
chr14:50739923 | T | C | 281 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(278): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.5449-436A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50739923 | |||||||
chr14:50739961 | T | C | 1 | a0003c0003t0001g0066 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.5449-474A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50739961 | |||||||
chr14:50740049 | T | C | 1 | a0001c0005t0001g0133 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.5449-562A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50740049 | |||||||
chr14:50740079 | A | T | 1 | a0004c0004t0001g0273 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.5449-592T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50740079 | |||||||
chr14:50740173 | G | A | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5449-686C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50740173 | |||||||
chr14:50740192 | C | CT | 111 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0046 others(108): Show |
113 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.5449-706dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50740192 | |||||||
chr14:50740318 | C | T | 44 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(41): Show |
46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.5449-831G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50740318 | |||||||
chr14:50740352 | C | CT | 56 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(53): Show |
58 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.5449-866dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50740352 | |||||||
chr14:50740381 | C | T | 4 | a0009c0014t0005g0014 a0009c0014t0005g0015 a0009c0014t0022g0013 others(1): Show |
4 | HG01433.hp2 HG01891.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.5449-894G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50740381 | |||||||
chr14:50740435 | C | G | 172 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(169): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.5449-948G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50740435 | |||||||
chr14:50740442 | G | T | 2 | a0001c0027t0012g0023 a0001c0027t0012g0287 |
2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.5449-955C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50740442 | |||||||
chr14:50740538 | T | C | 56 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0147 others(53): Show |
58 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.5448+1044A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50740538 | |||||||
chr14:50740609 | A | G | 1 | a0001c0052t0005g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5448+973T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50740609 | |||||||
chr14:50740639 | T | G | 2 | a0004c0004t0001g0050 a0004c0004t0001g0052 |
2 | HG00642.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.5448+943A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50740639 | |||||||
chr14:50740679 | G | A | 1 | a0004c0026t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5448+903C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50740679 | |||||||
chr14:50740747 | G | A | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.5448+835C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50740747 | |||||||
chr14:50740966 | C | T | 1 | a0008c0036t0004g0069 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.5448+616G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50740966 | |||||||
chr14:50741264 | A | G | 3 | a0003c0003t0001g0091 a0012c0019t0001g0210 a0012c0019t0001g0269 |
3 | HG02738.hp2 HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.5448+318T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50741264 | |||||||
chr14:50741274 | A | T | 1 | a0004c0004t0001g0273 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.5448+308T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50741274 | |||||||
chr14:50741299 | T | C | 2 | a0001c0027t0012g0023 a0001c0027t0012g0287 |
2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.5448+283A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50741299 | |||||||
chr14:50741315 | T | C | 2 | a0001c0027t0012g0023 a0001c0027t0012g0287 |
2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.5448+267A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50741315 | |||||||
chr14:50741376 | T | A | 1 | a0004c0004t0001g0273 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.5448+206A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50741376 | |||||||
chr14:50741425 | T | G | 56 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0147 others(53): Show |
58 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.5448+157A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50741425 | |||||||
chr14:50741493 | C | T | 6 | a0001c0005t0001g0046 a0001c0012t0001g0039 a0001c0012t0001g0059 others(3): Show |
6 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.5448+89G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50741493 | |||||||
chr14:50741518 | T | TGTA | 283 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(280): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.5448+63_5448+64ins others(3): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50741518 | |||||||
chr14:50741557 | C | A | 3 | a0001c0011t0001g0008 a0001c0011t0001g0011 a0001c0011t0001g0227 |
3 | HG01884.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5448+25G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 25/30 | chr14 | 50741557 | |||||||
chr14:50741738 | G | A | 1 | a0018c0034t0024g0284 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.5302-10C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 24/30 | chr14 | 50741738 | |||||||
chr14:50741993 | C | A | 3 | a0001c0025t0010g0067 a0001c0025t0010g0135 a0020c0033t0010g0049 |
3 | HG02630.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5302-265G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 24/30 | chr14 | 50741993 | |||||||
chr14:50742392 | C | CT | 65 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(62): Show |
67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.5302-665dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 24/30 | chr14 | 50742392 | |||||||
chr14:50742392 | CT | C | 11 | a0001c0002t0008g0195 a0001c0002t0008g0198 a0001c0011t0001g0008 others(8): Show |
11 | HG01884.hp2 HG01891.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.5302-665delA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 24/30 | chr14 | 50742392 | |||||||
chr14:50742457 | G | A | 3 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 |
3 | HG02559.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5302-729C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 24/30 | chr14 | 50742457 | |||||||
chr14:50742550 | C | A | 4 | a0002c0001t0002g0191 a0002c0001t0002g0213 a0002c0001t0002g0214 others(1): Show |
4 | HG01070.hp1 HG01515.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.5302-822G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 24/30 | chr14 | 50742550 | |||||||
chr14:50742881 | A | G | 3 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 |
3 | HG02486.hp1 HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.5301+535T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 24/30 | chr14 | 50742881 | |||||||
chr14:50743129 | C | CT | 10 | a0001c0025t0010g0067 a0001c0025t0010g0135 a0001c0052t0005g0285 others(7): Show |
10 | HG01261.hp1 HG01358.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.5301+286dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 24/30 | chr14 | 50743129 | |||||||
chr14:50743142 | T | A | 1 | a0003c0008t0004g0095 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5301+274A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 24/30 | chr14 | 50743142 | |||||||
chr14:50743215 | T | C | 213 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(210): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.5301+201A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 24/30 | chr14 | 50743215 | |||||||
chr14:50743310 | A | C | 1 | a0004c0004t0001g0273 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.5301+106T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 24/30 | chr14 | 50743310 | |||||||
chr14:50743666 | T | C | 1 | a0003c0003t0001g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5188-137A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 23/30 | chr14 | 50743666 | |||||||
chr14:50743687 | G | A | 209 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(206): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.5188-158C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 23/30 | chr14 | 50743687 | |||||||
chr14:50743879 | G | A | 1 | a0003c0003t0001g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5188-350C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 23/30 | chr14 | 50743879 | |||||||
chr14:50743983 | G | A | 3 | a0001c0002t0003g0017 a0001c0002t0003g0018 a0001c0012t0001g0039 |
3 | HG02615.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.5187+260C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 23/30 | chr14 | 50743983 | |||||||
chr14:50744085 | AG | A | 6 | a0001c0005t0001g0046 a0001c0012t0001g0039 a0001c0012t0001g0059 others(3): Show |
6 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.5187+157delC | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 23/30 | chr14 | 50744085 | |||||||
chr14:50744107 | G | T | 1 | a0001c0002t0003g0212 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.5187+136C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 23/30 | chr14 | 50744107 | |||||||
chr14:50744135 | T | C | 68 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(65): Show |
71 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.5187+108A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 23/30 | chr14 | 50744135 | |||||||
chr14:50744187 | G | A | 3 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0186 |
3 | HG01257.hp1 HG01258.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.5187+56C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 23/30 | chr14 | 50744187 | |||||||
chr14:50744649 | T | C | 5 | a0001c0002t0003g0009 a0001c0002t0003g0017 a0001c0002t0003g0018 others(2): Show |
6 | HG01884.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.5065-284A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50744649 | |||||||
chr14:50744677 | C | T | 6 | a0001c0005t0001g0046 a0001c0012t0001g0039 a0001c0012t0001g0059 others(3): Show |
6 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.5065-312G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50744677 | |||||||
chr14:50744919 | T | C | 2 | a0001c0002t0005g0033 a0001c0002t0020g0173 |
2 | HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5065-554A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50744919 | |||||||
chr14:50744935 | CAAAA | C | 4 | a0009c0014t0005g0014 a0009c0014t0005g0015 a0009c0014t0022g0013 others(1): Show |
4 | HG01433.hp2 HG01891.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.5065-574_5065-571d others(6): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50744935 | |||||||
chr14:50744943 | C | A | 1 | a0002c0001t0002g0180 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5065-578G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50744943 | |||||||
chr14:50744983 | A | G | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5065-618T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50744983 | |||||||
chr14:50745137 | GT | G | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5065-773delA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50745137 | |||||||
chr14:50745186 | C | T | 2 | a0001c0002t0001g0226 a0001c0002t0001g0228 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5065-821G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50745186 | |||||||
chr14:50745325 | T | C | 24 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(21): Show |
25 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.5065-960A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50745325 | |||||||
chr14:50745573 | G | A | 6 | a0001c0005t0001g0046 a0001c0012t0001g0039 a0001c0012t0001g0059 others(3): Show |
6 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.5065-1208C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50745573 | |||||||
chr14:50745735 | G | A | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5065-1370C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50745735 | |||||||
chr14:50745816 | T | C | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.5065-1451A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50745816 | |||||||
chr14:50745829 | T | C | 1 | a0008c0021t0001g0019 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.5065-1464A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50745829 | |||||||
chr14:50745903 | T | C | 1 | a0002c0001t0002g0258 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5065-1538A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50745903 | |||||||
chr14:50746034 | TA | T | 67 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0005t0001g0072 others(64): Show |
67 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.5065-1670delT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50746034 | |||||||
chr14:50746034 | TAAAAAAA others(3): Show |
T | 1 | a0001c0006t0003g0271 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5065-1679_5065-167 others(14): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50746034 | |||||||
chr14:50746111 | C | T | 2 | a0001c0002t0003g0017 a0001c0002t0003g0018 |
2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.5065-1746G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50746111 | |||||||
chr14:50746151 | A | G | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5065-1786T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50746151 | |||||||
chr14:50746281 | G | A | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5064+1711C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50746281 | |||||||
chr14:50746373 | G | C | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5064+1619C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50746373 | |||||||
chr14:50746394 | A | G | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5064+1598T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50746394 | |||||||
chr14:50746427 | G | T | 11 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(8): Show |
12 | HG01433.hp2 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.5064+1565C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50746427 | |||||||
chr14:50746455 | A | C | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.5064+1537T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50746455 | |||||||
chr14:50746576 | G | T | 1 | a0001c0017t0003g0115 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5064+1416C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50746576 | |||||||
chr14:50746729 | T | C | 3 | a0001c0025t0010g0067 a0001c0025t0010g0135 a0020c0033t0010g0049 |
3 | HG02630.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5064+1263A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50746729 | |||||||
chr14:50746766 | TG | T | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5064+1225delC | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50746766 | |||||||
chr14:50746768 | T | G | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.5064+1224A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50746768 | |||||||
chr14:50746804 | T | C | 4 | a0009c0014t0005g0014 a0009c0014t0005g0015 a0009c0014t0022g0013 others(1): Show |
4 | HG01433.hp2 HG01891.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.5064+1188A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50746804 | |||||||
chr14:50746837 | A | G | 71 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(68): Show |
74 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.5064+1155T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50746837 | |||||||
chr14:50746879 | CAG | C | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5064+1111_5064+111 others(6): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50746879 | |||||||
chr14:50747081 | C | A | 1 | a0018c0034t0024g0284 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.5064+911G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747081 | |||||||
chr14:50747082 | T | G | 3 | a0001c0011t0001g0008 a0001c0011t0001g0011 a0001c0011t0001g0227 |
3 | HG01884.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5064+910A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747082 | |||||||
chr14:50747147 | G | A | 3 | a0001c0025t0010g0067 a0001c0025t0010g0135 a0020c0033t0010g0049 |
3 | HG02630.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5064+845C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747147 | |||||||
chr14:50747319 | AAAGTTAT | A | 6 | a0001c0005t0001g0046 a0001c0012t0001g0039 a0001c0012t0001g0059 others(3): Show |
6 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.5064+666_5064+672d others(9): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747319 | |||||||
chr14:50747360 | T | C | 1 | a0005c0007t0001g0044 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.5064+632A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747360 | |||||||
chr14:50747437 | T | C | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5064+555A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747437 | |||||||
chr14:50747456 | G | A | 1 | a0001c0002t0003g0021 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5064+536C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747456 | |||||||
chr14:50747482 | C | A | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5064+510G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747482 | |||||||
chr14:50747517 | T | C | 1 | a0001c0002t0005g0004 | 2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.5064+475A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747517 | |||||||
chr14:50747594 | C | T | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5064+398G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747594 | |||||||
chr14:50747612 | T | C | 5 | a0008c0020t0003g0232 a0008c0020t0004g0105 a0008c0021t0001g0010 others(2): Show |
5 | HG01261.hp1 HG01358.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.5064+380A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747612 | |||||||
chr14:50747738 | T | TAA | 21 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(18): Show |
21 | HG01884.hp2 HG01891.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.5064+252_5064+253d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747738 | |||||||
chr14:50747749 | AAG | A | 11 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(8): Show |
12 | HG01433.hp2 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.5064+241_5064+242d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747749 | |||||||
chr14:50747750 | A | AG | 90 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(87): Show |
94 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.5064+241dupC | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747750 | |||||||
chr14:50747750 | A | G | 1 | a0004c0004t0001g0050 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.5064+242T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747750 | |||||||
chr14:50747750 | AG | A | 15 | a0001c0005t0001g0046 a0001c0012t0001g0039 a0001c0012t0001g0059 others(12): Show |
15 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.5064+241delC | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747750 | |||||||
chr14:50747751 | G | A | 100 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(97): Show |
100 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.5064+241C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747751 | |||||||
chr14:50747752 | G | A | 8 | a0006c0010t0006g0092 a0006c0010t0006g0093 a0007c0009t0004g0025 others(5): Show |
8 | HG02055.hp2 HG02895.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.5064+240C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747752 | |||||||
chr14:50747966 | C | A | 1 | a0003c0003t0001g0096 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5064+26G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 22/30 | chr14 | 50747966 | |||||||
chr14:50748212 | T | C | 34 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.4951-107A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50748212 | |||||||
chr14:50748213 | G | T | 2 | a0003c0008t0004g0095 a0003c0008t0015g0036 |
2 | HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4951-108C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50748213 | |||||||
chr14:50748326 | C | A | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.4951-221G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50748326 | |||||||
chr14:50748364 | G | A | 1 | a0002c0001t0014g0264 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4951-259C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50748364 | |||||||
chr14:50748382 | G | A | 1 | a0002c0001t0014g0264 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4951-277C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50748382 | |||||||
chr14:50748866 | G | A | 110 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(107): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.4951-761C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50748866 | |||||||
chr14:50748920 | A | G | 3 | a0001c0025t0010g0067 a0001c0025t0010g0135 a0020c0033t0010g0049 |
3 | HG02630.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4951-815T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50748920 | |||||||
chr14:50749062 | A | G | 6 | a0001c0005t0001g0046 a0001c0012t0001g0039 a0001c0012t0001g0059 others(3): Show |
6 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.4951-957T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50749062 | |||||||
chr14:50749074 | C | T | 1 | a0004c0004t0001g0224 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4951-969G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50749074 | |||||||
chr14:50749097 | T | C | 117 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(114): Show |
120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.4951-992A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50749097 | |||||||
chr14:50749114 | T | C | 1 | a0014c0040t0003g0275 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4951-1009A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50749114 | |||||||
chr14:50749121 | C | G | 20 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(17): Show |
20 | HG01884.hp2 HG01891.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.4951-1016G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50749121 | |||||||
chr14:50749139 | G | A | 1 | a0003c0003t0001g0182 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4951-1034C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50749139 | |||||||
chr14:50749158 | A | C | 3 | a0001c0002t0003g0017 a0001c0002t0003g0018 a0001c0017t0003g0115 |
3 | HG02615.hp1 HG03098.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.4951-1053T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50749158 | |||||||
chr14:50749297 | T | C | 34 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.4951-1192A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50749297 | |||||||
chr14:50749360 | A | G | 7 | a0001c0005t0001g0046 a0001c0011t0006g0076 a0001c0012t0001g0039 others(4): Show |
7 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.4951-1255T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50749360 | |||||||
chr14:50749632 | T | C | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.4951-1527A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50749632 | |||||||
chr14:50749830 | T | C | 2 | a0001c0025t0010g0067 a0001c0025t0010g0135 |
2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.4951-1725A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50749830 | |||||||
chr14:50749846 | T | C | 11 | a0001c0002t0008g0195 a0001c0002t0008g0198 a0001c0011t0001g0008 others(8): Show |
11 | HG01884.hp2 HG01891.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.4951-1741A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50749846 | |||||||
chr14:50750015 | T | G | 1 | a0002c0001t0014g0264 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4951-1910A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50750015 | |||||||
chr14:50750115 | C | CT | 7 | a0001c0029t0001g0089 a0007c0009t0004g0025 a0007c0009t0004g0103 others(4): Show |
7 | HG02055.hp2 HG02809.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4951-2011dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50750115 | |||||||
chr14:50750124 | T | C | 23 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(20): Show |
23 | HG01884.hp2 HG01891.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.4951-2019A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50750124 | |||||||
chr14:50750146 | C | A | 1 | a0001c0002t0003g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4951-2041G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50750146 | |||||||
chr14:50750171 | C | T | 121 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(118): Show |
124 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.4951-2066G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50750171 | |||||||
chr14:50750341 | T | C | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.4950+2177A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50750341 | |||||||
chr14:50750363 | A | G | 25 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(22): Show |
25 | HG01884.hp2 HG01891.hp2 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4950+2155T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50750363 | |||||||
chr14:50750365 | G | C | 154 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(151): Show |
157 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.4950+2153C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50750365 | |||||||
chr14:50750412 | ACTT | A | 11 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(8): Show |
12 | HG01433.hp2 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.4950+2103_4950+210 others(7): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50750412 | |||||||
chr14:50750524 | T | C | 175 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(172): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.4950+1994A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50750524 | |||||||
chr14:50750581 | TC | T | 121 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(118): Show |
124 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.4950+1936delG | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50750581 | |||||||
chr14:50750670 | T | C | 1 | a0006c0010t0002g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4950+1848A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50750670 | |||||||
chr14:50750856 | T | G | 129 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.4950+1662A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50750856 | |||||||
chr14:50750889 | C | T | 129 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.4950+1629G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50750889 | |||||||
chr14:50750986 | C | T | 3 | a0001c0025t0010g0067 a0001c0025t0010g0135 a0020c0033t0010g0049 |
3 | HG02630.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4950+1532G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50750986 | |||||||
chr14:50750999 | A | G | 130 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(127): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.4950+1519T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50750999 | |||||||
chr14:50751024 | C | T | 129 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.4950+1494G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50751024 | |||||||
chr14:50751143 | A | AC | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.4950+1374_4950+137 others(5): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50751143 | |||||||
chr14:50751144 | A | C | 144 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(141): Show |
147 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.4950+1374T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50751144 | |||||||
chr14:50751175 | C | T | 75 | a0001c0002t0003g0086 a0001c0005t0001g0040 a0001c0005t0001g0041 others(72): Show |
77 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.4950+1343G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50751175 | |||||||
chr14:50751187 | T | C | 1 | a0010c0023t0002g0175 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.4950+1331A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50751187 | |||||||
chr14:50751263 | C | G | 131 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(128): Show |
134 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.4950+1255G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50751263 | |||||||
chr14:50751264 | G | A | 53 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0186 others(50): Show |
55 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.4950+1254C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50751264 | |||||||
chr14:50751357 | A | C | 2 | a0001c0006t0003g0187 a0001c0006t0003g0188 |
2 | HG00642.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.4950+1161T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50751357 | |||||||
chr14:50751366 | C | CG | 4 | a0001c0029t0001g0197 a0002c0001t0002g0129 a0005c0007t0001g0097 others(1): Show |
4 | HG01109.hp1 HG03486.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.4950+1151dupC | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50751366 | |||||||
chr14:50751372 | C | G | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.4950+1146G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50751372 | |||||||
chr14:50751384 | T | C | 1 | a0002c0043t0002g0247 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.4950+1134A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50751384 | |||||||
chr14:50751486 | A | AAC | 131 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(128): Show |
134 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.4950+1031_4950+103 others(6): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50751486 | |||||||
chr14:50751498 | A | C | 42 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(39): Show |
44 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.4950+1020T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50751498 | |||||||
chr14:50751725 | T | C | 135 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(132): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.4950+793A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50751725 | |||||||
chr14:50751799 | T | A | 1 | a0004c0004t0001g0055 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.4950+719A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50751799 | |||||||
chr14:50751808 | T | TGA | 3 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 |
3 | HG02486.hp1 HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4950+708_4950+709d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50751808 | |||||||
chr14:50751819 | G | A | 57 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0186 others(54): Show |
59 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.4950+699C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50751819 | |||||||
chr14:50752049 | AT | A | 3 | a0001c0025t0010g0067 a0001c0025t0010g0135 a0020c0033t0010g0049 |
3 | HG02630.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4950+468delA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50752049 | |||||||
chr14:50752053 | G | A | 131 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(128): Show |
134 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.4950+465C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50752053 | |||||||
chr14:50752156 | T | A | 1 | a0003c0003t0001g0206 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4950+362A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50752156 | |||||||
chr14:50752157 | A | G | 1 | a0003c0003t0001g0206 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4950+361T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50752157 | |||||||
chr14:50752158 | G | GT | 139 | a0001c0002t0003g0086 a0001c0002t0008g0195 a0001c0002t0008g0198 others(136): Show |
141 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.4950+359dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50752158 | |||||||
chr14:50752158 | G | GTT | 74 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(71): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.4950+358_4950+359d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50752158 | |||||||
chr14:50752158 | G | GTTT | 6 | a0001c0002t0003g0021 a0001c0002t0003g0099 a0001c0011t0001g0008 others(3): Show |
6 | HG01884.hp2 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.4950+357_4950+359d others(5): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50752158 | |||||||
chr14:50752158 | G | T | 1 | a0003c0003t0001g0206 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4950+360C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50752158 | |||||||
chr14:50752381 | C | T | 9 | a0001c0005t0001g0046 a0001c0012t0001g0039 a0001c0012t0001g0059 others(6): Show |
9 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.4950+137G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 21/30 | chr14 | 50752381 | |||||||
chr14:50752782 | T | TA | 53 | a0001c0002t0001g0242 a0001c0002t0002g0064 a0001c0002t0002g0203 others(50): Show |
56 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.4735-50dupT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50752782 | |||||||
chr14:50752782 | T | TAA | 7 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0003g0236 others(4): Show |
7 | HG00738.hp1 HG01106.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.4735-51_4735-50dup others(2): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50752782 | |||||||
chr14:50752782 | TA | T | 124 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0072 others(121): Show |
126 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.4735-50delT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50752782 | |||||||
chr14:50752828 | C | T | 4 | a0009c0014t0005g0014 a0009c0014t0005g0015 a0009c0014t0022g0013 others(1): Show |
4 | HG01433.hp2 HG01891.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4735-95G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50752828 | |||||||
chr14:50752945 | C | T | 2 | a0003c0003t0001g0192 a0015c0057t0018g0030 |
2 | HG01358.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.4735-212G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50752945 | |||||||
chr14:50753020 | T | G | 1 | a0002c0001t0002g0235 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.4735-287A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753020 | |||||||
chr14:50753162 | C | T | 2 | a0001c0002t0003g0021 a0001c0002t0003g0099 |
2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4735-429G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753162 | |||||||
chr14:50753166 | G | A | 1 | a0003c0003t0001g0208 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4735-433C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753166 | |||||||
chr14:50753266 | G | A | 1 | a0001c0005t0001g0170 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.4735-533C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753266 | |||||||
chr14:50753315 | G | A | 1 | a0002c0043t0002g0247 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.4735-582C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753315 | |||||||
chr14:50753406 | G | A | 211 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(208): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.4735-673C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753406 | |||||||
chr14:50753457 | T | A | 73 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0046 others(70): Show |
73 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.4735-724A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753457 | |||||||
chr14:50753520 | G | A | 212 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(209): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.4735-787C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753520 | |||||||
chr14:50753523 | GATAGAC | G | 62 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0046 others(59): Show |
62 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.4735-796_4735-791d others(8): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753523 | |||||||
chr14:50753532 | A | G | 1 | a0001c0047t0003g0007 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4735-799T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753532 | |||||||
chr14:50753565 | A | T | 53 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(50): Show |
56 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.4735-832T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753565 | |||||||
chr14:50753586 | T | C | 62 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0046 others(59): Show |
62 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.4735-853A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753586 | |||||||
chr14:50753596 | T | C | 212 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(209): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.4735-863A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753596 | |||||||
chr14:50753650 | G | C | 60 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(57): Show |
63 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.4734+913C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753650 | |||||||
chr14:50753737 | A | G | 1 | a0004c0004t0001g0119 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4734+826T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753737 | |||||||
chr14:50753788 | C | T | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.4734+775G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753788 | |||||||
chr14:50753810 | A | G | 3 | a0001c0025t0010g0067 a0001c0025t0010g0135 a0020c0033t0010g0049 |
3 | HG02630.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4734+753T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753810 | |||||||
chr14:50753849 | A | T | 1 | a0002c0001t0002g0109 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4734+714T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753849 | |||||||
chr14:50753870 | T | C | 11 | a0001c0011t0001g0008 a0001c0011t0001g0011 a0001c0011t0001g0227 others(8): Show |
11 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.4734+693A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753870 | |||||||
chr14:50753916 | T | C | 3 | a0001c0027t0012g0023 a0001c0027t0012g0287 a0002c0001t0002g0235 |
3 | HG02647.hp2 NA19004.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4734+647A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50753916 | |||||||
chr14:50754109 | G | A | 18 | a0001c0011t0001g0008 a0001c0011t0001g0011 a0001c0011t0001g0227 others(15): Show |
18 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.4734+454C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50754109 | |||||||
chr14:50754114 | G | A | 4 | a0001c0002t0003g0086 a0001c0028t0003g0012 a0001c0028t0003g0101 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.4734+449C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50754114 | |||||||
chr14:50754278 | T | C | 1 | a0004c0004t0001g0055 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.4734+285A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50754278 | |||||||
chr14:50754283 | C | T | 2 | a0003c0003t0001g0066 a0003c0003t0001g0256 |
2 | HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.4734+280G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50754283 | |||||||
chr14:50754352 | G | T | 3 | a0001c0011t0001g0008 a0001c0011t0001g0011 a0001c0011t0001g0227 |
3 | HG01884.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4734+211C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50754352 | |||||||
chr14:50754509 | A | C | 1 | a0001c0002t0003g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4734+54T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 20/30 | chr14 | 50754509 | |||||||
chr14:50754954 | A | C | 59 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(56): Show |
62 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.4539-87T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50754954 | |||||||
chr14:50754955 | G | A | 2 | a0001c0002t0003g0062 a0001c0002t0003g0063 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.4539-88C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50754955 | |||||||
chr14:50755236 | T | C | 5 | a0007c0009t0004g0103 a0007c0009t0004g0136 a0007c0009t0004g0137 others(2): Show |
5 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.4539-369A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755236 | |||||||
chr14:50755398 | G | A | 1 | a0001c0002t0003g0021 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4539-531C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755398 | |||||||
chr14:50755417 | A | G | 1 | a0001c0002t0003g0199 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4539-550T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755417 | |||||||
chr14:50755465 | G | GT | 12 | a0001c0017t0003g0115 a0003c0003t0001g0164 a0003c0003t0001g0279 others(9): Show |
12 | HG01433.hp2 HG02055.hp2 HG03139.hp2 others(9): Show |
intron_variant | MODIFIER | c.4539-599dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755465 | |||||||
chr14:50755648 | C | CT | 6 | a0001c0011t0001g0227 a0007c0009t0004g0103 a0007c0009t0004g0137 others(3): Show |
6 | HG02896.hp2 HG02897.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.4539-782dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755648 | |||||||
chr14:50755648 | CT | C | 12 | a0001c0027t0012g0023 a0001c0027t0012g0287 a0002c0001t0002g0106 others(9): Show |
12 | HG00438.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.4539-782delA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755648 | |||||||
chr14:50755648 | CTT | C | 57 | a0001c0017t0002g0079 a0002c0001t0002g0028 a0002c0001t0002g0032 others(54): Show |
57 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.4539-783_4539-782d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755648 | |||||||
chr14:50755648 | CTTT | C | 9 | a0002c0001t0002g0108 a0002c0001t0002g0117 a0002c0001t0002g0145 others(6): Show |
9 | HG00099.hp1 HG01975.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.4539-784_4539-782d others(5): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755648 | |||||||
chr14:50755648 | CTTTTTTT others(8): Show |
C | 1 | a0003c0003t0001g0223 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4539-796_4539-782d others(17): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755648 | |||||||
chr14:50755648 | CTTTTTTT others(9): Show |
C | 53 | a0003c0003t0001g0005 a0003c0003t0001g0029 a0003c0003t0001g0038 others(50): Show |
55 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.4539-797_4539-782d others(18): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755648 | |||||||
chr14:50755648 | CTTTTTTT others(10): Show |
C | 1 | a0003c0003t0001g0207 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4539-798_4539-782d others(19): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755648 | |||||||
chr14:50755649 | T | TC | 3 | a0001c0012t0001g0039 a0001c0012t0001g0061 a0001c0018t0001g0027 |
3 | HG01361.hp1 HG01433.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.4539-783_4539-782i others(3): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755649 | |||||||
chr14:50755650 | T | C | 2 | a0001c0012t0001g0059 a0001c0018t0001g0230 |
2 | HG01168.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.4539-783A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755650 | |||||||
chr14:50755664 | TTTTTTTT others(8): Show |
T | 1 | a0001c0002t0002g0204 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4539-812_4539-798d others(17): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755664 | |||||||
chr14:50755669 | TTTTTTTT others(3): Show |
T | 4 | a0001c0029t0001g0089 a0001c0029t0001g0197 a0004c0004t0001g0050 others(1): Show |
4 | HG00642.hp2 HG02258.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.4539-812_4539-803d others(12): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755669 | |||||||
chr14:50755674 | TTTTTA | T | 28 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(25): Show |
31 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.4539-812_4539-808d others(7): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755674 | |||||||
chr14:50755675 | TTTTA | T | 22 | a0001c0002t0003g0009 a0001c0002t0003g0034 a0001c0002t0003g0070 others(19): Show |
22 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.4539-812_4539-809d others(6): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755675 | |||||||
chr14:50755676 | TTTA | T | 56 | a0001c0002t0003g0086 a0001c0005t0001g0040 a0001c0005t0001g0041 others(53): Show |
56 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.4539-812_4539-810d others(5): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755676 | |||||||
chr14:50755677 | TTA | T | 10 | a0001c0005t0001g0072 a0001c0005t0001g0147 a0001c0028t0003g0012 others(7): Show |
10 | HG01261.hp1 HG01358.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.4539-812_4539-811d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755677 | |||||||
chr14:50755678 | T | A | 1 | a0003c0003t0001g0151 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4539-811A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755678 | |||||||
chr14:50755678 | TA | T | 6 | a0001c0011t0001g0011 a0001c0052t0005g0285 a0009c0014t0005g0014 others(3): Show |
6 | HG01433.hp2 HG01891.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.4539-812delT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755678 | |||||||
chr14:50755679 | A | T | 19 | a0001c0011t0001g0008 a0001c0011t0001g0227 a0001c0012t0001g0039 others(16): Show |
19 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.4539-812T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755679 | |||||||
chr14:50755821 | C | T | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.4538+671G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755821 | |||||||
chr14:50755882 | C | A | 4 | a0009c0014t0005g0014 a0009c0014t0005g0015 a0009c0014t0022g0013 others(1): Show |
4 | HG01433.hp2 HG01891.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4538+610G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755882 | |||||||
chr14:50755959 | G | A | 1 | a0003c0003t0001g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.4538+533C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50755959 | |||||||
chr14:50756030 | G | A | 1 | a0001c0054t0006g0196 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4538+462C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50756030 | |||||||
chr14:50756120 | T | A | 1 | a0002c0001t0002g0278 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.4538+372A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50756120 | |||||||
chr14:50756156 | A | AT | 5 | a0006c0010t0006g0092 a0006c0010t0006g0093 a0006c0010t0006g0094 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4538+335dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50756156 | |||||||
chr14:50756157 | T | TA | 206 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(203): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.4538+334dupT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50756157 | |||||||
chr14:50756388 | G | T | 90 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0046 others(87): Show |
90 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.4538+104C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 18/30 | chr14 | 50756388 | |||||||
chr14:50758903 | A | G | 70 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0046 others(67): Show |
70 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.2400-273T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 17/30 | chr14 | 50758903 | |||||||
chr14:50759006 | C | T | 68 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0046 others(65): Show |
68 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.2400-376G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 17/30 | chr14 | 50759006 | |||||||
chr14:50759101 | G | C | 5 | a0001c0052t0005g0285 a0009c0014t0005g0014 a0009c0014t0005g0015 others(2): Show |
5 | HG01433.hp2 HG01891.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2400-471C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 17/30 | chr14 | 50759101 | |||||||
chr14:50759335 | C | T | 2 | a0003c0016t0001g0003 a0003c0016t0001g0130 |
3 | HG01069.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.2399+522G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 17/30 | chr14 | 50759335 | |||||||
chr14:50759496 | CT | C | 144 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(141): Show |
147 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.2399+360delA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 17/30 | chr14 | 50759496 | |||||||
chr14:50759503 | T | C | 2 | a0001c0002t0003g0002 a0001c0002t0003g0102 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2399+354A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 17/30 | chr14 | 50759503 | |||||||
chr14:50759511 | TG | T | 3 | a0008c0020t0003g0232 a0008c0020t0004g0105 a0008c0036t0004g0069 |
3 | HG01261.hp1 HG01496.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2399+345delC | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 17/30 | chr14 | 50759511 | |||||||
chr14:50759552 | A | G | 1 | a0002c0001t0002g0191 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2399+305T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 17/30 | chr14 | 50759552 | |||||||
chr14:50759721 | C | G | 77 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0046 others(74): Show |
77 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.2399+136G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 17/30 | chr14 | 50759721 | |||||||
chr14:50759732 | G | A | 1 | a0004c0004t0019g0081 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2399+125C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 17/30 | chr14 | 50759732 | |||||||
chr14:50759820 | G | A | 1 | a0001c0002t0021g0246 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2399+37C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 17/30 | chr14 | 50759820 | |||||||
chr14:50760437 | C | CT | 18 | a0001c0002t0003g0062 a0001c0002t0003g0063 a0001c0002t0003g0212 others(15): Show |
18 | HG00280.hp2 HG00733.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.1897-79dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 16/30 | chr14 | 50760437 | |||||||
chr14:50760437 | CT | C | 8 | a0001c0002t0021g0246 a0001c0030t0004g0111 a0001c0030t0004g0274 others(5): Show |
8 | HG00741.hp1 HG01099.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.1897-79delA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 16/30 | chr14 | 50760437 | |||||||
chr14:50760437 | CTT | C | 46 | a0001c0029t0001g0089 a0001c0029t0001g0197 a0001c0060t0003g0035 others(43): Show |
48 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1897-80_1897-79del others(2): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 16/30 | chr14 | 50760437 | |||||||
chr14:50760457 | T | C | 8 | a0003c0003t0001g0164 a0003c0003t0001g0249 a0003c0003t0001g0255 others(5): Show |
8 | NA18939.hp1 NA18950.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.1897-98A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 16/30 | chr14 | 50760457 | |||||||
chr14:50760604 | T | C | 49 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(46): Show |
52 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.1897-245A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 16/30 | chr14 | 50760604 | |||||||
chr14:50760689 | T | C | 3 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 |
3 | HG02559.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1897-330A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 16/30 | chr14 | 50760689 | |||||||
chr14:50760698 | G | T | 1 | a0001c0006t0003g0219 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1897-339C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 16/30 | chr14 | 50760698 | |||||||
chr14:50760962 | C | T | 1 | a0002c0001t0002g0235 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1897-603G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 16/30 | chr14 | 50760962 | |||||||
chr14:50761016 | C | G | 1 | a0021c0032t0006g0286 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1897-657G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 16/30 | chr14 | 50761016 | |||||||
chr14:50761018 | G | T | 1 | a0002c0001t0002g0229 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1897-659C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 16/30 | chr14 | 50761018 | |||||||
chr14:50761083 | G | A | 2 | a0001c0011t0006g0076 a0001c0011t0006g0077 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1896+707C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 16/30 | chr14 | 50761083 | |||||||
chr14:50761202 | G | A | 6 | a0001c0011t0001g0008 a0001c0011t0001g0011 a0001c0011t0001g0227 others(3): Show |
6 | HG01884.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1896+588C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 16/30 | chr14 | 50761202 | |||||||
chr14:50761393 | C | T | 12 | a0001c0012t0001g0039 a0001c0012t0001g0059 a0001c0012t0001g0061 others(9): Show |
12 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1896+397G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 16/30 | chr14 | 50761393 | |||||||
chr14:50761479 | T | C | 3 | a0001c0028t0003g0012 a0001c0028t0003g0101 a0001c0047t0003g0007 |
3 | HG02258.hp1 HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1896+311A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 16/30 | chr14 | 50761479 | |||||||
chr14:50761701 | A | T | 1 | a0001c0002t0003g0199 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1896+89T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 16/30 | chr14 | 50761701 | |||||||
chr14:50761713 | A | T | 1 | a0018c0034t0024g0284 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1896+77T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 16/30 | chr14 | 50761713 | |||||||
chr14:50761937 | C | G | 55 | a0001c0002t0002g0233 a0003c0003t0001g0005 a0003c0003t0001g0029 others(52): Show |
57 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1775-26G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50761937 | |||||||
chr14:50761964 | G | A | 213 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(210): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1775-53C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50761964 | |||||||
chr14:50762005 | G | A | 50 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(47): Show |
53 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.1775-94C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50762005 | |||||||
chr14:50762043 | G | A | 1 | a0021c0032t0006g0286 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1775-132C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50762043 | |||||||
chr14:50762057 | C | G | 1 | a0004c0004t0001g0071 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1775-146G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50762057 | |||||||
chr14:50762194 | G | A | 5 | a0001c0052t0005g0285 a0009c0014t0005g0014 a0009c0014t0005g0015 others(2): Show |
5 | HG01433.hp2 HG01891.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1775-283C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50762194 | |||||||
chr14:50762303 | A | G | 3 | a0001c0028t0003g0012 a0001c0028t0003g0101 a0001c0047t0003g0007 |
3 | HG02258.hp1 HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1775-392T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50762303 | |||||||
chr14:50762353 | C | T | 5 | a0001c0052t0005g0285 a0009c0014t0005g0014 a0009c0014t0005g0015 others(2): Show |
5 | HG01433.hp2 HG01891.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1775-442G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50762353 | |||||||
chr14:50762407 | G | A | 146 | a0001c0002t0002g0233 a0001c0005t0001g0040 a0001c0005t0001g0041 others(143): Show |
148 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1775-496C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50762407 | |||||||
chr14:50762645 | G | A | 3 | a0001c0028t0003g0012 a0001c0028t0003g0101 a0001c0047t0003g0007 |
3 | HG02258.hp1 HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1775-734C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50762645 | |||||||
chr14:50762712 | G | A | 2 | a0003c0008t0004g0095 a0003c0008t0015g0036 |
2 | HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1775-801C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50762712 | |||||||
chr14:50762832 | T | C | 2 | a0001c0002t0003g0017 a0001c0002t0003g0018 |
2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1775-921A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50762832 | |||||||
chr14:50762874 | A | C | 283 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(280): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1774+952T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50762874 | |||||||
chr14:50762973 | A | G | 1 | a0001c0030t0004g0274 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1774+853T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50762973 | |||||||
chr14:50763150 | G | T | 2 | a0002c0001t0002g0028 a0022c0046t0001g0112 |
2 | HG00408.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1774+676C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50763150 | |||||||
chr14:50763216 | C | T | 1 | a0004c0004t0001g0071 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1774+610G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50763216 | |||||||
chr14:50763245 | G | A | 1 | a0002c0001t0002g0189 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1774+581C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50763245 | |||||||
chr14:50763258 | T | C | 7 | a0001c0027t0012g0023 a0001c0027t0012g0287 a0001c0052t0005g0285 others(4): Show |
7 | HG01433.hp2 HG01891.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1774+568A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50763258 | |||||||
chr14:50763389 | G | A | 2 | a0001c0029t0001g0089 a0001c0029t0001g0197 |
2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1774+437C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50763389 | |||||||
chr14:50763420 | A | T | 278 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(275): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1774+406T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50763420 | |||||||
chr14:50763506 | C | G | 8 | a0001c0028t0003g0012 a0001c0028t0003g0101 a0001c0047t0003g0007 others(5): Show |
8 | HG01891.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1774+320G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50763506 | |||||||
chr14:50763514 | C | T | 2 | a0001c0029t0001g0089 a0001c0029t0001g0197 |
2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1774+312G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50763514 | |||||||
chr14:50763533 | G | C | 138 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0046 others(135): Show |
138 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1774+293C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50763533 | |||||||
chr14:50763642 | T | C | 4 | a0001c0027t0012g0023 a0001c0027t0012g0287 a0003c0008t0004g0095 others(1): Show |
4 | HG02647.hp2 HG03130.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1774+184A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50763642 | |||||||
chr14:50763710 | ATTCT | A | 54 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(51): Show |
57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.1774+112_1774+115d others(6): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50763710 | |||||||
chr14:50763710 | ATTCTTTT others(8): Show |
A | 2 | a0001c0006t0003g0162 a0004c0004t0001g0224 |
2 | HG01943.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.1774+101_1774+115d others(17): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50763710 | |||||||
chr14:50763713 | CT | C | 64 | a0001c0002t0002g0233 a0001c0052t0005g0285 a0002c0015t0002g0174 others(61): Show |
66 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.1774+112delA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50763713 | |||||||
chr14:50763713 | CTT | C | 134 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0046 others(131): Show |
134 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1774+111_1774+112d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50763713 | |||||||
chr14:50763727 | T | G | 37 | a0001c0005t0001g0046 a0002c0001t0002g0082 a0003c0022t0001g0211 others(34): Show |
37 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1774+99A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 15/30 | chr14 | 50763727 | |||||||
chr14:50764228 | T | C | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1636-264A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50764228 | |||||||
chr14:50764456 | C | T | 1 | a0010c0035t0002g0026 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1636-492G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50764456 | |||||||
chr14:50764580 | C | A | 213 | a0001c0002t0002g0233 a0001c0005t0001g0040 a0001c0005t0001g0041 others(210): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1636-616G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50764580 | |||||||
chr14:50764587 | G | A | 1 | a0001c0025t0010g0135 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1636-623C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50764587 | |||||||
chr14:50764949 | C | A | 5 | a0004c0004t0001g0155 a0004c0004t0001g0183 a0004c0004t0001g0248 others(2): Show |
5 | HG00621.hp2 NA18951.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.1636-985G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50764949 | |||||||
chr14:50764953 | T | C | 2 | a0001c0002t0005g0033 a0001c0002t0020g0173 |
2 | HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1636-989A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50764953 | |||||||
chr14:50765061 | C | CT | 8 | a0004c0004t0001g0042 a0004c0004t0001g0043 a0004c0004t0001g0071 others(5): Show |
8 | HG00438.hp1 HG00741.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1636-1098dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765061 | |||||||
chr14:50765063 | T | TA | 16 | a0001c0002t0003g0225 a0001c0005t0001g0186 a0001c0030t0004g0111 others(13): Show |
16 | HG00621.hp2 HG00735.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.1636-1100dupT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765063 | |||||||
chr14:50765063 | T | TAAA | 8 | a0002c0001t0002g0185 a0002c0001t0002g0202 a0007c0009t0004g0025 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1636-1102_1636-110 others(7): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765063 | |||||||
chr14:50765063 | TA | T | 107 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(104): Show |
112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1636-1100delT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765063 | |||||||
chr14:50765063 | TAA | T | 7 | a0001c0002t0003g0062 a0001c0012t0001g0059 a0001c0018t0001g0230 others(4): Show |
7 | HG00408.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1636-1101_1636-110 others(6): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765063 | |||||||
chr14:50765063 | TAAAAAAA others(1): Show |
T | 6 | a0001c0011t0001g0008 a0001c0011t0001g0011 a0001c0011t0001g0227 others(3): Show |
6 | HG01884.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1636-1107_1636-110 others(12): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765063 | |||||||
chr14:50765063 | TAAAAAAA others(5): Show |
T | 4 | a0001c0006t0003g0187 a0001c0006t0003g0188 a0001c0060t0003g0035 others(1): Show |
4 | HG00408.hp2 HG00642.hp1 HG00733.hp2 others(1): Show |
intron_variant | MODIFIER | c.1636-1111_1636-110 others(16): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765063 | |||||||
chr14:50765078 | A | T | 3 | a0001c0005t0001g0133 a0001c0005t0001g0134 a0001c0005t0001g0252 |
3 | HG01099.hp2 HG03017.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1636-1114T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765078 | |||||||
chr14:50765080 | A | T | 2 | a0009c0014t0005g0015 a0009c0014t0022g0013 |
2 | HG01433.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1636-1116T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765080 | |||||||
chr14:50765094 | T | A | 204 | a0001c0002t0002g0233 a0001c0005t0001g0040 a0001c0005t0001g0041 others(201): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1636-1130A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765094 | |||||||
chr14:50765188 | G | A | 1 | a0005c0007t0001g0097 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1635+1119C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765188 | |||||||
chr14:50765343 | A | T | 1 | a0001c0006t0003g0037 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1635+964T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765343 | |||||||
chr14:50765436 | G | A | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | NA18957.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1635+871C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765436 | |||||||
chr14:50765555 | T | C | 1 | a0002c0001t0002g0191 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1635+752A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765555 | |||||||
chr14:50765617 | C | T | 210 | a0001c0002t0002g0233 a0001c0005t0001g0040 a0001c0005t0001g0041 others(207): Show |
212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1635+690G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765617 | |||||||
chr14:50765640 | C | T | 3 | a0001c0029t0001g0089 a0001c0029t0001g0197 a0001c0060t0003g0035 |
3 | HG02280.hp2 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1635+667G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765640 | |||||||
chr14:50765814 | G | T | 2 | a0007c0009t0004g0025 a0021c0032t0006g0286 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1635+493C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765814 | |||||||
chr14:50765832 | C | T | 1 | a0020c0033t0010g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1635+475G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765832 | |||||||
chr14:50765843 | G | GT | 94 | a0001c0002t0002g0233 a0001c0011t0001g0008 a0001c0011t0001g0011 others(91): Show |
96 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.1635+463dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765843 | |||||||
chr14:50765843 | G | GTT | 6 | a0001c0005t0001g0252 a0002c0001t0002g0176 a0002c0001t0002g0180 others(3): Show |
6 | HG01099.hp2 HG03017.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1635+462_1635+463d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765843 | |||||||
chr14:50765843 | G | GTTT | 129 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0046 others(126): Show |
129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1635+461_1635+463d others(5): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765843 | |||||||
chr14:50765843 | G | T | 1 | a0002c0001t0002g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1635+464C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765843 | |||||||
chr14:50765889 | T | C | 3 | a0008c0020t0003g0232 a0008c0020t0004g0105 a0008c0036t0004g0069 |
3 | HG01261.hp1 HG01496.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1635+418A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765889 | |||||||
chr14:50765955 | C | T | 3 | a0001c0028t0003g0012 a0001c0028t0003g0101 a0001c0047t0003g0007 |
3 | HG02258.hp1 HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1635+352G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765955 | |||||||
chr14:50765956 | G | A | 1 | a0002c0001t0002g0117 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1635+351C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765956 | |||||||
chr14:50765968 | C | T | 3 | a0001c0029t0001g0089 a0001c0029t0001g0197 a0001c0060t0003g0035 |
3 | HG02280.hp2 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1635+339G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50765968 | |||||||
chr14:50766006 | C | T | 3 | a0008c0020t0003g0232 a0008c0020t0004g0105 a0008c0036t0004g0069 |
3 | HG01261.hp1 HG01496.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1635+301G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50766006 | |||||||
chr14:50766127 | G | A | 2 | a0002c0001t0002g0057 a0002c0001t0002g0201 |
2 | NA19011.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1635+180C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50766127 | |||||||
chr14:50766147 | A | C | 283 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(280): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1635+160T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 14/30 | chr14 | 50766147 | |||||||
chr14:50766529 | A | C | 3 | a0001c0029t0001g0089 a0001c0029t0001g0197 a0001c0060t0003g0035 |
3 | HG02280.hp2 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1546-133T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 13/30 | chr14 | 50766529 | |||||||
chr14:50766907 | A | G | 1 | a0002c0001t0002g0270 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1435-17T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50766907 | |||||||
chr14:50766938 | C | T | 3 | a0008c0020t0003g0232 a0008c0020t0004g0105 a0008c0036t0004g0069 |
3 | HG01261.hp1 HG01496.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1435-48G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50766938 | |||||||
chr14:50766982 | G | A | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1435-92C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50766982 | |||||||
chr14:50767010 | C | G | 3 | a0001c0002t0003g0062 a0001c0002t0003g0063 a0001c0002t0003g0212 |
3 | HG00280.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1435-120G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767010 | |||||||
chr14:50767202 | C | G | 3 | a0001c0028t0003g0012 a0001c0028t0003g0101 a0001c0047t0003g0007 |
3 | HG02258.hp1 HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1435-312G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767202 | |||||||
chr14:50767208 | T | G | 1 | a0003c0003t0001g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1435-318A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767208 | |||||||
chr14:50767283 | TAG | T | 3 | a0001c0028t0003g0012 a0001c0028t0003g0101 a0001c0047t0003g0007 |
3 | HG02258.hp1 HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1435-395_1435-394d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767283 | |||||||
chr14:50767301 | C | G | 1 | a0009c0014t0005g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1435-411G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767301 | |||||||
chr14:50767363 | C | A | 1 | a0006c0062t0006g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1435-473G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767363 | |||||||
chr14:50767385 | G | A | 46 | a0001c0002t0002g0233 a0002c0015t0002g0254 a0003c0003t0001g0005 others(43): Show |
48 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1435-495C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767385 | |||||||
chr14:50767438 | C | T | 5 | a0001c0012t0001g0039 a0001c0012t0001g0059 a0001c0012t0001g0061 others(2): Show |
5 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1435-548G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767438 | |||||||
chr14:50767442 | A | G | 59 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(56): Show |
62 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1435-552T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767442 | |||||||
chr14:50767559 | T | A | 209 | a0001c0002t0002g0233 a0001c0005t0001g0040 a0001c0005t0001g0041 others(206): Show |
211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1435-669A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767559 | |||||||
chr14:50767560 | G | C | 3 | a0008c0020t0003g0232 a0008c0020t0004g0105 a0008c0036t0004g0069 |
3 | HG01261.hp1 HG01496.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1435-670C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767560 | |||||||
chr14:50767582 | C | T | 5 | a0001c0012t0001g0039 a0001c0012t0001g0059 a0001c0012t0001g0061 others(2): Show |
5 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1435-692G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767582 | |||||||
chr14:50767584 | A | G | 3 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 |
3 | HG02559.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1435-694T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767584 | |||||||
chr14:50767588 | T | C | 3 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 |
3 | HG02559.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1435-698A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767588 | |||||||
chr14:50767592 | C | T | 4 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 others(1): Show |
4 | HG02559.hp2 HG03195.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1435-702G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767592 | |||||||
chr14:50767599 | T | C | 4 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 others(1): Show |
4 | HG01346.hp1 HG02559.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1435-709A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767599 | |||||||
chr14:50767605 | C | A | 3 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 |
3 | HG02559.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1435-715G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767605 | |||||||
chr14:50767608 | G | A | 3 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 |
3 | HG02559.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1435-718C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767608 | |||||||
chr14:50767611 | A | G | 1 | a0002c0001t0002g0229 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1435-721T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767611 | |||||||
chr14:50767613 | C | T | 56 | a0001c0006t0003g0271 a0002c0001t0002g0028 a0002c0001t0002g0032 others(53): Show |
56 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.1435-723G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767613 | |||||||
chr14:50767628 | G | C | 1 | a0001c0002t0021g0246 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1435-738C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767628 | |||||||
chr14:50767628 | G | T | 265 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(262): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1435-738C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767628 | |||||||
chr14:50767648 | T | A | 135 | a0001c0002t0002g0064 a0001c0005t0001g0040 a0001c0005t0001g0041 others(132): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1435-758A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767648 | |||||||
chr14:50767674 | A | G | 1 | a0001c0005t0001g0170 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1435-784T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767674 | |||||||
chr14:50767677 | T | C | 1 | a0001c0005t0001g0170 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1435-787A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767677 | |||||||
chr14:50767684 | G | A | 62 | a0001c0002t0002g0064 a0001c0006t0003g0271 a0001c0030t0004g0111 others(59): Show |
62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.1435-794C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767684 | |||||||
chr14:50767685 | C | T | 1 | a0008c0020t0004g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1435-795G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767685 | |||||||
chr14:50767686 | G | A | 2 | a0008c0020t0003g0232 a0008c0036t0004g0069 |
2 | HG01261.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1435-796C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767686 | |||||||
chr14:50767689 | C | T | 1 | a0001c0002t0002g0204 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1435-799G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767689 | |||||||
chr14:50767691 | C | T | 1 | a0001c0002t0002g0204 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1435-801G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767691 | |||||||
chr14:50767990 | A | G | 2 | a0003c0003t0001g0066 a0003c0003t0001g0256 |
2 | HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1435-1100T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50767990 | |||||||
chr14:50768052 | A | AAC | 7 | a0001c0005t0004g0263 a0003c0003t0001g0207 a0003c0008t0002g0080 others(4): Show |
7 | HG01167.hp1 HG01346.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1435-1164_1435-116 others(6): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50768052 | |||||||
chr14:50768052 | A | AACAC | 6 | a0002c0001t0002g0278 a0003c0008t0002g0262 a0003c0008t0002g0265 others(3): Show |
6 | HG01099.hp1 HG01891.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.1435-1166_1435-116 others(8): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50768052 | |||||||
chr14:50768052 | AAC | A | 51 | a0001c0002t0002g0233 a0001c0060t0003g0035 a0002c0001t0002g0032 others(48): Show |
52 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1435-1164_1435-116 others(6): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50768052 | |||||||
chr14:50768052 | AACAC | A | 83 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(80): Show |
84 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1435-1166_1435-116 others(8): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50768052 | |||||||
chr14:50768052 | AACACAC | A | 63 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(60): Show |
66 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1435-1168_1435-116 others(10): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50768052 | |||||||
chr14:50768052 | AACACACA others(1): Show |
A | 34 | a0001c0002t0003g0017 a0001c0002t0003g0018 a0001c0005t0001g0147 others(31): Show |
34 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1435-1170_1435-116 others(12): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50768052 | |||||||
chr14:50768052 | AACACACA others(3): Show |
A | 11 | a0001c0002t0003g0178 a0001c0002t0003g0225 a0001c0002t0008g0195 others(8): Show |
11 | HG01261.hp1 HG01496.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.1435-1172_1435-116 others(14): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50768052 | |||||||
chr14:50768052 | AACACACA others(5): Show |
A | 11 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 others(8): Show |
11 | HG00639.hp1 HG01074.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1435-1174_1435-116 others(16): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50768052 | |||||||
chr14:50768052 | AACACACA others(9): Show |
A | 2 | a0001c0052t0005g0285 a0003c0003t0001g0164 |
2 | NA19043.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1435-1178_1435-116 others(20): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50768052 | |||||||
chr14:50768102 | C | T | 1 | a0006c0062t0006g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1435-1212G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50768102 | |||||||
chr14:50768192 | CAGTATAT others(4): Show |
C | 1 | a0001c0006t0003g0219 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1435-1313_1435-130 others(15): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50768192 | |||||||
chr14:50768453 | T | C | 6 | a0001c0012t0001g0039 a0001c0012t0001g0059 a0001c0012t0001g0061 others(3): Show |
6 | HG01106.hp1 HG01168.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1435-1563A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50768453 | |||||||
chr14:50768616 | G | A | 2 | a0002c0001t0002g0144 a0002c0001t0002g0145 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1435-1726C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50768616 | |||||||
chr14:50768784 | T | C | 2 | a0001c0054t0006g0196 a0003c0008t0004g0095 |
2 | HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1434+1604A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50768784 | |||||||
chr14:50768803 | G | C | 118 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(115): Show |
123 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.1434+1585C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50768803 | |||||||
chr14:50768947 | G | C | 1 | a0005c0007t0001g0045 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1434+1441C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50768947 | |||||||
chr14:50769017 | G | A | 283 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(280): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1434+1371C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50769017 | |||||||
chr14:50769040 | CAGTT | C | 9 | a0001c0012t0001g0039 a0001c0012t0001g0059 a0001c0012t0001g0061 others(6): Show |
9 | HG01106.hp1 HG01168.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1434+1344_1434+134 others(8): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50769040 | |||||||
chr14:50769498 | C | A | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1434+890G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50769498 | |||||||
chr14:50769701 | G | A | 1 | a0003c0008t0004g0095 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1434+687C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50769701 | |||||||
chr14:50769714 | C | A | 1 | a0001c0002t0003g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1434+674G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50769714 | |||||||
chr14:50769793 | A | G | 1 | a0018c0034t0024g0284 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1434+595T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50769793 | |||||||
chr14:50769808 | T | C | 1 | a0001c0002t0003g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1434+580A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50769808 | |||||||
chr14:50769821 | T | C | 17 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(14): Show |
17 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1434+567A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50769821 | |||||||
chr14:50769822 | A | G | 1 | a0002c0001t0002g0214 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1434+566T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50769822 | |||||||
chr14:50769898 | G | GCC | 3 | a0008c0020t0003g0232 a0008c0020t0004g0105 a0008c0036t0004g0069 |
3 | HG01261.hp1 HG01496.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1434+489_1434+490i others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50769898 | |||||||
chr14:50769903 | G | A | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1434+485C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50769903 | |||||||
chr14:50769942 | C | CA | 7 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(4): Show |
7 | HG01981.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1434+445dupT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50769942 | |||||||
chr14:50770038 | G | A | 1 | a0004c0039t0001g0146 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1434+350C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50770038 | |||||||
chr14:50770045 | C | T | 3 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 |
3 | HG02559.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1434+343G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50770045 | |||||||
chr14:50770048 | G | A | 1 | a0001c0006t0003g0037 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1434+340C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50770048 | |||||||
chr14:50770359 | G | A | 1 | a0002c0001t0002g0109 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1434+29C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 12/30 | chr14 | 50770359 | |||||||
chr14:50770633 | G | A | 1 | a0001c0028t0003g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1260-71C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 11/30 | chr14 | 50770633 | |||||||
chr14:50770720 | C | T | 50 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(47): Show |
53 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.1259+132G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 11/30 | chr14 | 50770720 | |||||||
chr14:50770795 | G | A | 1 | a0004c0004t0019g0081 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1259+57C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 11/30 | chr14 | 50770795 | |||||||
chr14:50771123 | A | C | 1 | a0001c0018t0001g0027 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1119-131T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 10/30 | chr14 | 50771123 | |||||||
chr14:50771163 | T | C | 13 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(10): Show |
13 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1118+169A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 10/30 | chr14 | 50771163 | |||||||
chr14:50771164 | A | T | 3 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 |
3 | HG02559.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1118+168T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 10/30 | chr14 | 50771164 | |||||||
chr14:50771179 | T | C | 2 | a0001c0002t0001g0226 a0001c0002t0001g0228 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1118+153A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 10/30 | chr14 | 50771179 | |||||||
chr14:50771684 | GA | G | 52 | a0001c0002t0002g0233 a0002c0001t0002g0201 a0002c0015t0002g0174 others(49): Show |
53 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.982-217delT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 9/30 | chr14 | 50771684 | |||||||
chr14:50771711 | T | G | 1 | a0002c0001t0002g0032 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.982-243A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 9/30 | chr14 | 50771711 | |||||||
chr14:50771724 | G | A | 9 | a0001c0012t0001g0039 a0001c0012t0001g0059 a0001c0012t0001g0061 others(6): Show |
9 | HG01106.hp1 HG01168.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.982-256C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 9/30 | chr14 | 50771724 | |||||||
chr14:50771812 | C | G | 3 | a0008c0020t0003g0232 a0008c0020t0004g0105 a0008c0036t0004g0069 |
3 | HG01261.hp1 HG01496.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.982-344G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 9/30 | chr14 | 50771812 | |||||||
chr14:50771973 | G | A | 3 | a0002c0001t0002g0032 a0002c0001t0002g0205 a0002c0001t0017g0031 |
3 | HG01361.hp2 HG03239.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.981+328C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 9/30 | chr14 | 50771973 | |||||||
chr14:50771985 | C | CA | 9 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 others(6): Show |
9 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.981+315dupT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 9/30 | chr14 | 50771985 | |||||||
chr14:50772010 | CA | C | 166 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.981+290delT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 9/30 | chr14 | 50772010 | |||||||
chr14:50772041 | C | A | 22 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.981+260G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 9/30 | chr14 | 50772041 | |||||||
chr14:50772598 | C | T | 3 | a0001c0011t0001g0008 a0001c0011t0001g0011 a0001c0011t0001g0227 |
3 | HG01884.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.814-130G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 8/30 | chr14 | 50772598 | |||||||
chr14:50772599 | A | T | 3 | a0001c0011t0001g0008 a0001c0011t0001g0011 a0001c0011t0001g0227 |
3 | HG01884.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.814-131T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 8/30 | chr14 | 50772599 | |||||||
chr14:50772664 | G | A | 36 | a0001c0002t0003g0002 a0001c0002t0003g0009 a0001c0002t0003g0017 others(33): Show |
39 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.814-196C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 8/30 | chr14 | 50772664 | |||||||
chr14:50772686 | C | T | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.814-218G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 8/30 | chr14 | 50772686 | |||||||
chr14:50772693 | T | C | 1 | a0001c0052t0005g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.814-225A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 8/30 | chr14 | 50772693 | |||||||
chr14:50773162 | G | A | 1 | a0001c0030t0004g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.667-67C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50773162 | |||||||
chr14:50773270 | C | A | 1 | a0001c0006t0003g0162 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.667-175G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50773270 | |||||||
chr14:50773741 | T | C | 3 | a0001c0027t0012g0023 a0001c0027t0012g0287 a0003c0008t0015g0036 |
3 | HG02647.hp2 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.667-646A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50773741 | |||||||
chr14:50773776 | A | AC | 5 | a0006c0010t0006g0092 a0006c0010t0006g0093 a0006c0010t0006g0094 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.667-682dupG | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50773776 | |||||||
chr14:50773985 | T | C | 1 | a0004c0004t0001g0055 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.667-890A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50773985 | |||||||
chr14:50774020 | A | G | 5 | a0006c0010t0006g0092 a0006c0010t0006g0093 a0006c0010t0006g0094 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.667-925T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50774020 | |||||||
chr14:50774369 | T | C | 6 | a0001c0012t0001g0039 a0001c0012t0001g0059 a0001c0012t0001g0061 others(3): Show |
6 | HG01106.hp1 HG01168.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.667-1274A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50774369 | |||||||
chr14:50774373 | C | T | 1 | a0004c0004t0001g0043 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.667-1278G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50774373 | |||||||
chr14:50774432 | G | C | 1 | a0001c0011t0006g0077 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.667-1337C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50774432 | |||||||
chr14:50774771 | G | A | 68 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0046 others(65): Show |
68 | HG00438.hp1 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.667-1676C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50774771 | |||||||
chr14:50775053 | C | T | 2 | a0001c0028t0003g0012 a0001c0028t0003g0101 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.666+1896G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50775053 | |||||||
chr14:50775092 | G | A | 1 | a0007c0055t0004g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.666+1857C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50775092 | |||||||
chr14:50775136 | G | A | 1 | a0003c0003t0001g0193 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.666+1813C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50775136 | |||||||
chr14:50775281 | C | T | 2 | a0001c0052t0005g0285 a0018c0034t0024g0284 |
2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.666+1668G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50775281 | |||||||
chr14:50775332 | C | T | 1 | a0002c0001t0002g0165 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.666+1617G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50775332 | |||||||
chr14:50775405 | C | T | 2 | a0004c0004t0001g0051 a0004c0004t0001g0055 |
2 | NA18944.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.666+1544G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50775405 | |||||||
chr14:50775439 | G | A | 1 | a0002c0001t0002g0189 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.666+1510C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50775439 | |||||||
chr14:50775558 | A | C | 5 | a0006c0010t0006g0092 a0006c0010t0006g0093 a0006c0010t0006g0094 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.666+1391T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50775558 | |||||||
chr14:50775830 | A | G | 1 | a0004c0004t0019g0081 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.666+1119T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50775830 | |||||||
chr14:50776032 | C | T | 1 | a0001c0012t0001g0059 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.666+917G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50776032 | |||||||
chr14:50776039 | T | A | 1 | a0001c0012t0001g0059 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.666+910A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50776039 | |||||||
chr14:50776113 | T | C | 2 | a0001c0029t0001g0089 a0001c0029t0001g0197 |
2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.666+836A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50776113 | |||||||
chr14:50776207 | T | G | 3 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0026c0038t0002g0167 |
3 | HG01257.hp1 HG01258.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.666+742A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50776207 | |||||||
chr14:50776221 | T | C | 1 | a0010c0035t0002g0026 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.666+728A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50776221 | |||||||
chr14:50776230 | T | G | 1 | a0002c0001t0002g0220 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.666+719A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50776230 | |||||||
chr14:50776377 | A | T | 2 | a0001c0030t0004g0111 a0001c0030t0004g0274 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.666+572T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50776377 | |||||||
chr14:50776599 | T | C | 2 | a0002c0001t0002g0057 a0002c0001t0002g0201 |
2 | NA19011.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.666+350A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50776599 | |||||||
chr14:50776656 | A | G | 4 | a0001c0011t0001g0008 a0001c0011t0001g0011 a0001c0011t0001g0227 others(1): Show |
4 | HG01884.hp2 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+293T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50776656 | |||||||
chr14:50776751 | G | A | 6 | a0001c0002t0005g0004 a0001c0002t0005g0033 a0001c0002t0005g0084 others(3): Show |
7 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.666+198C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50776751 | |||||||
chr14:50776844 | T | C | 4 | a0001c0027t0012g0023 a0001c0027t0012g0287 a0001c0052t0005g0285 others(1): Show |
4 | HG02647.hp2 HG03130.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+105A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 7/30 | chr14 | 50776844 | |||||||
chr14:50777181 | C | A | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.476-42G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 6/30 | chr14 | 50777181 | |||||||
chr14:50777302 | A | G | 1 | a0001c0030t0004g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.476-163T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 6/30 | chr14 | 50777302 | |||||||
chr14:50777375 | A | G | 1 | a0003c0008t0004g0095 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.476-236T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 6/30 | chr14 | 50777375 | |||||||
chr14:50777457 | T | C | 1 | a0001c0030t0004g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.476-318A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 6/30 | chr14 | 50777457 | |||||||
chr14:50777488 | C | T | 6 | a0001c0012t0001g0039 a0001c0012t0001g0059 a0001c0012t0001g0061 others(3): Show |
6 | HG01106.hp1 HG01168.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.476-349G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 6/30 | chr14 | 50777488 | |||||||
chr14:50777681 | T | TA | 159 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(156): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.476-543dupT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 6/30 | chr14 | 50777681 | |||||||
chr14:50777927 | G | A | 1 | a0001c0018t0001g0230 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.476-788C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 6/30 | chr14 | 50777927 | |||||||
chr14:50778058 | G | A | 133 | a0001c0002t0002g0233 a0001c0002t0003g0086 a0001c0005t0001g0040 others(130): Show |
133 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.475+707C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 6/30 | chr14 | 50778058 | |||||||
chr14:50778330 | A | G | 1 | a0001c0002t0003g0009 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.475+435T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 6/30 | chr14 | 50778330 | |||||||
chr14:50778402 | C | A | 104 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(101): Show |
109 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.475+363G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 6/30 | chr14 | 50778402 | |||||||
chr14:50778448 | G | A | 1 | a0001c0025t0010g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.475+317C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 6/30 | chr14 | 50778448 | |||||||
chr14:50778476 | C | T | 1 | a0001c0002t0002g0204 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.475+289G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 6/30 | chr14 | 50778476 | |||||||
chr14:50778547 | C | T | 2 | a0008c0021t0001g0010 a0008c0021t0001g0019 |
2 | HG01358.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.475+218G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 6/30 | chr14 | 50778547 | |||||||
chr14:50778948 | T | C | 136 | a0001c0002t0002g0233 a0001c0002t0003g0086 a0001c0005t0001g0040 others(133): Show |
136 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.436-144A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50778948 | |||||||
chr14:50779179 | A | G | 6 | a0001c0012t0001g0039 a0001c0012t0001g0059 a0001c0012t0001g0061 others(3): Show |
6 | HG01106.hp1 HG01168.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.436-375T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50779179 | |||||||
chr14:50779218 | T | C | 1 | a0003c0003t0001g0193 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.436-414A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50779218 | |||||||
chr14:50779236 | A | G | 2 | a0001c0029t0001g0089 a0001c0029t0001g0197 |
2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.436-432T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50779236 | |||||||
chr14:50779540 | C | T | 1 | a0001c0005t0001g0133 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.436-736G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50779540 | |||||||
chr14:50779588 | C | G | 3 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 |
3 | HG02559.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.436-784G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50779588 | |||||||
chr14:50779674 | C | T | 10 | a0001c0011t0001g0008 a0001c0011t0001g0011 a0001c0011t0001g0227 others(7): Show |
10 | HG01106.hp1 HG01168.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.436-870G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50779674 | |||||||
chr14:50779702 | A | G | 227 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(224): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.436-898T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50779702 | |||||||
chr14:50779706 | C | T | 1 | a0001c0002t0003g0034 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.436-902G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50779706 | |||||||
chr14:50779714 | C | T | 1 | a0011c0024t0003g0001 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.436-910G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50779714 | |||||||
chr14:50779745 | G | A | 49 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(46): Show |
52 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.436-941C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50779745 | |||||||
chr14:50779853 | A | T | 4 | a0003c0003t0001g0096 a0003c0003t0001g0148 a0003c0003t0001g0149 others(1): Show |
4 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.436-1049T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50779853 | |||||||
chr14:50780495 | C | T | 1 | a0002c0001t0002g0117 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.436-1691G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50780495 | |||||||
chr14:50780700 | A | T | 54 | a0001c0002t0003g0002 a0001c0002t0003g0009 a0001c0002t0003g0017 others(51): Show |
57 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.436-1896T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50780700 | |||||||
chr14:50780901 | C | T | 6 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0136 others(3): Show |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.436-2097G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50780901 | |||||||
chr14:50781238 | G | A | 1 | a0007c0055t0004g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.436-2434C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50781238 | |||||||
chr14:50781503 | T | A | 1 | a0002c0001t0002g0235 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.436-2699A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50781503 | |||||||
chr14:50782005 | TA | T | 41 | a0001c0002t0003g0002 a0001c0002t0003g0009 a0001c0002t0003g0017 others(38): Show |
44 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.436-3202delT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50782005 | |||||||
chr14:50782109 | C | A | 51 | a0002c0015t0002g0254 a0003c0003t0001g0005 a0003c0003t0001g0029 others(48): Show |
53 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.436-3305G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50782109 | |||||||
chr14:50782145 | G | T | 3 | a0001c0029t0001g0089 a0001c0029t0001g0197 a0003c0008t0015g0036 |
3 | HG02809.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.436-3341C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50782145 | |||||||
chr14:50782172 | A | G | 216 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(213): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.436-3368T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50782172 | |||||||
chr14:50782360 | A | G | 6 | a0001c0012t0001g0039 a0001c0012t0001g0059 a0001c0012t0001g0061 others(3): Show |
6 | HG01106.hp1 HG01168.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.436-3556T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50782360 | |||||||
chr14:50782365 | T | C | 1 | a0001c0052t0005g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.436-3561A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50782365 | |||||||
chr14:50782466 | A | G | 2 | a0001c0028t0003g0012 a0001c0028t0003g0101 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.436-3662T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50782466 | |||||||
chr14:50782518 | C | A | 221 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(218): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.436-3714G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50782518 | |||||||
chr14:50782520 | T | C | 139 | a0001c0002t0002g0233 a0001c0002t0003g0086 a0001c0005t0001g0040 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.436-3716A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50782520 | |||||||
chr14:50782566 | G | C | 2 | a0001c0029t0001g0089 a0001c0029t0001g0197 |
2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.436-3762C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50782566 | |||||||
chr14:50782636 | A | C | 232 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(229): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.436-3832T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50782636 | |||||||
chr14:50782922 | G | A | 49 | a0002c0015t0002g0254 a0003c0003t0001g0005 a0003c0003t0001g0029 others(46): Show |
51 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.436-4118C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50782922 | |||||||
chr14:50782947 | G | C | 221 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(218): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.436-4143C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50782947 | |||||||
chr14:50782955 | C | A | 221 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(218): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.436-4151G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50782955 | |||||||
chr14:50782966 | GCGT | G | 277 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(274): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.436-4165_436-4163d others(5): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50782966 | |||||||
chr14:50783114 | G | A | 221 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(218): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.436-4310C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50783114 | |||||||
chr14:50783198 | G | A | 1 | a0003c0008t0004g0095 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.436-4394C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50783198 | |||||||
chr14:50783223 | AT | A | 279 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(276): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.436-4420delA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50783223 | |||||||
chr14:50783319 | G | A | 1 | a0002c0001t0002g0088 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.436-4515C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50783319 | |||||||
chr14:50783586 | T | A | 1 | a0004c0004t0001g0055 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.436-4782A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50783586 | |||||||
chr14:50783619 | G | A | 13 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0002g0064 others(10): Show |
13 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.436-4815C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50783619 | |||||||
chr14:50783803 | G | A | 1 | a0003c0008t0015g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.436-4999C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50783803 | |||||||
chr14:50783871 | T | C | 4 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0138 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.436-5067A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50783871 | |||||||
chr14:50783926 | G | A | 1 | a0011c0024t0003g0001 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.436-5122C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50783926 | |||||||
chr14:50783954 | G | C | 2 | a0003c0016t0001g0003 a0003c0016t0001g0130 |
3 | HG01069.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.436-5150C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50783954 | |||||||
chr14:50783959 | G | GA | 56 | a0001c0002t0003g0002 a0001c0002t0003g0009 a0001c0002t0003g0017 others(53): Show |
59 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.436-5156dupT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50783959 | |||||||
chr14:50783965 | G | A | 1 | a0001c0002t0002g0064 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.436-5161C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50783965 | |||||||
chr14:50784059 | G | T | 224 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.436-5255C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784059 | |||||||
chr14:50784096 | A | T | 1 | a0003c0008t0004g0095 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.436-5292T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784096 | |||||||
chr14:50784103 | A | T | 224 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.436-5299T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784103 | |||||||
chr14:50784186 | C | T | 1 | a0017c0037t0001g0056 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.436-5382G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784186 | |||||||
chr14:50784204 | C | T | 54 | a0001c0011t0006g0076 a0001c0011t0006g0077 a0001c0029t0001g0089 others(51): Show |
56 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.436-5400G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784204 | |||||||
chr14:50784243 | G | A | 1 | a0002c0001t0002g0106 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.436-5439C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784243 | |||||||
chr14:50784321 | C | T | 1 | a0018c0034t0024g0284 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.436-5517G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784321 | |||||||
chr14:50784334 | C | A | 4 | a0007c0009t0004g0025 a0007c0009t0004g0103 a0007c0009t0004g0138 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.436-5530G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784334 | |||||||
chr14:50784360 | T | C | 1 | a0001c0005t0001g0252 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.436-5556A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784360 | |||||||
chr14:50784425 | A | C | 2 | a0002c0013t0004g0140 a0002c0013t0004g0194 |
2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.436-5621T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784425 | |||||||
chr14:50784427 | G | A | 1 | a0002c0001t0002g0144 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.436-5623C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784427 | |||||||
chr14:50784439 | G | A | 220 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(217): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.436-5635C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784439 | |||||||
chr14:50784625 | C | T | 4 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 others(1): Show |
4 | HG02559.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.436-5821G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784625 | |||||||
chr14:50784673 | T | G | 157 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0002g0064 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.436-5869A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784673 | |||||||
chr14:50784678 | A | G | 3 | a0001c0002t0003g0062 a0001c0002t0003g0063 a0001c0002t0003g0212 |
3 | HG00280.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.436-5874T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784678 | |||||||
chr14:50784712 | TG | T | 3 | a0001c0018t0001g0027 a0001c0018t0001g0230 a0010c0035t0002g0026 |
3 | HG01106.hp1 HG01168.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.436-5909delC | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784712 | |||||||
chr14:50784877 | C | T | 3 | a0001c0027t0012g0023 a0001c0027t0012g0287 a0003c0008t0015g0036 |
3 | HG02647.hp2 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.436-6073G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784877 | |||||||
chr14:50784885 | C | G | 230 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(227): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.436-6081G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784885 | |||||||
chr14:50784965 | A | C | 3 | a0001c0027t0012g0023 a0001c0027t0012g0287 a0003c0008t0015g0036 |
3 | HG02647.hp2 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.436-6161T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50784965 | |||||||
chr14:50785063 | G | C | 1 | a0003c0003t0001g0149 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.436-6259C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50785063 | |||||||
chr14:50785258 | C | T | 13 | a0001c0011t0001g0008 a0001c0011t0001g0011 a0001c0011t0001g0227 others(10): Show |
13 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.436-6454G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50785258 | |||||||
chr14:50785270 | T | G | 8 | a0001c0002t0001g0242 a0001c0012t0001g0039 a0001c0012t0001g0059 others(5): Show |
8 | HG01106.hp1 HG01168.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.436-6466A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50785270 | |||||||
chr14:50785306 | T | C | 1 | a0003c0003t0001g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.436-6502A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50785306 | |||||||
chr14:50785315 | C | T | 1 | a0001c0002t0003g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.436-6511G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50785315 | |||||||
chr14:50785329 | G | A | 1 | a0003c0008t0004g0095 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.436-6525C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50785329 | |||||||
chr14:50785534 | G | C | 1 | a0003c0008t0007g0267 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.436-6730C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50785534 | |||||||
chr14:50785740 | A | C | 4 | a0001c0011t0001g0008 a0001c0011t0001g0011 a0001c0011t0001g0227 others(1): Show |
4 | HG01884.hp2 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-6936T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50785740 | |||||||
chr14:50785823 | G | A | 1 | a0001c0002t0001g0242 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.435+6889C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50785823 | |||||||
chr14:50785841 | A | G | 1 | a0004c0004t0001g0224 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.435+6871T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50785841 | |||||||
chr14:50785915 | C | G | 283 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(280): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.435+6797G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50785915 | |||||||
chr14:50786110 | GC | G | 3 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 |
3 | HG02559.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.435+6601delG | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50786110 | |||||||
chr14:50786113 | G | A | 3 | a0001c0030t0004g0111 a0001c0030t0004g0274 a0002c0015t0002g0254 |
3 | HG03688.hp2 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.435+6599C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50786113 | |||||||
chr14:50786306 | G | A | 1 | a0002c0001t0002g0270 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.435+6406C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50786306 | |||||||
chr14:50786890 | T | C | 2 | a0001c0002t0003g0070 a0001c0002t0023g0068 |
2 | HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.435+5822A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50786890 | |||||||
chr14:50787197 | G | A | 1 | a0002c0001t0002g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.435+5515C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50787197 | |||||||
chr14:50787794 | G | T | 1 | a0003c0008t0004g0095 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.435+4918C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50787794 | |||||||
chr14:50788016 | G | A | 46 | a0003c0003t0001g0005 a0003c0003t0001g0029 a0003c0003t0001g0038 others(43): Show |
48 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.435+4696C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50788016 | |||||||
chr14:50788035 | T | TA | 7 | a0002c0001t0002g0176 a0002c0001t0002g0220 a0006c0010t0006g0092 others(4): Show |
7 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.435+4676dupT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50788035 | |||||||
chr14:50788132 | A | C | 3 | a0004c0004t0001g0042 a0004c0004t0001g0043 a0004c0004t0001g0179 |
3 | HG01074.hp1 HG01243.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.435+4580T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50788132 | |||||||
chr14:50788190 | T | C | 144 | a0001c0002t0002g0233 a0001c0002t0003g0086 a0001c0005t0001g0040 others(141): Show |
144 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.435+4522A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50788190 | |||||||
chr14:50788269 | T | C | 1 | a0001c0052t0005g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.435+4443A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50788269 | |||||||
chr14:50788803 | C | T | 1 | a0026c0038t0002g0167 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.435+3909G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50788803 | |||||||
chr14:50788841 | G | A | 3 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 |
3 | HG02559.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.435+3871C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50788841 | |||||||
chr14:50789213 | C | G | 3 | a0001c0030t0004g0111 a0001c0030t0004g0274 a0002c0015t0002g0254 |
3 | HG03688.hp2 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.435+3499G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50789213 | |||||||
chr14:50789248 | A | G | 1 | a0002c0001t0002g0214 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.435+3464T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50789248 | |||||||
chr14:50789297 | G | A | 210 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(207): Show |
212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.435+3415C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50789297 | |||||||
chr14:50789356 | TG | T | 58 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(55): Show |
60 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.435+3355delC | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50789356 | |||||||
chr14:50789357 | G | A | 1 | a0021c0032t0006g0286 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.435+3355C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50789357 | |||||||
chr14:50789390 | T | C | 228 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(225): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.435+3322A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50789390 | |||||||
chr14:50789519 | C | A | 21 | a0001c0002t0021g0246 a0001c0005t0001g0133 a0001c0005t0001g0134 others(18): Show |
21 | HG00408.hp2 HG01099.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.435+3193G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50789519 | |||||||
chr14:50789527 | C | A | 1 | a0001c0011t0001g0011 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.435+3185G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50789527 | |||||||
chr14:50789630 | T | C | 5 | a0006c0010t0006g0092 a0006c0010t0006g0093 a0006c0010t0006g0094 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.435+3082A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50789630 | |||||||
chr14:50789871 | C | T | 1 | a0002c0001t0002g0165 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.435+2841G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50789871 | |||||||
chr14:50790048 | G | A | 1 | a0001c0002t0003g0171 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.435+2664C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50790048 | |||||||
chr14:50790075 | G | A | 3 | a0001c0002t0003g0021 a0001c0002t0003g0099 a0003c0008t0004g0095 |
3 | HG02922.hp2 HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.435+2637C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50790075 | |||||||
chr14:50790238 | T | A | 1 | a0003c0008t0015g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.435+2474A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50790238 | |||||||
chr14:50790313 | C | T | 3 | a0001c0030t0004g0111 a0001c0030t0004g0274 a0002c0015t0002g0254 |
3 | HG03688.hp2 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.435+2399G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50790313 | |||||||
chr14:50790615 | G | A | 2 | a0009c0014t0005g0015 a0009c0014t0022g0013 |
2 | HG01433.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.435+2097C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50790615 | |||||||
chr14:50790921 | A | G | 1 | a0002c0001t0002g0116 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.435+1791T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50790921 | |||||||
chr14:50791239 | A | T | 2 | a0001c0002t0001g0242 a0001c0052t0005g0285 |
2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.435+1473T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791239 | |||||||
chr14:50791322 | A | G | 1 | a0001c0002t0003g0225 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.435+1390T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791322 | |||||||
chr14:50791559 | A | T | 5 | a0003c0003t0001g0029 a0003c0003t0001g0038 a0003c0003t0001g0250 others(2): Show |
5 | HG00408.hp1 HG00621.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.435+1153T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791559 | |||||||
chr14:50791714 | T | C | 4 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 others(1): Show |
4 | HG02559.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.435+998A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791714 | |||||||
chr14:50791717 | T | C | 1 | a0004c0004t0001g0042 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.435+995A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791717 | |||||||
chr14:50791807 | G | GCACACAC others(3): Show |
1 | a0002c0001t0002g0185 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.435+904_435+905ins others(10): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791807 | |||||||
chr14:50791807 | G | GCACACAC others(5): Show |
30 | a0001c0002t0003g0086 a0001c0018t0001g0027 a0001c0018t0001g0230 others(27): Show |
30 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.435+904_435+905ins others(12): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791807 | |||||||
chr14:50791807 | G | GCACACAC others(7): Show |
37 | a0001c0002t0001g0242 a0001c0002t0003g0021 a0001c0002t0003g0099 others(34): Show |
37 | HG00408.hp2 HG00639.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.435+904_435+905ins others(14): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791807 | |||||||
chr14:50791807 | G | GCACACAC others(11): Show |
14 | a0001c0002t0002g0233 a0001c0006t0003g0271 a0002c0001t0002g0032 others(11): Show |
14 | HG00099.hp1 HG01192.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.435+904_435+905ins others(18): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791807 | |||||||
chr14:50791807 | G | GCACACAC others(9): Show |
46 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0001c0005t0001g0046 others(43): Show |
46 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.435+904_435+905ins others(16): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791807 | |||||||
chr14:50791807 | G | GCACACAC others(11): Show |
8 | a0001c0012t0001g0039 a0002c0001t0002g0082 a0002c0001t0002g0189 others(5): Show |
8 | HG03041.hp2 HG03927.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.435+904_435+905ins others(18): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791807 | |||||||
chr14:50791807 | G | GCACACAC others(8): Show |
4 | a0002c0001t0002g0120 a0002c0001t0002g0176 a0002c0001t0002g0220 others(1): Show |
4 | HG03669.hp1 HG03669.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+904_435+905ins others(15): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791807 | |||||||
chr14:50791807 | G | GCACACAC others(7): Show |
1 | a0003c0022t0001g0211 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.435+891_435+904dup others(14): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791807 | |||||||
chr14:50791808 | C | CACACACA others(1): Show |
16 | a0001c0002t0003g0009 a0001c0002t0003g0073 a0001c0002t0003g0074 others(13): Show |
16 | HG01168.hp1 HG01169.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.435+903_435+904ins others(8): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791808 | |||||||
chr14:50791808 | C | CACACACA others(7): Show |
1 | a0002c0001t0002g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.435+903_435+904ins others(14): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791808 | |||||||
chr14:50791810 | C | CACACAA | 59 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0028t0003g0012 others(56): Show |
61 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.435+901_435+902ins others(6): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791810 | |||||||
chr14:50791812 | C | CACAA | 54 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(51): Show |
57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.435+899_435+900ins others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791812 | |||||||
chr14:50791814 | C | CAA | 4 | a0001c0030t0004g0111 a0001c0030t0004g0274 a0002c0015t0002g0254 others(1): Show |
4 | HG03688.hp2 HG04199.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.435+897_435+898ins others(2): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791814 | |||||||
chr14:50791914 | C | G | 1 | a0001c0025t0010g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.435+798G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50791914 | |||||||
chr14:50792386 | A | G | 3 | a0007c0009t0004g0103 a0007c0009t0004g0138 a0021c0032t0006g0286 |
3 | HG02896.hp2 HG02897.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.435+326T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50792386 | |||||||
chr14:50792408 | A | C | 1 | a0002c0015t0002g0174 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.435+304T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50792408 | |||||||
chr14:50792657 | T | C | 4 | a0001c0002t0003g0009 a0001c0027t0012g0023 a0001c0027t0012g0287 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.435+55A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50792657 | |||||||
chr14:50792660 | C | T | 3 | a0007c0009t0004g0103 a0007c0009t0004g0138 a0021c0032t0006g0286 |
3 | HG02896.hp2 HG02897.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.435+52G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 5/30 | chr14 | 50792660 | |||||||
chr14:50793021 | G | A | 2 | a0001c0029t0001g0089 a0001c0029t0001g0197 |
2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.266-140C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50793021 | |||||||
chr14:50793052 | C | T | 1 | a0002c0001t0002g0185 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.266-171G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50793052 | |||||||
chr14:50793083 | G | A | 52 | a0001c0028t0003g0012 a0001c0028t0003g0101 a0002c0001t0002g0191 others(49): Show |
54 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.266-202C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50793083 | |||||||
chr14:50793156 | T | A | 1 | a0004c0004t0001g0179 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.266-275A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50793156 | |||||||
chr14:50793281 | A | G | 40 | a0001c0002t0002g0064 a0001c0002t0002g0203 a0001c0002t0002g0204 others(37): Show |
42 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.266-400T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50793281 | |||||||
chr14:50793366 | ACCATTCC others(12): Show |
A | 3 | a0001c0030t0004g0111 a0001c0030t0004g0274 a0002c0015t0002g0254 |
3 | HG03688.hp2 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.266-504_266-486del others(19): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50793366 | |||||||
chr14:50793417 | G | A | 1 | a0002c0001t0002g0258 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.266-536C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50793417 | |||||||
chr14:50793547 | T | C | 1 | a0002c0001t0002g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.266-666A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50793547 | |||||||
chr14:50793606 | T | A | 4 | a0006c0010t0006g0092 a0006c0010t0006g0093 a0006c0010t0006g0094 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.266-725A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50793606 | |||||||
chr14:50793687 | C | T | 9 | a0001c0002t0003g0070 a0001c0002t0003g0099 a0001c0002t0023g0068 others(6): Show |
9 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.266-806G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50793687 | |||||||
chr14:50793706 | GCTGCCAT others(5): Show |
G | 1 | a0001c0002t0003g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.266-837_266-826del others(12): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50793706 | |||||||
chr14:50793751 | G | A | 2 | a0001c0002t0003g0021 a0003c0008t0004g0095 |
2 | HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.266-870C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50793751 | |||||||
chr14:50793837 | CTA | C | 4 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 others(1): Show |
4 | HG02559.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-958_266-957del others(2): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50793837 | |||||||
chr14:50793865 | A | G | 1 | a0002c0013t0004g0140 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.266-984T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50793865 | |||||||
chr14:50793880 | T | A | 1 | a0001c0002t0003g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.266-999A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50793880 | |||||||
chr14:50793934 | C | A | 3 | a0007c0009t0004g0103 a0007c0009t0004g0138 a0021c0032t0006g0286 |
3 | HG02896.hp2 HG02897.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.266-1053G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50793934 | |||||||
chr14:50793994 | T | A | 1 | a0020c0033t0010g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.266-1113A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50793994 | |||||||
chr14:50794027 | G | A | 4 | a0001c0018t0001g0027 a0001c0018t0001g0230 a0001c0047t0003g0007 others(1): Show |
4 | HG01106.hp1 HG01168.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.266-1146C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50794027 | |||||||
chr14:50794356 | T | C | 1 | a0002c0001t0002g0221 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.266-1475A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50794356 | |||||||
chr14:50794384 | T | C | 28 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0003g0002 others(25): Show |
29 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.266-1503A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50794384 | |||||||
chr14:50794396 | C | A | 27 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0003g0002 others(24): Show |
28 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.266-1515G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50794396 | |||||||
chr14:50794404 | A | G | 1 | a0008c0020t0004g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.266-1523T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50794404 | |||||||
chr14:50794437 | T | C | 1 | a0006c0010t0002g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.266-1556A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50794437 | |||||||
chr14:50794478 | G | A | 1 | a0002c0015t0002g0174 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.266-1597C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50794478 | |||||||
chr14:50794736 | T | C | 53 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0003g0002 others(50): Show |
55 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.266-1855A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50794736 | |||||||
chr14:50794761 | T | TA | 12 | a0001c0002t0001g0242 a0001c0002t0005g0033 a0001c0002t0020g0173 others(9): Show |
12 | HG01358.hp2 HG01433.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.266-1881dupT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50794761 | |||||||
chr14:50794761 | TA | T | 40 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0003g0002 others(37): Show |
41 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.266-1881delT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50794761 | |||||||
chr14:50794880 | C | T | 1 | a0001c0002t0001g0242 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.266-1999G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50794880 | |||||||
chr14:50794954 | T | C | 53 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0003g0002 others(50): Show |
55 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.266-2073A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50794954 | |||||||
chr14:50795239 | G | A | 27 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0003g0002 others(24): Show |
28 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.266-2358C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50795239 | |||||||
chr14:50795269 | G | A | 1 | a0020c0033t0010g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.266-2388C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50795269 | |||||||
chr14:50795374 | T | C | 57 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0028t0003g0101 others(54): Show |
59 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.266-2493A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50795374 | |||||||
chr14:50795433 | T | C | 57 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0028t0003g0101 others(54): Show |
59 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.266-2552A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50795433 | |||||||
chr14:50795462 | T | C | 57 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0028t0003g0101 others(54): Show |
59 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.266-2581A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50795462 | |||||||
chr14:50795604 | T | C | 1 | a0001c0002t0005g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.266-2723A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50795604 | |||||||
chr14:50795779 | A | G | 144 | a0001c0002t0002g0064 a0001c0002t0002g0233 a0001c0002t0003g0073 others(141): Show |
145 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.266-2898T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50795779 | |||||||
chr14:50795844 | C | T | 55 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0003g0002 others(52): Show |
57 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.266-2963G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50795844 | |||||||
chr14:50795921 | G | T | 1 | a0001c0005t0001g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.266-3040C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50795921 | |||||||
chr14:50796139 | C | T | 1 | a0002c0001t0002g0106 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.266-3258G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50796139 | |||||||
chr14:50796426 | C | T | 2 | a0001c0006t0003g0219 a0002c0001t0002g0218 |
2 | HG00639.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.266-3545G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50796426 | |||||||
chr14:50796428 | T | C | 56 | a0001c0002t0001g0242 a0001c0002t0002g0203 a0001c0002t0002g0204 others(53): Show |
58 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.266-3547A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50796428 | |||||||
chr14:50796446 | C | T | 2 | a0002c0001t0002g0181 a0002c0043t0002g0247 |
2 | HG00280.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.266-3565G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50796446 | |||||||
chr14:50796583 | C | T | 147 | a0001c0002t0002g0064 a0001c0002t0002g0233 a0001c0002t0003g0073 others(144): Show |
148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.266-3702G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50796583 | |||||||
chr14:50796662 | AAATATGG others(4): Show |
A | 1 | a0002c0001t0002g0122 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.266-3792_266-3782d others(13): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50796662 | |||||||
chr14:50796695 | T | A | 62 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0005g0033 others(59): Show |
64 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.266-3814A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50796695 | |||||||
chr14:50796698 | A | G | 1 | a0002c0051t0002g0245 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.266-3817T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50796698 | |||||||
chr14:50796727 | A | C | 283 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(280): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.266-3846T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50796727 | |||||||
chr14:50796734 | C | T | 1 | a0002c0001t0002g0181 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.266-3853G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50796734 | |||||||
chr14:50796781 | A | G | 6 | a0001c0002t0003g0070 a0001c0002t0023g0068 a0001c0025t0010g0067 others(3): Show |
6 | HG01261.hp1 HG02451.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.266-3900T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50796781 | |||||||
chr14:50796836 | AG | A | 6 | a0001c0002t0005g0033 a0001c0002t0020g0173 a0006c0010t0006g0092 others(3): Show |
6 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.266-3956delC | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50796836 | |||||||
chr14:50796910 | A | G | 2 | a0002c0001t0002g0181 a0002c0043t0002g0247 |
2 | HG00280.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.266-4029T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50796910 | |||||||
chr14:50796991 | A | C | 3 | a0001c0030t0004g0111 a0001c0030t0004g0274 a0002c0015t0002g0254 |
3 | HG03688.hp2 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.266-4110T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50796991 | |||||||
chr14:50797149 | G | A | 1 | a0006c0010t0002g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.266-4268C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50797149 | |||||||
chr14:50797260 | A | T | 1 | a0001c0002t0003g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.266-4379T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50797260 | |||||||
chr14:50797334 | C | T | 1 | a0001c0002t0003g0171 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.266-4453G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50797334 | |||||||
chr14:50797781 | A | G | 6 | a0001c0002t0003g0009 a0001c0002t0003g0090 a0001c0002t0003g0099 others(3): Show |
6 | HG01884.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.266-4900T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50797781 | |||||||
chr14:50797833 | G | A | 1 | a0002c0015t0002g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.266-4952C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50797833 | |||||||
chr14:50797941 | G | A | 3 | a0001c0002t0003g0086 a0001c0029t0001g0089 a0001c0029t0001g0197 |
3 | HG02809.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.266-5060C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50797941 | |||||||
chr14:50797995 | G | A | 1 | a0023c0050t0002g0244 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.266-5114C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50797995 | |||||||
chr14:50798103 | A | G | 1 | a0003c0003t0011g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.266-5222T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50798103 | |||||||
chr14:50798107 | C | T | 1 | a0001c0012t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.266-5226G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50798107 | |||||||
chr14:50798126 | C | T | 2 | a0002c0001t0002g0108 a0002c0001t0002g0113 |
2 | NA18960.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.266-5245G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50798126 | |||||||
chr14:50798232 | G | A | 1 | a0001c0005t0001g0252 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.266-5351C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50798232 | |||||||
chr14:50798267 | G | C | 6 | a0001c0002t0005g0033 a0001c0002t0020g0173 a0003c0008t0004g0095 others(3): Show |
6 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.266-5386C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50798267 | |||||||
chr14:50798359 | A | T | 1 | a0003c0003t0011g0169 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.266-5478T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50798359 | |||||||
chr14:50798402 | G | C | 3 | a0001c0030t0004g0274 a0002c0015t0002g0254 a0004c0004t0001g0087 |
3 | HG04199.hp1 HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.266-5521C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50798402 | |||||||
chr14:50798422 | G | A | 1 | a0001c0002t0003g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.266-5541C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50798422 | |||||||
chr14:50798437 | GGTGGATG others(3): Show |
G | 2 | a0001c0002t0003g0034 a0001c0002t0003g0110 |
2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.266-5566_266-5557d others(12): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50798437 | |||||||
chr14:50798488 | C | T | 11 | a0001c0002t0003g0009 a0001c0002t0003g0070 a0001c0002t0005g0084 others(8): Show |
11 | HG01261.hp1 HG01891.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.266-5607G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50798488 | |||||||
chr14:50798735 | C | T | 38 | a0001c0005t0001g0186 a0001c0005t0004g0263 a0002c0001t0002g0032 others(35): Show |
39 | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.266-5854G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50798735 | |||||||
chr14:50798773 | T | C | 3 | a0001c0030t0004g0274 a0002c0015t0002g0254 a0004c0004t0001g0087 |
3 | HG04199.hp1 HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.266-5892A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50798773 | |||||||
chr14:50798854 | C | T | 1 | a0001c0002t0003g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.266-5973G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50798854 | |||||||
chr14:50798858 | A | G | 1 | a0004c0004t0001g0152 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.266-5977T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50798858 | |||||||
chr14:50798882 | G | A | 3 | a0001c0002t0003g0086 a0001c0029t0001g0089 a0001c0029t0001g0197 |
3 | HG02809.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.266-6001C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50798882 | |||||||
chr14:50799011 | C | T | 1 | a0006c0062t0006g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.266-6130G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50799011 | |||||||
chr14:50799016 | C | T | 277 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(274): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.266-6135G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50799016 | |||||||
chr14:50799636 | G | T | 1 | a0002c0001t0002g0213 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.266-6755C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50799636 | |||||||
chr14:50799719 | C | T | 1 | a0002c0001t0002g0213 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.266-6838G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50799719 | |||||||
chr14:50799748 | G | A | 1 | a0001c0027t0012g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.266-6867C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50799748 | |||||||
chr14:50799847 | T | C | 1 | a0018c0034t0024g0284 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.265+6890A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50799847 | |||||||
chr14:50799868 | G | A | 3 | a0001c0030t0004g0274 a0002c0015t0002g0254 a0004c0004t0001g0087 |
3 | HG04199.hp1 HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.265+6869C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50799868 | |||||||
chr14:50799912 | T | G | 40 | a0001c0002t0003g0017 a0001c0005t0001g0186 a0001c0005t0004g0263 others(37): Show |
41 | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.265+6825A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50799912 | |||||||
chr14:50800007 | T | TAC | 11 | a0003c0003t0001g0047 a0003c0003t0001g0048 a0003c0003t0001g0054 others(8): Show |
11 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.265+6728_265+6729d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800007 | |||||||
chr14:50800007 | T | TACAC | 14 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0003g0021 others(11): Show |
14 | HG00741.hp1 HG01433.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.265+6726_265+6729d others(6): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800007 | |||||||
chr14:50800007 | T | TACACAC | 31 | a0001c0002t0003g0062 a0001c0002t0003g0063 a0001c0005t0001g0046 others(28): Show |
31 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.265+6724_265+6729d others(8): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800007 | |||||||
chr14:50800007 | T | TACACACA others(1): Show |
8 | a0001c0002t0003g0110 a0002c0001t0007g0268 a0002c0001t0007g0277 others(5): Show |
8 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.265+6722_265+6729d others(10): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800007 | |||||||
chr14:50800007 | T | TACACACA others(3): Show |
7 | a0001c0002t0002g0064 a0001c0002t0003g0034 a0001c0005t0001g0040 others(4): Show |
7 | HG00140.hp1 HG00140.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.265+6720_265+6729d others(12): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800007 | |||||||
chr14:50800007 | T | TACACACA others(5): Show |
1 | a0019c0042t0001g0283 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.265+6718_265+6729d others(14): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800007 | |||||||
chr14:50800007 | TAC | T | 14 | a0001c0002t0003g0070 a0001c0002t0005g0033 a0001c0002t0005g0084 others(11): Show |
14 | HG01261.hp1 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.265+6728_265+6729d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800007 | |||||||
chr14:50800007 | TACACAC | T | 3 | a0001c0030t0004g0274 a0002c0015t0002g0254 a0004c0004t0001g0087 |
3 | HG04199.hp1 HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.265+6724_265+6729d others(8): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800007 | |||||||
chr14:50800007 | TACACACA others(1): Show |
T | 10 | a0001c0002t0003g0009 a0001c0002t0003g0131 a0001c0002t0003g0236 others(7): Show |
10 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.265+6722_265+6729d others(10): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800007 | |||||||
chr14:50800007 | TACACACA others(3): Show |
T | 32 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0003g0073 others(29): Show |
33 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.265+6720_265+6729d others(12): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800007 | |||||||
chr14:50800007 | TACACACA others(5): Show |
T | 33 | a0001c0002t0002g0233 a0001c0002t0003g0002 a0001c0002t0003g0102 others(30): Show |
34 | HG00099.hp1 HG00621.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.265+6718_265+6729d others(14): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800007 | |||||||
chr14:50800007 | TACACACA others(7): Show |
T | 103 | a0001c0002t0003g0078 a0001c0002t0003g0172 a0001c0002t0003g0184 others(100): Show |
106 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.265+6716_265+6729d others(16): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800007 | |||||||
chr14:50800007 | TACACACA others(11): Show |
T | 5 | a0001c0002t0003g0086 a0001c0018t0001g0027 a0001c0029t0001g0089 others(2): Show |
5 | HG01106.hp1 HG01433.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+6712_265+6729d others(20): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800007 | |||||||
chr14:50800329 | G | C | 1 | a0008c0036t0004g0069 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.265+6408C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800329 | |||||||
chr14:50800497 | A | G | 1 | a0021c0032t0006g0286 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.265+6240T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800497 | |||||||
chr14:50800504 | T | C | 4 | a0001c0005t0001g0186 a0003c0003t0001g0222 a0003c0003t0001g0223 others(1): Show |
4 | HG01109.hp1 HG01255.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+6233A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800504 | |||||||
chr14:50800664 | A | G | 6 | a0001c0002t0003g0009 a0001c0027t0012g0023 a0001c0028t0003g0012 others(3): Show |
6 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+6073T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800664 | |||||||
chr14:50800785 | CT | C | 261 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(258): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.265+5951delA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800785 | |||||||
chr14:50800805 | G | A | 12 | a0001c0002t0003g0009 a0001c0002t0003g0070 a0001c0002t0005g0084 others(9): Show |
12 | HG01261.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.265+5932C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800805 | |||||||
chr14:50800813 | G | A | 1 | a0001c0052t0005g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.265+5924C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800813 | |||||||
chr14:50800868 | C | T | 1 | a0004c0004t0001g0224 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.265+5869G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800868 | |||||||
chr14:50800933 | C | T | 1 | a0001c0052t0005g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.265+5804G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800933 | |||||||
chr14:50800946 | C | T | 5 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 others(2): Show |
5 | HG01496.hp2 HG02559.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+5791G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50800946 | |||||||
chr14:50801080 | C | A | 1 | a0001c0030t0004g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.265+5657G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50801080 | |||||||
chr14:50801087 | CTT | C | 44 | a0001c0002t0003g0009 a0001c0002t0003g0070 a0001c0002t0003g0074 others(41): Show |
44 | HG00741.hp1 HG01261.hp1 HG01358.hp1 others(41): Show |
intron_variant | MODIFIER | c.265+5648_265+5649d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50801087 | |||||||
chr14:50801087 | CTTT | C | 198 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(195): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.265+5647_265+5649d others(5): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50801087 | |||||||
chr14:50801087 | CTTTT | C | 34 | a0001c0005t0004g0263 a0002c0001t0002g0032 a0002c0001t0002g0258 others(31): Show |
35 | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.265+5646_265+5649d others(6): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50801087 | |||||||
chr14:50801132 | T | C | 152 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0233 others(149): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.265+5605A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50801132 | |||||||
chr14:50801235 | C | T | 3 | a0002c0001t0002g0132 a0003c0016t0001g0003 a0003c0016t0001g0130 |
4 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+5502G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50801235 | |||||||
chr14:50801515 | C | A | 2 | a0001c0002t0003g0236 a0007c0009t0004g0025 |
2 | HG02818.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.265+5222G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50801515 | |||||||
chr14:50801586 | C | T | 4 | a0002c0001t0002g0153 a0004c0004t0001g0155 a0005c0007t0001g0154 others(1): Show |
4 | NA18943.hp1 NA18951.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+5151G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50801586 | |||||||
chr14:50801697 | G | T | 1 | a0002c0001t0002g0129 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.265+5040C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50801697 | |||||||
chr14:50802066 | A | G | 1 | a0001c0002t0003g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.265+4671T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50802066 | |||||||
chr14:50802223 | T | C | 277 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(274): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.265+4514A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50802223 | |||||||
chr14:50802378 | A | G | 277 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(274): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.265+4359T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50802378 | |||||||
chr14:50802404 | G | A | 277 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(274): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.265+4333C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50802404 | |||||||
chr14:50802489 | C | G | 1 | a0003c0003t0001g0257 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.265+4248G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50802489 | |||||||
chr14:50802492 | T | C | 97 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(94): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.265+4245A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50802492 | |||||||
chr14:50802518 | G | T | 82 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(79): Show |
83 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.265+4219C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50802518 | |||||||
chr14:50802552 | T | C | 12 | a0001c0002t0003g0009 a0001c0002t0003g0070 a0001c0002t0005g0084 others(9): Show |
12 | HG01261.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.265+4185A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50802552 | |||||||
chr14:50802558 | G | A | 13 | a0001c0005t0001g0133 a0001c0005t0001g0134 a0001c0005t0001g0252 others(10): Show |
13 | HG00738.hp1 HG01099.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.265+4179C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50802558 | |||||||
chr14:50802712 | A | AT | 40 | a0001c0005t0001g0186 a0001c0005t0004g0263 a0002c0001t0002g0032 others(37): Show |
41 | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.265+4024dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50802712 | |||||||
chr14:50802868 | T | G | 6 | a0001c0002t0003g0070 a0001c0002t0005g0084 a0001c0002t0023g0068 others(3): Show |
6 | HG01261.hp1 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+3869A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50802868 | |||||||
chr14:50802875 | C | T | 1 | a0001c0027t0012g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.265+3862G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50802875 | |||||||
chr14:50802905 | T | C | 8 | a0001c0002t0001g0242 a0001c0002t0005g0033 a0001c0002t0020g0173 others(5): Show |
8 | HG02647.hp1 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.265+3832A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50802905 | |||||||
chr14:50802965 | C | G | 1 | a0001c0002t0002g0233 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.265+3772G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50802965 | |||||||
chr14:50803114 | G | A | 1 | a0001c0030t0004g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.265+3623C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50803114 | |||||||
chr14:50803128 | T | C | 6 | a0001c0002t0003g0070 a0001c0002t0005g0084 a0001c0002t0023g0068 others(3): Show |
6 | HG01261.hp1 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+3609A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50803128 | |||||||
chr14:50803209 | C | T | 1 | a0004c0004t0001g0237 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.265+3528G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50803209 | |||||||
chr14:50803296 | T | A | 3 | a0001c0030t0004g0274 a0002c0015t0002g0254 a0004c0004t0001g0087 |
3 | HG04199.hp1 HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.265+3441A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50803296 | |||||||
chr14:50803370 | A | C | 1 | a0001c0002t0003g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.265+3367T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50803370 | |||||||
chr14:50803549 | G | C | 127 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0233 others(124): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.265+3188C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50803549 | |||||||
chr14:50803849 | C | T | 8 | a0001c0002t0001g0242 a0001c0002t0005g0033 a0001c0002t0020g0173 others(5): Show |
8 | HG02647.hp1 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.265+2888G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50803849 | |||||||
chr14:50803903 | C | CT | 160 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0233 others(157): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.265+2833dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50803903 | |||||||
chr14:50803958 | G | A | 1 | a0001c0018t0001g0230 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.265+2779C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50803958 | |||||||
chr14:50804072 | T | C | 2 | a0001c0052t0005g0285 a0007c0009t0004g0025 |
2 | HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.265+2665A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50804072 | |||||||
chr14:50804085 | C | T | 2 | a0003c0003t0001g0066 a0003c0003t0001g0256 |
2 | HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.265+2652G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50804085 | |||||||
chr14:50804098 | C | T | 277 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(274): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.265+2639G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50804098 | |||||||
chr14:50804186 | C | T | 7 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0006t0003g0187 others(4): Show |
7 | HG00099.hp2 HG00642.hp1 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.265+2551G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50804186 | |||||||
chr14:50804249 | C | T | 1 | a0003c0003t0001g0255 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.265+2488G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50804249 | |||||||
chr14:50804300 | AAAAGCAG others(2): Show |
A | 6 | a0001c0060t0003g0035 a0006c0010t0008g0139 a0009c0014t0005g0014 others(3): Show |
6 | HG01433.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.265+2428_265+2436d others(11): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50804300 | |||||||
chr14:50804312 | G | A | 1 | a0021c0032t0006g0286 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.265+2425C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50804312 | |||||||
chr14:50804330 | G | C | 1 | a0001c0002t0005g0142 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.265+2407C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50804330 | |||||||
chr14:50804488 | C | T | 5 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 others(2): Show |
5 | HG01496.hp2 HG02559.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+2249G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50804488 | |||||||
chr14:50804489 | G | A | 1 | a0001c0002t0003g0021 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.265+2248C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50804489 | |||||||
chr14:50804560 | G | A | 1 | a0003c0003t0001g0150 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.265+2177C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50804560 | |||||||
chr14:50804897 | C | G | 1 | a0001c0002t0003g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.265+1840G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50804897 | |||||||
chr14:50804913 | G | A | 6 | a0001c0002t0003g0009 a0001c0027t0012g0023 a0001c0028t0003g0012 others(3): Show |
6 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+1824C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50804913 | |||||||
chr14:50805178 | C | T | 1 | a0020c0033t0010g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.265+1559G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50805178 | |||||||
chr14:50805200 | C | T | 3 | a0001c0002t0003g0086 a0001c0029t0001g0089 a0001c0029t0001g0197 |
3 | HG02809.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.265+1537G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50805200 | |||||||
chr14:50805293 | T | A | 1 | a0001c0002t0003g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.265+1444A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50805293 | |||||||
chr14:50805365 | T | C | 1 | a0002c0001t0002g0189 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.265+1372A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50805365 | |||||||
chr14:50805507 | T | C | 203 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0002g0064 others(200): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.265+1230A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50805507 | |||||||
chr14:50805537 | C | T | 52 | a0001c0002t0003g0236 a0001c0002t0005g0004 a0001c0002t0005g0141 others(49): Show |
53 | HG00438.hp2 HG00738.hp1 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.265+1200G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50805537 | |||||||
chr14:50805720 | T | C | 6 | a0001c0002t0003g0086 a0001c0018t0001g0027 a0001c0029t0001g0089 others(3): Show |
6 | HG01106.hp1 HG01433.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.265+1017A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50805720 | |||||||
chr14:50805754 | A | G | 3 | a0001c0030t0004g0274 a0002c0015t0002g0254 a0004c0004t0001g0087 |
3 | HG04199.hp1 HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.265+983T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50805754 | |||||||
chr14:50805821 | T | A | 1 | a0002c0013t0004g0140 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.265+916A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50805821 | |||||||
chr14:50805951 | CCA | C | 6 | a0001c0002t0003g0070 a0001c0002t0005g0084 a0001c0002t0023g0068 others(3): Show |
6 | HG01261.hp1 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+784_265+785del others(2): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50805951 | |||||||
chr14:50805973 | T | C | 6 | a0001c0002t0003g0070 a0001c0002t0005g0084 a0001c0002t0023g0068 others(3): Show |
6 | HG01261.hp1 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+764A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50805973 | |||||||
chr14:50806018 | C | T | 3 | a0001c0002t0005g0004 a0001c0002t0005g0141 a0001c0002t0005g0142 |
4 | HG02257.hp1 HG02559.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+719G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50806018 | |||||||
chr14:50806051 | T | A | 1 | a0001c0005t0001g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.265+686A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50806051 | |||||||
chr14:50806080 | T | C | 18 | a0001c0002t0003g0009 a0001c0002t0003g0073 a0001c0002t0003g0074 others(15): Show |
18 | HG01496.hp2 HG01884.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.265+657A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50806080 | |||||||
chr14:50806106 | T | C | 35 | a0001c0005t0001g0186 a0001c0005t0004g0263 a0001c0006t0003g0276 others(32): Show |
35 | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.265+631A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50806106 | |||||||
chr14:50806109 | A | G | 1 | a0001c0002t0003g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.265+628T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50806109 | |||||||
chr14:50806217 | A | C | 1 | a0001c0002t0003g0070 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.265+520T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50806217 | |||||||
chr14:50806227 | T | C | 6 | a0001c0027t0012g0023 a0001c0028t0003g0012 a0002c0058t0002g0024 others(3): Show |
7 | HG01884.hp1 HG02258.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.265+510A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50806227 | |||||||
chr14:50806248 | T | C | 7 | a0001c0002t0003g0070 a0001c0002t0005g0084 a0001c0002t0023g0068 others(4): Show |
7 | HG01261.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.265+489A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50806248 | |||||||
chr14:50806688 | C | T | 1 | a0002c0001t0002g0129 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.265+49G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 4/30 | chr14 | 50806688 | |||||||
chr14:50807056 | A | G | 81 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0233 others(78): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.184-238T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50807056 | |||||||
chr14:50807196 | C | T | 2 | a0001c0027t0012g0287 a0001c0028t0003g0101 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.184-378G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50807196 | |||||||
chr14:50807291 | G | A | 35 | a0001c0005t0001g0186 a0001c0005t0004g0263 a0001c0006t0003g0276 others(32): Show |
35 | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.184-473C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50807291 | |||||||
chr14:50807347 | T | C | 1 | a0001c0056t0001g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.184-529A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50807347 | |||||||
chr14:50807554 | G | T | 6 | a0001c0002t0005g0033 a0003c0008t0004g0095 a0006c0010t0006g0092 others(3): Show |
6 | HG02280.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-736C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50807554 | |||||||
chr14:50807795 | T | C | 1 | a0001c0056t0001g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.184-977A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50807795 | |||||||
chr14:50807938 | TG | T | 4 | a0009c0014t0005g0014 a0009c0014t0005g0015 a0009c0014t0022g0013 others(1): Show |
4 | HG01433.hp2 HG01891.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-1121delC | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50807938 | |||||||
chr14:50808377 | G | A | 1 | a0005c0007t0001g0098 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.184-1559C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50808377 | |||||||
chr14:50808388 | G | A | 1 | a0003c0003t0001g0251 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.184-1570C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50808388 | |||||||
chr14:50808528 | A | G | 4 | a0009c0014t0005g0014 a0009c0014t0005g0015 a0009c0014t0022g0013 others(1): Show |
4 | HG01433.hp2 HG01891.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-1710T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50808528 | |||||||
chr14:50808616 | T | C | 6 | a0001c0002t0003g0070 a0001c0002t0005g0084 a0001c0002t0023g0068 others(3): Show |
6 | HG01261.hp1 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-1798A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50808616 | |||||||
chr14:50808907 | T | A | 18 | a0001c0002t0003g0009 a0001c0002t0003g0073 a0001c0002t0003g0074 others(15): Show |
18 | HG01496.hp2 HG01884.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.184-2089A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50808907 | |||||||
chr14:50808959 | G | A | 2 | a0001c0052t0005g0285 a0003c0008t0004g0095 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.184-2141C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50808959 | |||||||
chr14:50809092 | G | A | 68 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(65): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.184-2274C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50809092 | |||||||
chr14:50809105 | A | C | 277 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(274): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.184-2287T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50809105 | |||||||
chr14:50809207 | G | A | 2 | a0001c0002t0003g0172 a0001c0002t0003g0184 |
2 | HG01069.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.184-2389C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50809207 | |||||||
chr14:50809236 | A | G | 8 | a0001c0002t0003g0078 a0001c0011t0006g0076 a0001c0011t0006g0077 others(5): Show |
9 | HG01884.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-2418T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50809236 | |||||||
chr14:50809291 | T | A | 59 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0233 others(56): Show |
62 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.184-2473A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50809291 | |||||||
chr14:50809489 | G | A | 8 | a0001c0002t0003g0078 a0001c0011t0006g0076 a0001c0011t0006g0077 others(5): Show |
9 | HG01884.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-2671C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50809489 | |||||||
chr14:50809799 | T | C | 1 | a0003c0008t0015g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.184-2981A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50809799 | |||||||
chr14:50809846 | A | T | 76 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0002g0064 others(73): Show |
76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.184-3028T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50809846 | |||||||
chr14:50809925 | G | A | 3 | a0001c0027t0012g0287 a0001c0028t0003g0101 a0001c0047t0003g0007 |
3 | HG02572.hp2 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.184-3107C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50809925 | |||||||
chr14:50810099 | C | T | 1 | a0002c0001t0002g0191 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.184-3281G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50810099 | |||||||
chr14:50810148 | A | G | 1 | a0003c0003t0001g0192 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.184-3330T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50810148 | |||||||
chr14:50810155 | C | T | 56 | a0001c0002t0003g0236 a0001c0002t0005g0004 a0001c0002t0005g0141 others(53): Show |
57 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.184-3337G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50810155 | |||||||
chr14:50810217 | T | C | 7 | a0001c0002t0001g0242 a0001c0028t0003g0012 a0006c0062t0006g0100 others(4): Show |
7 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-3399A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50810217 | |||||||
chr14:50810230 | C | A | 1 | a0003c0008t0015g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.184-3412G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50810230 | |||||||
chr14:50810230 | C | CA | 73 | a0001c0002t0001g0228 a0001c0002t0001g0242 a0001c0002t0002g0203 others(70): Show |
74 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.184-3413dupT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50810230 | |||||||
chr14:50810230 | CA | C | 11 | a0001c0002t0003g0034 a0001c0002t0003g0078 a0001c0002t0003g0184 others(8): Show |
12 | HG01069.hp2 HG01167.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.184-3413delT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50810230 | |||||||
chr14:50810306 | T | C | 1 | a0001c0006t0003g0276 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.184-3488A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50810306 | |||||||
chr14:50810447 | T | C | 5 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 others(2): Show |
5 | HG01496.hp2 HG02559.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-3629A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50810447 | |||||||
chr14:50810574 | A | G | 2 | a0003c0003t0001g0047 a0003c0003t0001g0048 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.184-3756T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50810574 | |||||||
chr14:50810617 | A | C | 118 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.184-3799T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50810617 | |||||||
chr14:50810746 | C | T | 9 | a0001c0002t0003g0070 a0001c0002t0003g0078 a0001c0002t0005g0084 others(6): Show |
9 | HG01261.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-3928G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50810746 | |||||||
chr14:50810863 | C | T | 1 | a0022c0046t0001g0112 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.184-4045G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50810863 | |||||||
chr14:50810914 | G | A | 1 | a0002c0001t0002g0221 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.184-4096C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50810914 | |||||||
chr14:50811111 | C | CT | 60 | a0001c0002t0003g0078 a0001c0002t0003g0236 a0001c0002t0005g0004 others(57): Show |
61 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.184-4294dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811111 | |||||||
chr14:50811139 | G | T | 4 | a0009c0014t0005g0014 a0009c0014t0005g0015 a0009c0014t0022g0013 others(1): Show |
4 | HG01433.hp2 HG01891.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-4321C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811139 | |||||||
chr14:50811220 | T | C | 1 | a0001c0002t0003g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.184-4402A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811220 | |||||||
chr14:50811326 | C | G | 35 | a0001c0005t0001g0186 a0001c0005t0004g0263 a0001c0006t0003g0276 others(32): Show |
35 | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.184-4508G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811326 | |||||||
chr14:50811355 | C | T | 2 | a0002c0001t0002g0032 a0002c0001t0017g0031 |
2 | HG01361.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.184-4537G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811355 | |||||||
chr14:50811372 | G | A | 1 | a0018c0034t0024g0284 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.184-4554C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811372 | |||||||
chr14:50811400 | C | T | 36 | a0001c0005t0001g0186 a0001c0005t0004g0263 a0001c0006t0003g0276 others(33): Show |
36 | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.184-4582G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811400 | |||||||
chr14:50811404 | C | T | 3 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0011t0001g0227 |
3 | HG02486.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.184-4586G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811404 | |||||||
chr14:50811415 | G | T | 5 | a0001c0027t0012g0023 a0002c0058t0002g0024 a0007c0009t0004g0025 others(2): Show |
6 | HG01884.hp1 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-4597C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811415 | |||||||
chr14:50811453 | A | C | 4 | a0001c0060t0003g0035 a0006c0010t0008g0139 a0008c0020t0003g0232 others(1): Show |
4 | HG02257.hp2 HG02280.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-4635T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811453 | |||||||
chr14:50811544 | C | CT | 12 | a0001c0002t0003g0017 a0001c0002t0003g0073 a0001c0002t0003g0184 others(9): Show |
12 | HG01069.hp2 HG02572.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.184-4727dupA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811544 | |||||||
chr14:50811544 | C | CTT | 65 | a0001c0002t0002g0203 a0001c0002t0002g0233 a0001c0002t0003g0002 others(62): Show |
69 | HG00099.hp1 HG00621.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.184-4728_184-4727d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811544 | |||||||
chr14:50811544 | C | CTTT | 16 | a0001c0002t0003g0212 a0001c0002t0008g0195 a0001c0006t0013g0006 others(13): Show |
16 | HG00280.hp2 HG00735.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.184-4729_184-4727d others(5): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811544 | |||||||
chr14:50811544 | CT | C | 88 | a0001c0002t0001g0228 a0001c0002t0002g0064 a0001c0002t0003g0021 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.184-4727delA | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811544 | |||||||
chr14:50811544 | CTTTTTTT others(1): Show |
C | 63 | a0001c0002t0001g0242 a0001c0002t0002g0204 a0001c0002t0003g0236 others(60): Show |
64 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.184-4734_184-4727d others(10): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811544 | |||||||
chr14:50811631 | G | A | 6 | a0001c0002t0001g0242 a0006c0062t0006g0100 a0009c0014t0005g0014 others(3): Show |
6 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-4813C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811631 | |||||||
chr14:50811671 | G | C | 62 | a0001c0002t0001g0242 a0001c0002t0003g0236 a0001c0002t0005g0004 others(59): Show |
63 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.184-4853C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811671 | |||||||
chr14:50811717 | C | T | 23 | a0001c0002t0001g0242 a0001c0005t0001g0040 a0001c0005t0001g0041 others(20): Show |
23 | HG00438.hp2 HG01257.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.184-4899G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811717 | |||||||
chr14:50811790 | C | G | 4 | a0009c0014t0005g0014 a0009c0014t0005g0015 a0009c0014t0022g0013 others(1): Show |
4 | HG01433.hp2 HG01891.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-4972G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811790 | |||||||
chr14:50811832 | A | C | 92 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0002g0064 others(89): Show |
92 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.184-5014T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811832 | |||||||
chr14:50811867 | G | A | 2 | a0001c0028t0003g0012 a0001c0047t0003g0007 |
2 | HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.184-5049C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811867 | |||||||
chr14:50811919 | G | A | 56 | a0001c0002t0003g0236 a0001c0002t0005g0004 a0001c0002t0005g0141 others(53): Show |
57 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.184-5101C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811919 | |||||||
chr14:50811931 | T | G | 63 | a0001c0002t0001g0242 a0001c0002t0003g0236 a0001c0002t0005g0004 others(60): Show |
64 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.184-5113A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811931 | |||||||
chr14:50811943 | A | G | 62 | a0001c0002t0001g0242 a0001c0002t0003g0236 a0001c0002t0005g0004 others(59): Show |
63 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.184-5125T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811943 | |||||||
chr14:50811956 | CA | C | 217 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(214): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.184-5139delT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811956 | |||||||
chr14:50811982 | G | A | 1 | a0008c0021t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.184-5164C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50811982 | |||||||
chr14:50812077 | G | A | 1 | a0003c0003t0001g0151 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.184-5259C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50812077 | |||||||
chr14:50812233 | T | C | 281 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(278): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.184-5415A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50812233 | |||||||
chr14:50812274 | A | T | 9 | a0001c0002t0003g0070 a0001c0002t0003g0078 a0001c0002t0005g0084 others(6): Show |
9 | HG01261.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-5456T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50812274 | |||||||
chr14:50812390 | T | C | 93 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0002g0064 others(90): Show |
93 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.184-5572A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50812390 | |||||||
chr14:50812404 | C | T | 60 | a0001c0002t0001g0242 a0001c0002t0003g0236 a0001c0002t0005g0004 others(57): Show |
61 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.184-5586G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50812404 | |||||||
chr14:50812423 | C | T | 1 | a0001c0002t0003g0034 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.184-5605G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50812423 | |||||||
chr14:50812503 | C | T | 1 | a0002c0013t0004g0140 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.184-5685G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50812503 | |||||||
chr14:50812527 | C | A | 1 | a0002c0001t0002g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.184-5709G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50812527 | |||||||
chr14:50812576 | G | C | 1 | a0002c0001t0002g0145 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.184-5758C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50812576 | |||||||
chr14:50812661 | T | C | 34 | a0001c0005t0001g0186 a0001c0005t0004g0263 a0001c0006t0003g0276 others(31): Show |
34 | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.184-5843A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50812661 | |||||||
chr14:50812680 | A | G | 1 | a0001c0005t0001g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184-5862T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50812680 | |||||||
chr14:50812717 | A | G | 64 | a0001c0002t0003g0131 a0001c0002t0003g0171 a0001c0002t0003g0236 others(61): Show |
66 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.184-5899T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50812717 | |||||||
chr14:50812796 | G | T | 111 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0002g0064 others(108): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.184-5978C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50812796 | |||||||
chr14:50812837 | T | C | 1 | a0001c0028t0003g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.184-6019A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50812837 | |||||||
chr14:50812848 | A | G | 4 | a0003c0003t0001g0005 a0003c0003t0001g0192 a0003c0003t0001g0193 others(1): Show |
5 | HG02135.hp1 HG02683.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-6030T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50812848 | |||||||
chr14:50812892 | C | T | 1 | a0004c0004t0001g0042 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.184-6074G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50812892 | |||||||
chr14:50813263 | T | C | 64 | a0001c0002t0003g0131 a0001c0002t0003g0171 a0001c0002t0003g0236 others(61): Show |
66 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.184-6445A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50813263 | |||||||
chr14:50813267 | A | G | 3 | a0003c0003t0001g0206 a0003c0003t0001g0207 a0003c0003t0001g0208 |
3 | HG01106.hp2 HG01167.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.184-6449T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50813267 | |||||||
chr14:50813414 | C | A | 1 | a0001c0047t0003g0007 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.184-6596G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50813414 | |||||||
chr14:50813417 | G | A | 5 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0075 others(2): Show |
5 | HG01496.hp2 HG02559.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-6599C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50813417 | |||||||
chr14:50813574 | G | A | 1 | a0001c0005t0001g0170 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.184-6756C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50813574 | |||||||
chr14:50813669 | T | C | 1 | a0004c0004t0001g0224 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.184-6851A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50813669 | |||||||
chr14:50813954 | C | T | 70 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0233 others(67): Show |
72 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.184-7136G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50813954 | |||||||
chr14:50813956 | G | A | 1 | a0001c0002t0003g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.184-7138C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50813956 | |||||||
chr14:50814213 | G | C | 1 | a0001c0005t0001g0186 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.184-7395C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50814213 | |||||||
chr14:50814264 | C | G | 1 | a0001c0002t0003g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.184-7446G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50814264 | |||||||
chr14:50814280 | T | C | 5 | a0001c0027t0012g0023 a0002c0058t0002g0024 a0007c0009t0004g0025 others(2): Show |
6 | HG01884.hp1 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-7462A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50814280 | |||||||
chr14:50814622 | C | T | 1 | a0004c0004t0001g0224 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.183+7252G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50814622 | |||||||
chr14:50814704 | C | T | 281 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(278): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.183+7170G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50814704 | |||||||
chr14:50814752 | C | T | 1 | a0002c0001t0002g0205 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.183+7122G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50814752 | |||||||
chr14:50815044 | A | G | 1 | a0002c0015t0002g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.183+6830T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50815044 | |||||||
chr14:50815092 | G | C | 2 | a0003c0003t0001g0005 a0003c0003t0001g0200 |
3 | HG03490.hp2 HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.183+6782C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50815092 | |||||||
chr14:50815094 | G | A | 67 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0002g0064 others(64): Show |
67 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.183+6780C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50815094 | |||||||
chr14:50815282 | C | T | 56 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0233 others(53): Show |
58 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.183+6592G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50815282 | |||||||
chr14:50815468 | G | A | 5 | a0001c0002t0003g0009 a0001c0002t0003g0034 a0001c0011t0001g0008 others(2): Show |
5 | HG01884.hp2 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+6406C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50815468 | |||||||
chr14:50815574 | T | C | 1 | a0002c0001t0002g0129 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.183+6300A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50815574 | |||||||
chr14:50815599 | A | G | 7 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0006t0003g0187 others(4): Show |
7 | HG00099.hp2 HG00642.hp1 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+6275T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50815599 | |||||||
chr14:50815600 | T | C | 1 | a0001c0030t0004g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.183+6274A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50815600 | |||||||
chr14:50815646 | C | T | 32 | a0001c0005t0001g0186 a0001c0005t0004g0263 a0001c0006t0003g0276 others(29): Show |
32 | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.183+6228G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50815646 | |||||||
chr14:50815949 | T | G | 61 | a0001c0002t0003g0131 a0001c0002t0003g0171 a0001c0002t0003g0236 others(58): Show |
63 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.183+5925A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50815949 | |||||||
chr14:50815967 | T | C | 1 | a0003c0003t0001g0164 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.183+5907A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50815967 | |||||||
chr14:50816070 | G | A | 61 | a0001c0002t0003g0131 a0001c0002t0003g0171 a0001c0002t0003g0236 others(58): Show |
63 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.183+5804C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50816070 | |||||||
chr14:50816104 | C | G | 187 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0002g0064 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.183+5770G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50816104 | |||||||
chr14:50816205 | G | C | 56 | a0001c0002t0003g0236 a0001c0002t0005g0004 a0001c0002t0005g0141 others(53): Show |
57 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.183+5669C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50816205 | |||||||
chr14:50816206 | A | C | 1 | a0001c0002t0003g0225 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.183+5668T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50816206 | |||||||
chr14:50816251 | G | T | 1 | a0002c0001t0002g0165 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.183+5623C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50816251 | |||||||
chr14:50816315 | C | G | 5 | a0001c0027t0012g0023 a0002c0058t0002g0024 a0007c0009t0004g0025 others(2): Show |
6 | HG01884.hp1 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+5559G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50816315 | |||||||
chr14:50816344 | A | G | 1 | a0001c0028t0003g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+5530T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50816344 | |||||||
chr14:50816430 | C | T | 213 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(210): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.183+5444G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50816430 | |||||||
chr14:50816680 | C | A | 1 | a0002c0015t0002g0174 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.183+5194G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50816680 | |||||||
chr14:50816793 | G | A | 1 | a0002c0001t0002g0240 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.183+5081C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50816793 | |||||||
chr14:50816825 | C | G | 1 | a0004c0004t0001g0087 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.183+5049G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50816825 | |||||||
chr14:50816979 | A | C | 1 | a0003c0008t0002g0261 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.183+4895T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50816979 | |||||||
chr14:50817026 | G | C | 1 | a0001c0028t0003g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+4848C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50817026 | |||||||
chr14:50817126 | C | A | 6 | a0001c0002t0003g0070 a0001c0002t0005g0084 a0001c0002t0023g0068 others(3): Show |
6 | HG01261.hp1 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.183+4748G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50817126 | |||||||
chr14:50817200 | T | C | 1 | a0001c0005t0001g0186 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.183+4674A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50817200 | |||||||
chr14:50817453 | G | T | 4 | a0003c0008t0004g0095 a0006c0010t0006g0092 a0006c0010t0006g0093 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+4421C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50817453 | |||||||
chr14:50817541 | A | C | 1 | a0004c0039t0001g0146 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.183+4333T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50817541 | |||||||
chr14:50817797 | C | T | 87 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0002g0064 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.183+4077G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50817797 | |||||||
chr14:50817876 | G | A | 2 | a0001c0002t0003g0172 a0001c0002t0003g0184 |
2 | HG01069.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.183+3998C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50817876 | |||||||
chr14:50817922 | C | T | 32 | a0001c0005t0001g0186 a0001c0005t0004g0263 a0001c0006t0003g0276 others(29): Show |
32 | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.183+3952G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50817922 | |||||||
chr14:50817943 | T | G | 32 | a0001c0005t0001g0186 a0001c0005t0004g0263 a0001c0006t0003g0276 others(29): Show |
32 | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.183+3931A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50817943 | |||||||
chr14:50818018 | G | T | 81 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0002g0064 others(78): Show |
81 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.183+3856C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50818018 | |||||||
chr14:50818049 | C | T | 2 | a0001c0028t0003g0012 a0001c0047t0003g0007 |
2 | HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.183+3825G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50818049 | |||||||
chr14:50818148 | C | T | 1 | a0001c0047t0003g0007 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.183+3726G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50818148 | |||||||
chr14:50818236 | A | T | 134 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0233 others(131): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.183+3638T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50818236 | |||||||
chr14:50818239 | C | T | 134 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0233 others(131): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.183+3635G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50818239 | |||||||
chr14:50818271 | C | A | 2 | a0001c0018t0001g0027 a0010c0035t0002g0026 |
2 | HG01106.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.183+3603G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50818271 | |||||||
chr14:50818304 | C | T | 2 | a0001c0060t0003g0035 a0006c0010t0008g0139 |
2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.183+3570G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50818304 | |||||||
chr14:50818318 | CA | C | 178 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0233 others(175): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.183+3555delT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50818318 | |||||||
chr14:50818318 | CAA | C | 71 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0002g0064 others(68): Show |
71 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.183+3554_183+3555d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50818318 | |||||||
chr14:50818344 | G | T | 6 | a0001c0002t0001g0242 a0001c0027t0012g0023 a0002c0058t0002g0024 others(3): Show |
7 | HG01884.hp1 HG03139.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+3530C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50818344 | |||||||
chr14:50818417 | G | C | 32 | a0001c0005t0001g0186 a0001c0005t0004g0263 a0001c0006t0003g0276 others(29): Show |
32 | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.183+3457C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50818417 | |||||||
chr14:50818489 | T | G | 1 | a0004c0004t0001g0071 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.183+3385A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50818489 | |||||||
chr14:50818519 | G | A | 35 | a0001c0005t0001g0133 a0001c0005t0001g0134 a0001c0005t0001g0170 others(32): Show |
35 | HG00408.hp2 HG00738.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.183+3355C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50818519 | |||||||
chr14:50818642 | G | T | 1 | a0002c0001t0002g0109 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.183+3232C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50818642 | |||||||
chr14:50818653 | A | G | 1 | a0002c0001t0002g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.183+3221T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50818653 | |||||||
chr14:50818896 | CA | C | 107 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0233 others(104): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.183+2977delT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50818896 | |||||||
chr14:50818896 | CAAA | C | 164 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(161): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.183+2975_183+2977d others(5): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50818896 | |||||||
chr14:50819004 | T | C | 1 | a0001c0052t0005g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.183+2870A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50819004 | |||||||
chr14:50819251 | A | G | 62 | a0001c0002t0002g0064 a0001c0002t0003g0062 a0001c0002t0003g0063 others(59): Show |
62 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.183+2623T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50819251 | |||||||
chr14:50819286 | T | G | 5 | a0001c0002t0003g0009 a0001c0011t0001g0008 a0001c0011t0001g0011 others(2): Show |
5 | HG01884.hp2 HG02258.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+2588A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50819286 | |||||||
chr14:50819377 | G | A | 11 | a0001c0002t0001g0242 a0001c0002t0003g0086 a0001c0005t0001g0040 others(8): Show |
12 | HG01257.hp1 HG01258.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.183+2497C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50819377 | |||||||
chr14:50819381 | T | G | 6 | a0001c0002t0001g0242 a0001c0027t0012g0023 a0002c0058t0002g0024 others(3): Show |
7 | HG01884.hp1 HG03139.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+2493A>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50819381 | |||||||
chr14:50819411 | G | A | 45 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0233 others(42): Show |
46 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.183+2463C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50819411 | |||||||
chr14:50819648 | A | G | 1 | a0001c0060t0003g0035 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.183+2226T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50819648 | |||||||
chr14:50819650 | G | A | 1 | a0003c0008t0004g0095 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.183+2224C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50819650 | |||||||
chr14:50820160 | T | A | 3 | a0001c0027t0012g0023 a0002c0058t0002g0024 a0011c0024t0003g0001 |
4 | HG01884.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+1714A>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50820160 | |||||||
chr14:50820352 | G | A | 3 | a0001c0027t0012g0023 a0002c0058t0002g0024 a0011c0024t0003g0001 |
4 | HG01884.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+1522C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50820352 | |||||||
chr14:50820402 | T | C | 1 | a0001c0002t0003g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.183+1472A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50820402 | |||||||
chr14:50820562 | G | T | 1 | a0003c0003t0001g0038 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.183+1312C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50820562 | |||||||
chr14:50821010 | C | T | 2 | a0002c0001t0002g0180 a0004c0004t0001g0179 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.183+864G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50821010 | |||||||
chr14:50821167 | G | A | 1 | a0001c0060t0003g0035 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.183+707C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50821167 | |||||||
chr14:50821240 | G | A | 1 | a0001c0006t0003g0037 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.183+634C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50821240 | |||||||
chr14:50821265 | T | C | 4 | a0003c0008t0004g0095 a0006c0010t0006g0092 a0006c0010t0006g0093 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+609A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50821265 | |||||||
chr14:50821412 | G | A | 1 | a0001c0002t0003g0171 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.183+462C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50821412 | |||||||
chr14:50821550 | C | T | 5 | a0001c0002t0003g0086 a0001c0005t0001g0040 a0001c0005t0001g0041 others(2): Show |
5 | HG01257.hp1 HG01258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+324G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50821550 | |||||||
chr14:50821715 | A | G | 3 | a0001c0002t0003g0009 a0001c0028t0003g0012 a0008c0021t0001g0010 |
3 | HG02258.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.183+159T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50821715 | |||||||
chr14:50821804 | G | A | 1 | a0001c0060t0003g0035 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.183+70C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 3/30 | chr14 | 50821804 | |||||||
chr14:50822102 | C | A | 1 | a0001c0002t0005g0084 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-21-25G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50822102 | |||||||
chr14:50822130 | C | T | 1 | a0002c0001t0002g0229 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-21-53G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50822130 | |||||||
chr14:50822155 | G | A | 1 | a0018c0034t0024g0284 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-21-78C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50822155 | |||||||
chr14:50822163 | T | C | 1 | a0003c0003t0001g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-21-86A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50822163 | |||||||
chr14:50822228 | C | T | 1 | a0001c0060t0003g0035 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-21-151G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50822228 | |||||||
chr14:50822386 | G | A | 2 | a0001c0005t0001g0133 a0001c0005t0001g0134 |
2 | HG03017.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-21-309C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50822386 | |||||||
chr14:50822487 | T | C | 2 | a0001c0002t0005g0033 a0006c0062t0006g0100 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-21-410A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50822487 | |||||||
chr14:50822604 | C | G | 7 | a0001c0052t0005g0285 a0001c0060t0003g0035 a0003c0008t0004g0095 others(4): Show |
7 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-527G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50822604 | |||||||
chr14:50822664 | G | C | 15 | a0001c0002t0003g0002 a0001c0002t0003g0102 a0001c0002t0003g0236 others(12): Show |
17 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-587C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50822664 | |||||||
chr14:50822684 | C | T | 23 | a0001c0002t0003g0021 a0001c0002t0003g0034 a0001c0002t0003g0090 others(20): Show |
23 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.-21-607G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50822684 | |||||||
chr14:50822853 | T | C | 1 | a0002c0001t0002g0088 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-21-776A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50822853 | |||||||
chr14:50823004 | G | A | 7 | a0001c0002t0003g0086 a0001c0005t0001g0040 a0001c0005t0001g0041 others(4): Show |
7 | HG01106.hp1 HG01257.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-21-927C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50823004 | |||||||
chr14:50823092 | A | G | 5 | a0001c0027t0012g0023 a0002c0058t0002g0024 a0007c0009t0004g0025 others(2): Show |
6 | HG01884.hp1 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-1015T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50823092 | |||||||
chr14:50823132 | C | T | 3 | a0001c0002t0003g0099 a0001c0027t0012g0287 a0001c0028t0003g0101 |
3 | HG02572.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-21-1055G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50823132 | |||||||
chr14:50823154 | TG | T | 3 | a0001c0002t0003g0178 a0001c0030t0004g0274 a0003c0003t0001g0091 |
3 | HG02738.hp2 HG04199.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-21-1078delC | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50823154 | |||||||
chr14:50823154 | TGG | T | 29 | a0001c0005t0001g0252 a0001c0005t0004g0263 a0001c0006t0003g0271 others(26): Show |
29 | HG00408.hp1 HG00738.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.-21-1079_-21-1078d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50823154 | |||||||
chr14:50823156 | G | T | 252 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(249): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.-21-1079C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50823156 | |||||||
chr14:50823208 | G | A | 1 | a0004c0004t0001g0224 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-21-1131C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50823208 | |||||||
chr14:50823289 | C | T | 1 | a0002c0001t0002g0176 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-21-1212G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50823289 | |||||||
chr14:50823419 | G | A | 1 | a0001c0002t0003g0225 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-21-1342C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50823419 | |||||||
chr14:50823423 | A | G | 272 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(269): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-21-1346T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50823423 | |||||||
chr14:50823521 | C | T | 1 | a0002c0001t0002g0165 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-21-1444G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50823521 | |||||||
chr14:50823537 | T | C | 4 | a0003c0008t0004g0095 a0006c0010t0006g0092 a0006c0010t0006g0093 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-1460A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50823537 | |||||||
chr14:50823944 | C | T | 1 | a0001c0028t0003g0101 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-21-1867G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50823944 | |||||||
chr14:50824069 | C | A | 3 | a0001c0027t0012g0023 a0002c0058t0002g0024 a0011c0024t0003g0001 |
4 | HG01884.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-1992G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50824069 | |||||||
chr14:50824197 | C | T | 1 | a0004c0004t0001g0248 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-21-2120G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50824197 | |||||||
chr14:50824386 | C | T | 2 | a0001c0052t0005g0285 a0018c0034t0024g0284 |
2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-21-2309G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50824386 | |||||||
chr14:50824555 | T | C | 2 | a0002c0001t0002g0144 a0002c0001t0002g0145 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-21-2478A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50824555 | |||||||
chr14:50824630 | G | A | 2 | a0001c0002t0005g0033 a0006c0062t0006g0100 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-21-2553C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50824630 | |||||||
chr14:50824687 | A | T | 73 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0002g0203 others(70): Show |
74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.-21-2610T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50824687 | |||||||
chr14:50824909 | A | C | 75 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0002g0203 others(72): Show |
76 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.-21-2832T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50824909 | |||||||
chr14:50825105 | G | A | 1 | a0001c0002t0003g0225 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-21-3028C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50825105 | |||||||
chr14:50825115 | G | A | 3 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0011t0001g0227 |
3 | HG02486.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-21-3038C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50825115 | |||||||
chr14:50825310 | G | A | 1 | a0003c0003t0001g0164 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-21-3233C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50825310 | |||||||
chr14:50825387 | G | T | 3 | a0001c0002t0003g0099 a0001c0027t0012g0287 a0001c0028t0003g0101 |
3 | HG02572.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-21-3310C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50825387 | |||||||
chr14:50825469 | G | A | 6 | a0001c0002t0001g0242 a0001c0027t0012g0023 a0002c0058t0002g0024 others(3): Show |
7 | HG01884.hp1 HG03139.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.-21-3392C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50825469 | |||||||
chr14:50825552 | G | A | 3 | a0001c0002t0003g0099 a0001c0027t0012g0287 a0001c0028t0003g0101 |
3 | HG02572.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-21-3475C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50825552 | |||||||
chr14:50825817 | C | T | 74 | a0001c0002t0003g0002 a0001c0002t0003g0099 a0001c0002t0003g0102 others(71): Show |
77 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-21-3740G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50825817 | |||||||
chr14:50825907 | C | T | 3 | a0008c0020t0003g0232 a0008c0020t0004g0105 a0021c0032t0006g0286 |
3 | HG01496.hp2 HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-21-3830G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50825907 | |||||||
chr14:50826026 | T | C | 16 | a0001c0005t0001g0158 a0001c0006t0003g0162 a0002c0001t0002g0153 others(13): Show |
16 | HG00438.hp1 HG00438.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.-21-3949A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50826026 | |||||||
chr14:50826321 | A | G | 34 | a0001c0002t0001g0242 a0001c0005t0001g0252 a0001c0005t0004g0263 others(31): Show |
34 | HG00408.hp1 HG00738.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.-22+4143T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50826321 | |||||||
chr14:50826335 | G | A | 2 | a0008c0020t0003g0232 a0021c0032t0006g0286 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-22+4129C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50826335 | |||||||
chr14:50826361 | G | A | 1 | a0010c0023t0002g0175 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-22+4103C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50826361 | |||||||
chr14:50826390 | A | G | 1 | a0001c0047t0003g0007 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-22+4074T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50826390 | |||||||
chr14:50826421 | C | G | 6 | a0001c0002t0003g0009 a0001c0011t0001g0008 a0001c0011t0001g0011 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+4043G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50826421 | |||||||
chr14:50826968 | T | C | 1 | a0002c0001t0002g0240 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-22+3496A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50826968 | |||||||
chr14:50826988 | C | T | 84 | a0001c0002t0003g0002 a0001c0002t0003g0099 a0001c0002t0003g0102 others(81): Show |
87 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-22+3476G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50826988 | |||||||
chr14:50827227 | T | C | 1 | a0001c0047t0003g0007 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-22+3237A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50827227 | |||||||
chr14:50827365 | A | C | 2 | a0001c0002t0003g0017 a0001c0002t0003g0018 |
2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-22+3099T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50827365 | |||||||
chr14:50827591 | CA | C | 64 | a0001c0002t0002g0064 a0001c0002t0003g0062 a0001c0002t0003g0063 others(61): Show |
64 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.-22+2872delT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50827591 | |||||||
chr14:50827591 | CAA | C | 137 | a0001c0002t0001g0242 a0001c0002t0003g0002 a0001c0002t0003g0009 others(134): Show |
141 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-22+2871_-22+2872d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50827591 | |||||||
chr14:50827591 | CAAA | C | 75 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0002g0203 others(72): Show |
76 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.-22+2870_-22+2872d others(5): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50827591 | |||||||
chr14:50827689 | A | G | 278 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(275): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.-22+2775T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50827689 | |||||||
chr14:50827724 | TCCAGC | T | 2 | a0001c0002t0003g0002 a0001c0002t0003g0102 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-22+2735_-22+2739d others(7): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50827724 | |||||||
chr14:50827752 | G | T | 1 | a0001c0047t0003g0007 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-22+2712C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50827752 | |||||||
chr14:50827756 | C | CA | 105 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(102): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.-22+2707dupT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50827756 | |||||||
chr14:50827756 | C | CAA | 88 | a0001c0002t0003g0002 a0001c0002t0003g0099 a0001c0002t0003g0110 others(85): Show |
92 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-22+2706_-22+2707d others(4): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50827756 | |||||||
chr14:50827756 | C | CAAA | 6 | a0001c0002t0003g0171 a0001c0005t0001g0170 a0001c0027t0012g0287 others(3): Show |
6 | HG01346.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+2705_-22+2707d others(5): Show |
NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50827756 | |||||||
chr14:50827850 | C | T | 1 | a0018c0034t0024g0284 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-22+2614G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50827850 | |||||||
chr14:50827906 | G | A | 2 | a0001c0002t0002g0233 a0002c0001t0016g0234 |
2 | HG01981.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-22+2558C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50827906 | |||||||
chr14:50827963 | G | A | 1 | a0001c0002t0003g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-22+2501C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50827963 | |||||||
chr14:50827970 | G | GA | 84 | a0001c0002t0003g0002 a0001c0002t0003g0102 a0001c0002t0003g0110 others(81): Show |
87 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-22+2493dupT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50827970 | |||||||
chr14:50827979 | A | C | 2 | a0006c0010t0006g0092 a0006c0010t0006g0093 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-22+2485T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50827979 | |||||||
chr14:50828040 | G | A | 277 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(274): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-22+2424C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50828040 | |||||||
chr14:50828102 | C | CA | 76 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0002g0203 others(73): Show |
77 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.-22+2361dupT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50828102 | |||||||
chr14:50828102 | CA | C | 84 | a0001c0002t0001g0242 a0001c0002t0002g0064 a0001c0002t0003g0009 others(81): Show |
85 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.-22+2361delT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50828102 | |||||||
chr14:50828156 | T | C | 1 | a0001c0002t0005g0033 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-22+2308A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50828156 | |||||||
chr14:50828198 | T | C | 37 | a0001c0005t0001g0252 a0001c0005t0004g0263 a0001c0006t0003g0271 others(34): Show |
37 | HG00408.hp1 HG00738.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.-22+2266A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50828198 | |||||||
chr14:50828782 | G | T | 98 | a0001c0002t0002g0064 a0001c0002t0003g0021 a0001c0002t0003g0034 others(95): Show |
98 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.-22+1682C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50828782 | |||||||
chr14:50828945 | A | T | 1 | a0001c0060t0003g0035 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-22+1519T>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50828945 | |||||||
chr14:50828967 | CA | C | 6 | a0001c0002t0003g0009 a0001c0002t0003g0034 a0001c0011t0001g0008 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+1496delT | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50828967 | |||||||
chr14:50828995 | G | A | 3 | a0004c0004t0001g0237 a0004c0004t0001g0238 a0004c0004t0001g0239 |
3 | HG01952.hp2 HG01978.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.-22+1469C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50828995 | |||||||
chr14:50829251 | A | G | 1 | a0001c0002t0005g0033 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-22+1213T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50829251 | |||||||
chr14:50829349 | A | C | 1 | a0019c0042t0001g0283 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-22+1115T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50829349 | |||||||
chr14:50829635 | A | C | 1 | a0002c0043t0002g0247 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-22+829T>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50829635 | |||||||
chr14:50829745 | A | G | 6 | a0001c0002t0021g0246 a0002c0001t0002g0032 a0002c0001t0017g0031 others(3): Show |
6 | HG01358.hp1 HG01361.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+719T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50829745 | |||||||
chr14:50829750 | G | C | 1 | a0002c0001t0002g0240 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-22+714C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50829750 | |||||||
chr14:50829751 | G | C | 1 | a0001c0005t0001g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-22+713C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50829751 | |||||||
chr14:50829895 | G | T | 1 | a0001c0047t0003g0007 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-22+569C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50829895 | |||||||
chr14:50830008 | T | C | 6 | a0001c0002t0001g0242 a0001c0027t0012g0023 a0002c0058t0002g0024 others(3): Show |
7 | HG01884.hp1 HG03139.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.-22+456A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50830008 | |||||||
chr14:50830035 | A | G | 1 | a0002c0001t0002g0028 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-22+429T>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50830035 | |||||||
chr14:50830048 | T | C | 4 | a0003c0003t0001g0279 a0003c0003t0001g0280 a0003c0003t0001g0281 others(1): Show |
4 | NA18950.hp1 NA18963.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+416A>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50830048 | |||||||
chr14:50830096 | C | G | 1 | a0023c0050t0002g0244 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-22+368G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50830096 | |||||||
chr14:50830111 | G | C | 1 | a0003c0003t0011g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-22+353C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50830111 | |||||||
chr14:50830242 | G | C | 1 | a0007c0009t0004g0025 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-22+222C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50830242 | |||||||
chr14:50830263 | G | T | 2 | a0001c0018t0001g0027 a0010c0035t0002g0026 |
2 | HG01106.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-22+201C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50830263 | |||||||
chr14:50830336 | G | A | 39 | a0001c0002t0021g0246 a0001c0005t0001g0252 a0001c0005t0004g0263 others(36): Show |
39 | HG00408.hp1 HG00738.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.-22+128C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50830336 | |||||||
chr14:50830353 | C | A | 1 | a0019c0042t0001g0283 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-22+111G>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50830353 | |||||||
chr14:50830376 | C | T | 5 | a0001c0027t0012g0023 a0002c0058t0002g0024 a0007c0009t0004g0025 others(2): Show |
6 | HG01884.hp1 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+88G>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50830376 | |||||||
chr14:50830425 | C | G | 1 | a0001c0011t0001g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-22+39G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 2/30 | chr14 | 50830425 | |||||||
chr14:50830602 | C | G | 1 | a0001c0002t0003g0021 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-75-85G>C | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 1/30 | chr14 | 50830602 | |||||||
chr14:50830621 | G | A | 2 | a0001c0052t0005g0285 a0018c0034t0024g0284 |
2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-75-104C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 1/30 | chr14 | 50830621 | |||||||
chr14:50830730 | G | GC | 272 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0242 others(269): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-75-214dupG | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 1/30 | chr14 | 50830730 | |||||||
chr14:50830757 | G | C | 1 | a0021c0032t0006g0286 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-75-240C>G | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 1/30 | chr14 | 50830757 | |||||||
chr14:50830804 | G | T | 1 | a0001c0047t0003g0007 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-76+202C>A | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 1/30 | chr14 | 50830804 | |||||||
chr14:50830936 | G | A | 1 | a0001c0027t0012g0287 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-76+70C>T | NIN | ENSG00000100503.27 | transcript | ENST00000530997.7 | protein_coding | 1/30 | chr14 | 50830936 |