Item | Value |
---|---|
geneid | 22795 |
ensemblid | ENSG00000087303.19 |
hgncid | 13389 |
symbol | NID2 |
name | nidogen 2 |
refseq_nuc | NM_007361.4 |
refseq_prot | NP_031387.3 |
ensembl_nuc | ENST00000216286.10 |
ensembl_prot | ENSP00000216286.4 |
mane_status | MANE Select |
chr | chr14 |
start | 52004809 |
end | 52069059 |
strand | - |
ver | v1.2 |
region | chr14:52004809-52069059 |
region5000 | chr14:51999809-52074059 |
regionname0 | NID2_chr14_52004809_52069059 |
regionname5000 | NID2_chr14_51999809_52074059 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1375 | 114 | 20 | 21 | 45 | 7 | 20 | 34 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0002 | 0/0 | 1375 | 103 | 8 | 18 | 67 | 1 | 9 | 53 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0003 | 0/0 | 1375 | 51 | 0 | 10 | 37 | 1 | 3 | 31 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0004 | 0/0 | 1375 | 22 | 15 | 5 | 0 | 1 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0005 | 0/0 | 1375 | 10 | 0 | 7 | 0 | 2 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0006 | 0/0 | 1375 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0007 | 0/0 | 1375 | 8 | 1 | 1 | 5 | 0 | 1 | 4 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0008 | 0/0 | 1375 | 6 | 1 | 4 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0009 | 0/0 | 1375 | 5 | 4 | 0 | 1 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0010 | 1/0 | 1375 | 4 | 3 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0011 | 0/0 | 1375 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0012 | 0/0 | 1375 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0013 | 0/0 | 1375 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0014 | 0/0 | 1375 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0015 | 0/0 | 1375 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0016 | 0/0 | 1375 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0017 | 0/0 | 1375 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0018 | 0/0 | 1375 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0019 | 0/0 | 1375 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0020 | 0/0 | 1375 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0021 | 0/0 | 1375 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0022 | 0/0 | 1375 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0023 | 0/0 | 1375 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0024 | 0/0 | 1375 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0025 | 0/0 | 1375 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0026 | 0/0 | 1375 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0027 | 0/0 | 1375 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0028 | 0/0 | 1375 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0029 | 0/0 | 1375 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0030 | 0/0 | 1375 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0031 | 0/0 | 1375 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0032 | 0/0 | 1375 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0033 | 0/0 | 1375 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0034 | 0/0 | 1375 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0035 | 0/0 | 1375 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0036 | 0/0 | 1375 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0037 | 0/0 | 1375 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
a0038 | 0/0 | 1375 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | MEGDR others(1370): Show |
chr14 | 51999809 | 52074059 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 4125 | 76 | 11 | 13 | 35 | 7 | 9 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0001c0005 | 0/0 | 4125 | 15 | 3 | 5 | 5 | 0 | 2 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0001c0007 | 0/0 | 4125 | 9 | 4 | 0 | 2 | 0 | 3 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0001c0010 | 0/0 | 4125 | 8 | 0 | 3 | 3 | 0 | 2 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0001c0022 | 0/0 | 4125 | 2 | 2 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0001c0023 | 0/0 | 4125 | 2 | 0 | 0 | 0 | 0 | 2 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0001c0032 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0001c0033 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0002c0003 | 0/0 | 4125 | 45 | 0 | 10 | 32 | 0 | 3 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0002c0004 | 0/0 | 4125 | 44 | 7 | 4 | 30 | 1 | 2 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0002c0015 | 0/0 | 4125 | 4 | 0 | 1 | 0 | 0 | 3 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0002c0025 | 0/0 | 4125 | 2 | 0 | 0 | 2 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0002c0027 | 0/0 | 4125 | 2 | 0 | 2 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0002c0039 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0002c0040 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0002c0041 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0002c0044 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0002c0048 | 0/0 | 4125 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0002c0050 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0003c0002 | 0/0 | 4125 | 49 | 0 | 10 | 35 | 1 | 3 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0003c0035 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0003c0036 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0004c0006 | 0/0 | 4125 | 11 | 9 | 1 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0004c0012 | 0/0 | 4125 | 5 | 1 | 3 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0004c0020 | 0/0 | 4125 | 3 | 3 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0004c0053 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0004c0055 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0004c0060 | 0/0 | 4125 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0005c0009 | 0/0 | 4125 | 8 | 0 | 5 | 0 | 2 | 1 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0005c0021 | 0/0 | 4125 | 2 | 0 | 2 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0006c0008 | 0/0 | 4125 | 9 | 9 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0007c0011 | 0/0 | 4125 | 7 | 1 | 1 | 4 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0007c0051 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0008c0013 | 0/0 | 4125 | 5 | 1 | 3 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0008c0052 | 0/0 | 4125 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0009c0014 | 0/0 | 4125 | 4 | 4 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0009c0038 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0010c0019 | 0/0 | 4125 | 3 | 3 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0010c0065 | 1/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0011c0016 | 0/0 | 4125 | 4 | 4 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0012c0018 | 0/0 | 4125 | 3 | 0 | 3 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0013c0017 | 0/0 | 4125 | 3 | 3 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0014c0024 | 0/0 | 4125 | 2 | 0 | 2 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0015c0056 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0015c0058 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0016c0064 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0016c0069 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0017c0026 | 0/0 | 4125 | 2 | 2 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0018c0028 | 0/0 | 4125 | 2 | 2 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0019c0031 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0020c0045 | 0/0 | 4125 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0021c0063 | 0/0 | 4125 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0022c0046 | 0/0 | 4125 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0023c0049 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0024c0067 | 0/0 | 4125 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0025c0042 | 0/0 | 4125 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0026c0037 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0027c0059 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0028c0029 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0029c0061 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0030c0030 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0031c0068 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0032c0043 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0033c0062 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0034c0057 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0035c0047 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0036c0066 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0037c0054 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 | ||
a0038c0034 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | ATGGA others(4120): Show |
chr14 | 51999809 | 52074059 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4870 | 76 | 11 | 13 | 35 | 7 | 9 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0001c0005t0001 | 0/0 | 4870 | 15 | 3 | 5 | 5 | 0 | 2 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0001c0007t0001 | 0/0 | 4870 | 8 | 3 | 0 | 2 | 0 | 3 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0001c0007t0002 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0001c0010t0001 | 0/0 | 4870 | 8 | 0 | 3 | 3 | 0 | 2 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0001c0022t0001 | 0/0 | 4870 | 2 | 2 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0001c0023t0001 | 0/0 | 4870 | 2 | 0 | 0 | 0 | 0 | 2 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0001c0032t0001 | 0/0 | 4870 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0001c0033t0001 | 0/0 | 4870 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0002c0003t0001 | 0/0 | 4870 | 45 | 0 | 10 | 32 | 0 | 3 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0002c0004t0001 | 0/0 | 4870 | 44 | 7 | 4 | 30 | 1 | 2 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0002c0015t0001 | 0/0 | 4870 | 4 | 0 | 1 | 0 | 0 | 3 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0002c0025t0001 | 0/0 | 4870 | 2 | 0 | 0 | 2 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0002c0027t0001 | 0/0 | 4870 | 2 | 0 | 2 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0002c0039t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0002c0040t0001 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0002c0041t0001 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0002c0044t0001 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0002c0048t0002 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0002c0050t0001 | 0/0 | 4870 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0003c0002t0001 | 0/0 | 4870 | 49 | 0 | 10 | 35 | 1 | 3 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0003c0035t0001 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0003c0036t0001 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0004c0006t0001 | 0/0 | 4870 | 10 | 8 | 1 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0004c0006t0002 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0004c0012t0002 | 0/0 | 4870 | 5 | 1 | 3 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0004c0020t0001 | 0/0 | 4870 | 3 | 3 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0004c0053t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0004c0055t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0004c0060t0001 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0005c0009t0001 | 0/0 | 4870 | 8 | 0 | 5 | 0 | 2 | 1 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0005c0021t0001 | 0/0 | 4870 | 2 | 0 | 2 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0006c0008t0001 | 0/0 | 4870 | 9 | 9 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0007c0011t0001 | 0/0 | 4870 | 7 | 1 | 1 | 4 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0007c0051t0001 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0008c0013t0001 | 0/0 | 4870 | 5 | 1 | 3 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0008c0052t0001 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0009c0014t0001 | 0/0 | 4870 | 4 | 4 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0009c0038t0001 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0010c0019t0001 | 0/0 | 4870 | 3 | 3 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0010c0065t0001 | 1/0 | 4870 | 1 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0011c0016t0001 | 0/0 | 4870 | 4 | 4 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0012c0018t0001 | 0/0 | 4870 | 3 | 0 | 3 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0013c0017t0001 | 0/0 | 4870 | 3 | 3 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0014c0024t0001 | 0/0 | 4870 | 2 | 0 | 2 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0015c0056t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0015c0058t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0016c0064t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0016c0069t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0017c0026t0001 | 0/0 | 4870 | 2 | 2 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0018c0028t0001 | 0/0 | 4870 | 2 | 2 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0019c0031t0001 | 0/0 | 4870 | 1 | 0 | 0 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0020c0045t0001 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0021c0063t0001 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0022c0046t0001 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0023c0049t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0024c0067t0002 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0025c0042t0001 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0026c0037t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0027c0059t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0028c0029t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0029c0061t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0030c0030t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0031c0068t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0032c0043t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0033c0062t0002 | 0/0 | 4870 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0034c0057t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0035c0047t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0036c0066t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0037c0054t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
a0038c0034t0001 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | GGAGA others(4865): Show |
chr14 | 51999809 | 52074059 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0235 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0005t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0005t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0005t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0005t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0005t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0005t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0005t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0005t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0005t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0005t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0005t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0005t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0005t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0005t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0007t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0007t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0007t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0007t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0007t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0007t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0007t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0007t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0007t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0010t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0010t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0010t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0010t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0010t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0010t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0022t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0022t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0023t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0023t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0032t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0001c0033t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0015t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0015t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0015t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0015t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0025t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0025t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0027t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0027t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0039t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0040t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0041t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0044t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0048t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0002c0050t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0035t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0003c0036t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0006t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0006t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0006t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0006t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0006t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0006t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0006t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0006t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0006t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0006t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0006t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0012t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0012t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0012t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0012t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0012t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0020t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0020t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0020t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0053t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0055t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0004c0060t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0005c0009t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0005c0009t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0005c0009t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0005c0009t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0005c0009t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0005c0009t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0005c0009t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0005c0021t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0005c0021t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0006c0008t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0006c0008t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0006c0008t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0006c0008t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0006c0008t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0006c0008t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0007c0011t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0007c0011t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0007c0011t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0007c0011t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0007c0011t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0007c0011t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0007c0011t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0007c0051t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0008c0013t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0008c0013t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0008c0013t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0008c0013t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0008c0013t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0008c0052t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0009c0014t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0009c0014t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0009c0014t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0009c0014t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0009c0038t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0010c0019t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0010c0019t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0010c0019t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0010c0065t0001g0337 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0011c0016t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0011c0016t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0011c0016t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0011c0016t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0012c0018t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0012c0018t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0013c0017t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0013c0017t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0014c0024t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0014c0024t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0015c0056t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0015c0058t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0016c0064t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0016c0069t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0017c0026t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0017c0026t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0018c0028t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0018c0028t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0019c0031t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0020c0045t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0021c0063t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0022c0046t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0023c0049t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0024c0067t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0025c0042t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0026c0037t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0027c0059t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0028c0029t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0029c0061t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0030c0030t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0031c0068t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0032c0043t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0033c0062t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0034c0057t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0035c0047t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0036c0066t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0037c0054t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
a0038c0034t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00099 | hp2 | a0004 | c0006 | t0001 | g0297 | EUR | GBR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0267 | EUR | GBR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00140 | hp2 | a0002 | c0004 | t0001 | g0023 | EUR | GBR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00280 | hp2 | a0019 | c0031 | t0001 | g0025 | EUR | FIN | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00323 | hp1 | a0008 | c0013 | t0001 | g0319 | EUR | FIN | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | FIN | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00423 | hp1 | a0003 | c0002 | t0001 | g0141 | EAS | CHS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00423 | hp2 | a0002 | c0004 | t0001 | g0097 | EAS | CHS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00438 | hp2 | a0007 | c0011 | t0001 | g0180 | EAS | CHS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00544 | hp2 | a0002 | c0003 | t0001 | g0116 | EAS | CHS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00558 | hp1 | a0002 | c0004 | t0001 | g0096 | EAS | CHS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00558 | hp2 | a0002 | c0003 | t0001 | g0098 | EAS | CHS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00597 | hp1 | a0002 | c0040 | t0001 | g0168 | EAS | CHS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00609 | hp1 | a0002 | c0004 | t0001 | g0162 | EAS | CHS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00609 | hp2 | a0002 | c0004 | t0001 | g0130 | EAS | CHS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00621 | hp2 | a0001 | c0010 | t0001 | g0034 | EAS | CHS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00639 | hp1 | a0004 | c0012 | t0002 | g0304 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00639 | hp2 | a0005 | c0009 | t0001 | g0224 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00642 | hp2 | a0008 | c0013 | t0001 | g0318 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00673 | hp1 | a0003 | c0002 | t0001 | g0081 | EAS | CHS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00673 | hp2 | a0002 | c0003 | t0001 | g0125 | EAS | CHS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00735 | hp1 | a0004 | c0060 | t0001 | g0298 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00738 | hp1 | a0001 | c0005 | t0001 | g0212 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00738 | hp2 | a0003 | c0002 | t0001 | g0014 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00741 | hp1 | a0003 | c0002 | t0001 | g0014 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG00741 | hp2 | a0005 | c0009 | t0001 | g0015 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01069 | hp1 | a0005 | c0021 | t0001 | g0283 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01069 | hp2 | a0001 | c0010 | t0001 | g0001 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01070 | hp1 | a0003 | c0002 | t0001 | g0271 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01070 | hp2 | a0020 | c0045 | t0001 | g0055 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01071 | hp1 | a0001 | c0010 | t0001 | g0001 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01071 | hp2 | a0002 | c0003 | t0001 | g0058 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01074 | hp1 | a0021 | c0063 | t0001 | g0343 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01074 | hp2 | a0005 | c0009 | t0001 | g0223 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01099 | hp1 | a0012 | c0018 | t0001 | g0045 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01099 | hp2 | a0001 | c0005 | t0001 | g0276 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01109 | hp2 | a0004 | c0012 | t0002 | g0299 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01167 | hp1 | a0022 | c0046 | t0001 | g0182 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01169 | hp2 | a0003 | c0002 | t0001 | g0205 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01175 | hp2 | a0005 | c0009 | t0001 | g0222 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01192 | hp1 | a0001 | c0010 | t0001 | g0001 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01192 | hp2 | a0002 | c0004 | t0001 | g0155 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01255 | hp2 | a0014 | c0024 | t0001 | g0269 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01256 | hp1 | a0008 | c0013 | t0001 | g0320 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01256 | hp2 | a0001 | c0005 | t0001 | g0281 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01257 | hp1 | a0002 | c0027 | t0001 | g0188 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01257 | hp2 | a0001 | c0005 | t0001 | g0220 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01258 | hp1 | a0002 | c0027 | t0001 | g0189 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01258 | hp2 | a0001 | c0005 | t0001 | g0263 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01261 | hp1 | a0004 | c0006 | t0001 | g0310 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01261 | hp2 | a0005 | c0009 | t0001 | g0273 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01346 | hp1 | a0003 | c0002 | t0001 | g0215 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01346 | hp2 | a0014 | c0024 | t0001 | g0270 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01358 | hp1 | a0008 | c0013 | t0001 | g0347 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01358 | hp2 | a0007 | c0011 | t0001 | g0289 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01361 | hp1 | a0004 | c0012 | t0002 | g0301 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01361 | hp2 | a0003 | c0002 | t0001 | g0018 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01433 | hp1 | a0008 | c0052 | t0001 | g0306 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01496 | hp1 | a0002 | c0003 | t0001 | g0118 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01496 | hp2 | a0002 | c0048 | t0002 | g0040 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01516 | hp2 | a0005 | c0009 | t0001 | g0282 | EUR | IBS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01517 | hp1 | a0005 | c0009 | t0001 | g0225 | EUR | IBS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01891 | hp1 | a0023 | c0049 | t0001 | g0090 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01891 | hp2 | a0004 | c0006 | t0001 | g0309 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01928 | hp1 | a0002 | c0003 | t0001 | g0057 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01928 | hp2 | a0005 | c0021 | t0001 | g0218 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01952 | hp1 | a0012 | c0018 | t0001 | g0004 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01952 | hp2 | a0003 | c0002 | t0001 | g0013 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01975 | hp1 | a0002 | c0003 | t0001 | g0117 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01978 | hp1 | a0024 | c0067 | t0002 | g0305 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01978 | hp2 | a0003 | c0002 | t0001 | g0217 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01981 | hp1 | a0002 | c0004 | t0001 | g0154 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01981 | hp2 | a0002 | c0003 | t0001 | g0054 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01993 | hp1 | a0002 | c0004 | t0001 | g0149 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01993 | hp2 | a0012 | c0018 | t0001 | g0004 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02004 | hp1 | a0002 | c0015 | t0001 | g0127 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02004 | hp2 | a0003 | c0002 | t0001 | g0013 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02056 | hp1 | a0002 | c0004 | t0001 | g0159 | EAS | KHV | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02056 | hp2 | a0001 | c0005 | t0001 | g0177 | EAS | KHV | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02074 | hp1 | a0003 | c0002 | t0001 | g0065 | EAS | KHV | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02074 | hp2 | a0002 | c0004 | t0001 | g0022 | EAS | KHV | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02080 | hp2 | a0002 | c0004 | t0001 | g0103 | EAS | KHV | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02083 | hp2 | a0002 | c0004 | t0001 | g0171 | EAS | KHV | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02132 | hp1 | a0003 | c0002 | t0001 | g0076 | EAS | KHV | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02135 | hp1 | a0003 | c0002 | t0001 | g0085 | EAS | KHV | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02145 | hp1 | a0004 | c0006 | t0001 | g0308 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02148 | hp2 | a0002 | c0003 | t0001 | g0056 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02155 | hp1 | a0002 | c0003 | t0001 | g0161 | EAS | CDX | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02155 | hp2 | a0003 | c0002 | t0001 | g0082 | EAS | CDX | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CDX | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02165 | hp2 | a0002 | c0004 | t0001 | g0170 | EAS | CDX | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02257 | hp1 | a0002 | c0039 | t0001 | g0089 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02257 | hp2 | a0006 | c0008 | t0001 | g0002 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02258 | hp1 | a0004 | c0006 | t0001 | g0317 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02273 | hp1 | a0002 | c0003 | t0001 | g0053 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02273 | hp2 | a0002 | c0003 | t0001 | g0128 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02280 | hp1 | a0013 | c0017 | t0001 | g0008 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02280 | hp2 | a0004 | c0020 | t0001 | g0335 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02293 | hp1 | a0002 | c0003 | t0001 | g0129 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02293 | hp2 | a0002 | c0004 | t0001 | g0169 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02300 | hp2 | a0025 | c0042 | t0001 | g0144 | AMR | PEL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02451 | hp1 | a0004 | c0020 | t0001 | g0336 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02451 | hp2 | a0006 | c0008 | t0001 | g0020 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02572 | hp1 | a0001 | c0005 | t0001 | g0287 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02572 | hp2 | a0001 | c0007 | t0001 | g0200 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02602 | hp2 | a0007 | c0011 | t0001 | g0031 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02615 | hp1 | a0004 | c0053 | t0001 | g0321 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02615 | hp2 | a0002 | c0004 | t0001 | g0042 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02622 | hp1 | a0002 | c0004 | t0001 | g0148 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02622 | hp2 | a0011 | c0016 | t0001 | g0344 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02630 | hp1 | a0004 | c0006 | t0001 | g0311 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02630 | hp2 | a0026 | c0037 | t0001 | g0026 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02647 | hp1 | a0001 | c0005 | t0001 | g0275 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02647 | hp2 | a0004 | c0006 | t0001 | g0312 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02683 | hp1 | a0001 | c0005 | t0001 | g0274 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02683 | hp2 | a0001 | c0007 | t0001 | g0133 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02698 | hp1 | a0005 | c0009 | t0001 | g0015 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02698 | hp2 | a0002 | c0015 | t0001 | g0131 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02717 | hp1 | a0011 | c0016 | t0001 | g0338 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02717 | hp2 | a0006 | c0008 | t0001 | g0342 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02723 | hp1 | a0015 | c0056 | t0001 | g0331 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02723 | hp2 | a0027 | c0059 | t0001 | g0349 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02735 | hp1 | a0002 | c0003 | t0001 | g0094 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02809 | hp2 | a0006 | c0008 | t0001 | g0002 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02818 | hp2 | a0016 | c0069 | t0001 | g0332 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02886 | hp1 | a0009 | c0014 | t0001 | g0292 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02886 | hp2 | a0011 | c0016 | t0001 | g0339 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02895 | hp1 | a0028 | c0029 | t0001 | g0142 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02895 | hp2 | a0002 | c0004 | t0001 | g0151 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02896 | hp1 | a0017 | c0026 | t0001 | g0293 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02896 | hp2 | a0009 | c0014 | t0001 | g0291 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02897 | hp1 | a0002 | c0004 | t0001 | g0152 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02897 | hp2 | a0009 | c0014 | t0001 | g0290 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02922 | hp1 | a0018 | c0028 | t0001 | g0324 | AFR | ESN | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02922 | hp2 | a0004 | c0006 | t0001 | g0313 | AFR | ESN | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02976 | hp1 | a0016 | c0064 | t0001 | g0328 | AFR | ESN | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02976 | hp2 | a0013 | c0017 | t0001 | g0186 | AFR | ESN | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03017 | hp2 | a0003 | c0002 | t0001 | g0277 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03041 | hp2 | a0029 | c0061 | t0001 | g0329 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03098 | hp1 | a0004 | c0006 | t0001 | g0325 | AFR | MSL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03098 | hp2 | a0018 | c0028 | t0001 | g0326 | AFR | MSL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03130 | hp1 | a0002 | c0004 | t0001 | g0043 | AFR | ESN | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03130 | hp2 | a0006 | c0008 | t0001 | g0346 | AFR | ESN | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03139 | hp1 | a0007 | c0011 | t0001 | g0288 | AFR | ESN | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03139 | hp2 | a0006 | c0008 | t0001 | g0323 | AFR | ESN | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03195 | hp1 | a0030 | c0030 | t0001 | g0221 | AFR | ESN | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03195 | hp2 | a0004 | c0006 | t0001 | g0316 | AFR | ESN | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03209 | hp1 | a0031 | c0068 | t0001 | g0334 | AFR | MSL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03225 | hp1 | a0010 | c0019 | t0001 | g0341 | AFR | MSL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03225 | hp2 | a0032 | c0043 | t0001 | g0146 | AFR | MSL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03239 | hp1 | a0001 | c0010 | t0001 | g0032 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03239 | hp2 | a0002 | c0004 | t0001 | g0101 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03486 | hp1 | a0009 | c0014 | t0001 | g0087 | AFR | MSL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03491 | hp1 | a0033 | c0062 | t0002 | g0303 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03491 | hp2 | a0001 | c0033 | t0001 | g0286 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03516 | hp1 | a0013 | c0017 | t0001 | g0008 | AFR | ESN | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03516 | hp2 | a0010 | c0019 | t0001 | g0307 | AFR | ESN | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03540 | hp1 | a0034 | c0057 | t0001 | g0314 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03540 | hp2 | a0001 | c0007 | t0002 | g0204 | AFR | GWD | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03579 | hp1 | a0004 | c0020 | t0001 | g0333 | AFR | MSL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03579 | hp2 | a0006 | c0008 | t0001 | g0002 | AFR | MSL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03654 | hp2 | a0004 | c0012 | t0002 | g0302 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03669 | hp1 | a0001 | c0005 | t0001 | g0246 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03669 | hp2 | a0002 | c0003 | t0001 | g0138 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03688 | hp1 | a0002 | c0015 | t0001 | g0107 | SAS | STU | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | STU | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03704 | hp1 | a0001 | c0007 | t0001 | g0181 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03704 | hp2 | a0002 | c0015 | t0001 | g0106 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03710 | hp1 | a0002 | c0004 | t0001 | g0156 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03710 | hp2 | a0003 | c0002 | t0001 | g0272 | SAS | PJL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03831 | hp1 | a0001 | c0010 | t0001 | g0183 | SAS | BEB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03927 | hp1 | a0001 | c0007 | t0001 | g0278 | SAS | BEB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03927 | hp2 | a0001 | c0023 | t0001 | g0033 | SAS | BEB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG04184 | hp1 | a0001 | c0023 | t0001 | g0039 | SAS | BEB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG04199 | hp2 | a0002 | c0003 | t0001 | g0187 | SAS | STU | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG04228 | hp1 | a0002 | c0050 | t0001 | g0294 | SAS | STU | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG04228 | hp2 | a0003 | c0002 | t0001 | g0021 | SAS | STU | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18522 | hp1 | a0010 | c0019 | t0001 | g0327 | AFR | YRI | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | YRI | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18906 | hp1 | a0036 | c0066 | t0001 | g0322 | AFR | YRI | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18906 | hp2 | a0002 | c0004 | t0001 | g0147 | AFR | YRI | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18941 | hp1 | a0002 | c0004 | t0001 | g0164 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18944 | hp1 | a0002 | c0003 | t0001 | g0122 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18945 | hp1 | a0003 | c0002 | t0001 | g0048 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18945 | hp2 | a0002 | c0003 | t0001 | g0099 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18946 | hp2 | a0002 | c0003 | t0001 | g0136 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18949 | hp1 | a0002 | c0003 | t0001 | g0095 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18949 | hp2 | a0003 | c0002 | t0001 | g0074 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18950 | hp1 | a0002 | c0003 | t0001 | g0114 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18950 | hp2 | a0003 | c0002 | t0001 | g0214 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18952 | hp1 | a0003 | c0002 | t0001 | g0069 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18952 | hp2 | a0002 | c0003 | t0001 | g0112 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18953 | hp1 | a0002 | c0003 | t0001 | g0160 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18953 | hp2 | a0002 | c0003 | t0001 | g0109 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18954 | hp1 | a0003 | c0002 | t0001 | g0079 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18954 | hp2 | a0002 | c0004 | t0001 | g0121 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18956 | hp1 | a0002 | c0004 | t0001 | g0102 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18956 | hp2 | a0002 | c0025 | t0001 | g0030 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18957 | hp1 | a0002 | c0004 | t0001 | g0185 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18957 | hp2 | a0003 | c0002 | t0001 | g0195 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18959 | hp1 | a0001 | c0010 | t0001 | g0086 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18959 | hp2 | a0003 | c0002 | t0001 | g0049 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18961 | hp1 | a0002 | c0003 | t0001 | g0193 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18963 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18965 | hp1 | a0002 | c0041 | t0001 | g0046 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18965 | hp2 | a0002 | c0003 | t0001 | g0123 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18967 | hp1 | a0002 | c0004 | t0001 | g0088 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18967 | hp2 | a0003 | c0002 | t0001 | g0194 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18968 | hp1 | a0003 | c0002 | t0001 | g0006 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18968 | hp2 | a0002 | c0004 | t0001 | g0178 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18969 | hp1 | a0002 | c0003 | t0001 | g0093 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18971 | hp2 | a0003 | c0002 | t0001 | g0184 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18973 | hp1 | a0002 | c0003 | t0001 | g0135 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18975 | hp1 | a0002 | c0003 | t0001 | g0163 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18975 | hp2 | a0007 | c0011 | t0001 | g0036 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18977 | hp2 | a0003 | c0002 | t0001 | g0070 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18978 | hp1 | a0003 | c0002 | t0001 | g0068 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18978 | hp2 | a0002 | c0025 | t0001 | g0028 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18979 | hp1 | a0003 | c0002 | t0001 | g0075 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18980 | hp1 | a0003 | c0002 | t0001 | g0280 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18980 | hp2 | a0002 | c0004 | t0001 | g0104 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18981 | hp1 | a0002 | c0003 | t0001 | g0172 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18982 | hp1 | a0003 | c0002 | t0001 | g0006 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18983 | hp1 | a0002 | c0004 | t0001 | g0158 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18983 | hp2 | a0002 | c0003 | t0001 | g0115 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18985 | hp1 | a0002 | c0004 | t0001 | g0150 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18985 | hp2 | a0002 | c0003 | t0001 | g0192 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18986 | hp1 | a0002 | c0004 | t0001 | g0179 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18986 | hp2 | a0003 | c0002 | t0001 | g0230 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18988 | hp1 | a0002 | c0003 | t0001 | g0124 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18988 | hp2 | a0002 | c0004 | t0001 | g0166 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18989 | hp2 | a0001 | c0007 | t0001 | g0084 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18990 | hp1 | a0003 | c0002 | t0001 | g0052 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18990 | hp2 | a0001 | c0005 | t0001 | g0236 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18994 | hp1 | a0003 | c0002 | t0001 | g0072 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18994 | hp2 | a0002 | c0004 | t0001 | g0105 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18998 | hp1 | a0002 | c0004 | t0001 | g0134 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18998 | hp2 | a0001 | c0005 | t0001 | g0237 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19001 | hp2 | a0002 | c0003 | t0001 | g0191 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19004 | hp1 | a0001 | c0007 | t0001 | g0243 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19004 | hp2 | a0002 | c0004 | t0001 | g0167 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19005 | hp1 | a0003 | c0002 | t0001 | g0213 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19007 | hp1 | a0003 | c0002 | t0001 | g0231 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19007 | hp2 | a0003 | c0002 | t0001 | g0080 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19009 | hp1 | a0003 | c0036 | t0001 | g0176 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19009 | hp2 | a0002 | c0004 | t0001 | g0139 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19010 | hp1 | a0003 | c0002 | t0001 | g0229 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19010 | hp2 | a0007 | c0011 | t0001 | g0047 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19030 | hp1 | a0001 | c0022 | t0001 | g0029 | AFR | LWK | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19030 | hp2 | a0011 | c0016 | t0001 | g0340 | AFR | LWK | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19043 | hp1 | a0015 | c0058 | t0001 | g0330 | AFR | LWK | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19043 | hp2 | a0037 | c0054 | t0001 | g0315 | AFR | LWK | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19055 | hp1 | a0002 | c0003 | t0001 | g0137 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19056 | hp1 | a0002 | c0004 | t0001 | g0143 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19057 | hp1 | a0003 | c0002 | t0001 | g0228 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19057 | hp2 | a0001 | c0010 | t0001 | g0145 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19058 | hp1 | a0038 | c0034 | t0001 | g0066 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19058 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19060 | hp1 | a0002 | c0004 | t0001 | g0174 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19063 | hp1 | a0003 | c0035 | t0001 | g0232 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19063 | hp2 | a0002 | c0003 | t0001 | g0190 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19064 | hp1 | a0002 | c0003 | t0001 | g0100 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19066 | hp2 | a0003 | c0002 | t0001 | g0071 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19067 | hp1 | a0009 | c0038 | t0001 | g0035 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19067 | hp2 | a0002 | c0004 | t0001 | g0132 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19068 | hp1 | a0001 | c0005 | t0001 | g0244 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19068 | hp2 | a0002 | c0044 | t0001 | g0157 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19070 | hp2 | a0003 | c0002 | t0001 | g0083 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19077 | hp1 | a0002 | c0003 | t0001 | g0111 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19077 | hp2 | a0002 | c0003 | t0001 | g0108 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19079 | hp1 | a0007 | c0051 | t0001 | g0295 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19079 | hp2 | a0002 | c0003 | t0001 | g0110 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19081 | hp1 | a0003 | c0002 | t0001 | g0051 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19081 | hp2 | a0002 | c0003 | t0001 | g0173 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19084 | hp1 | a0002 | c0004 | t0001 | g0165 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19086 | hp1 | a0003 | c0002 | t0001 | g0073 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19087 | hp1 | a0002 | c0004 | t0001 | g0153 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19087 | hp2 | a0001 | c0005 | t0001 | g0064 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19088 | hp2 | a0003 | c0002 | t0001 | g0050 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19089 | hp1 | a0002 | c0003 | t0001 | g0113 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19091 | hp1 | a0002 | c0004 | t0001 | g0120 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19091 | hp2 | a0007 | c0011 | t0001 | g0027 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19240 | hp1 | a0004 | c0055 | t0001 | g0296 | AFR | YRI | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA19240 | hp2 | a0006 | c0008 | t0001 | g0345 | AFR | YRI | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA20752 | hp1 | a0003 | c0002 | t0001 | g0018 | EUR | TSI | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | TSI | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA20905 | hp1 | a0001 | c0032 | t0001 | g0279 | SAS | GIH | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | GIH | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01123 | hp1 | a0003 | c0002 | t0001 | g0216 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG01123 | hp2 | a0002 | c0003 | t0001 | g0119 | AMR | CLM | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02109 | hp1 | a0001 | c0007 | t0001 | g0092 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02109 | hp2 | a0004 | c0012 | t0002 | g0300 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02559 | hp1 | a0006 | c0008 | t0001 | g0020 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG02559 | hp2 | a0001 | c0007 | t0001 | g0201 | AFR | ACB | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03471 | hp1 | a0001 | c0005 | t0001 | g0175 | AFR | MSL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG03471 | hp2 | a0008 | c0013 | t0001 | g0348 | AFR | MSL | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG06807 | hp1 | a0017 | c0026 | t0001 | g0037 | AFR | USA | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
HG06807 | hp2 | a0035 | c0047 | t0001 | g0044 | AFR | USA | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA18955 | hp2 | a0003 | c0002 | t0001 | g0067 | EAS | JPT | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | USA | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA20300 | hp2 | a0002 | c0004 | t0001 | g0041 | AFR | USA | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA21309 | hp1 | a0001 | c0022 | t0001 | g0091 | AFR | LWK | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
NA21309 | hp2 | a0004 | c0006 | t0002 | g0350 | AFR | LWK | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0235 | REF | REF | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
homoSapiens | grch38p0 | a0010 | c0065 | t0001 | g0337 | REF | REF | NID2_chr14_51999809_52074059 | NID2 | chr14 | 51999809 | 52074059 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:52005823 | T | C | 1 | a0038 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.4031A>G | p.His1344Arg | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 21/22 | 4096/4870 | 4031/4128 | 1344/1375 | chr14 | 52005823 | |||
chr14:52011008 | C | T | 1 | a0021 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.3590G>A | p.Arg1197His | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/22 | 3655/4870 | 3590/4128 | 1197/1375 | chr14 | 52011008 | |||
chr14:52011639 | C | A | 2 | a0028 a0031 |
2 | HG02895.hp1 HG03209.hp1 |
missense_variant | MODERATE | c.3465G>T | p.Met1155Ile | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 17/22 | 3530/4870 | 3465/4128 | 1155/1375 | chr14 | 52011639 | |||
chr14:52011650 | G | A | 1 | a0029 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.3454C>T | p.Arg1152Trp | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 17/22 | 3519/4870 | 3454/4128 | 1152/1375 | chr14 | 52011650 | |||
chr14:52015056 | G | A | 1 | a0033 | 1 | HG03491.hp1 | missense_variant&splice_region_variant | MODERATE | c.3248C>T | p.Ala1083Val | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 15/22 | 3313/4870 | 3248/4128 | 1083/1375 | chr14 | 52015056 | |||
chr14:52015200 | C | G | 1 | a0020 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.3104G>C | p.Arg1035Pro | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 15/22 | 3169/4870 | 3104/4128 | 1035/1375 | chr14 | 52015200 | |||
chr14:52019281 | G | C | 1 | a0026 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.2808C>G | p.Ser936Arg | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/22 | 2873/4870 | 2808/4128 | 936/1375 | chr14 | 52019281 | |||
chr14:52027278 | C | T | 2 | a0011 a0036 |
5 | HG02622.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
missense_variant | MODERATE | c.2597G>A | p.Arg866Gln | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/22 | 2662/4870 | 2597/4128 | 866/1375 | chr14 | 52027278 | |||
chr14:52028741 | A | T | 1 | a0027 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.2511T>A | p.Asp837Glu | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/22 | 2576/4870 | 2511/4128 | 837/1375 | chr14 | 52028741 | |||
chr14:52028763 | C | T | 1 | a0007 | 8 | HG00438.hp2 HG01358.hp2 HG02602.hp2 others(5): Show |
missense_variant | MODERATE | c.2489G>A | p.Arg830Gln | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/22 | 2554/4870 | 2489/4128 | 830/1375 | chr14 | 52028763 | |||
chr14:52029569 | C | A | 1 | a0016 | 2 | HG02818.hp2 HG02976.hp1 |
missense_variant | MODERATE | c.2379G>T | p.Gln793His | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 10/22 | 2444/4870 | 2379/4128 | 793/1375 | chr14 | 52029569 | |||
chr14:52029624 | C | T | 1 | a0023 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.2324G>A | p.Arg775Gln | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 10/22 | 2389/4870 | 2324/4128 | 775/1375 | chr14 | 52029624 | |||
chr14:52029655 | C | T | 1 | a0037 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.2293G>A | p.Asp765Asn | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 10/22 | 2358/4870 | 2293/4128 | 765/1375 | chr14 | 52029655 | |||
chr14:52029669 | C | A | 26 | a0001 a0002 a0003 others(23): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
missense_variant | MODERATE | c.2279G>T | p.Gly760Val | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 10/22 | 2344/4870 | 2279/4128 | 760/1375 | chr14 | 52029669 | |||
chr14:52029672 | G | A | 1 | a0015 | 2 | HG02723.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.2276C>T | p.Pro759Leu | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 10/22 | 2341/4870 | 2276/4128 | 759/1375 | chr14 | 52029672 | |||
chr14:52038828 | C | T | 1 | a0019 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.2176G>A | p.Val726Met | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/22 | 2241/4870 | 2176/4128 | 726/1375 | chr14 | 52038828 | |||
chr14:52040711 | A | G | 30 | a0001 a0002 a0004 others(27): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
missense_variant | MODERATE | c.1966T>C | p.Ser656Pro | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/22 | 2031/4870 | 1966/4128 | 656/1375 | chr14 | 52040711 | |||
chr14:52040783 | T | C | 2 | a0016 a0032 |
3 | HG02818.hp2 HG02976.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.1894A>G | p.Thr632Ala | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/22 | 1959/4870 | 1894/4128 | 632/1375 | chr14 | 52040783 | |||
chr14:52040794 | C | T | 2 | a0015 a0034 |
3 | HG02723.hp1 HG03540.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.1883G>A | p.Arg628His | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/22 | 1948/4870 | 1883/4128 | 628/1375 | chr14 | 52040794 | |||
chr14:52042124 | C | A | 3 | a0008 a0021 a0022 |
8 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(5): Show |
missense_variant | MODERATE | c.1806G>T | p.Glu602Asp | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 7/22 | 1871/4870 | 1806/4128 | 602/1375 | chr14 | 52042124 | |||
chr14:52042345 | G | A | 1 | a0014 | 2 | HG01255.hp2 HG01346.hp2 |
missense_variant | MODERATE | c.1585C>T | p.Pro529Ser | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 7/22 | 1650/4870 | 1585/4128 | 529/1375 | chr14 | 52042345 | |||
chr14:52053650 | C | T | 15 | a0001 a0003 a0005 others(12): Show |
206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
missense_variant | MODERATE | c.1358G>A | p.Gly453Asp | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/22 | 1423/4870 | 1358/4128 | 453/1375 | chr14 | 52053650 | |||
chr14:52054028 | G | T | 1 | a0005 | 10 | HG00639.hp2 HG00741.hp2 HG01069.hp1 others(7): Show |
missense_variant | MODERATE | c.1061C>A | p.Pro354His | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 4/22 | 1126/4870 | 1061/4128 | 354/1375 | chr14 | 52054028 | |||
chr14:52054041 | C | T | 1 | a0030 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.1048G>A | p.Val350Met | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 4/22 | 1113/4870 | 1048/4128 | 350/1375 | chr14 | 52054041 | |||
chr14:52054151 | T | C | 2 | a0013 a0036 |
4 | HG02280.hp1 HG02976.hp2 HG03516.hp1 others(1): Show |
missense_variant | MODERATE | c.938A>G | p.Asp313Gly | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 4/22 | 1003/4870 | 938/4128 | 313/1375 | chr14 | 52054151 | |||
chr14:52060173 | G | A | 1 | a0024 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.718C>T | p.Pro240Ser | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/22 | 783/4870 | 718/4128 | 240/1375 | chr14 | 52060173 | |||
chr14:52060287 | T | C | 1 | a0012 | 3 | HG01099.hp1 HG01952.hp1 HG01993.hp2 |
missense_variant | MODERATE | c.604A>G | p.Asn202Asp | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/22 | 669/4870 | 604/4128 | 202/1375 | chr14 | 52060287 | |||
chr14:52068930 | G | T | 21 | a0001 a0002 a0003 others(18): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
missense_variant | MODERATE | c.65C>A | p.Pro22Gln | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 1/22 | 130/4870 | 65/4128 | 22/1375 | chr14 | 52068930 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:52011597 | A | G | 58 | a0001c0005 a0001c0007 a0001c0010 others(55): Show |
267 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(264): Show |
synonymous_variant | LOW | c.3507T>C | p.Ala1169Ala | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 17/22 | 3572/4870 | 3507/4128 | 1169/1375 | chr14 | 52011597 | |||
chr14:52015142 | G | A | 1 | a0001c0023 | 2 | HG03927.hp2 HG04184.hp1 |
synonymous_variant | LOW | c.3162C>T | p.Cys1054Cys | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 15/22 | 3227/4870 | 3162/4128 | 1054/1375 | chr14 | 52015142 | |||
chr14:52015181 | G | T | 2 | a0002c0039 a0004c0055 |
2 | HG02257.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.3123C>A | p.Pro1041Pro | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 15/22 | 3188/4870 | 3123/4128 | 1041/1375 | chr14 | 52015181 | |||
chr14:52015199 | C | T | 24 | a0001c0007 a0001c0022 a0001c0032 others(21): Show |
198 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(195): Show |
synonymous_variant | LOW | c.3105G>A | p.Arg1035Arg | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 15/22 | 3170/4870 | 3105/4128 | 1035/1375 | chr14 | 52015199 | |||
chr14:52020132 | G | A | 3 | a0009c0014 a0011c0016 a0036c0066 |
9 | HG02622.hp2 HG02717.hp1 HG02886.hp1 others(6): Show |
synonymous_variant | LOW | c.2721C>T | p.Cys907Cys | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 13/22 | 2786/4870 | 2721/4128 | 907/1375 | chr14 | 52020132 | |||
chr14:52029557 | C | A | 3 | a0004c0012 a0024c0067 a0033c0062 |
7 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(4): Show |
synonymous_variant | LOW | c.2391G>T | p.Arg797Arg | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 10/22 | 2456/4870 | 2391/4128 | 797/1375 | chr14 | 52029557 | |||
chr14:52029665 | A | G | 3 | a0016c0064 a0016c0069 a0032c0043 |
3 | HG02818.hp2 HG02976.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.2283T>C | p.Asn761Asn | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 10/22 | 2348/4870 | 2283/4128 | 761/1375 | chr14 | 52029665 | |||
chr14:52029689 | C | T | 48 | a0001c0001 a0001c0005 a0001c0007 others(45): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
splice_region_variant&synonymous_variant | LOW | c.2259G>A | p.Glu753Glu | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 10/22 | 2324/4870 | 2259/4128 | 753/1375 | chr14 | 52029689 | |||
chr14:52038799 | G | A | 6 | a0001c0032 a0002c0003 a0002c0015 others(3): Show |
54 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(51): Show |
synonymous_variant | LOW | c.2205C>T | p.Asp735Asp | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/22 | 2270/4870 | 2205/4128 | 735/1375 | chr14 | 52038799 | |||
chr14:52038871 | G | A | 8 | a0001c0010 a0001c0022 a0001c0023 others(5): Show |
23 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(20): Show |
synonymous_variant | LOW | c.2133C>T | p.His711His | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/22 | 2198/4870 | 2133/4128 | 711/1375 | chr14 | 52038871 | |||
chr14:52038976 | A | G | 1 | a0015c0056 | 1 | HG02723.hp1 | splice_region_variant&synonymous_variant | LOW | c.2028T>C | p.Thr676Thr | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/22 | 2093/4870 | 2028/4128 | 676/1375 | chr14 | 52038976 | |||
chr14:52042783 | T | C | 28 | a0002c0003 a0002c0004 a0002c0015 others(25): Show |
146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
splice_region_variant&synonymous_variant | LOW | c.1578A>G | p.Glu526Glu | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 6/22 | 1643/4870 | 1578/4128 | 526/1375 | chr14 | 52042783 | |||
chr14:52054093 | T | C | 2 | a0016c0064 a0016c0069 |
2 | HG02818.hp2 HG02976.hp1 |
synonymous_variant | LOW | c.996A>G | p.Pro332Pro | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 4/22 | 1061/4870 | 996/4128 | 332/1375 | chr14 | 52054093 | |||
chr14:52054135 | A | G | 65 | a0001c0001 a0001c0005 a0001c0007 others(62): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
synonymous_variant | LOW | c.954T>C | p.Tyr318Tyr | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 4/22 | 1019/4870 | 954/4128 | 318/1375 | chr14 | 52054135 | |||
chr14:52054285 | G | A | 2 | a0002c0048 a0023c0049 |
2 | HG01496.hp2 HG01891.hp1 |
synonymous_variant | LOW | c.804C>T | p.Phe268Phe | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 4/22 | 869/4870 | 804/4128 | 268/1375 | chr14 | 52054285 | |||
chr14:52060231 | C | T | 3 | a0004c0053 a0028c0029 a0031c0068 |
3 | HG02615.hp1 HG02895.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.660G>A | p.Gln220Gln | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/22 | 725/4870 | 660/4128 | 220/1375 | chr14 | 52060231 | |||
chr14:52067873 | C | G | 1 | a0008c0052 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.519G>C | p.Ala173Ala | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/22 | 584/4870 | 519/4128 | 173/1375 | chr14 | 52067873 | |||
chr14:52068047 | C | A | 1 | a0002c0050 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.345G>T | p.Thr115Thr | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/22 | 410/4870 | 345/4128 | 115/1375 | chr14 | 52068047 | |||
chr14:52068092 | G | A | 3 | a0004c0020 a0016c0069 a0031c0068 |
5 | HG02280.hp2 HG02451.hp1 HG02818.hp2 others(2): Show |
synonymous_variant | LOW | c.300C>T | p.Pro100Pro | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/22 | 365/4870 | 300/4128 | 100/1375 | chr14 | 52068092 | |||
chr14:52068116 | C | A | 1 | a0007c0051 | 1 | NA19079.hp1 | synonymous_variant | LOW | c.276G>T | p.Thr92Thr | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/22 | 341/4870 | 276/4128 | 92/1375 | chr14 | 52068116 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:52005219 | T | A | 6 | a0001c0007t0002 a0002c0048t0002 a0004c0006t0002 others(3): Show |
10 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*267A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 22/22 | 267 | chr14 | 52005219 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:52005902 | AAGTC | A | 158 | a0001c0001t0001g0078 a0001c0001t0001g0254 a0001c0005t0001g0175 others(155): Show |
159 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.4005-57_4005-54del others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 20/21 | chr14 | 52005902 | |||||||
chr14:52006030 | AGCT | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
5 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.4005-184_4005-182d others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 20/21 | chr14 | 52006030 | |||||||
chr14:52006150 | C | T | 25 | a0001c0005t0001g0175 a0001c0005t0001g0246 a0002c0027t0001g0188 others(22): Show |
25 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.4005-301G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 20/21 | chr14 | 52006150 | |||||||
chr14:52006155 | C | T | 1 | a0008c0013t0001g0348 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4005-306G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 20/21 | chr14 | 52006155 | |||||||
chr14:52006207 | G | A | 1 | a0007c0011t0001g0288 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4004+330C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 20/21 | chr14 | 52006207 | |||||||
chr14:52006400 | G | A | 1 | a0005c0021t0001g0283 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.4004+137C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 20/21 | chr14 | 52006400 | |||||||
chr14:52006468 | G | T | 11 | a0001c0007t0001g0200 a0004c0006t0001g0308 a0004c0006t0001g0309 others(8): Show |
11 | HG01261.hp1 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.4004+69C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 20/21 | chr14 | 52006468 | |||||||
chr14:52006715 | A | G | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3881-55T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 19/21 | chr14 | 52006715 | |||||||
chr14:52006815 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3881-155T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 19/21 | chr14 | 52006815 | |||||||
chr14:52007011 | A | G | 60 | a0001c0001t0001g0024 a0001c0005t0001g0220 a0001c0007t0002g0204 others(57): Show |
64 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.3881-351T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 19/21 | chr14 | 52007011 | |||||||
chr14:52007020 | G | A | 1 | a0018c0028t0001g0324 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3881-360C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 19/21 | chr14 | 52007020 | |||||||
chr14:52007106 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0262 a0001c0005t0001g0263 others(1): Show |
5 | HG00099.hp1 HG00735.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.3881-446G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 19/21 | chr14 | 52007106 | |||||||
chr14:52007388 | T | A | 1 | a0001c0010t0001g0034 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3880+422A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 19/21 | chr14 | 52007388 | |||||||
chr14:52007496 | C | T | 1 | a0007c0011t0001g0288 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3880+314G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 19/21 | chr14 | 52007496 | |||||||
chr14:52007497 | G | A | 113 | a0001c0007t0001g0084 a0001c0007t0001g0133 a0001c0007t0001g0181 others(110): Show |
114 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.3880+313C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 19/21 | chr14 | 52007497 | |||||||
chr14:52007518 | A | G | 1 | a0026c0037t0001g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3880+292T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 19/21 | chr14 | 52007518 | |||||||
chr14:52007739 | A | T | 2 | a0016c0064t0001g0328 a0016c0069t0001g0332 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3880+71T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 19/21 | chr14 | 52007739 | |||||||
chr14:52007999 | T | G | 1 | a0010c0019t0001g0327 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3723-32A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52007999 | |||||||
chr14:52008003 | C | T | 174 | a0001c0007t0001g0084 a0001c0007t0001g0133 a0001c0007t0001g0181 others(171): Show |
179 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.3723-36G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52008003 | |||||||
chr14:52008100 | TTAG | T | 116 | a0001c0007t0001g0084 a0001c0007t0001g0133 a0001c0007t0001g0181 others(113): Show |
117 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.3723-136_3723-134d others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52008100 | |||||||
chr14:52008119 | T | G | 9 | a0007c0011t0001g0027 a0007c0011t0001g0031 a0007c0011t0001g0036 others(6): Show |
9 | HG00438.hp2 HG01358.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.3723-152A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52008119 | |||||||
chr14:52008125 | G | A | 3 | a0001c0001t0001g0233 a0001c0001t0001g0245 a0002c0015t0001g0127 |
3 | HG02004.hp1 HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.3723-158C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52008125 | |||||||
chr14:52008162 | G | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0207 |
3 | HG01167.hp2 HG01169.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.3723-195C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52008162 | |||||||
chr14:52008163 | A | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0207 |
3 | HG01167.hp2 HG01169.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.3723-196T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52008163 | |||||||
chr14:52008336 | A | G | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3723-369T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52008336 | |||||||
chr14:52008357 | C | T | 2 | a0001c0007t0001g0181 a0004c0006t0001g0297 |
2 | HG00099.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.3723-390G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52008357 | |||||||
chr14:52008376 | A | T | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3723-409T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52008376 | |||||||
chr14:52008436 | C | T | 1 | a0026c0037t0001g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3723-469G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52008436 | |||||||
chr14:52008680 | G | A | 1 | a0032c0043t0001g0146 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3723-713C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52008680 | |||||||
chr14:52008695 | G | A | 1 | a0003c0002t0001g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3723-728C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52008695 | |||||||
chr14:52008749 | C | T | 1 | a0001c0001t0001g0003 | 2 | NA18963.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.3723-782G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52008749 | |||||||
chr14:52008918 | TATATTC | T | 3 | a0007c0011t0001g0027 a0007c0011t0001g0036 a0007c0011t0001g0047 |
3 | NA18975.hp2 NA19010.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3723-957_3723-952d others(8): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52008918 | |||||||
chr14:52008946 | A | T | 1 | a0002c0003t0001g0138 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3723-979T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52008946 | |||||||
chr14:52008996 | C | A | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3723-1029G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52008996 | |||||||
chr14:52008997 | G | A | 1 | a0021c0063t0001g0343 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3723-1030C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52008997 | |||||||
chr14:52009054 | A | G | 1 | a0001c0033t0001g0286 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3723-1087T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009054 | |||||||
chr14:52009055 | T | C | 1 | a0014c0024t0001g0269 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3723-1088A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009055 | |||||||
chr14:52009154 | C | T | 1 | a0005c0009t0001g0225 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3723-1187G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009154 | |||||||
chr14:52009205 | A | G | 1 | a0004c0006t0002g0350 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3723-1238T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009205 | |||||||
chr14:52009261 | C | G | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3723-1294G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009261 | |||||||
chr14:52009297 | A | G | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3723-1330T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009297 | |||||||
chr14:52009394 | A | G | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3723-1427T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009394 | |||||||
chr14:52009483 | A | G | 1 | a0001c0007t0001g0201 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3722+1393T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009483 | |||||||
chr14:52009489 | T | G | 2 | a0002c0027t0001g0188 a0002c0027t0001g0189 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3722+1387A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009489 | |||||||
chr14:52009491 | C | T | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3722+1385G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009491 | |||||||
chr14:52009492 | A | G | 1 | a0001c0001t0001g0003 | 2 | NA18963.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.3722+1384T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009492 | |||||||
chr14:52009591 | G | T | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3722+1285C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009591 | |||||||
chr14:52009651 | T | A | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3722+1225A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009651 | |||||||
chr14:52009722 | G | A | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3722+1154C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009722 | |||||||
chr14:52009781 | G | A | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3722+1095C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009781 | |||||||
chr14:52009820 | C | T | 1 | a0026c0037t0001g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3722+1056G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009820 | |||||||
chr14:52009821 | G | T | 47 | a0002c0003t0001g0123 a0003c0002t0001g0006 a0003c0002t0001g0013 others(44): Show |
51 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.3722+1055C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009821 | |||||||
chr14:52009867 | G | A | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3722+1009C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009867 | |||||||
chr14:52009923 | G | C | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3722+953C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009923 | |||||||
chr14:52009940 | CTG | C | 12 | a0009c0014t0001g0087 a0009c0014t0001g0290 a0009c0014t0001g0291 others(9): Show |
12 | HG01891.hp1 HG02622.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.3722+934_3722+935d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52009940 | |||||||
chr14:52010020 | C | T | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3722+856G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52010020 | |||||||
chr14:52010024 | A | T | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3722+852T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52010024 | |||||||
chr14:52010206 | A | G | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3722+670T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52010206 | |||||||
chr14:52010239 | G | A | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3722+637C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52010239 | |||||||
chr14:52010261 | G | A | 1 | a0037c0054t0001g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3722+615C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52010261 | |||||||
chr14:52010341 | A | G | 15 | a0001c0005t0001g0175 a0001c0005t0001g0246 a0002c0027t0001g0188 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.3722+535T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52010341 | |||||||
chr14:52010349 | C | T | 1 | a0014c0024t0001g0269 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3722+527G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52010349 | |||||||
chr14:52010407 | AT | A | 10 | a0009c0014t0001g0087 a0009c0014t0001g0290 a0009c0014t0001g0291 others(7): Show |
10 | HG01074.hp1 HG02622.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.3722+468delA | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52010407 | |||||||
chr14:52010488 | C | T | 118 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0078 others(115): Show |
119 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.3722+388G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52010488 | |||||||
chr14:52010584 | T | C | 6 | a0002c0039t0001g0089 a0004c0055t0001g0296 a0010c0019t0001g0307 others(3): Show |
6 | HG02257.hp1 HG03225.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.3722+292A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52010584 | |||||||
chr14:52010759 | A | C | 12 | a0001c0001t0001g0016 a0001c0001t0001g0202 a0001c0001t0001g0234 others(9): Show |
13 | HG00621.hp1 HG02132.hp2 NA18946.hp1 others(10): Show |
intron_variant | MODIFIER | c.3722+117T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52010759 | |||||||
chr14:52010833 | C | T | 1 | a0003c0002t0001g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3722+43G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 18/21 | chr14 | 52010833 | |||||||
chr14:52011064 | G | T | 21 | a0002c0039t0001g0089 a0004c0055t0001g0296 a0007c0011t0001g0031 others(18): Show |
21 | HG01358.hp2 HG02257.hp1 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.3551-17C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 17/21 | chr14 | 52011064 | |||||||
chr14:52011117 | G | A | 128 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(125): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.3551-70C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 17/21 | chr14 | 52011117 | |||||||
chr14:52011144 | G | C | 3 | a0023c0049t0001g0090 a0028c0029t0001g0142 a0031c0068t0001g0334 |
3 | HG01891.hp1 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3551-97C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 17/21 | chr14 | 52011144 | |||||||
chr14:52011149 | G | A | 127 | a0001c0001t0001g0009 a0001c0001t0001g0140 a0001c0001t0001g0211 others(124): Show |
131 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.3551-102C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 17/21 | chr14 | 52011149 | |||||||
chr14:52011440 | C | G | 1 | a0001c0005t0001g0237 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3550+114G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 17/21 | chr14 | 52011440 | |||||||
chr14:52011491 | T | TAAAGTAG others(320): Show |
1 | a0016c0064t0001g0328 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3550+62_3550+63ins others(327): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 17/21 | chr14 | 52011491 | |||||||
chr14:52011823 | A | G | 50 | a0001c0001t0001g0202 a0001c0001t0001g0264 a0002c0003t0001g0123 others(47): Show |
54 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.3421-140T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52011823 | |||||||
chr14:52011940 | T | C | 18 | a0001c0005t0001g0175 a0001c0005t0001g0246 a0002c0027t0001g0188 others(15): Show |
18 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.3421-257A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52011940 | |||||||
chr14:52011951 | T | G | 47 | a0002c0003t0001g0123 a0003c0002t0001g0006 a0003c0002t0001g0013 others(44): Show |
51 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.3421-268A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52011951 | |||||||
chr14:52011992 | G | C | 1 | a0019c0031t0001g0025 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3421-309C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52011992 | |||||||
chr14:52012040 | A | T | 1 | a0002c0004t0001g0174 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3421-357T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012040 | |||||||
chr14:52012043 | T | TA | 23 | a0001c0001t0001g0140 a0001c0001t0001g0234 a0001c0001t0001g0248 others(20): Show |
24 | HG02080.hp1 HG02109.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.3421-361dupT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012043 | |||||||
chr14:52012043 | T | TAAA | 16 | a0001c0005t0001g0175 a0001c0005t0001g0246 a0002c0027t0001g0188 others(13): Show |
16 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.3421-363_3421-361d others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012043 | |||||||
chr14:52012043 | TA | T | 52 | a0001c0001t0001g0196 a0001c0001t0001g0264 a0002c0003t0001g0123 others(49): Show |
56 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.3421-361delT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012043 | |||||||
chr14:52012044 | A | T | 2 | a0016c0064t0001g0328 a0016c0069t0001g0332 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3421-361T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012044 | |||||||
chr14:52012057 | AATC | A | 7 | a0007c0011t0001g0027 a0007c0011t0001g0031 a0007c0011t0001g0036 others(4): Show |
7 | HG00438.hp2 HG01358.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.3421-377_3421-375d others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012057 | |||||||
chr14:52012117 | A | C | 2 | a0016c0064t0001g0328 a0016c0069t0001g0332 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3421-434T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012117 | |||||||
chr14:52012129 | CTG | C | 3 | a0001c0001t0001g0012 a0002c0039t0001g0089 a0004c0055t0001g0296 |
4 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.3421-448_3421-447d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012129 | |||||||
chr14:52012271 | C | G | 1 | a0002c0003t0001g0093 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3421-588G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012271 | |||||||
chr14:52012359 | G | A | 16 | a0001c0005t0001g0175 a0001c0005t0001g0246 a0002c0027t0001g0188 others(13): Show |
16 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.3421-676C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012359 | |||||||
chr14:52012499 | G | A | 1 | a0002c0015t0001g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3421-816C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012499 | |||||||
chr14:52012546 | C | T | 2 | a0001c0007t0002g0204 a0004c0006t0002g0350 |
2 | HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3421-863G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012546 | |||||||
chr14:52012581 | C | CA | 128 | a0001c0001t0001g0017 a0001c0001t0001g0061 a0001c0001t0001g0062 others(125): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.3421-899dupT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012581 | |||||||
chr14:52012605 | A | G | 2 | a0028c0029t0001g0142 a0031c0068t0001g0334 |
2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3421-922T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012605 | |||||||
chr14:52012658 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3421-975T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012658 | |||||||
chr14:52012677 | TCTC | T | 18 | a0001c0005t0001g0175 a0001c0005t0001g0246 a0002c0027t0001g0188 others(15): Show |
18 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.3421-997_3421-995d others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012677 | |||||||
chr14:52012712 | TA | T | 18 | a0001c0005t0001g0175 a0001c0005t0001g0246 a0002c0027t0001g0188 others(15): Show |
18 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.3421-1030delT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012712 | |||||||
chr14:52012757 | C | T | 1 | a0007c0011t0001g0288 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3421-1074G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012757 | |||||||
chr14:52012760 | C | T | 1 | a0008c0052t0001g0306 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3421-1077G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012760 | |||||||
chr14:52012844 | C | T | 2 | a0002c0004t0001g0149 a0002c0004t0001g0150 |
2 | HG01993.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.3421-1161G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52012844 | |||||||
chr14:52013008 | C | T | 1 | a0002c0003t0001g0108 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3420+1279G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52013008 | |||||||
chr14:52013052 | G | T | 1 | a0002c0003t0001g0187 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3420+1235C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52013052 | |||||||
chr14:52013110 | G | A | 1 | a0001c0007t0001g0181 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3420+1177C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52013110 | |||||||
chr14:52013198 | C | A | 1 | a0026c0037t0001g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3420+1089G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52013198 | |||||||
chr14:52013235 | C | T | 5 | a0011c0016t0001g0338 a0011c0016t0001g0339 a0011c0016t0001g0340 others(2): Show |
5 | HG02622.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3420+1052G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52013235 | |||||||
chr14:52013257 | C | G | 47 | a0002c0003t0001g0123 a0003c0002t0001g0006 a0003c0002t0001g0013 others(44): Show |
51 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.3420+1030G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52013257 | |||||||
chr14:52013267 | A | G | 1 | a0002c0003t0001g0098 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3420+1020T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52013267 | |||||||
chr14:52013421 | A | C | 2 | a0007c0011t0001g0288 a0007c0011t0001g0289 |
2 | HG01358.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3420+866T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52013421 | |||||||
chr14:52013474 | C | T | 1 | a0021c0063t0001g0343 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3420+813G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52013474 | |||||||
chr14:52013524 | C | T | 210 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0078 others(207): Show |
215 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.3420+763G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52013524 | |||||||
chr14:52013673 | G | A | 1 | a0004c0020t0001g0336 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3420+614C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52013673 | |||||||
chr14:52013793 | G | A | 1 | a0001c0007t0002g0204 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3420+494C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52013793 | |||||||
chr14:52013806 | A | T | 1 | a0026c0037t0001g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3420+481T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52013806 | |||||||
chr14:52013879 | C | T | 186 | a0001c0007t0001g0084 a0001c0007t0001g0092 a0001c0007t0001g0133 others(183): Show |
192 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.3420+408G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52013879 | |||||||
chr14:52013903 | A | G | 89 | a0001c0005t0001g0175 a0001c0005t0001g0246 a0001c0007t0001g0092 others(86): Show |
94 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.3420+384T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52013903 | |||||||
chr14:52013927 | A | C | 1 | a0003c0002t0001g0230 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3420+360T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52013927 | |||||||
chr14:52014034 | A | G | 27 | a0001c0005t0001g0175 a0001c0005t0001g0246 a0002c0027t0001g0188 others(24): Show |
27 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.3420+253T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52014034 | |||||||
chr14:52014107 | C | G | 1 | a0031c0068t0001g0334 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3420+180G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52014107 | |||||||
chr14:52014157 | G | A | 45 | a0001c0007t0001g0084 a0001c0007t0001g0133 a0001c0007t0001g0201 others(42): Show |
45 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.3420+130C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52014157 | |||||||
chr14:52014196 | A | C | 1 | a0026c0037t0001g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3420+91T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52014196 | |||||||
chr14:52014247 | G | A | 7 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(4): Show |
7 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.3420+40C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52014247 | |||||||
chr14:52014252 | G | A | 1 | a0032c0043t0001g0146 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3420+35C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 16/21 | chr14 | 52014252 | |||||||
chr14:52014806 | G | T | 53 | a0001c0007t0001g0092 a0001c0022t0001g0029 a0001c0022t0001g0091 others(50): Show |
58 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.3250+248C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 15/21 | chr14 | 52014806 | |||||||
chr14:52014861 | T | C | 9 | a0009c0014t0001g0087 a0009c0014t0001g0290 a0009c0014t0001g0291 others(6): Show |
9 | HG02622.hp2 HG02717.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.3250+193A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 15/21 | chr14 | 52014861 | |||||||
chr14:52014998 | T | A | 1 | a0003c0002t0001g0214 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3250+56A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 15/21 | chr14 | 52014998 | |||||||
chr14:52015280 | G | A | 1 | a0001c0010t0001g0001 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp1 |
splice_region_variant&intron_variant | LOW | c.3029-5C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52015280 | |||||||
chr14:52015443 | A | C | 1 | a0031c0068t0001g0334 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3029-168T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52015443 | |||||||
chr14:52015458 | A | G | 1 | a0002c0004t0001g0143 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3029-183T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52015458 | |||||||
chr14:52015518 | G | A | 15 | a0001c0005t0001g0175 a0002c0027t0001g0188 a0002c0027t0001g0189 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.3029-243C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52015518 | |||||||
chr14:52015556 | C | G | 15 | a0001c0005t0001g0175 a0002c0027t0001g0188 a0002c0027t0001g0189 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.3029-281G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52015556 | |||||||
chr14:52015645 | C | T | 1 | a0002c0004t0001g0139 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3029-370G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52015645 | |||||||
chr14:52015696 | C | T | 4 | a0009c0014t0001g0087 a0009c0014t0001g0290 a0009c0014t0001g0291 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3029-421G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52015696 | |||||||
chr14:52015730 | C | T | 1 | a0005c0009t0001g0273 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3029-455G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52015730 | |||||||
chr14:52015831 | C | T | 4 | a0002c0004t0001g0154 a0002c0004t0001g0155 a0002c0004t0001g0156 others(1): Show |
4 | HG01069.hp1 HG01192.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.3029-556G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52015831 | |||||||
chr14:52015980 | G | A | 15 | a0001c0005t0001g0175 a0002c0027t0001g0188 a0002c0027t0001g0189 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.3029-705C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52015980 | |||||||
chr14:52015998 | G | A | 6 | a0001c0007t0001g0084 a0001c0007t0001g0243 a0002c0004t0001g0102 others(3): Show |
6 | NA18954.hp2 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.3029-723C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52015998 | |||||||
chr14:52016035 | G | A | 1 | a0026c0037t0001g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3029-760C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52016035 | |||||||
chr14:52016050 | C | T | 223 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0078 others(220): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.3029-775G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52016050 | |||||||
chr14:52016316 | C | T | 15 | a0001c0005t0001g0175 a0002c0027t0001g0188 a0002c0027t0001g0189 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.3029-1041G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52016316 | |||||||
chr14:52016685 | T | C | 188 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0078 others(185): Show |
194 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.3029-1410A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52016685 | |||||||
chr14:52016737 | A | G | 61 | a0001c0005t0001g0287 a0001c0007t0001g0092 a0001c0022t0001g0029 others(58): Show |
66 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.3029-1462T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52016737 | |||||||
chr14:52016799 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0060 |
3 | NA18969.hp2 NA19055.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.3029-1524T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52016799 | |||||||
chr14:52016884 | G | T | 1 | a0018c0028t0001g0324 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3029-1609C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52016884 | |||||||
chr14:52016981 | G | A | 15 | a0001c0005t0001g0175 a0002c0027t0001g0188 a0002c0027t0001g0189 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.3029-1706C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52016981 | |||||||
chr14:52017088 | G | A | 4 | a0010c0019t0001g0307 a0010c0019t0001g0327 a0010c0019t0001g0341 others(1): Show |
4 | HG03225.hp1 HG03516.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3029-1813C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52017088 | |||||||
chr14:52017096 | T | C | 15 | a0001c0005t0001g0175 a0002c0027t0001g0188 a0002c0027t0001g0189 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.3029-1821A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52017096 | |||||||
chr14:52017242 | C | T | 1 | a0003c0002t0001g0069 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3028+1819G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52017242 | |||||||
chr14:52017332 | G | A | 2 | a0001c0007t0002g0204 a0004c0006t0002g0350 |
2 | HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3028+1729C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52017332 | |||||||
chr14:52017365 | G | A | 5 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 others(2): Show |
5 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3028+1696C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52017365 | |||||||
chr14:52017523 | C | A | 4 | a0002c0004t0001g0154 a0002c0004t0001g0155 a0002c0004t0001g0156 others(1): Show |
4 | HG01069.hp1 HG01192.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.3028+1538G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52017523 | |||||||
chr14:52017525 | C | G | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3028+1536G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52017525 | |||||||
chr14:52017632 | T | C | 15 | a0001c0005t0001g0175 a0002c0027t0001g0188 a0002c0027t0001g0189 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.3028+1429A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52017632 | |||||||
chr14:52017703 | T | C | 1 | a0001c0001t0001g0241 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3028+1358A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52017703 | |||||||
chr14:52017715 | T | C | 1 | a0001c0001t0001g0254 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3028+1346A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52017715 | |||||||
chr14:52017833 | C | CAA | 15 | a0001c0005t0001g0175 a0002c0027t0001g0188 a0002c0027t0001g0189 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.3028+1226_3028+122 others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52017833 | |||||||
chr14:52017855 | T | G | 9 | a0002c0003t0001g0054 a0002c0003t0001g0056 a0002c0003t0001g0057 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.3028+1206A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52017855 | |||||||
chr14:52017944 | G | A | 2 | a0001c0022t0001g0029 a0001c0022t0001g0091 |
2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3028+1117C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52017944 | |||||||
chr14:52018063 | C | T | 1 | a0002c0004t0001g0143 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3028+998G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52018063 | |||||||
chr14:52018064 | G | A | 1 | a0037c0054t0001g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3028+997C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52018064 | |||||||
chr14:52018092 | C | T | 1 | a0003c0002t0001g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3028+969G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52018092 | |||||||
chr14:52018147 | CTA | C | 1 | a0001c0010t0001g0001 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.3028+912_3028+913d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52018147 | |||||||
chr14:52018287 | C | G | 1 | a0004c0006t0001g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3028+774G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52018287 | |||||||
chr14:52018479 | G | A | 150 | a0001c0005t0001g0175 a0001c0007t0001g0084 a0001c0007t0001g0181 others(147): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.3028+582C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52018479 | |||||||
chr14:52018526 | T | C | 15 | a0001c0005t0001g0175 a0002c0027t0001g0188 a0002c0027t0001g0189 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.3028+535A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52018526 | |||||||
chr14:52018571 | T | C | 1 | a0001c0007t0001g0084 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3028+490A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52018571 | |||||||
chr14:52018674 | T | C | 2 | a0028c0029t0001g0142 a0031c0068t0001g0334 |
2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3028+387A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52018674 | |||||||
chr14:52018764 | C | T | 1 | a0024c0067t0002g0305 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3028+297G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52018764 | |||||||
chr14:52018773 | G | C | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3028+288C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52018773 | |||||||
chr14:52018956 | T | C | 1 | a0003c0002t0001g0277 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3028+105A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52018956 | |||||||
chr14:52018979 | G | C | 15 | a0001c0005t0001g0175 a0002c0027t0001g0188 a0002c0027t0001g0189 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.3028+82C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 14/21 | chr14 | 52018979 | |||||||
chr14:52019405 | C | G | 15 | a0001c0005t0001g0175 a0002c0027t0001g0188 a0002c0027t0001g0189 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.2795-111G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 13/21 | chr14 | 52019405 | |||||||
chr14:52019550 | G | A | 15 | a0001c0005t0001g0175 a0002c0027t0001g0188 a0002c0027t0001g0189 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.2795-256C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 13/21 | chr14 | 52019550 | |||||||
chr14:52019601 | T | A | 1 | a0032c0043t0001g0146 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2795-307A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 13/21 | chr14 | 52019601 | |||||||
chr14:52019651 | C | T | 4 | a0001c0001t0001g0226 a0001c0001t0001g0265 a0001c0001t0001g0266 others(1): Show |
4 | HG00140.hp1 HG02735.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.2795-357G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 13/21 | chr14 | 52019651 | |||||||
chr14:52019653 | GCACTCAC | G | 15 | a0001c0005t0001g0175 a0002c0027t0001g0188 a0002c0027t0001g0189 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.2795-366_2795-360d others(9): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 13/21 | chr14 | 52019653 | |||||||
chr14:52019733 | C | T | 1 | a0001c0007t0001g0201 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2794+326G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 13/21 | chr14 | 52019733 | |||||||
chr14:52019800 | C | T | 2 | a0003c0002t0001g0074 a0003c0002t0001g0076 |
2 | HG02132.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.2794+259G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 13/21 | chr14 | 52019800 | |||||||
chr14:52019861 | C | T | 15 | a0001c0005t0001g0175 a0002c0027t0001g0188 a0002c0027t0001g0189 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.2794+198G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 13/21 | chr14 | 52019861 | |||||||
chr14:52019969 | C | A | 2 | a0028c0029t0001g0142 a0031c0068t0001g0334 |
2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2794+90G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 13/21 | chr14 | 52019969 | |||||||
chr14:52020243 | C | T | 47 | a0002c0003t0001g0123 a0003c0002t0001g0006 a0003c0002t0001g0013 others(44): Show |
51 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.2675-65G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52020243 | |||||||
chr14:52020373 | G | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0207 |
3 | HG01167.hp2 HG01169.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.2675-195C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52020373 | |||||||
chr14:52020390 | C | T | 3 | a0016c0064t0001g0328 a0016c0069t0001g0332 a0032c0043t0001g0146 |
3 | HG02818.hp2 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2675-212G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52020390 | |||||||
chr14:52020519 | C | T | 1 | a0004c0012t0002g0304 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2675-341G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52020519 | |||||||
chr14:52020711 | T | C | 1 | a0003c0002t0001g0228 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2675-533A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52020711 | |||||||
chr14:52020797 | A | G | 69 | a0001c0005t0001g0175 a0001c0005t0001g0287 a0001c0007t0001g0092 others(66): Show |
74 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.2675-619T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52020797 | |||||||
chr14:52020946 | A | G | 1 | a0002c0004t0001g0139 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2675-768T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52020946 | |||||||
chr14:52021036 | CTG | C | 115 | a0001c0007t0001g0084 a0001c0007t0001g0181 a0001c0007t0001g0201 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.2675-860_2675-859d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52021036 | |||||||
chr14:52021048 | T | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(127): Show |
146 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.2675-870A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52021048 | |||||||
chr14:52021222 | GA | G | 256 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(253): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.2675-1045delT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52021222 | |||||||
chr14:52021222 | GAA | G | 75 | a0001c0001t0001g0227 a0001c0001t0001g0254 a0001c0005t0001g0175 others(72): Show |
82 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.2675-1046_2675-104 others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52021222 | |||||||
chr14:52021291 | C | T | 53 | a0001c0007t0001g0092 a0001c0022t0001g0029 a0001c0022t0001g0091 others(50): Show |
58 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.2675-1113G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52021291 | |||||||
chr14:52021667 | A | G | 53 | a0001c0007t0001g0092 a0001c0022t0001g0029 a0001c0022t0001g0091 others(50): Show |
58 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.2675-1489T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52021667 | |||||||
chr14:52021970 | C | T | 68 | a0001c0005t0001g0175 a0001c0007t0001g0092 a0001c0022t0001g0029 others(65): Show |
73 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.2675-1792G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52021970 | |||||||
chr14:52022188 | T | TAAGAATT others(314): Show |
1 | a0023c0049t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2675-2011_2675-201 others(325): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52022188 | |||||||
chr14:52022188 | T | TAAGAATT others(338): Show |
1 | a0031c0068t0001g0334 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2675-2011_2675-201 others(349): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52022188 | |||||||
chr14:52022188 | T | TAAGAATT others(339): Show |
1 | a0028c0029t0001g0142 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2675-2011_2675-201 others(350): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52022188 | |||||||
chr14:52022403 | G | T | 9 | a0002c0004t0001g0149 a0002c0004t0001g0150 a0002c0004t0001g0153 others(6): Show |
9 | HG00609.hp1 HG01993.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.2675-2225C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52022403 | |||||||
chr14:52022562 | T | C | 10 | a0002c0003t0001g0010 a0002c0003t0001g0108 a0002c0003t0001g0135 others(7): Show |
11 | NA18946.hp2 NA18953.hp1 NA18961.hp1 others(8): Show |
intron_variant | MODIFIER | c.2675-2384A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52022562 | |||||||
chr14:52022600 | G | A | 9 | a0009c0014t0001g0087 a0009c0014t0001g0290 a0009c0014t0001g0291 others(6): Show |
9 | HG02622.hp2 HG02717.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.2675-2422C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52022600 | |||||||
chr14:52022695 | G | A | 68 | a0001c0005t0001g0175 a0001c0007t0001g0092 a0001c0022t0001g0029 others(65): Show |
73 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.2675-2517C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52022695 | |||||||
chr14:52022735 | C | T | 115 | a0001c0007t0001g0084 a0001c0007t0001g0181 a0001c0007t0001g0201 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.2675-2557G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52022735 | |||||||
chr14:52022736 | G | A | 8 | a0007c0011t0001g0027 a0007c0011t0001g0031 a0007c0011t0001g0036 others(5): Show |
8 | HG00438.hp2 HG01358.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.2675-2558C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52022736 | |||||||
chr14:52022973 | T | G | 1 | a0001c0001t0001g0226 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2675-2795A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52022973 | |||||||
chr14:52023000 | A | G | 336 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(333): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.2675-2822T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023000 | |||||||
chr14:52023069 | C | T | 3 | a0023c0049t0001g0090 a0028c0029t0001g0142 a0031c0068t0001g0334 |
3 | HG01891.hp1 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2675-2891G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023069 | |||||||
chr14:52023186 | G | C | 3 | a0016c0064t0001g0328 a0016c0069t0001g0332 a0032c0043t0001g0146 |
3 | HG02818.hp2 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2675-3008C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023186 | |||||||
chr14:52023224 | C | A | 9 | a0009c0014t0001g0087 a0009c0014t0001g0290 a0009c0014t0001g0291 others(6): Show |
9 | HG02622.hp2 HG02717.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.2675-3046G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023224 | |||||||
chr14:52023246 | G | C | 1 | a0015c0056t0001g0331 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2675-3068C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023246 | |||||||
chr14:52023257 | G | A | 1 | a0002c0003t0001g0098 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2675-3079C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023257 | |||||||
chr14:52023259 | T | C | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2675-3081A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023259 | |||||||
chr14:52023346 | TG | T | 183 | a0001c0005t0001g0175 a0001c0005t0001g0287 a0001c0007t0001g0084 others(180): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.2675-3169delC | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023346 | |||||||
chr14:52023348 | G | C | 1 | a0001c0001t0001g0261 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2675-3170C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023348 | |||||||
chr14:52023352 | G | A | 3 | a0016c0064t0001g0328 a0016c0069t0001g0332 a0032c0043t0001g0146 |
3 | HG02818.hp2 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2675-3174C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023352 | |||||||
chr14:52023386 | C | T | 202 | a0001c0005t0001g0175 a0001c0005t0001g0287 a0001c0007t0001g0084 others(199): Show |
208 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.2675-3208G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023386 | |||||||
chr14:52023396 | A | C | 54 | a0001c0005t0001g0287 a0001c0007t0001g0092 a0001c0022t0001g0029 others(51): Show |
59 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.2675-3218T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023396 | |||||||
chr14:52023436 | T | C | 69 | a0001c0005t0001g0175 a0001c0005t0001g0287 a0001c0007t0001g0092 others(66): Show |
74 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.2675-3258A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023436 | |||||||
chr14:52023450 | G | A | 1 | a0003c0035t0001g0232 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2675-3272C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023450 | |||||||
chr14:52023480 | T | TA | 7 | a0001c0001t0001g0233 a0002c0004t0001g0041 a0002c0004t0001g0042 others(4): Show |
7 | HG02280.hp2 HG02300.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2675-3303dupT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023480 | |||||||
chr14:52023568 | T | G | 3 | a0002c0003t0001g0109 a0002c0004t0001g0149 a0002c0004t0001g0150 |
3 | HG01993.hp1 NA18953.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.2675-3390A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023568 | |||||||
chr14:52023619 | T | A | 1 | a0001c0001t0001g0061 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2675-3441A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023619 | |||||||
chr14:52023620 | C | G | 1 | a0001c0001t0001g0061 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2675-3442G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023620 | |||||||
chr14:52023621 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2675-3443G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023621 | |||||||
chr14:52023624 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2675-3446C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023624 | |||||||
chr14:52023851 | G | A | 69 | a0001c0005t0001g0175 a0001c0005t0001g0287 a0001c0007t0001g0092 others(66): Show |
74 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.2674+3350C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023851 | |||||||
chr14:52023912 | G | A | 114 | a0001c0007t0001g0084 a0001c0007t0001g0181 a0001c0007t0001g0243 others(111): Show |
115 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.2674+3289C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023912 | |||||||
chr14:52023972 | T | G | 54 | a0001c0005t0001g0287 a0001c0007t0001g0092 a0001c0022t0001g0029 others(51): Show |
59 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.2674+3229A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023972 | |||||||
chr14:52023979 | C | G | 1 | a0001c0007t0001g0084 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2674+3222G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52023979 | |||||||
chr14:52024012 | A | T | 6 | a0001c0005t0001g0287 a0001c0007t0001g0092 a0001c0022t0001g0029 others(3): Show |
7 | HG02109.hp1 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2674+3189T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52024012 | |||||||
chr14:52024350 | G | T | 113 | a0001c0007t0001g0181 a0001c0007t0001g0243 a0001c0007t0001g0278 others(110): Show |
114 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.2674+2851C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52024350 | |||||||
chr14:52024491 | T | C | 1 | a0007c0011t0001g0036 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2674+2710A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52024491 | |||||||
chr14:52024580 | C | A | 1 | a0001c0001t0001g0268 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2674+2621G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52024580 | |||||||
chr14:52024581 | C | T | 16 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(13): Show |
16 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.2674+2620G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52024581 | |||||||
chr14:52024661 | A | G | 1 | a0003c0002t0001g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2674+2540T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52024661 | |||||||
chr14:52024752 | A | G | 4 | a0002c0004t0001g0154 a0002c0004t0001g0155 a0002c0004t0001g0156 others(1): Show |
4 | HG01069.hp1 HG01192.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.2674+2449T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52024752 | |||||||
chr14:52024754 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2674+2447C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52024754 | |||||||
chr14:52024865 | A | G | 54 | a0001c0005t0001g0287 a0001c0007t0001g0092 a0001c0022t0001g0029 others(51): Show |
59 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.2674+2336T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52024865 | |||||||
chr14:52024882 | G | C | 1 | a0002c0004t0001g0143 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2674+2319C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52024882 | |||||||
chr14:52024937 | T | C | 247 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(244): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2674+2264A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52024937 | |||||||
chr14:52024957 | T | C | 335 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(332): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.2674+2244A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52024957 | |||||||
chr14:52025036 | T | C | 247 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(244): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2674+2165A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52025036 | |||||||
chr14:52025585 | G | A | 69 | a0001c0005t0001g0175 a0001c0005t0001g0287 a0001c0007t0001g0092 others(66): Show |
74 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.2674+1616C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52025585 | |||||||
chr14:52025641 | G | C | 332 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(329): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.2674+1560C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52025641 | |||||||
chr14:52025845 | AT | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(122): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.2674+1355delA | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52025845 | |||||||
chr14:52025848 | A | T | 1 | a0001c0005t0001g0177 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2674+1353T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52025848 | |||||||
chr14:52025907 | G | A | 336 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(333): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.2674+1294C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52025907 | |||||||
chr14:52025953 | C | T | 1 | a0007c0011t0001g0031 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2674+1248G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52025953 | |||||||
chr14:52026296 | C | T | 3 | a0016c0064t0001g0328 a0016c0069t0001g0332 a0032c0043t0001g0146 |
3 | HG02818.hp2 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2674+905G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52026296 | |||||||
chr14:52026311 | C | T | 4 | a0001c0005t0001g0212 a0001c0005t0001g0274 a0001c0005t0001g0275 others(1): Show |
4 | HG00738.hp1 HG01099.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2674+890G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52026311 | |||||||
chr14:52026350 | G | A | 128 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(125): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.2674+851C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52026350 | |||||||
chr14:52026366 | A | C | 2 | a0028c0029t0001g0142 a0031c0068t0001g0334 |
2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2674+835T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52026366 | |||||||
chr14:52026443 | T | C | 69 | a0001c0005t0001g0175 a0001c0005t0001g0287 a0001c0007t0001g0092 others(66): Show |
74 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.2674+758A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52026443 | |||||||
chr14:52026471 | G | A | 2 | a0012c0018t0001g0004 a0012c0018t0001g0045 |
3 | HG01099.hp1 HG01952.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.2674+730C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52026471 | |||||||
chr14:52026491 | G | C | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2674+710C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52026491 | |||||||
chr14:52026492 | A | T | 1 | a0001c0001t0001g0009 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2674+709T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52026492 | |||||||
chr14:52026510 | T | A | 119 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0078 others(116): Show |
120 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.2674+691A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52026510 | |||||||
chr14:52026844 | G | T | 16 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(13): Show |
16 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.2674+357C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52026844 | |||||||
chr14:52026857 | A | G | 1 | a0032c0043t0001g0146 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2674+344T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52026857 | |||||||
chr14:52026883 | G | A | 1 | a0002c0004t0001g0149 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2674+318C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52026883 | |||||||
chr14:52027005 | G | A | 16 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(13): Show |
16 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.2674+196C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52027005 | |||||||
chr14:52027005 | G | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0203 a0001c0007t0001g0200 others(3): Show |
7 | HG01243.hp1 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2674+196C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 12/21 | chr14 | 52027005 | |||||||
chr14:52027354 | G | A | 119 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0078 others(116): Show |
120 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.2531-10C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027354 | |||||||
chr14:52027374 | G | C | 16 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(13): Show |
16 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.2531-30C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027374 | |||||||
chr14:52027582 | C | T | 54 | a0001c0005t0001g0287 a0001c0007t0001g0092 a0001c0022t0001g0029 others(51): Show |
59 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.2531-238G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027582 | |||||||
chr14:52027589 | T | TA | 69 | a0001c0005t0001g0175 a0001c0005t0001g0287 a0001c0007t0001g0092 others(66): Show |
74 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.2531-246dupT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027589 | |||||||
chr14:52027633 | T | TAC | 91 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(88): Show |
105 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.2531-291_2531-290d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027633 | |||||||
chr14:52027633 | T | TACAC | 23 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0077 others(20): Show |
25 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.2531-293_2531-290d others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027633 | |||||||
chr14:52027633 | T | TACACAC | 29 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0001g0251 others(26): Show |
29 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.2531-295_2531-290d others(8): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027633 | |||||||
chr14:52027633 | T | TACACACA others(1): Show |
36 | a0001c0001t0001g0061 a0001c0001t0001g0078 a0001c0001t0001g0140 others(33): Show |
37 | HG00544.hp2 HG00558.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.2531-297_2531-290d others(10): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027633 | |||||||
chr14:52027633 | T | TACACACA others(3): Show |
25 | a0001c0001t0001g0062 a0001c0007t0001g0084 a0001c0007t0001g0243 others(22): Show |
25 | HG00544.hp1 HG00609.hp1 HG01993.hp1 others(22): Show |
intron_variant | MODIFIER | c.2531-299_2531-290d others(12): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027633 | |||||||
chr14:52027633 | T | TACACACA others(5): Show |
13 | a0002c0003t0001g0093 a0002c0003t0001g0118 a0002c0003t0001g0128 others(10): Show |
13 | HG01496.hp1 HG02165.hp2 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.2531-301_2531-290d others(14): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027633 | |||||||
chr14:52027633 | T | TACACACA others(7): Show |
9 | a0002c0003t0001g0054 a0002c0003t0001g0056 a0002c0003t0001g0057 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.2531-303_2531-290d others(16): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027633 | |||||||
chr14:52027633 | T | TACACACA others(9): Show |
1 | a0002c0003t0001g0172 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2531-305_2531-290d others(18): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027633 | |||||||
chr14:52027633 | T | TACACACA others(15): Show |
1 | a0002c0004t0001g0022 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2531-311_2531-290d others(24): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027633 | |||||||
chr14:52027633 | TAC | T | 62 | a0001c0001t0001g0260 a0001c0005t0001g0212 a0001c0005t0001g0275 others(59): Show |
67 | HG00099.hp2 HG00639.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.2531-291_2531-290d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027633 | |||||||
chr14:52027633 | TACAC | T | 20 | a0002c0003t0001g0123 a0002c0039t0001g0089 a0003c0002t0001g0184 others(17): Show |
20 | HG00438.hp2 HG00642.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.2531-293_2531-290d others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027633 | |||||||
chr14:52027633 | TACACAC | T | 15 | a0001c0005t0001g0175 a0002c0003t0001g0138 a0002c0027t0001g0188 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.2531-295_2531-290d others(8): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027633 | |||||||
chr14:52027680 | G | A | 332 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(329): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.2531-336C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027680 | |||||||
chr14:52027726 | C | CT | 10 | a0001c0005t0001g0287 a0001c0007t0001g0092 a0001c0022t0001g0029 others(7): Show |
11 | HG00423.hp1 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2531-383dupA | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027726 | |||||||
chr14:52027726 | CTT | C | 7 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(4): Show |
7 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.2531-384_2531-383d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027726 | |||||||
chr14:52027726 | CTTT | C | 9 | a0009c0014t0001g0087 a0009c0014t0001g0290 a0009c0014t0001g0291 others(6): Show |
9 | HG02622.hp2 HG02717.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.2531-385_2531-383d others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027726 | |||||||
chr14:52027845 | T | A | 1 | a0005c0021t0001g0218 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2531-501A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027845 | |||||||
chr14:52027919 | C | A | 15 | a0001c0005t0001g0175 a0002c0027t0001g0188 a0002c0027t0001g0189 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.2531-575G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027919 | |||||||
chr14:52027954 | A | T | 4 | a0023c0049t0001g0090 a0026c0037t0001g0026 a0028c0029t0001g0142 others(1): Show |
4 | HG01891.hp1 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2531-610T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027954 | |||||||
chr14:52027989 | C | T | 336 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(333): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.2531-645G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52027989 | |||||||
chr14:52028006 | T | A | 1 | a0002c0003t0001g0095 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2531-662A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52028006 | |||||||
chr14:52028071 | T | C | 336 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(333): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.2530+651A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52028071 | |||||||
chr14:52028112 | G | A | 16 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(13): Show |
16 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.2530+610C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52028112 | |||||||
chr14:52028279 | T | TTTG | 8 | a0001c0001t0001g0254 a0003c0002t0001g0067 a0003c0002t0001g0068 others(5): Show |
8 | HG03017.hp2 NA18955.hp2 NA18978.hp1 others(5): Show |
intron_variant | MODIFIER | c.2530+442_2530+443i others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52028279 | |||||||
chr14:52028280 | T | TTG | 171 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(168): Show |
192 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.2530+441_2530+442i others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52028280 | |||||||
chr14:52028281 | T | TG | 137 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0078 others(134): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2530+440_2530+441i others(3): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52028281 | |||||||
chr14:52028282 | T | G | 28 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(25): Show |
28 | HG00438.hp2 HG00639.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.2530+440A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52028282 | |||||||
chr14:52028285 | G | T | 336 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(333): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.2530+437C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52028285 | |||||||
chr14:52028324 | G | T | 1 | a0030c0030t0001g0221 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2530+398C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52028324 | |||||||
chr14:52028341 | G | T | 1 | a0001c0007t0001g0084 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2530+381C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52028341 | |||||||
chr14:52028464 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2530+258G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52028464 | |||||||
chr14:52028513 | C | A | 114 | a0001c0007t0001g0084 a0001c0007t0001g0181 a0001c0007t0001g0243 others(111): Show |
115 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.2530+209G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52028513 | |||||||
chr14:52028636 | T | G | 69 | a0001c0005t0001g0175 a0001c0005t0001g0287 a0001c0007t0001g0092 others(66): Show |
74 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.2530+86A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52028636 | |||||||
chr14:52028657 | C | T | 336 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(333): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.2530+65G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 11/21 | chr14 | 52028657 | |||||||
chr14:52028918 | C | T | 9 | a0009c0014t0001g0087 a0009c0014t0001g0290 a0009c0014t0001g0291 others(6): Show |
9 | HG02622.hp2 HG02717.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.2402-68G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 10/21 | chr14 | 52028918 | |||||||
chr14:52029009 | G | C | 115 | a0001c0007t0001g0084 a0001c0007t0001g0181 a0001c0007t0001g0243 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.2402-159C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 10/21 | chr14 | 52029009 | |||||||
chr14:52029017 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2402-167C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 10/21 | chr14 | 52029017 | |||||||
chr14:52029306 | G | A | 47 | a0002c0003t0001g0123 a0003c0002t0001g0006 a0003c0002t0001g0013 others(44): Show |
51 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.2401+241C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 10/21 | chr14 | 52029306 | |||||||
chr14:52029332 | C | G | 2 | a0011c0016t0001g0339 a0011c0016t0001g0340 |
2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2401+215G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 10/21 | chr14 | 52029332 | |||||||
chr14:52029373 | A | C | 344 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(341): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.2401+174T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 10/21 | chr14 | 52029373 | |||||||
chr14:52029404 | T | A | 4 | a0023c0049t0001g0090 a0026c0037t0001g0026 a0028c0029t0001g0142 others(1): Show |
4 | HG01891.hp1 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2401+143A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 10/21 | chr14 | 52029404 | |||||||
chr14:52029513 | C | T | 7 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(4): Show |
7 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.2401+34G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 10/21 | chr14 | 52029513 | |||||||
chr14:52029529 | C | G | 4 | a0023c0049t0001g0090 a0026c0037t0001g0026 a0028c0029t0001g0142 others(1): Show |
4 | HG01891.hp1 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2401+18G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 10/21 | chr14 | 52029529 | |||||||
chr14:52029727 | C | G | 3 | a0015c0056t0001g0331 a0015c0058t0001g0330 a0034c0057t0001g0314 |
3 | HG02723.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2258-37G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52029727 | |||||||
chr14:52029747 | C | CAGAT | 10 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2258-58_2258-57ins others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52029747 | |||||||
chr14:52029801 | G | T | 10 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2258-111C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52029801 | |||||||
chr14:52029885 | GC | G | 7 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(4): Show |
7 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.2258-196delG | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52029885 | |||||||
chr14:52029891 | C | A | 7 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(4): Show |
7 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.2258-201G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52029891 | |||||||
chr14:52030027 | G | T | 50 | a0002c0003t0001g0123 a0003c0002t0001g0006 a0003c0002t0001g0013 others(47): Show |
55 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.2258-337C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030027 | |||||||
chr14:52030030 | T | G | 316 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(313): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.2258-340A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030030 | |||||||
chr14:52030067 | A | G | 316 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(313): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.2258-377T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030067 | |||||||
chr14:52030159 | G | A | 7 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(4): Show |
7 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.2258-469C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030159 | |||||||
chr14:52030180 | A | G | 3 | a0016c0064t0001g0328 a0016c0069t0001g0332 a0032c0043t0001g0146 |
3 | HG02818.hp2 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2258-490T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030180 | |||||||
chr14:52030218 | T | C | 332 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(329): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.2258-528A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030218 | |||||||
chr14:52030220 | T | C | 7 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(4): Show |
7 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.2258-530A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030220 | |||||||
chr14:52030325 | G | A | 316 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(313): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.2258-635C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030325 | |||||||
chr14:52030336 | C | T | 332 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(329): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.2258-646G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030336 | |||||||
chr14:52030383 | A | G | 7 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(4): Show |
7 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.2258-693T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030383 | |||||||
chr14:52030474 | G | GAGAAAGA others(2): Show |
85 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(82): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.2258-793_2258-785d others(11): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030474 | |||||||
chr14:52030481 | A | AAAAGAAA others(28): Show |
1 | a0004c0012t0002g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2258-792_2258-791i others(37): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030481 | |||||||
chr14:52030481 | A | AAAAGAAA others(32): Show |
3 | a0004c0012t0002g0302 a0004c0012t0002g0304 a0024c0067t0002g0305 |
3 | HG00639.hp1 HG01978.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.2258-792_2258-791i others(41): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030481 | |||||||
chr14:52030481 | A | AAAAGAAA others(40): Show |
3 | a0004c0012t0002g0299 a0004c0012t0002g0301 a0033c0062t0002g0303 |
3 | HG01109.hp2 HG01361.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.2258-792_2258-791i others(49): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030481 | |||||||
chr14:52030481 | A | AAAAGAAA others(15): Show |
2 | a0015c0058t0001g0330 a0034c0057t0001g0314 |
2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2258-792_2258-791i others(24): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030481 | |||||||
chr14:52030481 | A | AAAAGAAA others(19): Show |
1 | a0015c0056t0001g0331 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2258-792_2258-791i others(28): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030481 | |||||||
chr14:52030481 | A | AAAAGAAA others(6): Show |
49 | a0001c0001t0001g0238 a0003c0002t0001g0006 a0003c0002t0001g0013 others(46): Show |
54 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.2258-792_2258-791i others(15): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030481 | |||||||
chr14:52030481 | AAAAGAAA others(19): Show |
A | 2 | a0002c0004t0001g0170 a0004c0053t0001g0321 |
2 | HG02165.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2258-817_2258-792d others(28): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030481 | |||||||
chr14:52030485 | G | GAAAGA | 25 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(22): Show |
28 | HG01243.hp1 HG01255.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.2258-800_2258-796d others(7): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030485 | |||||||
chr14:52030489 | G | GA | 56 | a0001c0001t0001g0210 a0001c0001t0001g0241 a0001c0001t0001g0258 others(53): Show |
57 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.2258-800dupT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030489 | |||||||
chr14:52030489 | GAAAGAAA others(9): Show |
G | 1 | a0002c0003t0001g0054 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2258-815_2258-800d others(18): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030489 | |||||||
chr14:52030490 | AAAG | A | 30 | a0001c0007t0001g0243 a0001c0010t0001g0001 a0001c0010t0001g0032 others(27): Show |
32 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.2258-803_2258-801d others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030490 | |||||||
chr14:52030490 | AAAGAAAG others(6): Show |
A | 18 | a0002c0003t0001g0057 a0002c0003t0001g0112 a0002c0003t0001g0115 others(15): Show |
18 | HG00544.hp2 HG00558.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.2258-813_2258-801d others(15): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030490 | |||||||
chr14:52030490 | AAAGAAAG others(10): Show |
A | 9 | a0002c0003t0001g0095 a0002c0003t0001g0124 a0002c0004t0001g0105 others(6): Show |
9 | HG00099.hp2 HG01192.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2258-817_2258-801d others(19): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030490 | |||||||
chr14:52030490 | AAAGAAAG others(14): Show |
A | 7 | a0002c0003t0001g0058 a0002c0003t0001g0093 a0002c0003t0001g0136 others(4): Show |
7 | HG00423.hp2 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.2258-821_2258-801d others(23): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030490 | |||||||
chr14:52030490 | AAAGAAAG others(27): Show |
A | 1 | a0001c0007t0002g0204 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2258-834_2258-801d others(36): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030490 | |||||||
chr14:52030490 | AAAGAAAG others(31): Show |
A | 1 | a0004c0006t0002g0350 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2258-838_2258-801d others(40): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030490 | |||||||
chr14:52030492 | AGAAAGAA others(2): Show |
A | 25 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(22): Show |
26 | HG00609.hp1 HG00609.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2258-811_2258-803d others(11): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030492 | |||||||
chr14:52030493 | G | A | 1 | a0002c0004t0001g0158 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2258-803C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030493 | |||||||
chr14:52030494 | A | G | 1 | a0002c0004t0001g0158 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2258-804T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030494 | |||||||
chr14:52030499 | AAG | A | 56 | a0001c0007t0001g0181 a0001c0007t0001g0243 a0001c0010t0001g0001 others(53): Show |
58 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.2258-811_2258-810d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030499 | |||||||
chr14:52030501 | G | A | 1 | a0026c0037t0001g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2258-811C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030501 | |||||||
chr14:52030501 | G | GAA | 17 | a0001c0005t0001g0175 a0001c0007t0001g0084 a0001c0032t0001g0279 others(14): Show |
17 | HG00140.hp2 HG02083.hp2 HG02273.hp1 others(14): Show |
intron_variant | MODIFIER | c.2258-812_2258-811i others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030501 | |||||||
chr14:52030501 | GAGAAAGA others(8): Show |
G | 1 | a0002c0004t0001g0158 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2258-826_2258-812d others(17): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030501 | |||||||
chr14:52030503 | G | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(35): Show |
42 | HG00621.hp2 HG01099.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.2258-813C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030503 | |||||||
chr14:52030505 | A | G | 38 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(35): Show |
42 | HG00621.hp2 HG01099.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.2258-815T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030505 | |||||||
chr14:52030507 | G | A | 13 | a0001c0001t0001g0210 a0001c0001t0001g0241 a0001c0001t0001g0258 others(10): Show |
14 | HG00621.hp2 HG01099.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.2258-817C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030507 | |||||||
chr14:52030509 | A | G | 13 | a0001c0001t0001g0210 a0001c0001t0001g0241 a0001c0001t0001g0258 others(10): Show |
14 | HG00621.hp2 HG01099.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.2258-819T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030509 | |||||||
chr14:52030515 | G | A | 2 | a0001c0005t0001g0175 a0008c0013t0001g0348 |
2 | HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2258-825C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030515 | |||||||
chr14:52030515 | GA | G | 118 | a0001c0001t0001g0210 a0001c0001t0001g0241 a0001c0001t0001g0258 others(115): Show |
120 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.2258-826delT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030515 | |||||||
chr14:52030516 | A | AAAG | 7 | a0001c0007t0001g0084 a0001c0032t0001g0279 a0002c0003t0001g0108 others(4): Show |
7 | HG02293.hp1 HG02293.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.2258-827_2258-826i others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030516 | |||||||
chr14:52030516 | A | AG | 14 | a0001c0010t0001g0001 a0001c0010t0001g0032 a0002c0003t0001g0123 others(11): Show |
16 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.2258-827_2258-826i others(3): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030516 | |||||||
chr14:52030516 | A | G | 2 | a0001c0005t0001g0175 a0008c0013t0001g0348 |
2 | HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2258-826T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030516 | |||||||
chr14:52030516 | AAAAG | A | 4 | a0007c0011t0001g0027 a0007c0011t0001g0180 a0010c0019t0001g0307 others(1): Show |
4 | HG00438.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2258-830_2258-827d others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030516 | |||||||
chr14:52030516 | AAAAGAAA others(1): Show |
A | 3 | a0001c0001t0001g0199 a0001c0022t0001g0029 a0001c0022t0001g0091 |
3 | HG02055.hp1 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2258-834_2258-827d others(10): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030516 | |||||||
chr14:52030516 | AAAAGAAA others(13): Show |
A | 2 | a0007c0011t0001g0288 a0007c0011t0001g0289 |
2 | HG01358.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2258-846_2258-827d others(22): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030516 | |||||||
chr14:52030519 | A | G | 23 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0060 others(20): Show |
25 | HG01243.hp1 HG01255.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.2258-829T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030519 | |||||||
chr14:52030520 | G | A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0060 others(20): Show |
25 | HG01243.hp1 HG01255.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.2258-830C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030520 | |||||||
chr14:52030522 | A | G | 2 | a0002c0027t0001g0188 a0002c0027t0001g0189 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2258-832T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030522 | |||||||
chr14:52030524 | G | GA | 13 | a0001c0001t0001g0210 a0001c0001t0001g0241 a0001c0001t0001g0258 others(10): Show |
14 | HG00621.hp2 HG01099.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.2258-835dupT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030524 | |||||||
chr14:52030528 | G | GA | 5 | a0001c0010t0001g0001 a0001c0010t0001g0032 a0002c0003t0001g0123 others(2): Show |
7 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.2258-839dupT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030528 | |||||||
chr14:52030538 | A | AAG | 7 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(4): Show |
7 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.2258-850_2258-849d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030538 | |||||||
chr14:52030552 | G | GAAAGAAA others(26): Show |
1 | a0034c0057t0001g0314 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2258-863_2258-862i others(35): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030552 | |||||||
chr14:52030552 | G | GAAAGAAA others(22): Show |
2 | a0015c0056t0001g0331 a0015c0058t0001g0330 |
2 | HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2258-863_2258-862i others(31): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030552 | |||||||
chr14:52030562 | A | G | 1 | a0023c0049t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2258-872T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030562 | |||||||
chr14:52030563 | A | C | 12 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(9): Show |
12 | HG00673.hp1 HG02109.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2258-873T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030563 | |||||||
chr14:52030564 | G | A | 2 | a0028c0029t0001g0142 a0031c0068t0001g0334 |
2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2258-874C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030564 | |||||||
chr14:52030565 | A | G | 6 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(3): Show |
6 | HG02109.hp1 HG02622.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2258-875T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030565 | |||||||
chr14:52030567 | A | AGAAAGAA others(46): Show |
2 | a0004c0012t0002g0301 a0033c0062t0002g0303 |
2 | HG01361.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.2258-878_2258-877i others(55): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030567 | |||||||
chr14:52030567 | A | AGAAAGAA others(9): Show |
1 | a0007c0011t0001g0036 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2258-878_2258-877i others(18): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030567 | |||||||
chr14:52030567 | A | AGAAAGAA others(42): Show |
3 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0304 |
3 | HG00639.hp1 HG01109.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.2258-878_2258-877i others(51): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030567 | |||||||
chr14:52030567 | A | AGAAAGAA others(38): Show |
2 | a0004c0012t0002g0302 a0024c0067t0002g0305 |
2 | HG01978.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.2258-878_2258-877i others(47): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030567 | |||||||
chr14:52030567 | A | AGAAAGAA others(1): Show |
3 | a0007c0051t0001g0295 a0009c0038t0001g0035 a0017c0026t0001g0293 |
3 | HG02896.hp1 NA19067.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2258-878_2258-877i others(10): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030567 | |||||||
chr14:52030567 | A | AGAAC | 3 | a0007c0011t0001g0031 a0007c0011t0001g0047 a0029c0061t0001g0329 |
3 | HG02602.hp2 HG03041.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2258-878_2258-877i others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030567 | |||||||
chr14:52030567 | A | C | 208 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(205): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.2258-877T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030567 | |||||||
chr14:52030567 | AG | A | 32 | a0001c0001t0001g0017 a0001c0001t0001g0126 a0001c0001t0001g0242 others(29): Show |
34 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.2258-878delC | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030567 | |||||||
chr14:52030568 | G | A | 2 | a0028c0029t0001g0142 a0031c0068t0001g0334 |
2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2258-878C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030568 | |||||||
chr14:52030568 | G | GAAA | 9 | a0001c0001t0001g0227 a0001c0001t0001g0233 a0001c0001t0001g0245 others(6): Show |
9 | HG01358.hp1 HG02056.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.2258-879_2258-878i others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030568 | |||||||
chr14:52030568 | G | GAAAGAAA others(4): Show |
1 | a0003c0002t0001g0229 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2258-879_2258-878i others(13): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030568 | |||||||
chr14:52030568 | G | GAAAGAAA others(8): Show |
1 | a0003c0002t0001g0214 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2258-879_2258-878i others(17): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030568 | |||||||
chr14:52030568 | G | GAAAGAAA others(4): Show |
1 | a0003c0002t0001g0205 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2258-879_2258-878i others(13): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030568 | |||||||
chr14:52030568 | G | GAAC | 6 | a0003c0002t0001g0013 a0003c0002t0001g0014 a0003c0002t0001g0216 others(3): Show |
9 | HG00738.hp2 HG00741.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.2258-879_2258-878i others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030568 | |||||||
chr14:52030569 | G | A | 54 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(51): Show |
60 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.2258-879C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030569 | |||||||
chr14:52030571 | A | C | 49 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(46): Show |
55 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.2258-881T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030571 | |||||||
chr14:52030572 | G | A | 22 | a0001c0001t0001g0017 a0001c0001t0001g0126 a0001c0001t0001g0227 others(19): Show |
23 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.2258-882C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030572 | |||||||
chr14:52030572 | G | C | 29 | a0002c0003t0001g0123 a0003c0002t0001g0013 a0003c0002t0001g0014 others(26): Show |
33 | HG00738.hp2 HG00741.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.2258-882C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030572 | |||||||
chr14:52030573 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0239 |
2 | HG03017.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2258-883C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030573 | |||||||
chr14:52030573 | GAAGGGAA others(1): Show |
G | 3 | a0001c0007t0001g0092 a0011c0016t0001g0344 a0036c0066t0001g0322 |
3 | HG02109.hp1 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2258-891_2258-884d others(10): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030573 | |||||||
chr14:52030573 | GAAGGGAA others(9): Show |
G | 3 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02818.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2258-899_2258-884d others(18): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030573 | |||||||
chr14:52030576 | G | A | 1 | a0013c0017t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2258-886C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030576 | |||||||
chr14:52030576 | G | C | 53 | a0001c0001t0001g0017 a0001c0001t0001g0126 a0001c0001t0001g0227 others(50): Show |
58 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.2258-886C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030576 | |||||||
chr14:52030577 | G | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0239 a0013c0017t0001g0186 |
3 | HG02976.hp2 HG03017.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2258-887C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030577 | |||||||
chr14:52030577 | GGA | G | 17 | a0002c0039t0001g0089 a0003c0002t0001g0006 a0003c0002t0001g0048 others(14): Show |
18 | HG00423.hp1 HG00642.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.2258-889_2258-888d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030577 | |||||||
chr14:52030577 | GGAAA | G | 7 | a0001c0022t0001g0029 a0001c0022t0001g0091 a0002c0003t0001g0094 others(4): Show |
7 | HG01891.hp1 HG02630.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2258-891_2258-888d others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030577 | |||||||
chr14:52030577 | GGAAAGA | G | 29 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(26): Show |
34 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.2258-893_2258-888d others(8): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030577 | |||||||
chr14:52030577 | GGAAAGAA others(1): Show |
G | 126 | a0001c0005t0001g0175 a0001c0007t0001g0084 a0001c0007t0001g0181 others(123): Show |
126 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.2258-895_2258-888d others(10): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030577 | |||||||
chr14:52030577 | GGAAAGAA others(5): Show |
G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(68): Show |
81 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.2258-899_2258-888d others(14): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030577 | |||||||
chr14:52030578 | G | A | 5 | a0009c0014t0001g0087 a0009c0014t0001g0292 a0011c0016t0001g0338 others(2): Show |
5 | HG02717.hp1 HG02886.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2258-888C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030578 | |||||||
chr14:52030580 | A | G | 5 | a0009c0014t0001g0087 a0009c0014t0001g0292 a0011c0016t0001g0338 others(2): Show |
5 | HG02717.hp1 HG02886.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2258-890T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030580 | |||||||
chr14:52030581 | A | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0239 |
2 | HG03017.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2258-891T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030581 | |||||||
chr14:52030581 | A | G | 58 | a0001c0001t0001g0017 a0001c0001t0001g0126 a0001c0001t0001g0227 others(55): Show |
63 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.2258-891T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030581 | |||||||
chr14:52030582 | GAA | G | 17 | a0002c0039t0001g0089 a0003c0002t0001g0006 a0003c0002t0001g0048 others(14): Show |
18 | HG00423.hp1 HG00642.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.2258-894_2258-893d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030582 | |||||||
chr14:52030583 | A | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0239 |
2 | HG03017.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2258-893T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030583 | |||||||
chr14:52030584 | A | AG | 34 | a0002c0003t0001g0123 a0003c0002t0001g0013 a0003c0002t0001g0014 others(31): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.2258-895_2258-894i others(3): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030584 | |||||||
chr14:52030585 | A | AGAACGAA others(15): Show |
1 | a0013c0017t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2258-896_2258-895i others(24): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030585 | |||||||
chr14:52030585 | A | G | 70 | a0001c0001t0001g0017 a0001c0001t0001g0126 a0001c0001t0001g0227 others(67): Show |
76 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.2258-895T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030585 | |||||||
chr14:52030586 | GAA | G | 29 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(26): Show |
34 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.2258-898_2258-897d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030586 | |||||||
chr14:52030586 | GAAA | G | 19 | a0001c0001t0001g0017 a0001c0001t0001g0126 a0001c0001t0001g0227 others(16): Show |
20 | HG00099.hp1 HG00738.hp1 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.2258-899_2258-897d others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030586 | |||||||
chr14:52030587 | A | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0239 |
2 | HG03017.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2258-897T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030587 | |||||||
chr14:52030589 | A | G | 29 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(26): Show |
34 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.2258-899T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030589 | |||||||
chr14:52030594 | G | GAAAGAGA others(1): Show |
10 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2258-905_2258-904i others(10): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030594 | |||||||
chr14:52030598 | GAA | G | 5 | a0002c0003t0001g0010 a0002c0003t0001g0190 a0002c0003t0001g0191 others(2): Show |
6 | NA18961.hp1 NA18963.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.2258-910_2258-909d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030598 | |||||||
chr14:52030608 | G | A | 5 | a0002c0003t0001g0010 a0002c0003t0001g0190 a0002c0003t0001g0191 others(2): Show |
6 | NA18961.hp1 NA18963.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.2258-918C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030608 | |||||||
chr14:52030614 | AAAAG | A | 109 | a0001c0007t0001g0084 a0001c0007t0001g0181 a0001c0007t0001g0243 others(106): Show |
109 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.2258-928_2258-925d others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030614 | |||||||
chr14:52030616 | A | G | 15 | a0002c0003t0001g0010 a0002c0003t0001g0190 a0002c0003t0001g0191 others(12): Show |
16 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.2258-926T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030616 | |||||||
chr14:52030616 | AAG | A | 4 | a0023c0049t0001g0090 a0026c0037t0001g0026 a0028c0029t0001g0142 others(1): Show |
4 | HG01891.hp1 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2258-928_2258-927d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030616 | |||||||
chr14:52030616 | AAGAAAGA others(3): Show |
A | 1 | a0001c0001t0001g0227 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2258-936_2258-927d others(12): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030616 | |||||||
chr14:52030626 | G | GAA | 10 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2258-937_2258-936i others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030626 | |||||||
chr14:52030634 | A | AAAAGAGA others(3): Show |
1 | a0002c0004t0001g0178 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2258-945_2258-944i others(12): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030634 | |||||||
chr14:52030634 | A | G | 10 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2258-944T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030634 | |||||||
chr14:52030636 | G | A | 11 | a0002c0004t0001g0178 a0004c0012t0002g0299 a0004c0012t0002g0300 others(8): Show |
11 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.2258-946C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030636 | |||||||
chr14:52030648 | G | GAGAA | 3 | a0023c0049t0001g0090 a0028c0029t0001g0142 a0031c0068t0001g0334 |
3 | HG01891.hp1 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2258-962_2258-959d others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030648 | |||||||
chr14:52030663 | A | AAAAAGAA others(13): Show |
4 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(1): Show |
4 | HG02055.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2258-993_2258-974d others(22): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030663 | |||||||
chr14:52030665 | A | G | 62 | a0001c0005t0001g0175 a0002c0003t0001g0123 a0002c0027t0001g0188 others(59): Show |
67 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.2258-975T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030665 | |||||||
chr14:52030755 | G | A | 306 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(303): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.2258-1065C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030755 | |||||||
chr14:52030898 | T | G | 10 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2258-1208A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030898 | |||||||
chr14:52030913 | T | C | 10 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2258-1223A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030913 | |||||||
chr14:52030946 | A | C | 2 | a0002c0003t0001g0100 a0002c0003t0001g0113 |
2 | NA19064.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.2258-1256T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030946 | |||||||
chr14:52030975 | C | A | 1 | a0001c0001t0001g0078 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2258-1285G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030975 | |||||||
chr14:52030978 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2258-1288A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52030978 | |||||||
chr14:52031000 | G | A | 7 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(4): Show |
7 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.2258-1310C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031000 | |||||||
chr14:52031013 | A | C | 1 | a0001c0001t0001g0226 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2258-1323T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031013 | |||||||
chr14:52031022 | G | C | 10 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2258-1332C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031022 | |||||||
chr14:52031024 | G | A | 3 | a0015c0056t0001g0331 a0015c0058t0001g0330 a0034c0057t0001g0314 |
3 | HG02723.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2258-1334C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031024 | |||||||
chr14:52031059 | A | G | 10 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2258-1369T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031059 | |||||||
chr14:52031088 | A | T | 10 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2258-1398T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031088 | |||||||
chr14:52031168 | T | C | 3 | a0015c0056t0001g0331 a0015c0058t0001g0330 a0034c0057t0001g0314 |
3 | HG02723.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2258-1478A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031168 | |||||||
chr14:52031207 | C | CG | 10 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2258-1518_2258-151 others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031207 | |||||||
chr14:52031209 | A | C | 119 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0078 others(116): Show |
120 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.2258-1519T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031209 | |||||||
chr14:52031262 | C | A | 1 | a0004c0012t0002g0304 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2258-1572G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031262 | |||||||
chr14:52031262 | C | T | 9 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(6): Show |
9 | HG01109.hp2 HG01361.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.2258-1572G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031262 | |||||||
chr14:52031265 | G | A | 10 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2258-1575C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031265 | |||||||
chr14:52031269 | A | G | 1 | a0018c0028t0001g0324 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2258-1579T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031269 | |||||||
chr14:52031349 | C | T | 1 | a0001c0001t0001g0019 | 2 | HG00642.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.2258-1659G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031349 | |||||||
chr14:52031393 | C | A | 51 | a0002c0003t0001g0123 a0003c0002t0001g0006 a0003c0002t0001g0013 others(48): Show |
56 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.2258-1703G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031393 | |||||||
chr14:52031414 | T | G | 2 | a0003c0002t0001g0018 a0003c0002t0001g0271 |
3 | HG01070.hp1 HG01361.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2258-1724A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031414 | |||||||
chr14:52031510 | C | T | 10 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2258-1820G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031510 | |||||||
chr14:52031615 | T | G | 8 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0302 others(5): Show |
8 | HG01109.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2258-1925A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031615 | |||||||
chr14:52031678 | C | A | 1 | a0002c0003t0001g0099 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2258-1988G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031678 | |||||||
chr14:52031689 | C | T | 3 | a0015c0056t0001g0331 a0015c0058t0001g0330 a0034c0057t0001g0314 |
3 | HG02723.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2258-1999G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031689 | |||||||
chr14:52031744 | G | A | 10 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.2258-2054C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031744 | |||||||
chr14:52031983 | T | C | 1 | a0011c0016t0001g0344 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2258-2293A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52031983 | |||||||
chr14:52032031 | A | G | 12 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(9): Show |
12 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2258-2341T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032031 | |||||||
chr14:52032213 | T | C | 2 | a0003c0002t0001g0014 a0003c0002t0001g0205 |
3 | HG00738.hp2 HG00741.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2258-2523A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032213 | |||||||
chr14:52032227 | G | A | 2 | a0013c0017t0001g0008 a0013c0017t0001g0186 |
3 | HG02280.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2258-2537C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032227 | |||||||
chr14:52032287 | C | T | 332 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(329): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.2258-2597G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032287 | |||||||
chr14:52032296 | T | A | 1 | a0032c0043t0001g0146 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2258-2606A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032296 | |||||||
chr14:52032320 | G | A | 121 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(118): Show |
137 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.2258-2630C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032320 | |||||||
chr14:52032408 | G | C | 303 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(300): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.2258-2718C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032408 | |||||||
chr14:52032430 | G | C | 14 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(11): Show |
15 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2258-2740C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032430 | |||||||
chr14:52032431 | G | A | 14 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(11): Show |
15 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2258-2741C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032431 | |||||||
chr14:52032450 | C | T | 15 | a0004c0006t0001g0297 a0004c0012t0002g0299 a0004c0012t0002g0300 others(12): Show |
16 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.2258-2760G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032450 | |||||||
chr14:52032543 | T | C | 318 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(315): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.2258-2853A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032543 | |||||||
chr14:52032578 | GATCATCT others(3): Show |
G | 125 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(122): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.2258-2898_2258-288 others(14): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032578 | |||||||
chr14:52032585 | T | C | 14 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(11): Show |
15 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2258-2895A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032585 | |||||||
chr14:52032619 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0060 |
3 | NA18969.hp2 NA19055.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2258-2929G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032619 | |||||||
chr14:52032691 | T | A | 12 | a0001c0007t0001g0092 a0001c0022t0001g0029 a0001c0022t0001g0091 others(9): Show |
12 | HG02109.hp1 HG02622.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.2258-3001A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032691 | |||||||
chr14:52032698 | C | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0262 a0001c0005t0001g0263 others(1): Show |
5 | HG00099.hp1 HG00735.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.2258-3008G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032698 | |||||||
chr14:52032804 | G | GAAAAA | 56 | a0001c0001t0001g0196 a0001c0001t0001g0238 a0001c0005t0001g0220 others(53): Show |
61 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.2258-3119_2258-311 others(9): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032804 | |||||||
chr14:52032804 | G | GAAAAAA | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.2258-3120_2258-311 others(10): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032804 | |||||||
chr14:52032804 | G | GAAAAAAA | 116 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0078 others(113): Show |
117 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.2258-3121_2258-311 others(11): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032804 | |||||||
chr14:52032804 | G | GAAAAAAA others(7): Show |
1 | a0026c0037t0001g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2258-3115_2258-311 others(18): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032804 | |||||||
chr14:52032804 | G | GAAAAAGA others(6): Show |
2 | a0028c0029t0001g0142 a0031c0068t0001g0334 |
2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2258-3115_2258-311 others(17): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032804 | |||||||
chr14:52032812 | A | AAAAACAA others(12): Show |
2 | a0013c0017t0001g0008 a0013c0017t0001g0186 |
3 | HG02280.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2258-3123_2258-312 others(23): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032812 | |||||||
chr14:52032812 | A | AAAACAAA others(11): Show |
12 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(9): Show |
12 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2258-3123_2258-312 others(22): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032812 | |||||||
chr14:52032952 | T | A | 12 | a0001c0005t0001g0175 a0002c0027t0001g0188 a0002c0027t0001g0189 others(9): Show |
12 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.2258-3262A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032952 | |||||||
chr14:52032955 | C | A | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2258-3265G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032955 | |||||||
chr14:52032986 | T | G | 14 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(11): Show |
15 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2258-3296A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52032986 | |||||||
chr14:52033049 | T | G | 2 | a0011c0016t0001g0339 a0011c0016t0001g0340 |
2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2258-3359A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52033049 | |||||||
chr14:52033117 | A | G | 12 | a0001c0007t0001g0092 a0001c0022t0001g0029 a0001c0022t0001g0091 others(9): Show |
12 | HG02109.hp1 HG02622.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.2258-3427T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52033117 | |||||||
chr14:52033251 | G | A | 9 | a0002c0003t0001g0010 a0002c0003t0001g0135 a0002c0003t0001g0136 others(6): Show |
10 | NA18946.hp2 NA18953.hp1 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.2258-3561C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52033251 | |||||||
chr14:52033460 | G | A | 190 | a0001c0005t0001g0175 a0001c0007t0001g0084 a0001c0007t0001g0181 others(187): Show |
196 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.2258-3770C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52033460 | |||||||
chr14:52033462 | T | TG | 14 | a0002c0004t0001g0147 a0002c0004t0001g0148 a0007c0011t0001g0027 others(11): Show |
14 | HG00438.hp2 HG01358.hp2 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.2258-3773dupC | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52033462 | |||||||
chr14:52033523 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(117): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.2258-3833C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52033523 | |||||||
chr14:52033549 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2258-3859C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52033549 | |||||||
chr14:52033561 | C | T | 9 | a0002c0003t0001g0118 a0002c0004t0001g0088 a0002c0004t0001g0134 others(6): Show |
9 | HG01496.hp1 HG02083.hp2 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.2258-3871G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52033561 | |||||||
chr14:52033610 | T | C | 48 | a0002c0003t0001g0123 a0003c0002t0001g0006 a0003c0002t0001g0013 others(45): Show |
52 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2258-3920A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52033610 | |||||||
chr14:52033616 | A | AAG | 344 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(341): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.2258-3927_2258-392 others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52033616 | |||||||
chr14:52033618 | C | T | 344 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(341): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.2258-3928G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52033618 | |||||||
chr14:52033619 | T | G | 344 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(341): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.2258-3929A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52033619 | |||||||
chr14:52033622 | C | A | 344 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(341): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.2258-3932G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52033622 | |||||||
chr14:52033754 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2258-4064A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52033754 | |||||||
chr14:52033774 | G | C | 1 | a0001c0001t0001g0242 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2258-4084C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52033774 | |||||||
chr14:52033986 | A | G | 125 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(122): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.2258-4296T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52033986 | |||||||
chr14:52034069 | A | G | 299 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(296): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.2258-4379T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034069 | |||||||
chr14:52034111 | C | G | 298 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(295): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.2258-4421G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034111 | |||||||
chr14:52034134 | G | T | 3 | a0016c0064t0001g0328 a0016c0069t0001g0332 a0032c0043t0001g0146 |
3 | HG02818.hp2 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2258-4444C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034134 | |||||||
chr14:52034140 | G | A | 2 | a0016c0064t0001g0328 a0016c0069t0001g0332 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2258-4450C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034140 | |||||||
chr14:52034235 | A | C | 1 | a0001c0010t0001g0032 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2257+4512T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034235 | |||||||
chr14:52034235 | A | G | 297 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(294): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.2257+4512T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034235 | |||||||
chr14:52034265 | T | A | 1 | a0023c0049t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2257+4482A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034265 | |||||||
chr14:52034301 | G | A | 6 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 others(3): Show |
6 | HG02280.hp2 HG02615.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2257+4446C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034301 | |||||||
chr14:52034309 | A | AATT | 298 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(295): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.2257+4435_2257+443 others(7): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034309 | |||||||
chr14:52034400 | T | A | 1 | a0003c0002t0001g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2257+4347A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034400 | |||||||
chr14:52034431 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2257+4316T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034431 | |||||||
chr14:52034496 | T | C | 298 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(295): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.2257+4251A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034496 | |||||||
chr14:52034517 | A | C | 298 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(295): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.2257+4230T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034517 | |||||||
chr14:52034573 | G | C | 1 | a0002c0044t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2257+4174C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034573 | |||||||
chr14:52034693 | C | T | 297 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(294): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.2257+4054G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034693 | |||||||
chr14:52034721 | G | A | 1 | a0001c0007t0001g0181 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2257+4026C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034721 | |||||||
chr14:52034764 | T | C | 1 | a0001c0007t0001g0181 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2257+3983A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034764 | |||||||
chr14:52034781 | G | C | 13 | a0001c0005t0001g0287 a0001c0007t0001g0092 a0001c0022t0001g0029 others(10): Show |
13 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.2257+3966C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52034781 | |||||||
chr14:52035016 | T | C | 14 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(11): Show |
15 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2257+3731A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035016 | |||||||
chr14:52035018 | C | CA | 294 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(291): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.2257+3728_2257+372 others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035018 | |||||||
chr14:52035089 | A | G | 17 | a0003c0002t0001g0013 a0003c0002t0001g0014 a0003c0002t0001g0065 others(14): Show |
19 | HG00738.hp2 HG00741.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.2257+3658T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035089 | |||||||
chr14:52035114 | C | G | 1 | a0002c0003t0001g0100 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2257+3633G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035114 | |||||||
chr14:52035201 | A | T | 1 | a0002c0015t0001g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2257+3546T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035201 | |||||||
chr14:52035305 | C | T | 1 | a0008c0013t0001g0347 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2257+3442G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035305 | |||||||
chr14:52035335 | C | G | 142 | a0001c0007t0002g0204 a0001c0032t0001g0279 a0002c0003t0001g0010 others(139): Show |
143 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.2257+3412G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035335 | |||||||
chr14:52035497 | A | G | 343 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(340): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.2257+3250T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035497 | |||||||
chr14:52035509 | C | T | 8 | a0008c0013t0001g0318 a0008c0013t0001g0319 a0008c0013t0001g0320 others(5): Show |
8 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.2257+3238G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035509 | |||||||
chr14:52035527 | C | T | 1 | a0008c0052t0001g0306 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2257+3220G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035527 | |||||||
chr14:52035528 | G | A | 1 | a0002c0004t0001g0147 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2257+3219C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035528 | |||||||
chr14:52035627 | C | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(138): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.2257+3120G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035627 | |||||||
chr14:52035635 | G | A | 1 | a0018c0028t0001g0326 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2257+3112C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035635 | |||||||
chr14:52035668 | C | G | 11 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(8): Show |
11 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2257+3079G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035668 | |||||||
chr14:52035764 | C | T | 16 | a0001c0010t0001g0001 a0001c0010t0001g0032 a0001c0010t0001g0034 others(13): Show |
19 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2257+2983G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035764 | |||||||
chr14:52035825 | C | A | 8 | a0008c0013t0001g0318 a0008c0013t0001g0319 a0008c0013t0001g0320 others(5): Show |
8 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.2257+2922G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035825 | |||||||
chr14:52035856 | G | A | 8 | a0008c0013t0001g0318 a0008c0013t0001g0319 a0008c0013t0001g0320 others(5): Show |
8 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.2257+2891C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTA | 4 | a0002c0004t0001g0101 a0010c0019t0001g0341 a0025c0042t0001g0144 others(1): Show |
4 | HG02300.hp2 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2257+2889_2257+289 others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATA | 3 | a0002c0004t0001g0178 a0002c0048t0002g0040 a0023c0049t0001g0090 |
3 | HG01496.hp2 HG01891.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.2257+2887_2257+289 others(8): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATA | 3 | a0004c0006t0001g0316 a0004c0020t0001g0336 a0028c0029t0001g0142 |
3 | HG02451.hp1 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2257+2885_2257+289 others(10): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(1): Show |
20 | a0002c0003t0001g0108 a0002c0003t0001g0122 a0002c0003t0001g0125 others(17): Show |
20 | HG00099.hp2 HG00673.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.2257+2883_2257+289 others(12): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(3): Show |
38 | a0001c0032t0001g0279 a0002c0003t0001g0010 a0002c0003t0001g0053 others(35): Show |
39 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.2257+2881_2257+289 others(14): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(5): Show |
13 | a0002c0003t0001g0098 a0002c0003t0001g0100 a0002c0003t0001g0113 others(10): Show |
13 | HG00558.hp2 HG02004.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.2257+2879_2257+289 others(16): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(7): Show |
4 | a0002c0003t0001g0095 a0002c0003t0001g0116 a0002c0004t0001g0170 others(1): Show |
4 | HG00544.hp2 HG02165.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2257+2877_2257+289 others(18): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(13): Show |
5 | a0002c0003t0001g0093 a0002c0003t0001g0119 a0002c0004t0001g0022 others(2): Show |
5 | HG01123.hp2 HG01993.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.2257+2871_2257+289 others(24): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(15): Show |
7 | a0002c0004t0001g0041 a0002c0004t0001g0103 a0002c0004t0001g0104 others(4): Show |
7 | HG02080.hp2 HG02280.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.2257+2869_2257+289 others(26): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(17): Show |
9 | a0002c0004t0001g0042 a0002c0004t0001g0043 a0002c0004t0001g0164 others(6): Show |
9 | HG01361.hp1 HG01978.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2257+2890_2257+289 others(28): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(19): Show |
3 | a0002c0004t0001g0088 a0002c0004t0001g0165 a0002c0004t0001g0167 |
3 | NA18967.hp1 NA19004.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2257+2890_2257+289 others(30): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(21): Show |
2 | a0002c0003t0001g0117 a0002c0004t0001g0162 |
2 | HG00609.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.2257+2890_2257+289 others(32): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(23): Show |
7 | a0002c0004t0001g0096 a0002c0004t0001g0134 a0002c0004t0001g0153 others(4): Show |
7 | HG00558.hp1 HG02083.hp2 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.2257+2890_2257+289 others(34): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(25): Show |
3 | a0002c0004t0001g0121 a0002c0004t0001g0159 a0033c0062t0002g0303 |
3 | HG02056.hp1 HG03491.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.2257+2890_2257+289 others(36): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(27): Show |
3 | a0002c0003t0001g0118 a0002c0004t0001g0130 a0004c0012t0002g0299 |
3 | HG00609.hp2 HG01109.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.2257+2890_2257+289 others(38): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(29): Show |
1 | a0002c0004t0001g0097 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2257+2890_2257+289 others(40): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(31): Show |
2 | a0004c0012t0002g0300 a0004c0012t0002g0304 |
2 | HG00639.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2257+2890_2257+289 others(42): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(33): Show |
1 | a0002c0004t0001g0105 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2257+2890_2257+289 others(44): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(37): Show |
2 | a0002c0004t0001g0139 a0004c0060t0001g0298 |
2 | HG00735.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2257+2890_2257+289 others(48): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(9): Show |
14 | a0001c0010t0001g0001 a0001c0010t0001g0032 a0001c0010t0001g0034 others(11): Show |
17 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2257+2890_2257+289 others(20): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTATATAT others(11): Show |
1 | a0001c0010t0001g0183 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2257+2890_2257+289 others(22): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTGTATAT others(7): Show |
1 | a0016c0064t0001g0328 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2257+2890_2257+289 others(18): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | G | GTGTATAT others(21): Show |
1 | a0016c0069t0001g0332 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2257+2890_2257+289 others(32): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035856 | GTA | G | 11 | a0002c0004t0001g0147 a0002c0004t0001g0148 a0003c0002t0001g0049 others(8): Show |
11 | HG00438.hp2 HG02622.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2257+2889_2257+289 others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035856 | |||||||
chr14:52035865 | T | TATGTGTA others(17): Show |
2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2257+2881_2257+288 others(28): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035865 | |||||||
chr14:52035868 | A | G | 114 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(111): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.2257+2879T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035868 | |||||||
chr14:52035878 | A | ATACATAT others(19): Show |
110 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(107): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.2257+2868_2257+286 others(30): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035878 | |||||||
chr14:52035878 | A | ATACATAT others(45): Show |
1 | a0001c0001t0001g0007 | 2 | NA18944.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.2257+2868_2257+286 others(56): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035878 | |||||||
chr14:52035878 | A | ATATATAT others(29): Show |
1 | a0008c0013t0001g0348 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2257+2868_2257+286 others(40): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035878 | |||||||
chr14:52035878 | A | ATATATAT others(29): Show |
1 | a0013c0017t0001g0008 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2257+2868_2257+286 others(40): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035878 | |||||||
chr14:52035878 | A | ATATATAT others(17): Show |
1 | a0008c0013t0001g0347 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2257+2868_2257+286 others(28): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035878 | |||||||
chr14:52035878 | A | ATATATAT others(11): Show |
1 | a0008c0013t0001g0320 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2257+2868_2257+286 others(22): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035878 | |||||||
chr14:52035878 | A | ATATATAT others(7): Show |
1 | a0021c0063t0001g0343 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2257+2868_2257+286 others(18): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035878 | |||||||
chr14:52035878 | A | ATATATAT others(5): Show |
3 | a0008c0013t0001g0318 a0008c0013t0001g0319 a0022c0046t0001g0182 |
3 | HG00323.hp1 HG00642.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.2257+2868_2257+286 others(16): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035878 | |||||||
chr14:52035878 | A | ATATATAT others(9): Show |
1 | a0001c0033t0001g0286 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2257+2868_2257+286 others(20): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035878 | |||||||
chr14:52035878 | A | ATATATTT others(5): Show |
1 | a0013c0017t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2257+2868_2257+286 others(16): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035878 | |||||||
chr14:52035878 | A | T | 18 | a0001c0010t0001g0001 a0001c0010t0001g0032 a0001c0010t0001g0034 others(15): Show |
21 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2257+2869T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52035878 | |||||||
chr14:52036074 | C | A | 278 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(275): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2257+2673G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036074 | |||||||
chr14:52036077 | C | A | 278 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(275): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2257+2670G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036077 | |||||||
chr14:52036086 | G | A | 1 | a0002c0004t0001g0043 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2257+2661C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036086 | |||||||
chr14:52036158 | C | T | 1 | a0008c0013t0001g0348 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2257+2589G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036158 | |||||||
chr14:52036181 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2257+2566A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036181 | |||||||
chr14:52036207 | A | G | 1 | a0026c0037t0001g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2257+2540T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036207 | |||||||
chr14:52036213 | T | C | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(137): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2257+2534A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036213 | |||||||
chr14:52036340 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(137): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2257+2407G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036340 | |||||||
chr14:52036369 | A | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(137): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2257+2378T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036369 | |||||||
chr14:52036441 | C | G | 2 | a0011c0016t0001g0339 a0011c0016t0001g0340 |
2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2257+2306G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036441 | |||||||
chr14:52036537 | C | A | 2 | a0006c0008t0001g0345 a0006c0008t0001g0346 |
2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2257+2210G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036537 | |||||||
chr14:52036612 | T | C | 8 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(5): Show |
8 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2257+2135A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036612 | |||||||
chr14:52036651 | T | C | 250 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(247): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.2257+2096A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036651 | |||||||
chr14:52036678 | G | A | 250 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(247): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.2257+2069C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036678 | |||||||
chr14:52036741 | T | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(38): Show |
45 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.2257+2006A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036741 | |||||||
chr14:52036827 | T | C | 280 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(277): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2257+1920A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036827 | |||||||
chr14:52036872 | A | AG | 280 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(277): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2257+1874_2257+187 others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036872 | |||||||
chr14:52036879 | G | A | 1 | a0004c0006t0001g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2257+1868C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52036879 | |||||||
chr14:52037167 | C | T | 2 | a0007c0011t0001g0288 a0007c0011t0001g0289 |
2 | HG01358.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2257+1580G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037167 | |||||||
chr14:52037213 | C | G | 1 | a0002c0003t0001g0093 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2257+1534G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037213 | |||||||
chr14:52037224 | A | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(137): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2257+1523T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037224 | |||||||
chr14:52037229 | T | A | 2 | a0001c0005t0001g0263 a0001c0005t0001g0281 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2257+1518A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037229 | |||||||
chr14:52037264 | T | TTTTTG | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(137): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2257+1478_2257+148 others(9): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037264 | |||||||
chr14:52037347 | GGTTT | G | 3 | a0008c0013t0001g0318 a0008c0013t0001g0319 a0008c0013t0001g0320 |
3 | HG00323.hp1 HG00642.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.2257+1396_2257+139 others(8): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037347 | |||||||
chr14:52037363 | G | C | 1 | a0003c0002t0001g0271 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2257+1384C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037363 | |||||||
chr14:52037418 | A | G | 1 | a0008c0013t0001g0348 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2257+1329T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037418 | |||||||
chr14:52037471 | T | A | 1 | a0005c0021t0001g0218 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2257+1276A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037471 | |||||||
chr14:52037543 | G | C | 140 | a0001c0032t0001g0279 a0002c0003t0001g0010 a0002c0003t0001g0053 others(137): Show |
141 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.2257+1204C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037543 | |||||||
chr14:52037572 | C | T | 1 | a0002c0015t0001g0127 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2257+1175G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037572 | |||||||
chr14:52037598 | T | G | 9 | a0004c0053t0001g0321 a0008c0013t0001g0318 a0008c0013t0001g0319 others(6): Show |
9 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.2257+1149A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037598 | |||||||
chr14:52037679 | T | G | 284 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(281): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2257+1068A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037679 | |||||||
chr14:52037724 | A | T | 1 | a0002c0004t0001g0132 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2257+1023T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037724 | |||||||
chr14:52037780 | T | C | 8 | a0008c0013t0001g0318 a0008c0013t0001g0319 a0008c0013t0001g0320 others(5): Show |
8 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.2257+967A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037780 | |||||||
chr14:52037844 | A | G | 140 | a0001c0032t0001g0279 a0002c0003t0001g0010 a0002c0003t0001g0053 others(137): Show |
141 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.2257+903T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037844 | |||||||
chr14:52037863 | C | A | 1 | a0001c0007t0001g0133 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2257+884G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037863 | |||||||
chr14:52037906 | T | C | 280 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(277): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2257+841A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037906 | |||||||
chr14:52037915 | C | T | 1 | a0030c0030t0001g0221 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2257+832G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52037915 | |||||||
chr14:52038042 | G | A | 1 | a0002c0004t0001g0023 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2257+705C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52038042 | |||||||
chr14:52038150 | C | T | 14 | a0001c0010t0001g0001 a0001c0010t0001g0032 a0001c0010t0001g0034 others(11): Show |
17 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2257+597G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52038150 | |||||||
chr14:52038183 | G | A | 3 | a0004c0006t0002g0350 a0028c0029t0001g0142 a0031c0068t0001g0334 |
3 | HG02895.hp1 HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2257+564C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52038183 | |||||||
chr14:52038232 | T | C | 111 | a0001c0032t0001g0279 a0002c0003t0001g0010 a0002c0003t0001g0053 others(108): Show |
112 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.2257+515A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52038232 | |||||||
chr14:52038237 | G | T | 9 | a0004c0053t0001g0321 a0008c0013t0001g0318 a0008c0013t0001g0319 others(6): Show |
9 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.2257+510C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52038237 | |||||||
chr14:52038515 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(129): Show |
148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.2257+232T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52038515 | |||||||
chr14:52038553 | G | A | 1 | a0003c0002t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2257+194C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52038553 | |||||||
chr14:52038642 | A | G | 280 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(277): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2257+105T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52038642 | |||||||
chr14:52038657 | A | G | 280 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(277): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2257+90T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 9/21 | chr14 | 52038657 | |||||||
chr14:52038999 | T | C | 8 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(5): Show |
8 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2027-22A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52038999 | |||||||
chr14:52039053 | T | A | 343 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(340): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.2027-76A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52039053 | |||||||
chr14:52039054 | T | G | 343 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(340): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.2027-77A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52039054 | |||||||
chr14:52039068 | T | A | 1 | a0002c0003t0001g0119 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2027-91A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52039068 | |||||||
chr14:52039082 | C | A | 2 | a0028c0029t0001g0142 a0031c0068t0001g0334 |
2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2027-105G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52039082 | |||||||
chr14:52039093 | C | T | 280 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(277): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2027-116G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52039093 | |||||||
chr14:52039191 | T | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(128): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.2027-214A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52039191 | |||||||
chr14:52039352 | C | T | 280 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(277): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2027-375G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52039352 | |||||||
chr14:52039459 | G | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(137): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2027-482C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52039459 | |||||||
chr14:52039541 | G | C | 1 | a0004c0006t0002g0350 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2027-564C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52039541 | |||||||
chr14:52039569 | C | T | 1 | a0001c0033t0001g0286 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2027-592G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52039569 | |||||||
chr14:52039616 | G | A | 1 | a0035c0047t0001g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2027-639C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52039616 | |||||||
chr14:52039723 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0262 a0001c0005t0001g0263 others(2): Show |
6 | HG00099.hp1 HG00735.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.2027-746C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52039723 | |||||||
chr14:52039729 | A | G | 1 | a0002c0044t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2027-752T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52039729 | |||||||
chr14:52039752 | G | A | 1 | a0002c0004t0001g0179 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2027-775C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52039752 | |||||||
chr14:52039768 | T | C | 280 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(277): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2027-791A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52039768 | |||||||
chr14:52040187 | C | A | 1 | a0018c0028t0001g0326 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2026+464G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52040187 | |||||||
chr14:52040251 | A | AT | 39 | a0001c0001t0001g0196 a0001c0001t0001g0211 a0001c0005t0001g0275 others(36): Show |
39 | HG00438.hp2 HG00639.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.2026+399dupA | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52040251 | |||||||
chr14:52040251 | A | ATT | 110 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(107): Show |
111 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2026+398_2026+399d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52040251 | |||||||
chr14:52040251 | A | ATTT | 8 | a0002c0003t0001g0100 a0002c0003t0001g0125 a0002c0004t0001g0132 others(5): Show |
8 | HG00673.hp2 HG01433.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2026+397_2026+399d others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52040251 | |||||||
chr14:52040251 | AT | A | 6 | a0002c0039t0001g0089 a0003c0036t0001g0176 a0004c0055t0001g0296 others(3): Show |
7 | HG01099.hp1 HG01952.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.2026+399delA | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52040251 | |||||||
chr14:52040389 | C | T | 1 | a0011c0016t0001g0344 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2026+262G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52040389 | |||||||
chr14:52040405 | G | T | 7 | a0007c0011t0001g0027 a0007c0011t0001g0031 a0007c0011t0001g0036 others(4): Show |
7 | HG00438.hp2 HG02602.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.2026+246C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52040405 | |||||||
chr14:52040423 | A | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(107): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2026+228T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52040423 | |||||||
chr14:52040488 | G | A | 139 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(136): Show |
140 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.2026+163C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52040488 | |||||||
chr14:52040519 | A | C | 1 | a0026c0037t0001g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2026+132T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52040519 | |||||||
chr14:52040616 | C | G | 8 | a0008c0013t0001g0318 a0008c0013t0001g0319 a0008c0013t0001g0320 others(5): Show |
8 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.2026+35G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 8/21 | chr14 | 52040616 | |||||||
chr14:52040884 | A | G | 1 | a0002c0003t0001g0099 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1826-33T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 7/21 | chr14 | 52040884 | |||||||
chr14:52041029 | T | C | 3 | a0004c0006t0002g0350 a0028c0029t0001g0142 a0031c0068t0001g0334 |
3 | HG02895.hp1 HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1826-178A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 7/21 | chr14 | 52041029 | |||||||
chr14:52041114 | G | A | 1 | a0002c0003t0001g0124 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1826-263C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 7/21 | chr14 | 52041114 | |||||||
chr14:52041179 | C | CA | 111 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(108): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1826-329dupT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 7/21 | chr14 | 52041179 | |||||||
chr14:52041305 | A | G | 1 | a0001c0005t0001g0287 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1826-454T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 7/21 | chr14 | 52041305 | |||||||
chr14:52041346 | G | A | 1 | a0002c0004t0001g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1826-495C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 7/21 | chr14 | 52041346 | |||||||
chr14:52041347 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0264 |
2 | NA18971.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1826-496C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 7/21 | chr14 | 52041347 | |||||||
chr14:52041596 | C | T | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1825+509G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 7/21 | chr14 | 52041596 | |||||||
chr14:52041823 | G | T | 39 | a0002c0004t0001g0147 a0002c0004t0001g0148 a0002c0048t0002g0040 others(36): Show |
39 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1825+282C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 7/21 | chr14 | 52041823 | |||||||
chr14:52041960 | G | C | 30 | a0002c0004t0001g0147 a0002c0004t0001g0148 a0002c0048t0002g0040 others(27): Show |
30 | HG00438.hp2 HG00639.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1825+145C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 7/21 | chr14 | 52041960 | |||||||
chr14:52042077 | T | C | 2 | a0028c0029t0001g0142 a0031c0068t0001g0334 |
2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1825+28A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 7/21 | chr14 | 52042077 | |||||||
chr14:52042079 | C | G | 2 | a0028c0029t0001g0142 a0031c0068t0001g0334 |
2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1825+26G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 7/21 | chr14 | 52042079 | |||||||
chr14:52042383 | G | A | 280 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(277): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1580-33C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 6/21 | chr14 | 52042383 | |||||||
chr14:52042413 | G | A | 36 | a0002c0004t0001g0147 a0002c0004t0001g0148 a0002c0048t0002g0040 others(33): Show |
36 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1580-63C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 6/21 | chr14 | 52042413 | |||||||
chr14:52042541 | TA | T | 279 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(276): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1580-192delT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 6/21 | chr14 | 52042541 | |||||||
chr14:52042765 | T | A | 1 | a0002c0004t0001g0178 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1579+17A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 6/21 | chr14 | 52042765 | |||||||
chr14:52042765 | T | C | 279 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(276): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1579+17A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 6/21 | chr14 | 52042765 | |||||||
chr14:52042766 | G | A | 279 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(276): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1579+16C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 6/21 | chr14 | 52042766 | |||||||
chr14:52042767 | G | C | 1 | a0002c0004t0001g0178 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1579+15C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 6/21 | chr14 | 52042767 | |||||||
chr14:52042939 | A | G | 1 | a0001c0005t0001g0275 | 1 | HG02647.hp1 | splice_region_variant&intron_variant | LOW | c.1430-8T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52042939 | |||||||
chr14:52043061 | C | T | 4 | a0003c0002t0001g0048 a0015c0056t0001g0331 a0015c0058t0001g0330 others(1): Show |
4 | HG02723.hp1 HG03540.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.1430-130G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043061 | |||||||
chr14:52043070 | A | G | 58 | a0003c0002t0001g0006 a0003c0002t0001g0013 a0003c0002t0001g0014 others(55): Show |
63 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.1430-139T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043070 | |||||||
chr14:52043140 | C | T | 145 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(142): Show |
146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1430-209G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043140 | |||||||
chr14:52043169 | A | G | 145 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(142): Show |
146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1430-238T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043169 | |||||||
chr14:52043177 | C | T | 8 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(5): Show |
8 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1430-246G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043177 | |||||||
chr14:52043373 | G | T | 145 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(142): Show |
146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1430-442C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043373 | |||||||
chr14:52043494 | G | T | 25 | a0001c0010t0001g0001 a0001c0010t0001g0032 a0001c0010t0001g0034 others(22): Show |
29 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1430-563C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043494 | |||||||
chr14:52043495 | G | C | 25 | a0001c0010t0001g0001 a0001c0010t0001g0032 a0001c0010t0001g0034 others(22): Show |
29 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1430-564C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043495 | |||||||
chr14:52043619 | C | A | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1430-688G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043619 | |||||||
chr14:52043622 | C | G | 1 | a0001c0005t0001g0236 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1430-691G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043622 | |||||||
chr14:52043742 | G | A | 25 | a0001c0010t0001g0001 a0001c0010t0001g0032 a0001c0010t0001g0034 others(22): Show |
29 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1430-811C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043742 | |||||||
chr14:52043761 | A | G | 1 | a0019c0031t0001g0025 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1430-830T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043761 | |||||||
chr14:52043779 | G | A | 2 | a0002c0003t0001g0192 a0002c0004t0001g0150 |
2 | NA18985.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1430-848C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043779 | |||||||
chr14:52043779 | G | T | 2 | a0002c0004t0001g0147 a0002c0004t0001g0148 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1430-848C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043779 | |||||||
chr14:52043794 | G | A | 123 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(120): Show |
124 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1430-863C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043794 | |||||||
chr14:52043827 | C | A | 1 | a0029c0061t0001g0329 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1430-896G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043827 | |||||||
chr14:52043849 | A | G | 57 | a0003c0002t0001g0006 a0003c0002t0001g0013 a0003c0002t0001g0014 others(54): Show |
62 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.1430-918T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043849 | |||||||
chr14:52043860 | G | T | 2 | a0002c0048t0002g0040 a0023c0049t0001g0090 |
2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1430-929C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043860 | |||||||
chr14:52043878 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0284 |
3 | HG00642.hp1 HG01243.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1430-947G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043878 | |||||||
chr14:52043984 | G | A | 2 | a0028c0029t0001g0142 a0031c0068t0001g0334 |
2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1430-1053C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52043984 | |||||||
chr14:52044121 | G | T | 11 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(8): Show |
11 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1430-1190C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044121 | |||||||
chr14:52044162 | T | C | 1 | a0003c0002t0001g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1430-1231A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044162 | |||||||
chr14:52044266 | C | CT | 163 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(160): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1430-1336dupA | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044266 | |||||||
chr14:52044266 | C | CTT | 33 | a0001c0001t0001g0012 a0001c0001t0001g0077 a0001c0001t0001g0210 others(30): Show |
36 | HG00280.hp2 HG00438.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1430-1337_1430-133 others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044266 | |||||||
chr14:52044266 | C | CTTTT | 11 | a0002c0004t0001g0147 a0002c0004t0001g0148 a0007c0011t0001g0027 others(8): Show |
11 | HG00438.hp2 HG02602.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1430-1339_1430-133 others(8): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044266 | |||||||
chr14:52044266 | CTTT | C | 102 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(99): Show |
103 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1430-1338_1430-133 others(7): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044266 | |||||||
chr14:52044266 | CTTTT | C | 21 | a0002c0003t0001g0129 a0002c0004t0001g0174 a0002c0048t0002g0040 others(18): Show |
21 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1430-1339_1430-133 others(8): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044266 | |||||||
chr14:52044348 | C | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(104): Show |
119 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.1430-1417G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044348 | |||||||
chr14:52044384 | C | G | 128 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(125): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1430-1453G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044384 | |||||||
chr14:52044411 | AG | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(141): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1430-1481delC | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044411 | |||||||
chr14:52044470 | C | T | 131 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(128): Show |
132 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1430-1539G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044470 | |||||||
chr14:52044484 | A | G | 2 | a0003c0002t0001g0072 a0003c0002t0001g0073 |
2 | NA18994.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1430-1553T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044484 | |||||||
chr14:52044562 | G | A | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1430-1631C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044562 | |||||||
chr14:52044565 | C | T | 1 | a0002c0003t0001g0125 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1430-1634G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044565 | |||||||
chr14:52044605 | A | G | 3 | a0013c0017t0001g0008 a0013c0017t0001g0186 a0036c0066t0001g0322 |
4 | HG02280.hp1 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1430-1674T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044605 | |||||||
chr14:52044610 | CT | C | 276 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(273): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1430-1680delA | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044610 | |||||||
chr14:52044692 | A | T | 1 | a0026c0037t0001g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1430-1761T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044692 | |||||||
chr14:52044697 | C | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0196 a0001c0001t0001g0197 others(8): Show |
12 | HG01243.hp1 HG02055.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1430-1766G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044697 | |||||||
chr14:52044800 | G | T | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1430-1869C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044800 | |||||||
chr14:52044807 | G | C | 1 | a0002c0004t0001g0130 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1430-1876C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044807 | |||||||
chr14:52044821 | T | C | 118 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(115): Show |
119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1430-1890A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044821 | |||||||
chr14:52044828 | G | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(141): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1430-1897C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044828 | |||||||
chr14:52044843 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1430-1912G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044843 | |||||||
chr14:52044878 | C | G | 129 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(126): Show |
130 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1430-1947G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044878 | |||||||
chr14:52044920 | G | T | 2 | a0001c0007t0001g0278 a0019c0031t0001g0025 |
2 | HG00280.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1430-1989C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044920 | |||||||
chr14:52044923 | A | C | 22 | a0001c0010t0001g0001 a0001c0010t0001g0032 a0001c0010t0001g0034 others(19): Show |
25 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1430-1992T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044923 | |||||||
chr14:52044991 | T | C | 133 | a0001c0032t0001g0279 a0002c0003t0001g0010 a0002c0003t0001g0053 others(130): Show |
134 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.1430-2060A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52044991 | |||||||
chr14:52045063 | C | G | 8 | a0008c0013t0001g0318 a0008c0013t0001g0319 a0008c0013t0001g0320 others(5): Show |
8 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1430-2132G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045063 | |||||||
chr14:52045118 | C | T | 276 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(273): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1430-2187G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045118 | |||||||
chr14:52045128 | G | A | 8 | a0008c0013t0001g0318 a0008c0013t0001g0319 a0008c0013t0001g0320 others(5): Show |
8 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1430-2197C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045128 | |||||||
chr14:52045130 | G | A | 3 | a0016c0064t0001g0328 a0016c0069t0001g0332 a0032c0043t0001g0146 |
3 | HG02818.hp2 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1430-2199C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045130 | |||||||
chr14:52045160 | C | T | 109 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(106): Show |
122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1430-2229G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045160 | |||||||
chr14:52045179 | T | C | 4 | a0007c0011t0001g0288 a0007c0011t0001g0289 a0028c0029t0001g0142 others(1): Show |
4 | HG01358.hp2 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1430-2248A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045179 | |||||||
chr14:52045193 | G | C | 26 | a0003c0002t0001g0006 a0003c0002t0001g0048 a0003c0002t0001g0049 others(23): Show |
27 | HG00423.hp1 HG00673.hp1 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1430-2262C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045193 | |||||||
chr14:52045244 | A | G | 8 | a0008c0013t0001g0318 a0008c0013t0001g0319 a0008c0013t0001g0320 others(5): Show |
8 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1430-2313T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045244 | |||||||
chr14:52045251 | G | T | 26 | a0003c0002t0001g0006 a0003c0002t0001g0048 a0003c0002t0001g0049 others(23): Show |
27 | HG00423.hp1 HG00673.hp1 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1430-2320C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045251 | |||||||
chr14:52045456 | T | C | 1 | a0005c0009t0001g0224 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1430-2525A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045456 | |||||||
chr14:52045557 | A | AAT | 111 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(108): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1430-2627_1430-262 others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045557 | |||||||
chr14:52045558 | A | AT | 165 | a0001c0001t0001g0060 a0001c0010t0001g0001 a0001c0010t0001g0032 others(162): Show |
169 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1430-2628_1430-262 others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045558 | |||||||
chr14:52045564 | A | T | 3 | a0001c0001t0001g0226 a0001c0001t0001g0265 a0002c0004t0001g0169 |
3 | HG02293.hp2 HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1430-2633T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045564 | |||||||
chr14:52045620 | ACTGT | A | 111 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(108): Show |
112 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1430-2693_1430-269 others(8): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045620 | |||||||
chr14:52045659 | G | A | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1430-2728C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045659 | |||||||
chr14:52045773 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(138): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1430-2842C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045773 | |||||||
chr14:52045856 | C | T | 1 | a0001c0023t0001g0033 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1430-2925G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045856 | |||||||
chr14:52045866 | C | A | 1 | a0036c0066t0001g0322 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1430-2935G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045866 | |||||||
chr14:52045892 | A | G | 283 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(280): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1430-2961T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045892 | |||||||
chr14:52045899 | C | CTG | 283 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(280): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1430-2970_1430-296 others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52045899 | |||||||
chr14:52046068 | A | C | 112 | a0001c0032t0001g0279 a0002c0003t0001g0010 a0002c0003t0001g0053 others(109): Show |
113 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1430-3137T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046068 | |||||||
chr14:52046139 | C | T | 2 | a0002c0048t0002g0040 a0023c0049t0001g0090 |
2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1430-3208G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046139 | |||||||
chr14:52046151 | G | A | 252 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(249): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1430-3220C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046151 | |||||||
chr14:52046255 | G | A | 1 | a0004c0012t0002g0304 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1430-3324C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046255 | |||||||
chr14:52046278 | G | A | 1 | a0013c0017t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1430-3347C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046278 | |||||||
chr14:52046285 | T | C | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1430-3354A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046285 | |||||||
chr14:52046322 | C | CA | 51 | a0003c0002t0001g0006 a0003c0002t0001g0013 a0003c0002t0001g0014 others(48): Show |
56 | HG00639.hp2 HG00673.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.1430-3392dupT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046322 | |||||||
chr14:52046322 | C | CAA | 9 | a0001c0007t0001g0278 a0003c0002t0001g0052 a0003c0002t0001g0072 others(6): Show |
9 | HG00423.hp1 HG01261.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1430-3393_1430-339 others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046322 | |||||||
chr14:52046326 | A | G | 1 | a0011c0016t0001g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1430-3395T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046326 | |||||||
chr14:52046341 | A | AAAAGC | 36 | a0001c0010t0001g0001 a0001c0010t0001g0032 a0001c0010t0001g0034 others(33): Show |
39 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1430-3411_1430-341 others(9): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046341 | |||||||
chr14:52046341 | A | AAAGC | 122 | a0001c0001t0001g0024 a0001c0001t0001g0063 a0001c0001t0001g0203 others(119): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.1430-3411_1430-341 others(8): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046341 | |||||||
chr14:52046341 | A | AAGC | 108 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(105): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1430-3413_1430-341 others(7): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046341 | |||||||
chr14:52046341 | A | AGC | 9 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0008c0013t0001g0318 others(6): Show |
9 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1430-3411_1430-341 others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046341 | |||||||
chr14:52046346 | G | A | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1430-3415C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046346 | |||||||
chr14:52046465 | G | A | 1 | a0026c0037t0001g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1430-3534C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046465 | |||||||
chr14:52046473 | A | G | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1430-3542T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046473 | |||||||
chr14:52046484 | G | A | 272 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(269): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1430-3553C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046484 | |||||||
chr14:52046593 | C | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(128): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1430-3662G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046593 | |||||||
chr14:52046594 | G | A | 20 | a0004c0006t0002g0350 a0004c0012t0002g0299 a0004c0012t0002g0300 others(17): Show |
20 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.1430-3663C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046594 | |||||||
chr14:52046656 | C | G | 1 | a0001c0007t0001g0084 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1430-3725G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046656 | |||||||
chr14:52046855 | A | G | 1 | a0004c0006t0002g0350 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1430-3924T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046855 | |||||||
chr14:52046942 | C | T | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1430-4011G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52046942 | |||||||
chr14:52047039 | G | T | 1 | a0001c0001t0001g0059 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1430-4108C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52047039 | |||||||
chr14:52047109 | T | C | 3 | a0016c0064t0001g0328 a0016c0069t0001g0332 a0032c0043t0001g0146 |
3 | HG02818.hp2 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1430-4178A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52047109 | |||||||
chr14:52047365 | G | T | 2 | a0016c0064t0001g0328 a0016c0069t0001g0332 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1430-4434C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52047365 | |||||||
chr14:52047496 | C | T | 1 | a0004c0006t0001g0313 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1430-4565G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52047496 | |||||||
chr14:52047521 | G | A | 1 | a0011c0016t0001g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1430-4590C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52047521 | |||||||
chr14:52047526 | C | T | 1 | a0002c0044t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1430-4595G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52047526 | |||||||
chr14:52047648 | C | T | 8 | a0008c0013t0001g0318 a0008c0013t0001g0319 a0008c0013t0001g0320 others(5): Show |
8 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1430-4717G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52047648 | |||||||
chr14:52047787 | G | A | 2 | a0014c0024t0001g0269 a0014c0024t0001g0270 |
2 | HG01255.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1430-4856C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52047787 | |||||||
chr14:52047865 | G | A | 8 | a0008c0013t0001g0318 a0008c0013t0001g0319 a0008c0013t0001g0320 others(5): Show |
8 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1430-4934C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52047865 | |||||||
chr14:52047966 | G | A | 283 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(280): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1430-5035C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52047966 | |||||||
chr14:52047970 | C | T | 2 | a0031c0068t0001g0334 a0035c0047t0001g0044 |
2 | HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1430-5039G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52047970 | |||||||
chr14:52048015 | C | A | 150 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(147): Show |
166 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1430-5084G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048015 | |||||||
chr14:52048138 | G | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(139): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1430-5207C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048138 | |||||||
chr14:52048194 | T | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(149): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1430-5263A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048194 | |||||||
chr14:52048210 | G | T | 1 | a0001c0007t0001g0084 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1430-5279C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048210 | |||||||
chr14:52048217 | T | C | 1 | a0002c0003t0001g0173 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1430-5286A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048217 | |||||||
chr14:52048244 | G | A | 1 | a0002c0003t0001g0122 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1430-5313C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048244 | |||||||
chr14:52048263 | A | G | 151 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(148): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1429+5316T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048263 | |||||||
chr14:52048491 | A | G | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(140): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1429+5088T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048491 | |||||||
chr14:52048498 | C | A | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(140): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1429+5081G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048498 | |||||||
chr14:52048541 | T | G | 154 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(151): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.1429+5038A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048541 | |||||||
chr14:52048589 | T | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(128): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1429+4990A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048589 | |||||||
chr14:52048611 | T | C | 1 | a0002c0004t0001g0156 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1429+4968A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048611 | |||||||
chr14:52048751 | A | G | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(140): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1429+4828T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048751 | |||||||
chr14:52048798 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(103): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1429+4781C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048798 | |||||||
chr14:52048799 | G | A | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(140): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1429+4780C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048799 | |||||||
chr14:52048804 | A | G | 2 | a0002c0048t0002g0040 a0023c0049t0001g0090 |
2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1429+4775T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048804 | |||||||
chr14:52048842 | G | A | 1 | a0003c0002t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1429+4737C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048842 | |||||||
chr14:52048910 | C | T | 1 | a0006c0008t0001g0345 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1429+4669G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048910 | |||||||
chr14:52048998 | A | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(149): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1429+4581T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52048998 | |||||||
chr14:52049042 | T | C | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(140): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1429+4537A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049042 | |||||||
chr14:52049169 | ATC | A | 8 | a0008c0013t0001g0318 a0008c0013t0001g0319 a0008c0013t0001g0320 others(5): Show |
8 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1429+4408_1429+440 others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049169 | |||||||
chr14:52049173 | C | CT | 142 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(139): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1429+4405dupA | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049173 | |||||||
chr14:52049190 | TG | T | 9 | a0004c0006t0002g0350 a0008c0013t0001g0318 a0008c0013t0001g0319 others(6): Show |
9 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1429+4388delC | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049190 | |||||||
chr14:52049197 | TTTG | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(139): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1429+4379_1429+438 others(7): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049197 | |||||||
chr14:52049422 | C | T | 1 | a0001c0007t0001g0084 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1429+4157G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049422 | |||||||
chr14:52049445 | G | C | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(140): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1429+4134C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049445 | |||||||
chr14:52049453 | CAG | C | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(140): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1429+4124_1429+412 others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049453 | |||||||
chr14:52049575 | C | CA | 113 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(110): Show |
114 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.1429+4003dupT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049575 | |||||||
chr14:52049575 | CA | C | 149 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(146): Show |
165 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1429+4003delT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049575 | |||||||
chr14:52049630 | C | G | 1 | a0001c0010t0001g0032 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1429+3949G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049630 | |||||||
chr14:52049663 | A | G | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1429+3916T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049663 | |||||||
chr14:52049677 | C | T | 152 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(149): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1429+3902G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049677 | |||||||
chr14:52049700 | CCA | C | 142 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(139): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1429+3877_1429+387 others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049700 | |||||||
chr14:52049734 | G | C | 2 | a0028c0029t0001g0142 a0031c0068t0001g0334 |
2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1429+3845C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049734 | |||||||
chr14:52049805 | A | G | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1429+3774T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049805 | |||||||
chr14:52049849 | T | C | 132 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(129): Show |
133 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1429+3730A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049849 | |||||||
chr14:52049849 | T | G | 152 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(149): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1429+3730A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049849 | |||||||
chr14:52049883 | C | G | 142 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(139): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1429+3696G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049883 | |||||||
chr14:52049883 | C | T | 16 | a0003c0002t0001g0013 a0003c0002t0001g0014 a0003c0002t0001g0184 others(13): Show |
18 | HG00738.hp2 HG00741.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.1429+3696G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52049883 | |||||||
chr14:52050134 | G | A | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1429+3445C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52050134 | |||||||
chr14:52050220 | C | A | 2 | a0002c0027t0001g0188 a0002c0027t0001g0189 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1429+3359G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52050220 | |||||||
chr14:52050225 | T | A | 5 | a0002c0004t0001g0162 a0002c0004t0001g0164 a0002c0004t0001g0165 others(2): Show |
5 | HG00609.hp1 NA18941.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.1429+3354A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52050225 | |||||||
chr14:52050234 | G | A | 2 | a0002c0048t0002g0040 a0023c0049t0001g0090 |
2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1429+3345C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52050234 | |||||||
chr14:52050339 | G | A | 2 | a0002c0004t0001g0151 a0002c0004t0001g0152 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1429+3240C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52050339 | |||||||
chr14:52050472 | G | C | 118 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(115): Show |
119 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.1429+3107C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52050472 | |||||||
chr14:52050605 | AC | A | 11 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(8): Show |
11 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1429+2973delG | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52050605 | |||||||
chr14:52050614 | GACA | G | 12 | a0002c0025t0001g0028 a0002c0025t0001g0030 a0002c0041t0001g0046 others(9): Show |
12 | HG00438.hp2 HG02602.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.1429+2962_1429+296 others(7): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52050614 | |||||||
chr14:52050768 | C | T | 1 | a0001c0005t0001g0274 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1429+2811G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52050768 | |||||||
chr14:52050828 | C | T | 14 | a0002c0025t0001g0028 a0002c0025t0001g0030 a0002c0041t0001g0046 others(11): Show |
14 | HG00438.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1429+2751G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52050828 | |||||||
chr14:52050911 | A | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(198): Show |
222 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1429+2668T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52050911 | |||||||
chr14:52051004 | C | T | 3 | a0013c0017t0001g0008 a0013c0017t0001g0186 a0036c0066t0001g0322 |
4 | HG02280.hp1 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1429+2575G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52051004 | |||||||
chr14:52051136 | G | C | 1 | a0018c0028t0001g0324 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1429+2443C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52051136 | |||||||
chr14:52051139 | A | C | 3 | a0002c0004t0001g0154 a0002c0004t0001g0155 a0002c0004t0001g0156 |
3 | HG01192.hp2 HG01981.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1429+2440T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52051139 | |||||||
chr14:52051190 | GA | G | 200 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(197): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1429+2388delT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52051190 | |||||||
chr14:52051583 | A | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0227 |
4 | NA18963.hp1 NA18979.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1429+1996T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52051583 | |||||||
chr14:52051584 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0227 |
4 | NA18963.hp1 NA18979.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1429+1995T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52051584 | |||||||
chr14:52051619 | A | G | 1 | a0037c0054t0001g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1429+1960T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52051619 | |||||||
chr14:52051767 | T | C | 224 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(221): Show |
245 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1429+1812A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52051767 | |||||||
chr14:52051777 | G | A | 3 | a0016c0064t0001g0328 a0016c0069t0001g0332 a0032c0043t0001g0146 |
3 | HG02818.hp2 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1429+1802C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52051777 | |||||||
chr14:52051795 | A | G | 1 | a0028c0029t0001g0142 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1429+1784T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52051795 | |||||||
chr14:52051867 | T | C | 1 | a0001c0005t0001g0177 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1429+1712A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52051867 | |||||||
chr14:52051907 | T | C | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1429+1672A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52051907 | |||||||
chr14:52051965 | A | G | 212 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(209): Show |
233 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1429+1614T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52051965 | |||||||
chr14:52052082 | T | C | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1429+1497A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52052082 | |||||||
chr14:52052093 | G | A | 200 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(197): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1429+1486C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52052093 | |||||||
chr14:52052144 | G | A | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1429+1435C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52052144 | |||||||
chr14:52052419 | G | A | 2 | a0002c0004t0001g0023 a0004c0006t0001g0297 |
2 | HG00099.hp2 HG00140.hp2 |
intron_variant | MODIFIER | c.1429+1160C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52052419 | |||||||
chr14:52052485 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1429+1094T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52052485 | |||||||
chr14:52052536 | A | G | 165 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(162): Show |
182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1429+1043T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52052536 | |||||||
chr14:52052757 | C | G | 1 | a0002c0004t0001g0097 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1429+822G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52052757 | |||||||
chr14:52052837 | T | C | 191 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(188): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1429+742A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52052837 | |||||||
chr14:52052947 | C | T | 7 | a0002c0048t0002g0040 a0004c0020t0001g0336 a0004c0053t0001g0321 others(4): Show |
8 | HG01496.hp2 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1429+632G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52052947 | |||||||
chr14:52052967 | G | A | 5 | a0002c0004t0001g0162 a0002c0004t0001g0164 a0002c0004t0001g0165 others(2): Show |
5 | HG00609.hp1 NA18941.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.1429+612C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52052967 | |||||||
chr14:52053121 | G | A | 186 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(183): Show |
207 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1429+458C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52053121 | |||||||
chr14:52053172 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1429+407C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52053172 | |||||||
chr14:52053243 | T | C | 8 | a0008c0013t0001g0318 a0008c0013t0001g0319 a0008c0013t0001g0320 others(5): Show |
8 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1429+336A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52053243 | |||||||
chr14:52053263 | T | C | 4 | a0002c0048t0002g0040 a0004c0020t0001g0336 a0004c0053t0001g0321 others(1): Show |
4 | HG01496.hp2 HG01891.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1429+316A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52053263 | |||||||
chr14:52053295 | C | T | 3 | a0002c0048t0002g0040 a0004c0020t0001g0336 a0023c0049t0001g0090 |
3 | HG01496.hp2 HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1429+284G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52053295 | |||||||
chr14:52053335 | C | G | 4 | a0002c0048t0002g0040 a0004c0020t0001g0336 a0004c0053t0001g0321 others(1): Show |
4 | HG01496.hp2 HG01891.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1429+244G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52053335 | |||||||
chr14:52053359 | CATT | C | 4 | a0002c0048t0002g0040 a0004c0020t0001g0336 a0004c0053t0001g0321 others(1): Show |
4 | HG01496.hp2 HG01891.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1429+217_1429+219d others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52053359 | |||||||
chr14:52053428 | T | A | 8 | a0008c0013t0001g0318 a0008c0013t0001g0319 a0008c0013t0001g0320 others(5): Show |
8 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1429+151A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52053428 | |||||||
chr14:52053457 | T | C | 4 | a0002c0048t0002g0040 a0004c0020t0001g0336 a0004c0053t0001g0321 others(1): Show |
4 | HG01496.hp2 HG01891.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1429+122A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 5/21 | chr14 | 52053457 | |||||||
chr14:52054469 | A | T | 2 | a0002c0039t0001g0089 a0004c0055t0001g0296 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.768-148T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52054469 | |||||||
chr14:52054525 | G | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(165): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.768-204C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52054525 | |||||||
chr14:52054549 | T | C | 12 | a0002c0025t0001g0028 a0002c0025t0001g0030 a0002c0041t0001g0046 others(9): Show |
12 | HG00438.hp2 HG02602.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.768-228A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52054549 | |||||||
chr14:52054604 | A | T | 183 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(180): Show |
201 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.768-283T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52054604 | |||||||
chr14:52054638 | T | C | 1 | a0017c0026t0001g0037 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.768-317A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52054638 | |||||||
chr14:52054670 | C | A | 12 | a0002c0025t0001g0028 a0002c0025t0001g0030 a0002c0041t0001g0046 others(9): Show |
12 | HG00438.hp2 HG02602.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.768-349G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52054670 | |||||||
chr14:52054693 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.768-372T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52054693 | |||||||
chr14:52054709 | A | G | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.768-388T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52054709 | |||||||
chr14:52054718 | A | G | 188 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(185): Show |
209 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.768-397T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52054718 | |||||||
chr14:52054722 | A | C | 3 | a0016c0064t0001g0328 a0016c0069t0001g0332 a0032c0043t0001g0146 |
3 | HG02818.hp2 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.768-401T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52054722 | |||||||
chr14:52054901 | C | T | 342 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(339): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.768-580G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52054901 | |||||||
chr14:52055011 | T | C | 2 | a0001c0007t0001g0278 a0003c0002t0001g0277 |
2 | HG03017.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.768-690A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52055011 | |||||||
chr14:52055054 | C | T | 3 | a0002c0048t0002g0040 a0004c0053t0001g0321 a0023c0049t0001g0090 |
3 | HG01496.hp2 HG01891.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.768-733G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52055054 | |||||||
chr14:52055055 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(182): Show |
206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.768-734C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52055055 | |||||||
chr14:52055175 | A | G | 129 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(126): Show |
130 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.768-854T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52055175 | |||||||
chr14:52055220 | G | A | 1 | a0001c0007t0002g0204 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.768-899C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52055220 | |||||||
chr14:52055377 | C | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(182): Show |
206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.768-1056G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52055377 | |||||||
chr14:52055475 | C | G | 12 | a0002c0025t0001g0028 a0002c0025t0001g0030 a0002c0041t0001g0046 others(9): Show |
12 | HG00438.hp2 HG02602.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.768-1154G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52055475 | |||||||
chr14:52055519 | C | G | 12 | a0002c0025t0001g0028 a0002c0025t0001g0030 a0002c0041t0001g0046 others(9): Show |
12 | HG00438.hp2 HG02602.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.768-1198G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52055519 | |||||||
chr14:52055775 | A | G | 1 | a0015c0058t0001g0330 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.768-1454T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52055775 | |||||||
chr14:52055821 | A | G | 332 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(329): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.768-1500T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52055821 | |||||||
chr14:52055930 | C | CTTGTGTG others(3): Show |
154 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(151): Show |
155 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.768-1619_768-1610d others(12): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52055930 | |||||||
chr14:52055941 | T | TTGTGTGT others(5): Show |
24 | a0001c0010t0001g0001 a0001c0010t0001g0032 a0001c0010t0001g0034 others(21): Show |
28 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.768-1621_768-1620i others(14): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52055941 | |||||||
chr14:52055941 | T | TTGTGTGT others(7): Show |
162 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(159): Show |
179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.768-1621_768-1620i others(16): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52055941 | |||||||
chr14:52055941 | T | TTGTGTGT others(9): Show |
2 | a0001c0005t0001g0177 a0005c0021t0001g0283 |
2 | HG01069.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.768-1621_768-1620i others(18): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52055941 | |||||||
chr14:52056088 | G | A | 1 | a0002c0003t0001g0163 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.768-1767C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52056088 | |||||||
chr14:52056106 | A | C | 3 | a0002c0048t0002g0040 a0004c0053t0001g0321 a0023c0049t0001g0090 |
3 | HG01496.hp2 HG01891.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.768-1785T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52056106 | |||||||
chr14:52056216 | C | A | 3 | a0002c0048t0002g0040 a0004c0053t0001g0321 a0023c0049t0001g0090 |
3 | HG01496.hp2 HG01891.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.768-1895G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52056216 | |||||||
chr14:52056274 | A | G | 1 | a0001c0005t0001g0220 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.768-1953T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52056274 | |||||||
chr14:52056322 | A | G | 3 | a0015c0056t0001g0331 a0015c0058t0001g0330 a0034c0057t0001g0314 |
3 | HG02723.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.768-2001T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52056322 | |||||||
chr14:52056469 | G | T | 12 | a0002c0025t0001g0028 a0002c0025t0001g0030 a0002c0041t0001g0046 others(9): Show |
12 | HG00438.hp2 HG02602.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.768-2148C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52056469 | |||||||
chr14:52056570 | C | T | 4 | a0002c0048t0002g0040 a0004c0053t0001g0321 a0018c0028t0001g0324 others(1): Show |
4 | HG01496.hp2 HG01891.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.768-2249G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52056570 | |||||||
chr14:52056647 | T | C | 332 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(329): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.768-2326A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52056647 | |||||||
chr14:52056684 | C | T | 188 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(185): Show |
209 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.768-2363G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52056684 | |||||||
chr14:52056685 | T | G | 200 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(197): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.768-2364A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52056685 | |||||||
chr14:52056778 | C | T | 114 | a0002c0003t0001g0010 a0002c0003t0001g0053 a0002c0003t0001g0054 others(111): Show |
115 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.768-2457G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52056778 | |||||||
chr14:52056797 | A | C | 1 | a0001c0001t0001g0219 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.768-2476T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52056797 | |||||||
chr14:52056905 | T | C | 165 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(162): Show |
182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.768-2584A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52056905 | |||||||
chr14:52057000 | A | C | 1 | a0002c0004t0001g0169 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.768-2679T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057000 | |||||||
chr14:52057137 | G | A | 206 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(203): Show |
227 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.768-2816C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057137 | |||||||
chr14:52057169 | A | G | 332 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(329): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.768-2848T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057169 | |||||||
chr14:52057172 | G | C | 3 | a0002c0048t0002g0040 a0004c0020t0001g0336 a0023c0049t0001g0090 |
3 | HG01496.hp2 HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.768-2851C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057172 | |||||||
chr14:52057182 | C | T | 108 | a0002c0003t0001g0010 a0002c0003t0001g0093 a0002c0003t0001g0094 others(105): Show |
109 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.768-2861G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057182 | |||||||
chr14:52057183 | G | A | 1 | a0003c0002t0001g0076 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.768-2862C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057183 | |||||||
chr14:52057228 | A | G | 1 | a0002c0004t0001g0174 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.767+2896T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057228 | |||||||
chr14:52057239 | C | T | 2 | a0028c0029t0001g0142 a0031c0068t0001g0334 |
2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.767+2885G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057239 | |||||||
chr14:52057455 | C | A | 18 | a0001c0010t0001g0001 a0001c0010t0001g0032 a0001c0010t0001g0034 others(15): Show |
21 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.767+2669G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057455 | |||||||
chr14:52057477 | T | A | 206 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(203): Show |
227 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.767+2647A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057477 | |||||||
chr14:52057703 | CA | C | 21 | a0002c0003t0001g0095 a0002c0003t0001g0123 a0002c0003t0001g0124 others(18): Show |
21 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.767+2420delT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057703 | |||||||
chr14:52057703 | CAA | C | 98 | a0002c0003t0001g0010 a0002c0003t0001g0093 a0002c0003t0001g0094 others(95): Show |
99 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.767+2419_767+2420d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057703 | |||||||
chr14:52057703 | CAAAA | C | 36 | a0001c0001t0001g0077 a0001c0005t0001g0274 a0001c0005t0001g0275 others(33): Show |
38 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.767+2417_767+2420d others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057703 | |||||||
chr14:52057703 | CAAAAA | C | 166 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(163): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.767+2416_767+2420d others(7): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057703 | |||||||
chr14:52057703 | CAAAAAAA others(6): Show |
C | 2 | a0012c0018t0001g0004 a0012c0018t0001g0045 |
3 | HG01099.hp1 HG01952.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.767+2408_767+2420d others(15): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057703 | |||||||
chr14:52057721 | A | G | 12 | a0002c0039t0001g0089 a0004c0012t0002g0299 a0004c0012t0002g0300 others(9): Show |
12 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.767+2403T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057721 | |||||||
chr14:52057763 | T | A | 4 | a0002c0048t0002g0040 a0004c0020t0001g0336 a0004c0053t0001g0321 others(1): Show |
4 | HG01496.hp2 HG01891.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.767+2361A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057763 | |||||||
chr14:52057771 | A | G | 1 | a0008c0013t0001g0347 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.767+2353T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057771 | |||||||
chr14:52057803 | C | T | 206 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(203): Show |
227 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.767+2321G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52057803 | |||||||
chr14:52058061 | C | T | 15 | a0002c0025t0001g0028 a0002c0025t0001g0030 a0002c0041t0001g0046 others(12): Show |
15 | HG00438.hp2 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.767+2063G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52058061 | |||||||
chr14:52058093 | A | C | 205 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(202): Show |
226 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.767+2031T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52058093 | |||||||
chr14:52058255 | C | A | 8 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(5): Show |
8 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.767+1869G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52058255 | |||||||
chr14:52058275 | C | T | 2 | a0016c0064t0001g0328 a0016c0069t0001g0332 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.767+1849G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52058275 | |||||||
chr14:52058304 | C | A | 2 | a0016c0064t0001g0328 a0016c0069t0001g0332 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.767+1820G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52058304 | |||||||
chr14:52058690 | T | C | 343 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(340): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.767+1434A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52058690 | |||||||
chr14:52058807 | T | C | 1 | a0004c0006t0002g0350 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.767+1317A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52058807 | |||||||
chr14:52058844 | A | G | 96 | a0001c0001t0001g0009 a0002c0003t0001g0010 a0002c0003t0001g0093 others(93): Show |
98 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.767+1280T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52058844 | |||||||
chr14:52058893 | A | C | 116 | a0001c0001t0001g0009 a0002c0003t0001g0010 a0002c0003t0001g0093 others(113): Show |
118 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.767+1231T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52058893 | |||||||
chr14:52058916 | G | T | 2 | a0002c0048t0002g0040 a0023c0049t0001g0090 |
2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.767+1208C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52058916 | |||||||
chr14:52058987 | G | A | 2 | a0006c0008t0001g0345 a0006c0008t0001g0346 |
2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.767+1137C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52058987 | |||||||
chr14:52059102 | C | T | 1 | a0002c0004t0001g0096 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.767+1022G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52059102 | |||||||
chr14:52059309 | G | A | 2 | a0016c0064t0001g0328 a0016c0069t0001g0332 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.767+815C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52059309 | |||||||
chr14:52059330 | A | G | 5 | a0010c0019t0001g0307 a0010c0019t0001g0327 a0010c0019t0001g0341 others(2): Show |
5 | HG02622.hp2 HG03098.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.767+794T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52059330 | |||||||
chr14:52059451 | C | A | 3 | a0004c0053t0001g0321 a0028c0029t0001g0142 a0031c0068t0001g0334 |
3 | HG02615.hp1 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.767+673G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52059451 | |||||||
chr14:52059452 | C | A | 1 | a0035c0047t0001g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.767+672G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52059452 | |||||||
chr14:52059549 | T | C | 5 | a0009c0014t0001g0087 a0009c0014t0001g0290 a0009c0014t0001g0291 others(2): Show |
5 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.767+575A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52059549 | |||||||
chr14:52059590 | A | G | 3 | a0015c0056t0001g0331 a0015c0058t0001g0330 a0034c0057t0001g0314 |
3 | HG02723.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.767+534T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52059590 | |||||||
chr14:52059726 | T | G | 1 | a0001c0001t0001g0285 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.767+398A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52059726 | |||||||
chr14:52059881 | T | C | 3 | a0004c0053t0001g0321 a0028c0029t0001g0142 a0031c0068t0001g0334 |
3 | HG02615.hp1 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.767+243A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52059881 | |||||||
chr14:52059963 | T | G | 1 | a0003c0002t0001g0081 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.767+161A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52059963 | |||||||
chr14:52060110 | T | A | 1 | a0002c0003t0001g0125 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.767+14A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 3/21 | chr14 | 52060110 | |||||||
chr14:52060364 | G | GA | 108 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0007t0001g0133 others(105): Show |
114 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.535-9dupT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52060364 | |||||||
chr14:52060364 | GAAAA | G | 7 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(4): Show |
7 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.535-12_535-9delTTT others(1): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52060364 | |||||||
chr14:52060378 | A | G | 8 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(5): Show |
8 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.535-22T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52060378 | |||||||
chr14:52060380 | G | A | 151 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0038 others(148): Show |
160 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.535-24C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52060380 | |||||||
chr14:52060410 | A | G | 1 | a0001c0022t0001g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.535-54T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52060410 | |||||||
chr14:52060469 | C | T | 166 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0038 others(163): Show |
175 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.535-113G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52060469 | |||||||
chr14:52060470 | T | G | 150 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0038 others(147): Show |
159 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.535-114A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52060470 | |||||||
chr14:52060472 | C | A | 8 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 others(5): Show |
8 | HG01496.hp2 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.535-116G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52060472 | |||||||
chr14:52060557 | G | A | 4 | a0010c0019t0001g0307 a0010c0019t0001g0327 a0010c0019t0001g0341 others(1): Show |
4 | HG03098.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-201C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52060557 | |||||||
chr14:52060569 | A | T | 1 | a0004c0006t0002g0350 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.535-213T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52060569 | |||||||
chr14:52060622 | T | C | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.535-266A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52060622 | |||||||
chr14:52060682 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.535-326A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52060682 | |||||||
chr14:52060740 | G | A | 3 | a0015c0056t0001g0331 a0015c0058t0001g0330 a0034c0057t0001g0314 |
3 | HG02723.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.535-384C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52060740 | |||||||
chr14:52060776 | A | ATCAT | 5 | a0003c0002t0001g0013 a0003c0002t0001g0014 a0003c0002t0001g0205 others(2): Show |
7 | HG00738.hp2 HG00741.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.535-424_535-421dup others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52060776 | |||||||
chr14:52060779 | A | T | 2 | a0013c0017t0001g0008 a0013c0017t0001g0186 |
3 | HG02280.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.535-423T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52060779 | |||||||
chr14:52060806 | T | C | 10 | a0001c0007t0001g0092 a0004c0012t0002g0299 a0004c0012t0002g0300 others(7): Show |
10 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.535-450A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52060806 | |||||||
chr14:52061029 | C | T | 1 | a0002c0003t0001g0053 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.535-673G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52061029 | |||||||
chr14:52061411 | A | G | 1 | a0019c0031t0001g0025 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.535-1055T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52061411 | |||||||
chr14:52061457 | A | G | 2 | a0028c0029t0001g0142 a0031c0068t0001g0334 |
2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.535-1101T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52061457 | |||||||
chr14:52061483 | G | A | 2 | a0001c0007t0001g0092 a0023c0049t0001g0090 |
2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.535-1127C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52061483 | |||||||
chr14:52061726 | T | TTACCCTC others(54): Show |
1 | a0003c0002t0001g0214 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.535-1371_535-1370i others(63): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52061726 | |||||||
chr14:52061930 | C | T | 116 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0007t0001g0133 others(113): Show |
122 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.535-1574G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52061930 | |||||||
chr14:52062200 | T | C | 2 | a0007c0011t0001g0288 a0007c0011t0001g0289 |
2 | HG01358.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.535-1844A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52062200 | |||||||
chr14:52062246 | C | T | 1 | a0003c0002t0001g0215 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.535-1890G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52062246 | |||||||
chr14:52062339 | A | C | 2 | a0003c0002t0001g0213 a0003c0002t0001g0214 |
2 | NA18950.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.535-1983T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52062339 | |||||||
chr14:52062375 | A | C | 3 | a0001c0001t0001g0211 a0001c0005t0001g0175 a0001c0005t0001g0212 |
3 | HG00738.hp1 HG01255.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.535-2019T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52062375 | |||||||
chr14:52062403 | C | T | 1 | a0003c0002t0001g0082 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.535-2047G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52062403 | |||||||
chr14:52062444 | G | A | 4 | a0010c0019t0001g0307 a0010c0019t0001g0327 a0010c0019t0001g0341 others(1): Show |
4 | HG03098.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-2088C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52062444 | |||||||
chr14:52062478 | G | T | 156 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0038 others(153): Show |
165 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.535-2122C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52062478 | |||||||
chr14:52062524 | A | C | 2 | a0016c0064t0001g0328 a0016c0069t0001g0332 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.535-2168T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52062524 | |||||||
chr14:52062582 | C | A | 1 | a0004c0020t0001g0336 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.535-2226G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52062582 | |||||||
chr14:52062730 | A | G | 1 | a0002c0041t0001g0046 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.535-2374T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52062730 | |||||||
chr14:52062733 | G | C | 1 | a0002c0003t0001g0125 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.535-2377C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52062733 | |||||||
chr14:52062760 | T | A | 8 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(5): Show |
8 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.535-2404A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52062760 | |||||||
chr14:52062829 | T | G | 162 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0038 others(159): Show |
171 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.535-2473A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52062829 | |||||||
chr14:52062902 | C | T | 6 | a0003c0002t0001g0048 a0003c0002t0001g0049 a0003c0002t0001g0050 others(3): Show |
6 | HG00423.hp1 NA18945.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.535-2546G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52062902 | |||||||
chr14:52063145 | T | C | 23 | a0001c0005t0001g0287 a0001c0007t0001g0092 a0004c0012t0002g0299 others(20): Show |
24 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.535-2789A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52063145 | |||||||
chr14:52063205 | T | C | 127 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0007t0001g0133 others(124): Show |
133 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.535-2849A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52063205 | |||||||
chr14:52063266 | T | C | 127 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0007t0001g0133 others(124): Show |
133 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.535-2910A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52063266 | |||||||
chr14:52063445 | C | A | 1 | a0004c0006t0002g0350 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.535-3089G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52063445 | |||||||
chr14:52063564 | A | C | 113 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0007t0001g0133 others(110): Show |
119 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.535-3208T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52063564 | |||||||
chr14:52063633 | G | T | 11 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(8): Show |
11 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.535-3277C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52063633 | |||||||
chr14:52063802 | T | C | 26 | a0001c0001t0001g0038 a0001c0010t0001g0001 a0001c0010t0001g0032 others(23): Show |
29 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.535-3446A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52063802 | |||||||
chr14:52063825 | G | C | 111 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0007t0001g0133 others(108): Show |
117 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.535-3469C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52063825 | |||||||
chr14:52064411 | G | C | 1 | a0005c0021t0001g0283 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.534+3447C>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52064411 | |||||||
chr14:52064539 | C | A | 179 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0038 others(176): Show |
189 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.534+3319G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52064539 | |||||||
chr14:52064599 | A | T | 111 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0007t0001g0133 others(108): Show |
117 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.534+3259T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52064599 | |||||||
chr14:52064652 | T | C | 1 | a0003c0002t0001g0085 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.534+3206A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52064652 | |||||||
chr14:52064682 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0284 a0001c0001t0001g0285 |
4 | HG00642.hp1 HG01243.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.534+3176A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52064682 | |||||||
chr14:52064688 | T | G | 3 | a0015c0056t0001g0331 a0015c0058t0001g0330 a0034c0057t0001g0314 |
3 | HG02723.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.534+3170A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52064688 | |||||||
chr14:52064690 | C | T | 4 | a0008c0013t0001g0318 a0008c0013t0001g0319 a0008c0013t0001g0320 others(1): Show |
4 | HG00323.hp1 HG00642.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+3168G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52064690 | |||||||
chr14:52064705 | T | C | 1 | a0001c0033t0001g0286 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.534+3153A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52064705 | |||||||
chr14:52064855 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.534+3003G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52064855 | |||||||
chr14:52065087 | C | T | 1 | a0037c0054t0001g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.534+2771G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065087 | |||||||
chr14:52065090 | A | AT | 125 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0126 others(122): Show |
132 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.534+2767dupA | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065090 | |||||||
chr14:52065277 | C | A | 171 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0038 others(168): Show |
181 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.534+2581G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065277 | |||||||
chr14:52065287 | G | A | 2 | a0007c0011t0001g0288 a0007c0011t0001g0289 |
2 | HG01358.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.534+2571C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065287 | |||||||
chr14:52065303 | T | A | 4 | a0003c0002t0001g0006 a0003c0002t0001g0079 a0003c0002t0001g0080 others(1): Show |
5 | HG00673.hp1 NA18954.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.534+2555A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065303 | |||||||
chr14:52065456 | C | CTT | 13 | a0002c0003t0001g0128 a0002c0003t0001g0129 a0002c0004t0001g0130 others(10): Show |
13 | HG00609.hp2 HG01099.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.534+2400_534+2401d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065456 | |||||||
chr14:52065456 | C | CTTT | 106 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0126 others(103): Show |
112 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.534+2399_534+2401d others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065456 | |||||||
chr14:52065456 | CT | C | 8 | a0003c0002t0001g0082 a0003c0002t0001g0083 a0003c0002t0001g0141 others(5): Show |
9 | HG00423.hp1 HG02155.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+2401delA | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065456 | |||||||
chr14:52065471 | T | C | 18 | a0004c0006t0002g0350 a0006c0008t0001g0342 a0008c0013t0001g0318 others(15): Show |
19 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.534+2387A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065471 | |||||||
chr14:52065471 | T | TTC | 8 | a0004c0012t0002g0299 a0004c0012t0002g0300 a0004c0012t0002g0301 others(5): Show |
8 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.534+2386_534+2387i others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065471 | |||||||
chr14:52065472 | C | T | 18 | a0001c0010t0001g0001 a0001c0010t0001g0032 a0001c0010t0001g0034 others(15): Show |
21 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.534+2386G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065472 | |||||||
chr14:52065475 | C | A | 153 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0038 others(150): Show |
160 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.534+2383G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065475 | |||||||
chr14:52065475 | C | CA | 3 | a0001c0005t0001g0287 a0001c0007t0001g0092 a0023c0049t0001g0090 |
3 | HG01891.hp1 HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.534+2382_534+2383i others(3): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065475 | |||||||
chr14:52065475 | CTTTCTTT others(3): Show |
C | 18 | a0001c0010t0001g0001 a0001c0010t0001g0032 a0001c0010t0001g0034 others(15): Show |
21 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.534+2373_534+2382d others(12): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065475 | |||||||
chr14:52065482 | T | A | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.534+2376A>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065482 | |||||||
chr14:52065482 | T | TTTTA | 4 | a0001c0007t0001g0084 a0002c0003t0001g0187 a0002c0004t0001g0147 others(1): Show |
4 | HG02622.hp1 HG04199.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.534+2372_534+2375d others(6): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065482 | |||||||
chr14:52065482 | T | TTTTATTT others(1): Show |
8 | a0002c0004t0001g0149 a0002c0004t0001g0150 a0002c0004t0001g0151 others(5): Show |
8 | HG01257.hp1 HG01258.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.534+2368_534+2375d others(10): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065482 | |||||||
chr14:52065482 | T | TTTTATTT others(5): Show |
89 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0126 others(86): Show |
95 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.534+2364_534+2375d others(14): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065482 | |||||||
chr14:52065482 | T | TTTTATTT others(9): Show |
12 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0001g0137 others(9): Show |
12 | HG02083.hp2 HG02165.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.534+2360_534+2375d others(18): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065482 | |||||||
chr14:52065482 | T | TTTTATTT others(13): Show |
1 | a0002c0004t0001g0174 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.534+2356_534+2375d others(22): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065482 | |||||||
chr14:52065482 | TTTTATTT others(1): Show |
T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
7 | HG00280.hp1 HG01109.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.534+2368_534+2375d others(10): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065482 | |||||||
chr14:52065482 | TTTTATTT others(5): Show |
T | 8 | a0001c0001t0001g0038 a0001c0023t0001g0039 a0002c0025t0001g0028 others(5): Show |
8 | HG01099.hp1 HG03041.hp2 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.534+2364_534+2375d others(14): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065482 | |||||||
chr14:52065490 | A | C | 18 | a0001c0010t0001g0001 a0001c0010t0001g0032 a0001c0010t0001g0034 others(15): Show |
21 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.534+2368T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065490 | |||||||
chr14:52065493 | TA | T | 18 | a0001c0010t0001g0001 a0001c0010t0001g0032 a0001c0010t0001g0034 others(15): Show |
21 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.534+2364delT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065493 | |||||||
chr14:52065497 | TATTTA | T | 3 | a0015c0056t0001g0331 a0015c0058t0001g0330 a0034c0057t0001g0314 |
3 | HG02723.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.534+2356_534+2360d others(7): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065497 | |||||||
chr14:52065582 | C | T | 11 | a0001c0005t0001g0287 a0001c0007t0001g0092 a0004c0012t0002g0299 others(8): Show |
11 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.534+2276G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065582 | |||||||
chr14:52065655 | T | TC | 5 | a0002c0004t0001g0139 a0002c0041t0001g0046 a0004c0012t0002g0300 others(2): Show |
5 | HG01099.hp1 HG02109.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.534+2202dupG | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065655 | |||||||
chr14:52065661 | A | C | 173 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0038 others(170): Show |
183 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.534+2197T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065661 | |||||||
chr14:52065669 | C | A | 1 | a0004c0053t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.534+2189G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065669 | |||||||
chr14:52065751 | A | G | 193 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(190): Show |
204 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.534+2107T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065751 | |||||||
chr14:52065773 | C | T | 2 | a0002c0004t0001g0185 a0003c0002t0001g0184 |
2 | NA18957.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.534+2085G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065773 | |||||||
chr14:52065782 | A | G | 1 | a0001c0010t0001g0183 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.534+2076T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065782 | |||||||
chr14:52065847 | A | T | 1 | a0025c0042t0001g0144 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.534+2011T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065847 | |||||||
chr14:52065909 | G | A | 1 | a0003c0002t0001g0085 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.534+1949C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065909 | |||||||
chr14:52065915 | T | C | 1 | a0001c0001t0001g0009 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.534+1943A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065915 | |||||||
chr14:52065954 | G | A | 1 | a0010c0019t0001g0327 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.534+1904C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52065954 | |||||||
chr14:52066001 | G | A | 2 | a0002c0004t0001g0178 a0002c0004t0001g0179 |
2 | NA18968.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.534+1857C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52066001 | |||||||
chr14:52066051 | C | T | 1 | a0004c0012t0002g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.534+1807G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52066051 | |||||||
chr14:52066107 | T | G | 4 | a0001c0007t0001g0092 a0004c0053t0001g0321 a0023c0049t0001g0090 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+1751A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52066107 | |||||||
chr14:52066167 | C | A | 1 | a0015c0058t0001g0330 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.534+1691G>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52066167 | |||||||
chr14:52066249 | G | A | 1 | a0001c0005t0001g0287 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.534+1609C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52066249 | |||||||
chr14:52066252 | A | ACAG | 5 | a0004c0006t0001g0325 a0010c0019t0001g0307 a0010c0019t0001g0327 others(2): Show |
5 | HG03098.hp1 HG03098.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.534+1603_534+1605d others(5): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52066252 | |||||||
chr14:52066321 | C | CA | 20 | a0001c0010t0001g0086 a0004c0006t0001g0316 a0004c0012t0002g0300 others(17): Show |
20 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.534+1536dupT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52066321 | |||||||
chr14:52066321 | C | CAA | 6 | a0007c0011t0001g0288 a0007c0011t0001g0289 a0009c0014t0001g0290 others(3): Show |
6 | HG01358.hp2 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.534+1535_534+1536d others(4): Show |
NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52066321 | |||||||
chr14:52066321 | CA | C | 6 | a0002c0004t0001g0143 a0004c0020t0001g0335 a0006c0008t0001g0323 others(3): Show |
6 | HG02280.hp2 HG02895.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.534+1536delT | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52066321 | |||||||
chr14:52066369 | A | T | 62 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0126 others(59): Show |
64 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.534+1489T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52066369 | |||||||
chr14:52066381 | C | T | 72 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0059 others(69): Show |
77 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.534+1477G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52066381 | |||||||
chr14:52066407 | T | C | 1 | a0001c0001t0001g0009 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.534+1451A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52066407 | |||||||
chr14:52066444 | T | G | 4 | a0001c0007t0001g0092 a0001c0022t0001g0091 a0004c0006t0001g0317 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+1414A>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52066444 | |||||||
chr14:52066515 | A | T | 85 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0059 others(82): Show |
90 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.534+1343T>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52066515 | |||||||
chr14:52066696 | G | T | 1 | a0016c0064t0001g0328 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.534+1162C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52066696 | |||||||
chr14:52066725 | A | G | 208 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(205): Show |
219 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.534+1133T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52066725 | |||||||
chr14:52067052 | T | C | 335 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(332): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.534+806A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52067052 | |||||||
chr14:52067181 | C | T | 1 | a0026c0037t0001g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.534+677G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52067181 | |||||||
chr14:52067278 | G | T | 1 | a0019c0031t0001g0025 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.534+580C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52067278 | |||||||
chr14:52067331 | A | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0024 |
3 | NA18963.hp1 NA18979.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.534+527T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52067331 | |||||||
chr14:52067347 | A | G | 5 | a0004c0053t0001g0321 a0008c0013t0001g0318 a0008c0013t0001g0319 others(2): Show |
5 | HG00323.hp1 HG00642.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.534+511T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52067347 | |||||||
chr14:52067373 | G | T | 1 | a0002c0004t0001g0023 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.534+485C>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52067373 | |||||||
chr14:52067452 | A | G | 1 | a0002c0004t0001g0022 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.534+406T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52067452 | |||||||
chr14:52067666 | C | T | 13 | a0004c0006t0001g0308 a0004c0006t0001g0309 a0004c0006t0001g0310 others(10): Show |
16 | HG01261.hp1 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.534+192G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52067666 | |||||||
chr14:52067813 | C | T | 27 | a0004c0006t0001g0308 a0004c0006t0001g0309 a0004c0006t0001g0310 others(24): Show |
30 | HG00323.hp1 HG00642.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.534+45G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 2/21 | chr14 | 52067813 | |||||||
chr14:52068267 | C | G | 9 | a0004c0006t0001g0297 a0004c0012t0002g0299 a0004c0012t0002g0300 others(6): Show |
9 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.229-104G>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 1/21 | chr14 | 52068267 | |||||||
chr14:52068279 | T | C | 345 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(342): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.229-116A>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 1/21 | chr14 | 52068279 | |||||||
chr14:52068401 | C | T | 1 | a0004c0055t0001g0296 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.229-238G>A | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 1/21 | chr14 | 52068401 | |||||||
chr14:52068463 | A | G | 1 | a0003c0002t0001g0021 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.229-300T>C | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 1/21 | chr14 | 52068463 | |||||||
chr14:52068669 | A | C | 336 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(333): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.228+98T>G | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 1/21 | chr14 | 52068669 | |||||||
chr14:52068697 | G | A | 292 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(289): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.228+70C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 1/21 | chr14 | 52068697 | |||||||
chr14:52068708 | G | A | 1 | a0004c0006t0002g0350 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.228+59C>T | NID2 | ENSG00000087303.19 | transcript | ENST00000216286.10 | protein_coding | 1/21 | chr14 | 52068708 |