Item | Value |
---|---|
geneid | 26018 |
ensemblid | ENSG00000144749.14 |
hgncid | 17360 |
symbol | LRIG1 |
name | leucine rich repeats and immunoglobulin like domains 1 |
refseq_nuc | NM_015541.3 |
refseq_prot | NP_056356.2 |
ensembl_nuc | ENST00000273261.8 |
ensembl_prot | ENSP00000273261.3 |
mane_status | MANE Select |
chr | chr3 |
start | 66378797 |
end | 66501022 |
strand | - |
ver | v1.2 |
region | chr3:66378797-66501022 |
region5000 | chr3:66373797-66506022 |
regionname0 | LRIG1_chr3_66378797_66501022 |
regionname5000 | LRIG1_chr3_66373797_66506022 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1093 | 60 | 6 | 25 | 16 | 4 | 8 | 12 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0002 | 0/0 | 1093 | 58 | 3 | 13 | 38 | 0 | 4 | 25 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0003 | 1/0 | 1093 | 29 | 16 | 1 | 11 | 0 | 0 | 9 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0004 | 0/0 | 1093 | 19 | 4 | 1 | 4 | 1 | 9 | 2 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0005 | 0/0 | 1093 | 15 | 9 | 4 | 2 | 0 | 0 | 2 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0006 | 0/0 | 1093 | 13 | 12 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0007 | 0/0 | 1093 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0008 | 0/0 | 1093 | 12 | 5 | 0 | 5 | 0 | 2 | 4 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0009 | 0/0 | 1093 | 9 | 3 | 1 | 4 | 0 | 1 | 3 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0010 | 0/0 | 1093 | 6 | 1 | 1 | 2 | 1 | 1 | 2 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0011 | 0/0 | 1093 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0012 | 0/0 | 1093 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0013 | 0/0 | 1093 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0014 | 0/0 | 1093 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0015 | 0/0 | 1093 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0016 | 0/0 | 1093 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0017 | 0/0 | 1093 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0018 | 0/0 | 1093 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0019 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0020 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0021 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0022 | 0/0 | 1093 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0023 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0024 | 0/0 | 1093 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0025 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0026 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0027 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0028 | 0/0 | 1093 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0029 | 0/0 | 1093 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0030 | 0/0 | 1093 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0031 | 0/0 | 1093 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0032 | 0/0 | 1093 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0033 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
a0034 | 0/0 | 1093 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | MARPV others(1088): Show |
chr3 | 66373797 | 66506022 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/1 | 3279 | 40 | 4 | 14 | 12 | 3 | 6 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0001c0007 | 0/0 | 3279 | 12 | 0 | 10 | 0 | 1 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0001c0014 | 0/0 | 3279 | 5 | 0 | 1 | 3 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0001c0023 | 0/0 | 3279 | 2 | 2 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0001c0040 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0002c0001 | 0/0 | 3279 | 49 | 3 | 12 | 30 | 0 | 4 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0002c0018 | 0/0 | 3279 | 3 | 0 | 0 | 3 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0002c0021 | 0/0 | 3279 | 2 | 0 | 0 | 2 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0002c0022 | 0/0 | 3279 | 2 | 0 | 1 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0002c0041 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0002c0048 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0003c0005 | 1/0 | 3279 | 15 | 3 | 1 | 10 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0003c0010 | 0/0 | 3279 | 7 | 7 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0003c0012 | 0/0 | 3279 | 5 | 4 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0003c0031 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0003c0036 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0004c0003 | 0/0 | 3279 | 18 | 4 | 1 | 3 | 1 | 9 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0004c0053 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0005c0004 | 0/0 | 3279 | 15 | 9 | 4 | 2 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0006c0009 | 0/0 | 3279 | 8 | 7 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0006c0019 | 0/0 | 3279 | 2 | 2 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0006c0026 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0006c0027 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0006c0035 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0007c0006 | 0/0 | 3279 | 12 | 12 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0008c0008 | 0/0 | 3279 | 11 | 4 | 0 | 5 | 0 | 2 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0008c0033 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0009c0013 | 0/0 | 3279 | 5 | 0 | 1 | 3 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0009c0015 | 0/0 | 3279 | 3 | 3 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0009c0037 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0010c0011 | 0/0 | 3279 | 6 | 1 | 1 | 2 | 1 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0011c0016 | 0/0 | 3279 | 3 | 3 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0011c0030 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0012c0017 | 0/0 | 3279 | 3 | 0 | 0 | 3 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0013c0042 | 0/0 | 3279 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0013c0043 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0014c0020 | 0/0 | 3279 | 2 | 1 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0015c0051 | 0/0 | 3279 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0016c0050 | 0/0 | 3279 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0017c0025 | 0/0 | 3279 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0018c0055 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0019c0038 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0020c0046 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0021c0049 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0022c0054 | 0/0 | 3279 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0023c0052 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0024c0056 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0025c0047 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0026c0032 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0027c0028 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0028c0044 | 0/0 | 3279 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0029c0039 | 0/0 | 3279 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0030c0029 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0031c0024 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0032c0057 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0033c0034 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 | ||
a0034c0045 | 0/0 | 3279 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | ATGGC others(3274): Show |
chr3 | 66373797 | 66506022 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/1 | 5363 | 39 | 4 | 14 | 12 | 3 | 5 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0001c0002t0031 | 0/0 | 5363 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0001c0007t0001 | 0/0 | 5363 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0001c0007t0002 | 0/0 | 5362 | 11 | 0 | 10 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0001c0014t0010 | 0/0 | 5362 | 2 | 0 | 1 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0001c0014t0011 | 0/0 | 5362 | 2 | 0 | 0 | 2 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0001c0014t0028 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0001c0023t0002 | 0/0 | 5362 | 2 | 2 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0001c0040t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0002c0001t0001 | 0/0 | 5363 | 46 | 3 | 11 | 28 | 0 | 4 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0002c0001t0015 | 0/0 | 5363 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0002c0001t0016 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0002c0001t0032 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0002c0018t0001 | 0/0 | 5363 | 3 | 0 | 0 | 3 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0002c0021t0001 | 0/0 | 5363 | 2 | 0 | 0 | 2 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0002c0022t0001 | 0/0 | 5363 | 2 | 0 | 1 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0002c0041t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0002c0048t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0003c0005t0001 | 0/0 | 5363 | 4 | 3 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0003c0005t0003 | 1/0 | 5363 | 11 | 0 | 1 | 9 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0003c0010t0002 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0003c0010t0004 | 0/0 | 5362 | 6 | 6 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0003c0012t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0003c0012t0014 | 0/0 | 5362 | 2 | 2 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0003c0012t0017 | 0/0 | 5365 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5360): Show |
chr3 | 66373797 | 66506022 |
a0003c0012t0018 | 0/0 | 5364 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5359): Show |
chr3 | 66373797 | 66506022 |
a0003c0031t0001 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0003c0036t0034 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0004c0003t0001 | 0/0 | 5363 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0004c0003t0002 | 0/0 | 5362 | 15 | 3 | 1 | 3 | 1 | 7 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0004c0003t0026 | 0/0 | 5362 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0004c0003t0039 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0004c0053t0002 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0005c0004t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0005c0004t0006 | 0/0 | 5361 | 7 | 4 | 3 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5356): Show |
chr3 | 66373797 | 66506022 |
a0005c0004t0007 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5356): Show |
chr3 | 66373797 | 66506022 |
a0005c0004t0008 | 0/0 | 5361 | 5 | 4 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5356): Show |
chr3 | 66373797 | 66506022 |
a0005c0004t0021 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0006c0009t0002 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0006c0009t0004 | 0/0 | 5362 | 7 | 6 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0006c0019t0012 | 0/0 | 5363 | 2 | 2 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0006c0026t0036 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0006c0027t0004 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0006c0035t0033 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0007c0006t0005 | 0/0 | 5362 | 7 | 7 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0007c0006t0009 | 0/0 | 5362 | 4 | 4 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0007c0006t0020 | 0/0 | 5364 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5359): Show |
chr3 | 66373797 | 66506022 |
a0008c0008t0001 | 0/0 | 5363 | 5 | 1 | 0 | 4 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0008c0008t0003 | 0/0 | 5363 | 4 | 3 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0008c0008t0025 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0008c0008t0037 | 0/0 | 5363 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0008c0033t0001 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0009c0013t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0009c0013t0002 | 0/0 | 5362 | 3 | 0 | 1 | 2 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0009c0013t0004 | 0/0 | 5362 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0009c0015t0002 | 0/0 | 5362 | 3 | 3 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0009c0037t0002 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0010c0011t0001 | 0/0 | 5363 | 2 | 0 | 0 | 2 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0010c0011t0007 | 0/0 | 5361 | 3 | 0 | 1 | 0 | 1 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5356): Show |
chr3 | 66373797 | 66506022 |
a0010c0011t0024 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5356): Show |
chr3 | 66373797 | 66506022 |
a0011c0016t0013 | 0/0 | 5367 | 3 | 3 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5362): Show |
chr3 | 66373797 | 66506022 |
a0011c0030t0027 | 0/0 | 5367 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5362): Show |
chr3 | 66373797 | 66506022 |
a0012c0017t0002 | 0/0 | 5362 | 3 | 0 | 0 | 3 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0013c0042t0010 | 0/0 | 5362 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0013c0043t0022 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0014c0020t0029 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5356): Show |
chr3 | 66373797 | 66506022 |
a0014c0020t0035 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0015c0051t0002 | 0/0 | 5362 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0016c0050t0023 | 0/0 | 5362 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0017c0025t0012 | 0/0 | 5363 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0018c0055t0002 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0019c0038t0003 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0020c0046t0010 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0021c0049t0001 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0022c0054t0002 | 0/0 | 5362 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0023c0052t0038 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0024c0056t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0025c0047t0030 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0026c0032t0007 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5356): Show |
chr3 | 66373797 | 66506022 |
a0027c0028t0003 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0028c0044t0001 | 0/0 | 5363 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0029c0039t0001 | 0/0 | 5363 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0030c0029t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0031c0024t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
a0032c0057t0011 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5357): Show |
chr3 | 66373797 | 66506022 |
a0033c0034t0019 | 0/0 | 5364 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5359): Show |
chr3 | 66373797 | 66506022 |
a0034c0045t0001 | 0/0 | 5363 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | AGCAA others(5358): Show |
chr3 | 66373797 | 66506022 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0002t0031g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0007t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0007t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0007t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0007t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0007t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0007t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0007t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0007t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0007t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0007t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0007t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0007t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0014t0010g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0014t0010g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0014t0011g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0014t0011g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0014t0028g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0023t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0023t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0001c0040t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0015g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0016g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0001t0032g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0018t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0018t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0018t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0021t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0021t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0022t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0022t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0041t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0002c0048t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0005t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0005t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0005t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0005t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0005t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0005t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0005t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0005t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0005t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0005t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0005t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0005t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0005t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0005t0003g0249 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0010t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0010t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0010t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0010t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0010t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0010t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0010t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0012t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0012t0014g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0012t0014g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0012t0017g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0012t0018g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0031t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0003c0036t0034g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0026g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0003t0039g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0004c0053t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0005c0004t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0005c0004t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0005c0004t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0005c0004t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0005c0004t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0005c0004t0006g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0005c0004t0006g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0005c0004t0006g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0005c0004t0007g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0005c0004t0008g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0005c0004t0008g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0005c0004t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0005c0004t0008g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0005c0004t0008g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0005c0004t0021g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0006c0009t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0006c0009t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0006c0009t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0006c0009t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0006c0009t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0006c0009t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0006c0009t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0006c0009t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0006c0019t0012g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0006c0019t0012g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0006c0026t0036g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0006c0027t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0006c0035t0033g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0007c0006t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0007c0006t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0007c0006t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0007c0006t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0007c0006t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0007c0006t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0007c0006t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0007c0006t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0007c0006t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0007c0006t0009g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0007c0006t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0007c0006t0020g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0008c0008t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0008c0008t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0008c0008t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0008c0008t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0008c0008t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0008c0008t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0008c0008t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0008c0008t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0008c0008t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0008c0008t0025g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0008c0008t0037g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0008c0033t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0009c0013t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0009c0013t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0009c0013t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0009c0013t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0009c0013t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0009c0015t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0009c0015t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0009c0015t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0009c0037t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0010c0011t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0010c0011t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0010c0011t0007g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0010c0011t0007g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0010c0011t0007g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0010c0011t0024g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0011c0016t0013g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0011c0016t0013g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0011c0016t0013g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0011c0030t0027g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0012c0017t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0012c0017t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0012c0017t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0013c0042t0010g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0013c0043t0022g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0014c0020t0029g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0014c0020t0035g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0015c0051t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0016c0050t0023g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0017c0025t0012g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0018c0055t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0019c0038t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0020c0046t0010g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0021c0049t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0022c0054t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0023c0052t0038g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0024c0056t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0025c0047t0030g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0026c0032t0007g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0027c0028t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0028c0044t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0029c0039t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0030c0029t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0031c0024t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0032c0057t0011g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0033c0034t0019g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
a0034c0045t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0004 | c0003 | t0002 | g0080 | EUR | GBR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0078 | EUR | GBR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG00280 | hp1 | a0010 | c0011 | t0007 | g0174 | EUR | FIN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG00280 | hp2 | a0001 | c0007 | t0001 | g0118 | EUR | FIN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG00544 | hp1 | a0012 | c0017 | t0002 | g0019 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG00544 | hp2 | a0002 | c0001 | t0001 | g0047 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG00558 | hp1 | a0002 | c0001 | t0001 | g0146 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG00558 | hp2 | a0002 | c0021 | t0001 | g0115 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG00609 | hp1 | a0013 | c0043 | t0022 | g0009 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG00609 | hp2 | a0009 | c0037 | t0002 | g0017 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG00621 | hp1 | a0002 | c0001 | t0032 | g0199 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG00621 | hp2 | a0002 | c0001 | t0001 | g0147 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG00673 | hp2 | a0002 | c0018 | t0001 | g0050 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG00735 | hp1 | a0006 | c0009 | t0004 | g0228 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG00738 | hp1 | a0002 | c0001 | t0001 | g0170 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG00738 | hp2 | a0002 | c0001 | t0001 | g0151 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01069 | hp1 | a0002 | c0001 | t0001 | g0084 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01069 | hp2 | a0002 | c0001 | t0015 | g0002 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0053 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01070 | hp2 | a0003 | c0005 | t0003 | g0241 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01071 | hp2 | a0002 | c0001 | t0001 | g0086 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01074 | hp1 | a0002 | c0001 | t0001 | g0122 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01074 | hp2 | a0001 | c0007 | t0002 | g0157 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01099 | hp1 | a0005 | c0004 | t0006 | g0238 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01099 | hp2 | a0001 | c0007 | t0002 | g0155 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01167 | hp1 | a0002 | c0001 | t0001 | g0052 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0069 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0075 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01192 | hp2 | a0001 | c0007 | t0002 | g0160 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01243 | hp1 | a0002 | c0022 | t0001 | g0179 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01243 | hp2 | a0005 | c0004 | t0008 | g0254 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01255 | hp1 | a0001 | c0007 | t0002 | g0194 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01255 | hp2 | a0002 | c0001 | t0001 | g0112 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01256 | hp1 | a0004 | c0003 | t0002 | g0144 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01256 | hp2 | a0009 | c0013 | t0002 | g0024 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01261 | hp1 | a0001 | c0007 | t0002 | g0079 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0087 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0150 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01346 | hp2 | a0002 | c0001 | t0001 | g0165 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01358 | hp1 | a0005 | c0004 | t0006 | g0239 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01358 | hp2 | a0001 | c0007 | t0002 | g0161 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01433 | hp1 | a0001 | c0014 | t0010 | g0186 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01433 | hp2 | a0002 | c0001 | t0001 | g0163 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01496 | hp1 | a0015 | c0051 | t0002 | g0054 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01515 | hp1 | a0016 | c0050 | t0023 | g0081 | EUR | IBS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0062 | EUR | IBS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01884 | hp1 | a0003 | c0005 | t0001 | g0037 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01884 | hp2 | a0007 | c0006 | t0005 | g0242 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01891 | hp2 | a0009 | c0015 | t0002 | g0034 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0162 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01928 | hp2 | a0001 | c0007 | t0002 | g0154 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01934 | hp1 | a0001 | c0007 | t0002 | g0158 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01952 | hp1 | a0017 | c0025 | t0012 | g0253 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0085 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01981 | hp1 | a0002 | c0001 | t0001 | g0109 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01981 | hp2 | a0005 | c0004 | t0006 | g0240 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0167 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01993 | hp2 | a0001 | c0007 | t0002 | g0124 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02027 | hp2 | a0014 | c0020 | t0029 | g0029 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02040 | hp1 | a0002 | c0001 | t0001 | g0138 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02040 | hp2 | a0003 | c0005 | t0003 | g0210 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02055 | hp1 | a0003 | c0012 | t0014 | g0236 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0178 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02056 | hp1 | a0002 | c0018 | t0001 | g0192 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02071 | hp1 | a0002 | c0001 | t0001 | g0180 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02071 | hp2 | a0004 | c0003 | t0002 | g0102 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02132 | hp1 | a0018 | c0055 | t0002 | g0130 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02132 | hp2 | a0002 | c0001 | t0001 | g0195 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02135 | hp1 | a0004 | c0003 | t0002 | g0181 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02145 | hp1 | a0019 | c0038 | t0003 | g0235 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02145 | hp2 | a0020 | c0046 | t0010 | g0184 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02148 | hp1 | a0001 | c0007 | t0002 | g0159 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0117 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02165 | hp1 | a0003 | c0012 | t0001 | g0040 | EAS | CDX | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02165 | hp2 | a0002 | c0001 | t0001 | g0169 | EAS | CDX | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02258 | hp1 | a0005 | c0004 | t0008 | g0248 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02258 | hp2 | a0004 | c0003 | t0002 | g0152 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02280 | hp1 | a0021 | c0049 | t0001 | g0066 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02280 | hp2 | a0006 | c0019 | t0012 | g0244 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0131 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02300 | hp2 | a0022 | c0054 | t0002 | g0196 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02451 | hp1 | a0008 | c0008 | t0001 | g0038 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02451 | hp2 | a0005 | c0004 | t0008 | g0247 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02523 | hp1 | a0008 | c0008 | t0025 | g0043 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02523 | hp2 | a0024 | c0056 | t0001 | g0182 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02572 | hp1 | a0003 | c0036 | t0034 | g0203 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02572 | hp2 | a0005 | c0004 | t0008 | g0250 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02622 | hp1 | a0007 | c0006 | t0009 | g0014 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02630 | hp1 | a0014 | c0020 | t0035 | g0208 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02630 | hp2 | a0005 | c0004 | t0006 | g0222 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02647 | hp1 | a0003 | c0010 | t0004 | g0231 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02647 | hp2 | a0007 | c0006 | t0005 | g0219 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02698 | hp1 | a0004 | c0003 | t0002 | g0057 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02698 | hp2 | a0010 | c0011 | t0007 | g0168 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02717 | hp1 | a0006 | c0035 | t0033 | g0207 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02717 | hp2 | a0025 | c0047 | t0030 | g0153 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02723 | hp1 | a0002 | c0001 | t0001 | g0173 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02723 | hp2 | a0008 | c0008 | t0003 | g0256 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02735 | hp1 | a0001 | c0002 | t0031 | g0068 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02735 | hp2 | a0004 | c0003 | t0002 | g0104 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0103 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02738 | hp2 | a0002 | c0001 | t0001 | g0187 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02809 | hp1 | a0003 | c0005 | t0001 | g0039 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02809 | hp2 | a0006 | c0019 | t0012 | g0245 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02818 | hp1 | a0003 | c0010 | t0004 | g0260 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02818 | hp2 | a0005 | c0004 | t0006 | g0202 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02886 | hp1 | a0007 | c0006 | t0005 | g0230 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02886 | hp2 | a0005 | c0004 | t0021 | g0006 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02896 | hp1 | a0001 | c0023 | t0002 | g0067 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02896 | hp2 | a0026 | c0032 | t0007 | g0046 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02897 | hp1 | a0003 | c0010 | t0004 | g0258 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02897 | hp2 | a0001 | c0023 | t0002 | g0082 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02922 | hp1 | a0009 | c0015 | t0002 | g0033 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02922 | hp2 | a0003 | c0010 | t0004 | g0201 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02965 | hp1 | a0007 | c0006 | t0005 | g0215 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02965 | hp2 | a0011 | c0030 | t0027 | g0021 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02970 | hp1 | a0006 | c0009 | t0004 | g0226 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02970 | hp2 | a0006 | c0009 | t0004 | g0232 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02976 | hp1 | a0003 | c0012 | t0017 | g0004 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02976 | hp2 | a0003 | c0012 | t0018 | g0008 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03017 | hp1 | a0002 | c0001 | t0001 | g0059 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0077 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03041 | hp1 | a0007 | c0006 | t0005 | g0200 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03041 | hp2 | a0006 | c0026 | t0036 | g0234 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03098 | hp1 | a0005 | c0004 | t0006 | g0220 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03098 | hp2 | a0006 | c0009 | t0004 | g0251 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03130 | hp1 | a0007 | c0006 | t0009 | g0035 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03130 | hp2 | a0003 | c0012 | t0014 | g0233 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03139 | hp1 | a0010 | c0011 | t0024 | g0063 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03139 | hp2 | a0002 | c0001 | t0001 | g0171 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03195 | hp1 | a0008 | c0033 | t0001 | g0027 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03195 | hp2 | a0003 | c0010 | t0004 | g0229 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03209 | hp1 | a0002 | c0001 | t0001 | g0172 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03209 | hp2 | a0027 | c0028 | t0003 | g0259 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03225 | hp1 | a0004 | c0003 | t0002 | g0088 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03225 | hp2 | a0006 | c0009 | t0004 | g0224 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03239 | hp1 | a0008 | c0008 | t0003 | g0213 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03239 | hp2 | a0001 | c0007 | t0002 | g0099 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03453 | hp1 | a0008 | c0008 | t0003 | g0252 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03486 | hp1 | a0003 | c0031 | t0001 | g0036 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03486 | hp2 | a0007 | c0006 | t0005 | g0223 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03579 | hp1 | a0004 | c0003 | t0002 | g0089 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03579 | hp2 | a0003 | c0005 | t0001 | g0028 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03669 | hp1 | a0009 | c0013 | t0004 | g0214 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0113 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03688 | hp1 | a0002 | c0001 | t0001 | g0123 | SAS | STU | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03688 | hp2 | a0004 | c0003 | t0026 | g0190 | SAS | STU | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03704 | hp1 | a0004 | c0003 | t0001 | g0142 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03704 | hp2 | a0004 | c0003 | t0002 | g0105 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03710 | hp1 | a0004 | c0003 | t0002 | g0132 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03710 | hp2 | a0004 | c0003 | t0002 | g0193 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0074 | SAS | BEB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03834 | hp2 | a0013 | c0042 | t0010 | g0083 | SAS | BEB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0106 | SAS | BEB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03927 | hp2 | a0028 | c0044 | t0001 | g0185 | SAS | BEB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03942 | hp1 | a0008 | c0008 | t0037 | g0261 | SAS | BEB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03942 | hp2 | a0004 | c0003 | t0002 | g0100 | SAS | BEB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG04115 | hp1 | a0029 | c0039 | t0001 | g0072 | SAS | STU | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG04115 | hp2 | a0004 | c0003 | t0002 | g0107 | SAS | STU | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18522 | hp1 | a0005 | c0004 | t0006 | g0221 | AFR | YRI | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18522 | hp2 | a0007 | c0006 | t0009 | g0011 | AFR | YRI | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18747 | hp1 | a0002 | c0001 | t0001 | g0110 | EAS | CHB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18747 | hp2 | a0002 | c0022 | t0001 | g0176 | EAS | CHB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18906 | hp1 | a0006 | c0027 | t0004 | g0227 | AFR | YRI | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18906 | hp2 | a0004 | c0003 | t0039 | g0262 | AFR | YRI | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18939 | hp1 | a0002 | c0001 | t0001 | g0090 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18939 | hp2 | a0001 | c0014 | t0011 | g0058 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18943 | hp2 | a0002 | c0001 | t0001 | g0048 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18949 | hp1 | a0001 | c0014 | t0028 | g0120 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18950 | hp1 | a0005 | c0004 | t0001 | g0018 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18950 | hp2 | a0002 | c0001 | t0001 | g0183 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18951 | hp1 | a0002 | c0001 | t0001 | g0136 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18951 | hp2 | a0030 | c0029 | t0001 | g0022 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18953 | hp1 | a0008 | c0008 | t0001 | g0031 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18953 | hp2 | a0002 | c0001 | t0001 | g0121 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18961 | hp1 | a0003 | c0005 | t0003 | g0217 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18961 | hp2 | a0002 | c0001 | t0001 | g0191 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18966 | hp1 | a0002 | c0001 | t0001 | g0128 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18966 | hp2 | a0003 | c0005 | t0003 | g0001 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18969 | hp1 | a0002 | c0041 | t0001 | g0116 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18969 | hp2 | a0012 | c0017 | t0002 | g0023 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18970 | hp1 | a0010 | c0011 | t0001 | g0091 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18970 | hp2 | a0008 | c0008 | t0001 | g0030 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18974 | hp1 | a0002 | c0001 | t0001 | g0134 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18974 | hp2 | a0005 | c0004 | t0007 | g0016 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18975 | hp1 | a0002 | c0001 | t0001 | g0149 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18981 | hp1 | a0004 | c0053 | t0002 | g0197 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18981 | hp2 | a0010 | c0011 | t0001 | g0095 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18985 | hp1 | a0003 | c0005 | t0003 | g0218 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18985 | hp2 | a0002 | c0001 | t0001 | g0164 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18986 | hp1 | a0003 | c0005 | t0003 | g0001 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18986 | hp2 | a0002 | c0021 | t0001 | g0114 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18988 | hp2 | a0002 | c0001 | t0001 | g0101 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18989 | hp1 | a0002 | c0001 | t0001 | g0188 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18989 | hp2 | a0003 | c0005 | t0003 | g0216 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18991 | hp1 | a0002 | c0001 | t0016 | g0003 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18991 | hp2 | a0009 | c0013 | t0001 | g0041 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18992 | hp1 | a0002 | c0001 | t0001 | g0139 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18992 | hp2 | a0003 | c0005 | t0003 | g0209 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18993 | hp1 | a0001 | c0040 | t0001 | g0096 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18993 | hp2 | a0012 | c0017 | t0002 | g0015 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18994 | hp1 | a0003 | c0005 | t0001 | g0026 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA18994 | hp2 | a0002 | c0001 | t0001 | g0140 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19000 | hp1 | a0002 | c0018 | t0001 | g0175 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19000 | hp2 | a0009 | c0013 | t0002 | g0044 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19004 | hp1 | a0002 | c0001 | t0001 | g0145 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19004 | hp2 | a0008 | c0008 | t0001 | g0020 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19007 | hp1 | a0001 | c0014 | t0011 | g0119 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19007 | hp2 | a0002 | c0001 | t0001 | g0143 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19030 | hp1 | a0009 | c0015 | t0002 | g0032 | AFR | LWK | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19030 | hp2 | a0003 | c0010 | t0004 | g0257 | AFR | LWK | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19043 | hp1 | a0008 | c0008 | t0003 | g0237 | AFR | LWK | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19043 | hp2 | a0011 | c0016 | t0013 | g0206 | AFR | LWK | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19056 | hp1 | a0004 | c0003 | t0002 | g0097 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19056 | hp2 | a0002 | c0001 | t0001 | g0126 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19058 | hp1 | a0008 | c0008 | t0001 | g0013 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19064 | hp1 | a0002 | c0001 | t0001 | g0133 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19064 | hp2 | a0009 | c0013 | t0002 | g0042 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19065 | hp1 | a0003 | c0005 | t0003 | g0211 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19065 | hp2 | a0002 | c0048 | t0001 | g0098 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19077 | hp1 | a0002 | c0001 | t0001 | g0135 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19077 | hp2 | a0003 | c0005 | t0003 | g0212 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19079 | hp1 | a0031 | c0024 | t0001 | g0025 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19079 | hp2 | a0032 | c0057 | t0011 | g0129 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19085 | hp1 | a0002 | c0001 | t0001 | g0071 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19240 | hp1 | a0005 | c0004 | t0008 | g0255 | AFR | YRI | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA19240 | hp2 | a0003 | c0010 | t0002 | g0010 | AFR | YRI | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0070 | EUR | TSI | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA20805 | hp2 | a0034 | c0045 | t0001 | g0111 | EUR | TSI | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA20905 | hp1 | a0001 | c0014 | t0010 | g0125 | SAS | GIH | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA20905 | hp2 | a0002 | c0001 | t0001 | g0141 | SAS | GIH | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01123 | hp1 | a0010 | c0011 | t0007 | g0156 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG01123 | hp2 | a0002 | c0001 | t0001 | g0055 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02486 | hp1 | a0023 | c0052 | t0038 | g0263 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02486 | hp2 | a0011 | c0016 | t0013 | g0204 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02559 | hp1 | a0011 | c0016 | t0013 | g0205 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG02559 | hp2 | a0007 | c0006 | t0009 | g0012 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03471 | hp1 | a0007 | c0006 | t0005 | g0243 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG03471 | hp2 | a0006 | c0009 | t0002 | g0045 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG06807 | hp1 | a0006 | c0009 | t0004 | g0225 | AFR | USA | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
HG06807 | hp2 | a0007 | c0006 | t0020 | g0005 | AFR | USA | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA20300 | hp1 | a0006 | c0009 | t0004 | g0246 | AFR | USA | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
NA20300 | hp2 | a0033 | c0034 | t0019 | g0007 | AFR | USA | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0177 | REF | REF | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
homoSapiens | grch38p0 | a0003 | c0005 | t0003 | g0249 | REF | REF | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:66380387 | T | G | 8 | a0004 a0009 a0012 others(5): Show |
36 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(33): Show |
missense_variant | MODERATE | c.3158A>C | p.Gln1053Pro | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 3773/5363 | 3158/3282 | 1053/1093 | chr3 | 66380387 | |||
chr3:66380453 | G | C | 7 | a0005 a0010 a0014 others(4): Show |
27 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(24): Show |
missense_variant | MODERATE | c.3092C>G | p.Pro1031Arg | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 3707/5363 | 3092/3282 | 1031/1093 | chr3 | 66380453 | |||
chr3:66380598 | T | C | 1 | a0020 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.3034A>G | p.Met1012Val | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3649/5363 | 3034/3282 | 1012/1093 | chr3 | 66380598 | |||
chr3:66380635 | G | C | 1 | a0022 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.2997C>G | p.Asn999Lys | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3612/5363 | 2997/3282 | 999/1093 | chr3 | 66380635 | |||
chr3:66380654 | C | G | 2 | a0012 a0018 |
4 | HG00544.hp1 HG02132.hp1 NA18969.hp2 others(1): Show |
missense_variant | MODERATE | c.2978G>C | p.Gly993Ala | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3593/5363 | 2978/3282 | 993/1093 | chr3 | 66380654 | |||
chr3:66380763 | C | T | 5 | a0005 a0010 a0014 others(2): Show |
25 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(22): Show |
missense_variant | MODERATE | c.2869G>A | p.Ala957Thr | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3484/5363 | 2869/3282 | 957/1093 | chr3 | 66380763 | |||
chr3:66380770 | T | G | 1 | a0030 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.2862A>C | p.Arg954Ser | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3477/5363 | 2862/3282 | 954/1093 | chr3 | 66380770 | |||
chr3:66380855 | C | A | 1 | a0006 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.2777G>T | p.Gly926Val | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3392/5363 | 2777/3282 | 926/1093 | chr3 | 66380855 | |||
chr3:66380856 | C | T | 5 | a0006 a0007 a0016 others(2): Show |
28 | HG00735.hp1 HG01515.hp1 HG01884.hp2 others(25): Show |
missense_variant | MODERATE | c.2776G>A | p.Gly926Ser | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3391/5363 | 2776/3282 | 926/1093 | chr3 | 66380856 | |||
chr3:66381622 | G | A | 1 | a0015 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.2627C>T | p.Pro876Leu | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/19 | 3242/5363 | 2627/3282 | 876/1093 | chr3 | 66381622 | |||
chr3:66382293 | T | C | 1 | a0023 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.2597A>G | p.Asn866Ser | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/19 | 3212/5363 | 2597/3282 | 866/1093 | chr3 | 66382293 | |||
chr3:66382297 | C | T | 1 | a0034 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.2593G>A | p.Ala865Thr | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/19 | 3208/5363 | 2593/3282 | 865/1093 | chr3 | 66382297 | |||
chr3:66382309 | C | G | 1 | a0028 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.2581G>C | p.Gly861Arg | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/19 | 3196/5363 | 2581/3282 | 861/1093 | chr3 | 66382309 | |||
chr3:66383278 | G | A | 1 | a0033 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.2195C>T | p.Pro732Leu | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/19 | 2810/5363 | 2195/3282 | 732/1093 | chr3 | 66383278 | |||
chr3:66383311 | G | A | 2 | a0011 a0013 |
6 | HG00609.hp1 HG02486.hp2 HG02559.hp1 others(3): Show |
missense_variant | MODERATE | c.2162C>T | p.Pro721Leu | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/19 | 2777/5363 | 2162/3282 | 721/1093 | chr3 | 66383311 | |||
chr3:66383999 | G | C | 1 | a0023 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.2063C>G | p.Thr688Ser | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/19 | 2678/5363 | 2063/3282 | 688/1093 | chr3 | 66383999 | |||
chr3:66384219 | T | C | 11 | a0002 a0008 a0014 others(8): Show |
80 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(77): Show |
missense_variant | MODERATE | c.1843A>G | p.Met615Val | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/19 | 2458/5363 | 1843/3282 | 615/1093 | chr3 | 66384219 | |||
chr3:66386113 | C | T | 1 | a0033 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.1657G>A | p.Gly553Arg | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/19 | 2272/5363 | 1657/3282 | 553/1093 | chr3 | 66386113 | |||
chr3:66386121 | G | A | 1 | a0026 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.1649C>T | p.Ala550Val | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/19 | 2264/5363 | 1649/3282 | 550/1093 | chr3 | 66386121 | |||
chr3:66386122 | C | T | 1 | a0007 | 12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
missense_variant | MODERATE | c.1648G>A | p.Ala550Thr | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/19 | 2263/5363 | 1648/3282 | 550/1093 | chr3 | 66386122 | |||
chr3:66386255 | C | T | 1 | a0017 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.1515G>A | p.Met505Ile | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/19 | 2130/5363 | 1515/3282 | 505/1093 | chr3 | 66386255 | |||
chr3:66410216 | G | A | 1 | a0019 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.848C>T | p.Thr283Met | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/19 | 1463/5363 | 848/3282 | 283/1093 | chr3 | 66410216 | |||
chr3:66412879 | C | T | 1 | a0031 | 1 | NA19079.hp1 | missense_variant | MODERATE | c.783G>A | p.Met261Ile | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/19 | 1398/5363 | 783/3282 | 261/1093 | chr3 | 66412879 | |||
chr3:66412916 | T | C | 1 | a0024 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.746A>G | p.Lys249Arg | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/19 | 1361/5363 | 746/3282 | 249/1093 | chr3 | 66412916 | |||
chr3:66451607 | G | A | 1 | a0032 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.317C>T | p.Ala106Val | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/19 | 932/5363 | 317/3282 | 106/1093 | chr3 | 66451607 | |||
chr3:66500332 | G | C | 18 | a0001 a0002 a0004 others(15): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
missense_variant | MODERATE | c.76C>G | p.Leu26Val | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 691/5363 | 76/3282 | 26/1093 | chr3 | 66500332 | |||
chr3:66500338 | G | C | 18 | a0001 a0002 a0004 others(15): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
missense_variant | MODERATE | c.70C>G | p.Leu24Val | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 685/5363 | 70/3282 | 24/1093 | chr3 | 66500338 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:66380395 | C | T | 3 | a0009c0037 a0012c0017 a0018c0055 |
5 | HG00544.hp1 HG00609.hp2 HG02132.hp1 others(2): Show |
synonymous_variant | LOW | c.3150G>A | p.Ala1050Ala | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 3765/5363 | 3150/3282 | 1050/1093 | chr3 | 66380395 | |||
chr3:66380446 | G | A | 4 | a0001c0014 a0013c0042 a0020c0046 others(1): Show |
8 | HG01433.hp1 HG02145.hp2 HG03834.hp2 others(5): Show |
synonymous_variant | LOW | c.3099C>T | p.Ser1033Ser | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 3714/5363 | 3099/3282 | 1033/1093 | chr3 | 66380446 | |||
chr3:66380479 | G | C | 1 | a0003c0036 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.3066C>G | p.Ser1022Ser | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 3681/5363 | 3066/3282 | 1022/1093 | chr3 | 66380479 | |||
chr3:66380680 | G | A | 3 | a0006c0019 a0011c0030 a0017c0025 |
4 | HG01952.hp1 HG02280.hp2 HG02809.hp2 others(1): Show |
synonymous_variant | LOW | c.2952C>T | p.Ala984Ala | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3567/5363 | 2952/3282 | 984/1093 | chr3 | 66380680 | |||
chr3:66380737 | C | T | 1 | a0002c0021 | 2 | HG00558.hp2 NA18986.hp2 |
synonymous_variant | LOW | c.2895G>A | p.Pro965Pro | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3510/5363 | 2895/3282 | 965/1093 | chr3 | 66380737 | |||
chr3:66380851 | G | A | 2 | a0002c0018 a0024c0056 |
4 | HG00673.hp2 HG02056.hp1 HG02523.hp2 others(1): Show |
synonymous_variant | LOW | c.2781C>T | p.Gly927Gly | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3396/5363 | 2781/3282 | 927/1093 | chr3 | 66380851 | |||
chr3:66381519 | C | T | 1 | a0001c0007 | 12 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
synonymous_variant | LOW | c.2730G>A | p.Ala910Ala | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/19 | 3345/5363 | 2730/3282 | 910/1093 | chr3 | 66381519 | |||
chr3:66383034 | G | A | 3 | a0006c0009 a0006c0026 a0006c0027 |
10 | HG00735.hp1 HG02970.hp1 HG02970.hp2 others(7): Show |
synonymous_variant | LOW | c.2439C>T | p.Cys813Cys | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/19 | 3054/5363 | 2439/3282 | 813/1093 | chr3 | 66383034 | |||
chr3:66383252 | A | G | 42 | a0001c0007 a0001c0014 a0001c0023 others(39): Show |
176 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
synonymous_variant | LOW | c.2221T>C | p.Leu741Leu | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/19 | 2836/5363 | 2221/3282 | 741/1093 | chr3 | 66383252 | |||
chr3:66384097 | G | A | 1 | a0003c0031 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.1965C>T | p.Asp655Asp | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/19 | 2580/5363 | 1965/3282 | 655/1093 | chr3 | 66384097 | |||
chr3:66384244 | G | A | 1 | a0002c0022 | 2 | HG01243.hp1 NA18747.hp2 |
synonymous_variant | LOW | c.1818C>T | p.His606His | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/19 | 2433/5363 | 1818/3282 | 606/1093 | chr3 | 66384244 | |||
chr3:66386114 | G | A | 2 | a0004c0053 a0022c0054 |
2 | HG02300.hp2 NA18981.hp1 |
synonymous_variant | LOW | c.1656C>T | p.Asp552Asp | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/19 | 2271/5363 | 1656/3282 | 552/1093 | chr3 | 66386114 | |||
chr3:66386126 | G | C | 3 | a0009c0037 a0012c0017 a0018c0055 |
5 | HG00544.hp1 HG00609.hp2 HG02132.hp1 others(2): Show |
synonymous_variant | LOW | c.1644C>G | p.Val548Val | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/19 | 2259/5363 | 1644/3282 | 548/1093 | chr3 | 66386126 | |||
chr3:66386156 | G | A | 1 | a0008c0033 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.1614C>T | p.Thr538Thr | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/19 | 2229/5363 | 1614/3282 | 538/1093 | chr3 | 66386156 | |||
chr3:66394191 | G | A | 19 | a0001c0007 a0001c0023 a0003c0010 others(16): Show |
78 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(75): Show |
synonymous_variant | LOW | c.1317C>T | p.Ser439Ser | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/19 | 1932/5363 | 1317/3282 | 439/1093 | chr3 | 66394191 | |||
chr3:66417176 | C | T | 2 | a0001c0040 a0002c0041 |
2 | NA18969.hp1 NA18993.hp1 |
synonymous_variant | LOW | c.456G>A | p.Thr152Thr | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/19 | 1071/5363 | 456/3282 | 152/1093 | chr3 | 66417176 | |||
chr3:66462470 | A | G | 1 | a0029c0039 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.258T>C | p.Ala86Ala | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/19 | 873/5363 | 258/3282 | 86/1093 | chr3 | 66462470 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:66378812 | A | C | 1 | a0014c0020t0029 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1451T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 1451 | chr3 | 66378812 | ||||||
chr3:66379037 | G | A | 2 | a0006c0019t0012 a0017c0025t0012 |
3 | HG01952.hp1 HG02280.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1226C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 1226 | chr3 | 66379037 | ||||||
chr3:66379051 | C | G | 7 | a0001c0014t0011 a0001c0014t0028 a0003c0012t0018 others(4): Show |
17 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1212G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 1212 | chr3 | 66379051 | ||||||
chr3:66379132 | T | TTTAAG | 2 | a0011c0016t0013 a0011c0030t0027 |
4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1126_*1130dupCTTA others(1): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 1130 | chr3 | 66379132 | ||||||
chr3:66379145 | A | G | 1 | a0008c0008t0025 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1118T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 1118 | chr3 | 66379145 | ||||||
chr3:66379259 | C | T | 2 | a0003c0012t0014 a0004c0003t0026 |
3 | HG02055.hp1 HG03130.hp2 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1004G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 1004 | chr3 | 66379259 | ||||||
chr3:66379331 | C | T | 1 | a0006c0035t0033 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*932G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 932 | chr3 | 66379331 | ||||||
chr3:66379418 | A | C | 1 | a0003c0036t0034 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*845T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 845 | chr3 | 66379418 | ||||||
chr3:66379586 | G | A | 2 | a0003c0012t0014 a0033c0034t0019 |
3 | HG02055.hp1 HG03130.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*677C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 677 | chr3 | 66379586 | ||||||
chr3:66379598 | C | T | 1 | a0004c0003t0026 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*665G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 665 | chr3 | 66379598 | ||||||
chr3:66379705 | G | C | 3 | a0007c0006t0005 a0007c0006t0009 a0007c0006t0020 |
12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*558C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 558 | chr3 | 66379705 | ||||||
chr3:66379762 | C | A | 1 | a0003c0012t0014 | 2 | HG02055.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*501G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 501 | chr3 | 66379762 | ||||||
chr3:66379791 | G | A | 1 | a0003c0012t0014 | 2 | HG02055.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*472C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 472 | chr3 | 66379791 | ||||||
chr3:66379910 | AC | A | 36 | a0001c0007t0002 a0001c0014t0010 a0001c0014t0011 others(33): Show |
92 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*352delG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 352 | chr3 | 66379910 | ||||||
chr3:66379924 | T | A | 3 | a0001c0014t0010 a0013c0042t0010 a0020c0046t0010 |
4 | HG01433.hp1 HG02145.hp2 HG03834.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*339A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 339 | chr3 | 66379924 | ||||||
chr3:66379942 | G | A | 1 | a0001c0014t0028 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*321C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 321 | chr3 | 66379942 | ||||||
chr3:66379952 | ATT | A | 8 | a0005c0004t0006 a0005c0004t0007 a0005c0004t0008 others(5): Show |
20 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*309_*310delAA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 309 | chr3 | 66379952 | ||||||
chr3:66379953 | T | C | 1 | a0023c0052t0038 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*310A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 310 | chr3 | 66379953 | ||||||
chr3:66379957 | C | T | 2 | a0005c0004t0008 a0010c0011t0024 |
6 | HG01243.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*306G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 306 | chr3 | 66379957 | ||||||
chr3:66379966 | A | G | 1 | a0003c0012t0014 | 2 | HG02055.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*297T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 297 | chr3 | 66379966 | ||||||
chr3:66380043 | C | G | 1 | a0016c0050t0023 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*220G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 220 | chr3 | 66380043 | ||||||
chr3:66380044 | T | C | 2 | a0014c0020t0035 a0025c0047t0030 |
2 | HG02630.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*219A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 219 | chr3 | 66380044 | ||||||
chr3:66380047 | T | C | 1 | a0006c0026t0036 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*216A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 216 | chr3 | 66380047 | ||||||
chr3:66380151 | G | A | 1 | a0001c0002t0031 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*112C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 112 | chr3 | 66380151 | ||||||
chr3:66500512 | G | A | 1 | a0008c0008t0037 | 1 | HG03942.hp1 | 5_prime_UTR_variant | MODIFIER | c.-105C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 105 | chr3 | 66500512 | ||||||
chr3:66500574 | C | A | 1 | a0002c0001t0032 | 1 | HG00621.hp1 | 5_prime_UTR_variant | MODIFIER | c.-167G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 167 | chr3 | 66500574 | ||||||
chr3:66500652 | G | T | 67 | a0001c0002t0001 a0001c0002t0031 a0001c0007t0001 others(64): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
5_prime_UTR_variant | MODIFIER | c.-245C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 245 | chr3 | 66500652 | ||||||
chr3:66500920 | G | T | 1 | a0013c0043t0022 | 1 | HG00609.hp1 | 5_prime_UTR_variant | MODIFIER | c.-513C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 513 | chr3 | 66500920 | ||||||
chr3:66500929 | G | A | 2 | a0004c0003t0039 a0023c0052t0038 |
2 | HG02486.hp1 NA18906.hp2 |
5_prime_UTR_variant | MODIFIER | c.-522C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 522 | chr3 | 66500929 | ||||||
chr3:66500930 | A | AGC | 5 | a0003c0012t0017 a0003c0012t0018 a0005c0004t0021 others(2): Show |
5 | HG02886.hp2 HG02976.hp1 HG02976.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-525_-524dupGC | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 524 | chr3 | 66500930 | ||||||
chr3:66500942 | C | G | 1 | a0002c0001t0016 | 1 | NA18991.hp1 | 5_prime_UTR_variant | MODIFIER | c.-535G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 535 | chr3 | 66500942 | ||||||
chr3:66500955 | G | T | 1 | a0002c0001t0015 | 1 | HG01069.hp2 | 5_prime_UTR_variant | MODIFIER | c.-548C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 548 | chr3 | 66500955 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:66380873 | C | T | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2771-12G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66380873 | |||||||
chr3:66380971 | A | C | 4 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(1): Show |
4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.2771-110T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66380971 | |||||||
chr3:66381030 | A | C | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2771-169T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381030 | |||||||
chr3:66381108 | A | G | 204 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(201): Show |
204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2771-247T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381108 | |||||||
chr3:66381111 | G | A | 2 | a0008c0008t0001g0013 a0008c0008t0001g0030 |
2 | NA18970.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.2771-250C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381111 | |||||||
chr3:66381178 | A | G | 178 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(175): Show |
178 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.2770+301T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381178 | |||||||
chr3:66381180 | A | AATAGCCC others(16): Show |
1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2770+276_2770+298d others(25): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381180 | |||||||
chr3:66381186 | C | T | 2 | a0003c0012t0014g0233 a0003c0012t0014g0236 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2770+293G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381186 | |||||||
chr3:66381192 | G | A | 12 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(9): Show |
12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.2770+287C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381192 | |||||||
chr3:66381222 | G | A | 1 | a0026c0032t0007g0046 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2770+257C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381222 | |||||||
chr3:66381289 | C | T | 35 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(32): Show |
35 | HG00735.hp1 HG01884.hp2 HG01952.hp1 others(32): Show |
intron_variant | MODIFIER | c.2770+190G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381289 | |||||||
chr3:66381385 | A | G | 1 | a0001c0014t0010g0186 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2770+94T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381385 | |||||||
chr3:66381394 | G | C | 6 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(3): Show |
6 | HG00735.hp1 HG02970.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2770+85C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381394 | |||||||
chr3:66381663 | C | G | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2618-32G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381663 | |||||||
chr3:66381669 | T | G | 1 | a0004c0003t0002g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2618-38A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381669 | |||||||
chr3:66381732 | T | A | 1 | a0021c0049t0001g0066 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2618-101A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381732 | |||||||
chr3:66381851 | C | T | 1 | a0004c0003t0002g0100 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2618-220G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381851 | |||||||
chr3:66381852 | A | G | 174 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(171): Show |
174 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.2618-221T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381852 | |||||||
chr3:66381883 | G | A | 5 | a0001c0014t0010g0125 a0001c0014t0010g0186 a0003c0012t0018g0008 others(2): Show |
5 | HG01433.hp1 HG02145.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2618-252C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381883 | |||||||
chr3:66381953 | TC | T | 11 | a0003c0012t0018g0008 a0006c0009t0002g0045 a0006c0009t0004g0224 others(8): Show |
11 | HG00735.hp1 HG02970.hp1 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.2617+319delG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381953 | |||||||
chr3:66381991 | G | A | 1 | a0002c0001t0001g0123 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2617+282C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381991 | |||||||
chr3:66381996 | G | C | 3 | a0014c0020t0035g0208 a0023c0052t0038g0263 a0025c0047t0030g0153 |
3 | HG02486.hp1 HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2617+277C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381996 | |||||||
chr3:66382022 | A | G | 4 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(1): Show |
4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.2617+251T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66382022 | |||||||
chr3:66382077 | G | A | 2 | a0001c0002t0001g0069 a0001c0002t0001g0070 |
2 | HG01167.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2617+196C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66382077 | |||||||
chr3:66382114 | T | C | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2617+159A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66382114 | |||||||
chr3:66382256 | A | G | 204 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(201): Show |
204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2617+17T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66382256 | |||||||
chr3:66382421 | G | A | 55 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(52): Show |
55 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.2492-23C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382421 | |||||||
chr3:66382423 | A | C | 4 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2492-25T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382423 | |||||||
chr3:66382429 | G | A | 5 | a0009c0037t0002g0017 a0012c0017t0002g0015 a0012c0017t0002g0019 others(2): Show |
5 | HG00544.hp1 HG00609.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.2492-31C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382429 | |||||||
chr3:66382522 | T | TG | 28 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(25): Show |
28 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.2492-125dupC | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382522 | |||||||
chr3:66382545 | C | G | 4 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2492-147G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382545 | |||||||
chr3:66382563 | G | A | 6 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(3): Show |
6 | HG00735.hp1 HG02970.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2492-165C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382563 | |||||||
chr3:66382578 | A | ACACCCAG others(11): Show |
24 | a0005c0004t0001g0018 a0005c0004t0006g0202 a0005c0004t0006g0220 others(21): Show |
24 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.2492-198_2492-181d others(20): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382578 | |||||||
chr3:66382586 | C | T | 100 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(97): Show |
100 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2492-188G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382586 | |||||||
chr3:66382649 | G | A | 1 | a0001c0014t0010g0125 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2492-251C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382649 | |||||||
chr3:66382669 | A | G | 204 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(201): Show |
204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2492-271T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382669 | |||||||
chr3:66382717 | C | T | 1 | a0004c0003t0002g0102 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2491+265G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382717 | |||||||
chr3:66382752 | T | A | 177 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(174): Show |
177 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(174): Show |
intron_variant | MODIFIER | c.2491+230A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382752 | |||||||
chr3:66382753 | G | A | 4 | a0003c0005t0003g0001 a0003c0005t0003g0209 a0003c0005t0003g0211 others(1): Show |
5 | NA18966.hp2 NA18986.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.2491+229C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382753 | |||||||
chr3:66382776 | TGAGTATT others(21): Show |
T | 4 | a0002c0001t0001g0112 a0003c0012t0014g0233 a0003c0012t0014g0236 others(1): Show |
4 | HG01255.hp2 HG02055.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2491+178_2491+205d others(30): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382776 | |||||||
chr3:66382887 | C | T | 1 | a0004c0003t0002g0104 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2491+95G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382887 | |||||||
chr3:66382888 | A | G | 177 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(174): Show |
177 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(174): Show |
intron_variant | MODIFIER | c.2491+94T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382888 | |||||||
chr3:66383513 | T | G | 89 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(86): Show |
89 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.2072-112A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383513 | |||||||
chr3:66383611 | G | A | 1 | a0004c0053t0002g0197 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2072-210C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383611 | |||||||
chr3:66383666 | TTCTTGAC others(44): Show |
T | 23 | a0003c0012t0018g0008 a0005c0004t0006g0202 a0005c0004t0006g0220 others(20): Show |
23 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.2071+274_2072-266d others(53): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383666 | |||||||
chr3:66383732 | A | G | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2071+259T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383732 | |||||||
chr3:66383829 | T | G | 1 | a0006c0019t0012g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2071+162A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383829 | |||||||
chr3:66383941 | C | G | 3 | a0002c0001t0001g0084 a0002c0001t0001g0086 a0002c0001t0001g0138 |
3 | HG01069.hp1 HG01071.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.2071+50G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383941 | |||||||
chr3:66383948 | T | TCA | 24 | a0001c0002t0001g0065 a0001c0002t0001g0070 a0001c0002t0001g0085 others(21): Show |
24 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.2071+41_2071+42dup others(2): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | |||||||
chr3:66383948 | T | TCACA | 11 | a0005c0004t0006g0220 a0005c0004t0006g0222 a0005c0004t0008g0247 others(8): Show |
11 | HG01243.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2071+39_2071+42dup others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | |||||||
chr3:66383948 | T | TCACACA | 54 | a0002c0001t0001g0047 a0002c0001t0001g0048 a0002c0001t0001g0052 others(51): Show |
54 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2071+37_2071+42dup others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | |||||||
chr3:66383948 | T | TCACACAC others(1): Show |
28 | a0002c0001t0001g0071 a0002c0001t0001g0121 a0002c0001t0001g0126 others(25): Show |
28 | HG00621.hp1 HG00621.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.2071+35_2071+42dup others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | |||||||
chr3:66383948 | T | TCACACAC others(3): Show |
15 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0002c0001t0001g0140 others(12): Show |
15 | HG00280.hp1 HG00735.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.2071+33_2071+42dup others(10): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | |||||||
chr3:66383948 | T | TCACACAC others(5): Show |
20 | a0005c0004t0006g0238 a0005c0004t0007g0016 a0006c0009t0004g0232 others(17): Show |
20 | HG01099.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.2071+31_2071+42dup others(12): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | |||||||
chr3:66383948 | T | TCACACAC others(7): Show |
5 | a0001c0014t0010g0125 a0001c0014t0010g0186 a0007c0006t0005g0215 others(2): Show |
5 | HG01433.hp1 HG02145.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2071+29_2071+42dup others(14): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | |||||||
chr3:66383948 | T | TCACACAC others(9): Show |
2 | a0006c0009t0002g0045 a0020c0046t0010g0184 |
2 | HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2071+27_2071+42dup others(16): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | |||||||
chr3:66383948 | T | TCACACAC others(11): Show |
1 | a0029c0039t0001g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2071+25_2071+42dup others(18): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | |||||||
chr3:66383948 | TCACACAC others(1): Show |
T | 3 | a0005c0004t0006g0202 a0005c0004t0021g0006 a0027c0028t0003g0259 |
3 | HG02818.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2071+35_2071+42del others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | |||||||
chr3:66383948 | TCACACAC others(5): Show |
T | 1 | a0005c0004t0006g0221 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2071+31_2071+42del others(12): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | |||||||
chr3:66384307 | G | A | 1 | a0003c0012t0017g0004 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1790-35C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384307 | |||||||
chr3:66384440 | T | C | 1 | a0023c0052t0038g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1790-168A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384440 | |||||||
chr3:66384454 | T | C | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1790-182A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384454 | |||||||
chr3:66384460 | C | T | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1790-188G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384460 | |||||||
chr3:66384581 | TA | T | 4 | a0004c0003t0039g0262 a0009c0015t0002g0032 a0009c0015t0002g0033 others(1): Show |
4 | HG01891.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1790-310delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384581 | |||||||
chr3:66384656 | G | C | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1790-384C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384656 | |||||||
chr3:66384671 | G | C | 1 | a0002c0001t0001g0138 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1790-399C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384671 | |||||||
chr3:66384678 | CAATGGGA others(34): Show |
C | 2 | a0001c0002t0001g0074 a0010c0011t0007g0156 |
2 | HG01123.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1790-447_1790-407d others(43): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384678 | |||||||
chr3:66384693 | T | A | 50 | a0002c0001t0001g0047 a0002c0001t0001g0048 a0002c0001t0001g0059 others(47): Show |
50 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1790-421A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384693 | |||||||
chr3:66384696 | G | A | 1 | a0004c0003t0002g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1790-424C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384696 | |||||||
chr3:66384703 | T | C | 3 | a0001c0002t0001g0094 a0003c0005t0001g0026 a0030c0029t0001g0022 |
3 | NA18951.hp2 NA18994.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1790-431A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384703 | |||||||
chr3:66384821 | C | T | 1 | a0002c0001t0001g0143 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1790-549G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384821 | |||||||
chr3:66384905 | G | A | 1 | a0024c0056t0001g0182 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1790-633C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384905 | |||||||
chr3:66385152 | C | G | 1 | a0001c0002t0001g0062 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1789+829G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385152 | |||||||
chr3:66385457 | T | TTTTTA | 4 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1789+523_1789+524i others(7): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385457 | |||||||
chr3:66385457 | T | TTTTTG | 151 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(148): Show |
151 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.1789+519_1789+523d others(7): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385457 | |||||||
chr3:66385534 | C | T | 26 | a0002c0001t0001g0170 a0002c0001t0001g0171 a0002c0001t0001g0172 others(23): Show |
26 | HG00738.hp1 HG01099.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.1789+447G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385534 | |||||||
chr3:66385616 | C | T | 15 | a0006c0035t0033g0207 a0007c0006t0005g0200 a0007c0006t0005g0215 others(12): Show |
15 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1789+365G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385616 | |||||||
chr3:66385634 | G | A | 3 | a0002c0001t0001g0055 a0002c0001t0001g0151 a0008c0008t0003g0213 |
3 | HG00738.hp2 HG01123.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1789+347C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385634 | |||||||
chr3:66385667 | A | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1789+314T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385667 | |||||||
chr3:66385672 | C | T | 1 | a0001c0002t0001g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1789+309G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385672 | |||||||
chr3:66385758 | T | G | 97 | a0001c0014t0010g0125 a0001c0014t0010g0186 a0001c0014t0011g0058 others(94): Show |
97 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.1789+223A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385758 | |||||||
chr3:66386330 | G | A | 2 | a0004c0003t0002g0088 a0004c0003t0002g0089 |
2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1469-29C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386330 | |||||||
chr3:66386443 | C | A | 1 | a0002c0001t0001g0128 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1469-142G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386443 | |||||||
chr3:66386452 | G | T | 1 | a0002c0001t0001g0128 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1469-151C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386452 | |||||||
chr3:66386467 | T | C | 57 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(54): Show |
57 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1469-166A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386467 | |||||||
chr3:66386603 | C | G | 3 | a0006c0019t0012g0244 a0006c0019t0012g0245 a0017c0025t0012g0253 |
3 | HG01952.hp1 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1469-302G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386603 | |||||||
chr3:66386652 | G | A | 1 | a0020c0046t0010g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1469-351C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386652 | |||||||
chr3:66386662 | T | C | 93 | a0001c0014t0010g0125 a0001c0014t0010g0186 a0001c0014t0011g0058 others(90): Show |
93 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1469-361A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386662 | |||||||
chr3:66386692 | G | C | 10 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(7): Show |
10 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1469-391C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386692 | |||||||
chr3:66386760 | A | AC | 13 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(10): Show |
13 | HG01884.hp2 HG02145.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1469-460_1469-459i others(3): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386760 | |||||||
chr3:66386835 | G | A | 1 | a0001c0002t0001g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1469-534C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386835 | |||||||
chr3:66387010 | T | C | 1 | a0003c0012t0017g0004 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1469-709A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387010 | |||||||
chr3:66387032 | C | G | 1 | a0030c0029t0001g0022 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1469-731G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387032 | |||||||
chr3:66387097 | C | T | 22 | a0005c0004t0006g0202 a0005c0004t0006g0220 a0005c0004t0006g0221 others(19): Show |
22 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1469-796G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387097 | |||||||
chr3:66387204 | A | G | 1 | a0001c0007t0002g0194 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1469-903T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387204 | |||||||
chr3:66387246 | G | C | 1 | a0001c0002t0031g0068 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1469-945C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387246 | |||||||
chr3:66387321 | C | G | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1469-1020G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387321 | |||||||
chr3:66387407 | C | G | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1469-1106G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387407 | |||||||
chr3:66387413 | G | A | 1 | a0001c0002t0001g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1469-1112C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387413 | |||||||
chr3:66387473 | A | G | 13 | a0006c0035t0033g0207 a0007c0006t0005g0200 a0007c0006t0005g0215 others(10): Show |
13 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1469-1172T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387473 | |||||||
chr3:66387505 | G | A | 5 | a0007c0006t0005g0219 a0011c0016t0013g0204 a0011c0016t0013g0205 others(2): Show |
5 | HG02486.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1469-1204C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387505 | |||||||
chr3:66387532 | A | G | 23 | a0005c0004t0006g0202 a0005c0004t0006g0220 a0005c0004t0006g0221 others(20): Show |
23 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.1469-1231T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387532 | |||||||
chr3:66387566 | C | T | 5 | a0004c0003t0002g0102 a0004c0003t0002g0104 a0004c0003t0002g0193 others(2): Show |
5 | HG01256.hp2 HG02071.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1469-1265G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387566 | |||||||
chr3:66387608 | C | T | 2 | a0014c0020t0035g0208 a0025c0047t0030g0153 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1469-1307G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387608 | |||||||
chr3:66387738 | A | G | 6 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(3): Show |
6 | HG02055.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1469-1437T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387738 | |||||||
chr3:66387785 | C | G | 1 | a0023c0052t0038g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1469-1484G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387785 | |||||||
chr3:66387836 | G | A | 22 | a0002c0001t0001g0191 a0005c0004t0006g0202 a0005c0004t0006g0220 others(19): Show |
22 | HG01099.hp1 HG01123.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1469-1535C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387836 | |||||||
chr3:66387882 | G | A | 23 | a0004c0003t0001g0142 a0004c0003t0002g0057 a0004c0003t0002g0080 others(20): Show |
23 | HG00099.hp1 HG01256.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.1469-1581C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387882 | |||||||
chr3:66387883 | G | C | 70 | a0002c0001t0001g0047 a0002c0001t0001g0048 a0002c0001t0001g0059 others(67): Show |
70 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1469-1582C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387883 | |||||||
chr3:66387916 | G | T | 178 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(175): Show |
178 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1469-1615C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387916 | |||||||
chr3:66387941 | C | CA | 104 | a0001c0002t0001g0060 a0001c0007t0001g0118 a0001c0007t0002g0079 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1469-1641dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387941 | |||||||
chr3:66387964 | G | A | 73 | a0002c0001t0001g0047 a0002c0001t0001g0048 a0002c0001t0001g0052 others(70): Show |
73 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1469-1663C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387964 | |||||||
chr3:66388038 | C | T | 1 | a0003c0005t0003g0241 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1469-1737G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388038 | |||||||
chr3:66388064 | G | A | 1 | a0003c0005t0003g0211 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1469-1763C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388064 | |||||||
chr3:66388106 | C | CA | 14 | a0001c0002t0001g0178 a0001c0023t0002g0067 a0001c0023t0002g0082 others(11): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1469-1806dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388106 | |||||||
chr3:66388106 | C | CAA | 20 | a0001c0014t0010g0125 a0001c0014t0010g0186 a0003c0012t0014g0233 others(17): Show |
20 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1469-1807_1469-180 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388106 | |||||||
chr3:66388106 | C | CAAA | 9 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0005c0004t0007g0016 others(6): Show |
9 | HG01243.hp2 HG02572.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.1469-1808_1469-180 others(7): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388106 | |||||||
chr3:66388106 | CA | C | 142 | a0001c0002t0001g0051 a0001c0002t0001g0062 a0001c0002t0001g0064 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1469-1806delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388106 | |||||||
chr3:66388106 | CAA | C | 14 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0094 others(11): Show |
14 | HG00735.hp1 HG02300.hp1 HG02897.hp1 others(11): Show |
intron_variant | MODIFIER | c.1469-1807_1469-180 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388106 | |||||||
chr3:66388272 | A | C | 3 | a0004c0003t0002g0057 a0004c0003t0002g0105 a0004c0003t0002g0107 |
3 | HG02698.hp1 HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1469-1971T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388272 | |||||||
chr3:66388293 | G | A | 1 | a0001c0002t0001g0092 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1469-1992C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388293 | |||||||
chr3:66388449 | A | G | 6 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(3): Show |
6 | HG02055.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1469-2148T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388449 | |||||||
chr3:66388601 | G | A | 4 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(1): Show |
4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469-2300C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388601 | |||||||
chr3:66388649 | A | T | 4 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(1): Show |
4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469-2348T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388649 | |||||||
chr3:66388691 | T | C | 12 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(9): Show |
12 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1469-2390A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388691 | |||||||
chr3:66388708 | T | G | 11 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(8): Show |
11 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1469-2407A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388708 | |||||||
chr3:66388777 | A | G | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1469-2476T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388777 | |||||||
chr3:66388816 | G | A | 196 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(193): Show |
196 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1469-2515C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388816 | |||||||
chr3:66388900 | C | T | 1 | a0006c0026t0036g0234 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1469-2599G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388900 | |||||||
chr3:66389031 | T | C | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1469-2730A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389031 | |||||||
chr3:66389049 | G | A | 4 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(1): Show |
4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469-2748C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389049 | |||||||
chr3:66389230 | C | T | 1 | a0001c0002t0001g0060 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1469-2929G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389230 | |||||||
chr3:66389265 | A | C | 14 | a0001c0014t0010g0125 a0001c0014t0010g0186 a0001c0014t0011g0058 others(11): Show |
14 | HG01433.hp1 HG02145.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1469-2964T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389265 | |||||||
chr3:66389315 | G | GA | 4 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(1): Show |
4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469-3015dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389315 | |||||||
chr3:66389366 | T | A | 6 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(3): Show |
6 | HG02055.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1469-3065A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389366 | |||||||
chr3:66389367 | T | A | 6 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(3): Show |
6 | HG02055.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1469-3066A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389367 | |||||||
chr3:66389426 | T | C | 1 | a0031c0024t0001g0025 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1469-3125A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389426 | |||||||
chr3:66389471 | A | G | 1 | a0001c0002t0001g0051 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1469-3170T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389471 | |||||||
chr3:66389596 | A | G | 1 | a0003c0010t0004g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1469-3295T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389596 | |||||||
chr3:66389662 | C | G | 1 | a0004c0003t0002g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1469-3361G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389662 | |||||||
chr3:66389751 | T | C | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1469-3450A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389751 | |||||||
chr3:66389831 | A | C | 1 | a0004c0003t0002g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1469-3530T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389831 | |||||||
chr3:66389998 | T | C | 3 | a0004c0003t0002g0100 a0004c0003t0002g0132 a0004c0003t0026g0190 |
3 | HG03688.hp2 HG03710.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1469-3697A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389998 | |||||||
chr3:66390098 | T | G | 4 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1469-3797A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66390098 | |||||||
chr3:66390406 | A | G | 24 | a0005c0004t0006g0202 a0005c0004t0006g0220 a0005c0004t0006g0221 others(21): Show |
24 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1468+3634T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66390406 | |||||||
chr3:66390545 | A | C | 74 | a0002c0001t0001g0047 a0002c0001t0001g0048 a0002c0001t0001g0059 others(71): Show |
74 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1468+3495T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66390545 | |||||||
chr3:66390558 | T | G | 2 | a0004c0003t0002g0088 a0004c0003t0002g0089 |
2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1468+3482A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66390558 | |||||||
chr3:66390619 | T | C | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+3421A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66390619 | |||||||
chr3:66390769 | T | C | 4 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(1): Show |
4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+3271A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66390769 | |||||||
chr3:66390774 | T | C | 1 | a0006c0026t0036g0234 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1468+3266A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66390774 | |||||||
chr3:66390825 | C | T | 191 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(188): Show |
191 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1468+3215G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66390825 | |||||||
chr3:66391020 | GAT | G | 81 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1468+3018_1468+301 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391020 | |||||||
chr3:66391068 | C | T | 21 | a0005c0004t0006g0202 a0005c0004t0006g0220 a0005c0004t0006g0221 others(18): Show |
21 | HG01099.hp1 HG01123.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1468+2972G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391068 | |||||||
chr3:66391122 | C | T | 81 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1468+2918G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391122 | |||||||
chr3:66391166 | T | C | 2 | a0006c0009t0004g0232 a0006c0009t0004g0246 |
2 | HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1468+2874A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391166 | |||||||
chr3:66391237 | C | T | 174 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(171): Show |
174 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.1468+2803G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391237 | |||||||
chr3:66391454 | T | C | 2 | a0014c0020t0035g0208 a0025c0047t0030g0153 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1468+2586A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391454 | |||||||
chr3:66391455 | G | T | 87 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(84): Show |
87 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1468+2585C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391455 | |||||||
chr3:66391562 | G | C | 1 | a0004c0003t0026g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1468+2478C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391562 | |||||||
chr3:66391586 | A | G | 5 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 others(2): Show |
5 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1468+2454T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391586 | |||||||
chr3:66391588 | G | A | 2 | a0003c0012t0014g0233 a0003c0012t0014g0236 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1468+2452C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391588 | |||||||
chr3:66391681 | A | G | 1 | a0003c0010t0004g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1468+2359T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391681 | |||||||
chr3:66391686 | A | G | 1 | a0004c0003t0002g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1468+2354T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391686 | |||||||
chr3:66391756 | T | G | 71 | a0002c0001t0001g0047 a0002c0001t0001g0048 a0002c0001t0001g0059 others(68): Show |
71 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1468+2284A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391756 | |||||||
chr3:66391836 | A | T | 4 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(1): Show |
4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+2204T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391836 | |||||||
chr3:66391942 | T | C | 4 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(1): Show |
4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+2098A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391942 | |||||||
chr3:66392005 | C | A | 1 | a0010c0011t0024g0063 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1468+2035G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392005 | |||||||
chr3:66392011 | C | G | 195 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(192): Show |
195 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1468+2029G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392011 | |||||||
chr3:66392121 | A | C | 74 | a0002c0001t0001g0047 a0002c0001t0001g0048 a0002c0001t0001g0059 others(71): Show |
74 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1468+1919T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392121 | |||||||
chr3:66392359 | A | G | 4 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(1): Show |
4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+1681T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392359 | |||||||
chr3:66392454 | T | C | 4 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(1): Show |
4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+1586A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392454 | |||||||
chr3:66392540 | C | T | 1 | a0003c0010t0004g0229 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1468+1500G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392540 | |||||||
chr3:66392544 | A | C | 21 | a0005c0004t0006g0202 a0005c0004t0006g0220 a0005c0004t0006g0221 others(18): Show |
21 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1468+1496T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392544 | |||||||
chr3:66392577 | T | A | 54 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(51): Show |
54 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1468+1463A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392577 | |||||||
chr3:66392596 | T | C | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1468+1444A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392596 | |||||||
chr3:66392603 | G | C | 7 | a0003c0010t0002g0010 a0003c0010t0004g0201 a0003c0010t0004g0231 others(4): Show |
7 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+1437C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392603 | |||||||
chr3:66392757 | G | A | 54 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(51): Show |
54 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1468+1283C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392757 | |||||||
chr3:66392813 | T | C | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+1227A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392813 | |||||||
chr3:66392951 | T | G | 4 | a0003c0005t0003g0001 a0003c0005t0003g0209 a0003c0005t0003g0211 others(1): Show |
5 | NA18966.hp2 NA18986.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.1468+1089A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392951 | |||||||
chr3:66393138 | A | G | 59 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(56): Show |
59 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1468+902T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66393138 | |||||||
chr3:66393146 | A | T | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+894T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66393146 | |||||||
chr3:66393188 | T | A | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1468+852A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66393188 | |||||||
chr3:66393430 | T | C | 14 | a0006c0035t0033g0207 a0007c0006t0005g0200 a0007c0006t0005g0215 others(11): Show |
14 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1468+610A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66393430 | |||||||
chr3:66393519 | G | C | 4 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(1): Show |
4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+521C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66393519 | |||||||
chr3:66393714 | G | T | 84 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(81): Show |
84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1468+326C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66393714 | |||||||
chr3:66393906 | T | C | 29 | a0004c0003t0001g0142 a0004c0003t0002g0057 a0004c0003t0002g0080 others(26): Show |
29 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.1468+134A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66393906 | |||||||
chr3:66393929 | A | C | 1 | a0002c0001t0001g0135 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1468+111T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66393929 | |||||||
chr3:66394273 | A | C | 84 | a0001c0002t0001g0051 a0001c0014t0011g0058 a0001c0014t0011g0119 others(81): Show |
84 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.1305-70T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394273 | |||||||
chr3:66394327 | G | A | 1 | a0006c0035t0033g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1305-124C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394327 | |||||||
chr3:66394459 | A | G | 12 | a0006c0009t0002g0045 a0006c0009t0004g0224 a0006c0009t0004g0225 others(9): Show |
12 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.1305-256T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394459 | |||||||
chr3:66394552 | C | T | 1 | a0007c0006t0020g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1305-349G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394552 | |||||||
chr3:66394602 | C | T | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1305-399G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394602 | |||||||
chr3:66394710 | A | G | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1305-507T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394710 | |||||||
chr3:66394769 | T | C | 1 | a0001c0002t0001g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1305-566A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394769 | |||||||
chr3:66394840 | C | A | 5 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(2): Show |
5 | HG00735.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305-637G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394840 | |||||||
chr3:66394885 | A | G | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1305-682T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394885 | |||||||
chr3:66394896 | T | C | 10 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(7): Show |
10 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1305-693A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394896 | |||||||
chr3:66395099 | G | T | 1 | a0001c0002t0001g0131 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1305-896C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395099 | |||||||
chr3:66395144 | C | T | 1 | a0002c0001t0001g0149 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1305-941G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395144 | |||||||
chr3:66395166 | A | C | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305-963T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395166 | |||||||
chr3:66395177 | A | G | 12 | a0006c0009t0002g0045 a0006c0009t0004g0224 a0006c0009t0004g0225 others(9): Show |
12 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.1305-974T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395177 | |||||||
chr3:66395239 | G | A | 13 | a0006c0035t0033g0207 a0007c0006t0005g0200 a0007c0006t0005g0215 others(10): Show |
13 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1305-1036C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395239 | |||||||
chr3:66395310 | C | T | 1 | a0003c0005t0003g0218 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1305-1107G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395310 | |||||||
chr3:66395407 | A | T | 1 | a0001c0007t0002g0154 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1305-1204T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395407 | |||||||
chr3:66395509 | A | G | 2 | a0010c0011t0007g0168 a0010c0011t0007g0174 |
2 | HG00280.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1305-1306T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395509 | |||||||
chr3:66395518 | G | C | 57 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(54): Show |
57 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1305-1315C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395518 | |||||||
chr3:66395638 | C | T | 3 | a0004c0003t0002g0152 a0004c0003t0039g0262 a0023c0052t0038g0263 |
3 | HG02258.hp2 HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1305-1435G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395638 | |||||||
chr3:66395703 | G | A | 1 | a0001c0002t0031g0068 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1305-1500C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395703 | |||||||
chr3:66395738 | T | C | 13 | a0006c0009t0002g0045 a0006c0009t0004g0224 a0006c0009t0004g0225 others(10): Show |
13 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.1305-1535A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395738 | |||||||
chr3:66395850 | A | C | 12 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(9): Show |
12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1305-1647T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395850 | |||||||
chr3:66395979 | C | CA | 23 | a0005c0004t0006g0202 a0005c0004t0006g0220 a0005c0004t0006g0221 others(20): Show |
23 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.1305-1777dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395979 | |||||||
chr3:66396074 | C | A | 2 | a0014c0020t0035g0208 a0025c0047t0030g0153 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1305-1871G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396074 | |||||||
chr3:66396082 | C | T | 2 | a0001c0002t0001g0060 a0003c0010t0004g0258 |
2 | HG00735.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1305-1879G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396082 | |||||||
chr3:66396092 | G | A | 1 | a0005c0004t0001g0018 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1305-1889C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396092 | |||||||
chr3:66396182 | A | T | 12 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(9): Show |
12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1304+1930T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396182 | |||||||
chr3:66396396 | G | A | 20 | a0005c0004t0006g0202 a0005c0004t0006g0220 a0005c0004t0006g0221 others(17): Show |
20 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1304+1716C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396396 | |||||||
chr3:66396809 | T | G | 2 | a0006c0009t0004g0232 a0006c0009t0004g0246 |
2 | HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1304+1303A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396809 | |||||||
chr3:66396875 | A | T | 2 | a0001c0007t0002g0079 a0001c0007t0002g0099 |
2 | HG01261.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1304+1237T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396875 | |||||||
chr3:66396880 | A | G | 6 | a0003c0012t0014g0233 a0003c0012t0014g0236 a0011c0016t0013g0204 others(3): Show |
6 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1304+1232T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396880 | |||||||
chr3:66396929 | C | T | 1 | a0006c0009t0004g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1304+1183G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396929 | |||||||
chr3:66397070 | C | T | 1 | a0009c0013t0002g0024 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1304+1042G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397070 | |||||||
chr3:66397110 | C | T | 1 | a0011c0016t0013g0205 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1304+1002G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397110 | |||||||
chr3:66397237 | G | A | 4 | a0001c0014t0010g0125 a0001c0014t0010g0186 a0013c0042t0010g0083 others(1): Show |
4 | HG01433.hp1 HG02145.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304+875C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397237 | |||||||
chr3:66397440 | T | C | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1304+672A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397440 | |||||||
chr3:66397448 | T | TA | 90 | a0001c0002t0001g0049 a0001c0002t0001g0056 a0001c0002t0001g0060 others(87): Show |
91 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.1304+663dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397448 | |||||||
chr3:66397448 | T | TAA | 69 | a0001c0002t0001g0053 a0001c0002t0001g0127 a0001c0002t0001g0178 others(66): Show |
69 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1304+662_1304+663d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397448 | |||||||
chr3:66397678 | G | A | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304+434C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397678 | |||||||
chr3:66397737 | A | C | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304+375T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397737 | |||||||
chr3:66397782 | G | A | 234 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1304+330C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397782 | |||||||
chr3:66397811 | G | C | 1 | a0002c0001t0001g0135 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1304+301C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397811 | |||||||
chr3:66397842 | T | G | 2 | a0006c0019t0012g0244 a0006c0019t0012g0245 |
2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1304+270A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397842 | |||||||
chr3:66397883 | A | G | 94 | a0001c0002t0001g0051 a0001c0014t0010g0125 a0001c0014t0010g0186 others(91): Show |
94 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1304+229T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397883 | |||||||
chr3:66398007 | G | A | 1 | a0020c0046t0010g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1304+105C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66398007 | |||||||
chr3:66398040 | G | A | 2 | a0014c0020t0035g0208 a0025c0047t0030g0153 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1304+72C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66398040 | |||||||
chr3:66398646 | G | A | 5 | a0003c0012t0014g0233 a0003c0012t0014g0236 a0008c0008t0001g0038 others(2): Show |
5 | HG02055.hp1 HG02451.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1232+324C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 10/18 | chr3 | 66398646 | |||||||
chr3:66398652 | G | A | 8 | a0005c0004t0006g0238 a0005c0004t0006g0239 a0005c0004t0006g0240 others(5): Show |
8 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1232+318C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 10/18 | chr3 | 66398652 | |||||||
chr3:66398718 | G | A | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1232+252C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 10/18 | chr3 | 66398718 | |||||||
chr3:66398718 | G | C | 76 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(73): Show |
77 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.1232+252C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 10/18 | chr3 | 66398718 | |||||||
chr3:66399203 | C | T | 1 | a0002c0001t0001g0048 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1161-162G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399203 | |||||||
chr3:66399298 | C | T | 2 | a0004c0003t0002g0080 a0004c0003t0002g0144 |
2 | HG00099.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1161-257G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399298 | |||||||
chr3:66399355 | A | G | 12 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(9): Show |
12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1161-314T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399355 | |||||||
chr3:66399412 | A | G | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1161-371T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399412 | |||||||
chr3:66399470 | G | A | 2 | a0003c0012t0014g0233 a0006c0009t0002g0045 |
2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1161-429C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399470 | |||||||
chr3:66399559 | G | A | 1 | a0002c0001t0001g0055 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1161-518C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399559 | |||||||
chr3:66399751 | T | C | 5 | a0002c0001t0001g0052 a0002c0001t0001g0055 a0002c0001t0001g0151 others(2): Show |
5 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161-710A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399751 | |||||||
chr3:66399783 | A | C | 1 | a0002c0001t0001g0173 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1161-742T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399783 | |||||||
chr3:66399835 | C | T | 162 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(159): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1161-794G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399835 | |||||||
chr3:66399847 | G | T | 3 | a0001c0014t0010g0125 a0001c0014t0010g0186 a0013c0042t0010g0083 |
3 | HG01433.hp1 HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1161-806C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399847 | |||||||
chr3:66400998 | C | T | 1 | a0001c0002t0001g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1161-1957G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66400998 | |||||||
chr3:66401017 | A | T | 240 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1161-1976T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401017 | |||||||
chr3:66401059 | C | T | 13 | a0006c0009t0002g0045 a0006c0009t0004g0224 a0006c0009t0004g0225 others(10): Show |
13 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.1161-2018G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401059 | |||||||
chr3:66401098 | G | A | 33 | a0004c0003t0001g0142 a0004c0003t0002g0057 a0004c0003t0002g0080 others(30): Show |
33 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1161-2057C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401098 | |||||||
chr3:66401172 | G | A | 2 | a0004c0003t0039g0262 a0023c0052t0038g0263 |
2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1161-2131C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401172 | |||||||
chr3:66401261 | G | T | 238 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1161-2220C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401261 | |||||||
chr3:66401279 | G | A | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1161-2238C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401279 | |||||||
chr3:66401287 | G | A | 2 | a0007c0006t0005g0242 a0007c0006t0005g0243 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1161-2246C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401287 | |||||||
chr3:66401397 | A | C | 56 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(53): Show |
56 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1161-2356T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401397 | |||||||
chr3:66401475 | T | G | 10 | a0006c0009t0002g0045 a0006c0009t0004g0224 a0006c0009t0004g0225 others(7): Show |
10 | HG00735.hp1 HG02970.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.1161-2434A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401475 | |||||||
chr3:66401483 | T | C | 58 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(55): Show |
58 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1161-2442A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401483 | |||||||
chr3:66401529 | A | G | 1 | a0006c0027t0004g0227 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1161-2488T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401529 | |||||||
chr3:66401613 | C | T | 1 | a0003c0010t0004g0229 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1161-2572G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401613 | |||||||
chr3:66401628 | G | A | 1 | a0015c0051t0002g0054 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1161-2587C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401628 | |||||||
chr3:66401696 | A | G | 1 | a0019c0038t0003g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1161-2655T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401696 | |||||||
chr3:66401844 | C | T | 1 | a0004c0003t0026g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1161-2803G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401844 | |||||||
chr3:66401886 | G | A | 2 | a0014c0020t0035g0208 a0025c0047t0030g0153 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1161-2845C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401886 | |||||||
chr3:66402107 | T | G | 62 | a0001c0007t0001g0118 a0001c0007t0002g0124 a0001c0007t0002g0154 others(59): Show |
62 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1161-3066A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66402107 | |||||||
chr3:66402138 | A | G | 70 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(67): Show |
71 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.1160+3060T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66402138 | |||||||
chr3:66402167 | A | G | 1 | a0002c0001t0001g0138 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1160+3031T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66402167 | |||||||
chr3:66402301 | C | T | 2 | a0003c0012t0014g0233 a0003c0012t0014g0236 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1160+2897G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66402301 | |||||||
chr3:66402408 | A | ACTCT | 71 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(68): Show |
71 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.1160+2786_1160+278 others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66402408 | |||||||
chr3:66402493 | G | C | 1 | a0001c0002t0001g0103 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1160+2705C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66402493 | |||||||
chr3:66402549 | TTGCATGG others(16): Show |
T | 149 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(146): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1160+2626_1160+264 others(27): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66402549 | |||||||
chr3:66402602 | C | T | 13 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(10): Show |
13 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1160+2596G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66402602 | |||||||
chr3:66403040 | T | C | 9 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(6): Show |
9 | HG02055.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1160+2158A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403040 | |||||||
chr3:66403109 | C | A | 10 | a0006c0009t0002g0045 a0006c0009t0004g0224 a0006c0009t0004g0225 others(7): Show |
10 | HG00735.hp1 HG02970.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.1160+2089G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403109 | |||||||
chr3:66403126 | A | G | 3 | a0002c0001t0001g0170 a0002c0001t0001g0171 a0002c0001t0001g0172 |
3 | HG00738.hp1 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1160+2072T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403126 | |||||||
chr3:66403181 | T | TC | 4 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(1): Show |
4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1160+2016dupG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403181 | |||||||
chr3:66403217 | T | C | 12 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(9): Show |
12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1160+1981A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403217 | |||||||
chr3:66403347 | T | A | 56 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(53): Show |
56 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1160+1851A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403347 | |||||||
chr3:66403379 | G | A | 12 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(9): Show |
12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1160+1819C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403379 | |||||||
chr3:66403411 | CAG | C | 17 | a0001c0002t0001g0078 a0005c0004t0006g0238 a0005c0004t0006g0239 others(14): Show |
17 | HG00099.hp2 HG01099.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.1160+1785_1160+178 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403411 | |||||||
chr3:66403513 | A | T | 1 | a0002c0018t0001g0192 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1160+1685T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403513 | |||||||
chr3:66403584 | C | A | 4 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160+1614G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403584 | |||||||
chr3:66403699 | G | A | 3 | a0009c0013t0001g0041 a0009c0013t0002g0042 a0009c0013t0002g0044 |
3 | NA18991.hp2 NA19000.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1160+1499C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403699 | |||||||
chr3:66403767 | G | A | 67 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(64): Show |
68 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.1160+1431C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403767 | |||||||
chr3:66403872 | C | T | 54 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(51): Show |
54 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1160+1326G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403872 | |||||||
chr3:66403920 | C | T | 55 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(52): Show |
55 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1160+1278G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403920 | |||||||
chr3:66403982 | G | A | 1 | a0008c0033t0001g0027 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1160+1216C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403982 | |||||||
chr3:66403997 | G | C | 1 | a0002c0041t0001g0116 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1160+1201C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403997 | |||||||
chr3:66403998 | G | A | 4 | a0005c0004t0006g0220 a0005c0004t0006g0221 a0005c0004t0006g0222 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1160+1200C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403998 | |||||||
chr3:66403998 | G | C | 3 | a0003c0005t0001g0037 a0003c0005t0001g0039 a0003c0031t0001g0036 |
3 | HG01884.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1160+1200C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403998 | |||||||
chr3:66404028 | T | C | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1160+1170A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66404028 | |||||||
chr3:66404089 | T | C | 12 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(9): Show |
12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1160+1109A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66404089 | |||||||
chr3:66404106 | A | C | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1160+1092T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66404106 | |||||||
chr3:66404183 | C | T | 1 | a0002c0001t0001g0101 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1160+1015G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66404183 | |||||||
chr3:66404555 | C | T | 13 | a0006c0026t0036g0234 a0007c0006t0005g0200 a0007c0006t0005g0215 others(10): Show |
13 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1160+643G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66404555 | |||||||
chr3:66404570 | G | A | 232 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1160+628C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66404570 | |||||||
chr3:66404583 | T | C | 1 | a0003c0010t0004g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1160+615A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66404583 | |||||||
chr3:66405039 | C | G | 1 | a0001c0007t0002g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1160+159G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66405039 | |||||||
chr3:66405159 | G | A | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1160+39C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66405159 | |||||||
chr3:66405170 | G | A | 2 | a0005c0004t0007g0016 a0029c0039t0001g0072 |
2 | HG04115.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1160+28C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66405170 | |||||||
chr3:66405306 | C | T | 1 | a0002c0001t0032g0199 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1080-28G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405306 | |||||||
chr3:66405373 | T | C | 68 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(65): Show |
68 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.1080-95A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405373 | |||||||
chr3:66405463 | C | T | 58 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.1080-185G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405463 | |||||||
chr3:66405523 | G | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1080-245C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405523 | |||||||
chr3:66405618 | C | T | 13 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(10): Show |
13 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1080-340G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405618 | |||||||
chr3:66405674 | T | C | 13 | a0006c0026t0036g0234 a0007c0006t0005g0200 a0007c0006t0005g0215 others(10): Show |
13 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1080-396A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405674 | |||||||
chr3:66405689 | A | T | 1 | a0005c0004t0006g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1080-411T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405689 | |||||||
chr3:66405725 | C | T | 1 | a0001c0002t0001g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1080-447G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405725 | |||||||
chr3:66405749 | G | A | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1080-471C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405749 | |||||||
chr3:66406139 | C | T | 1 | a0002c0001t0001g0048 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1080-861G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406139 | |||||||
chr3:66406297 | A | T | 1 | a0002c0001t0001g0134 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1080-1019T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406297 | |||||||
chr3:66406407 | G | A | 9 | a0001c0002t0001g0094 a0001c0002t0001g0108 a0001c0002t0001g0127 others(6): Show |
9 | HG02056.hp2 HG02135.hp2 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.1079+941C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406407 | |||||||
chr3:66406484 | T | C | 8 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(5): Show |
8 | HG02055.hp1 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1079+864A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406484 | |||||||
chr3:66406498 | G | A | 4 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1079+850C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406498 | |||||||
chr3:66406532 | C | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1079+816G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406532 | |||||||
chr3:66406610 | C | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1079+738G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406610 | |||||||
chr3:66406638 | G | T | 1 | a0003c0012t0017g0004 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1079+710C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406638 | |||||||
chr3:66406652 | C | T | 59 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.1079+696G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406652 | |||||||
chr3:66406671 | T | C | 20 | a0001c0014t0010g0125 a0001c0014t0010g0186 a0006c0009t0004g0224 others(17): Show |
20 | HG00735.hp1 HG01433.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1079+677A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406671 | |||||||
chr3:66406769 | A | G | 1 | a0002c0001t0001g0101 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1079+579T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406769 | |||||||
chr3:66406943 | A | G | 3 | a0002c0001t0001g0126 a0002c0001t0001g0140 a0002c0001t0001g0145 |
3 | NA18994.hp2 NA19004.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1079+405T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406943 | |||||||
chr3:66407020 | C | T | 10 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(7): Show |
10 | HG00735.hp1 HG02922.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.1079+328G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66407020 | |||||||
chr3:66407159 | T | G | 1 | a0001c0002t0001g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1079+189A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66407159 | |||||||
chr3:66407167 | T | G | 1 | a0007c0006t0020g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1079+181A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66407167 | |||||||
chr3:66407303 | T | G | 2 | a0004c0003t0039g0262 a0023c0052t0038g0263 |
2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1079+45A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66407303 | |||||||
chr3:66407584 | A | G | 2 | a0001c0002t0001g0094 a0003c0005t0001g0026 |
2 | NA18994.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.936-93T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66407584 | |||||||
chr3:66407615 | G | A | 1 | a0001c0002t0031g0068 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.936-124C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66407615 | |||||||
chr3:66407622 | T | C | 245 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.936-131A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66407622 | |||||||
chr3:66407623 | G | GCA | 85 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(82): Show |
86 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.936-134_936-133dup others(2): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66407623 | |||||||
chr3:66407695 | A | C | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.936-204T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66407695 | |||||||
chr3:66407714 | T | C | 2 | a0006c0009t0002g0045 a0027c0028t0003g0259 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.936-223A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66407714 | |||||||
chr3:66407804 | C | T | 1 | a0001c0002t0001g0077 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.936-313G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66407804 | |||||||
chr3:66407881 | C | T | 4 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.936-390G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66407881 | |||||||
chr3:66408042 | C | G | 13 | a0006c0026t0036g0234 a0007c0006t0005g0200 a0007c0006t0005g0215 others(10): Show |
13 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.936-551G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408042 | |||||||
chr3:66408085 | G | A | 5 | a0002c0001t0001g0052 a0002c0001t0001g0055 a0002c0001t0001g0151 others(2): Show |
5 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.936-594C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408085 | |||||||
chr3:66408106 | C | T | 10 | a0001c0007t0001g0118 a0001c0007t0002g0124 a0001c0007t0002g0154 others(7): Show |
10 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.936-615G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408106 | |||||||
chr3:66408169 | T | C | 2 | a0001c0002t0001g0056 a0001c0002t0001g0073 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.936-678A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408169 | |||||||
chr3:66408179 | A | G | 7 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(4): Show |
7 | HG02055.hp1 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.936-688T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408179 | |||||||
chr3:66408209 | T | C | 59 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.936-718A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408209 | |||||||
chr3:66408219 | G | A | 1 | a0008c0008t0001g0020 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.936-728C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408219 | |||||||
chr3:66408277 | T | C | 75 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(72): Show |
76 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.936-786A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408277 | |||||||
chr3:66408521 | C | T | 173 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(170): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.936-1030G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408521 | |||||||
chr3:66408683 | G | A | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.936-1192C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408683 | |||||||
chr3:66408683 | G | C | 5 | a0001c0014t0010g0125 a0001c0014t0010g0186 a0013c0042t0010g0083 others(2): Show |
5 | HG01433.hp1 HG02145.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.936-1192C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408683 | |||||||
chr3:66408808 | C | T | 1 | a0002c0001t0001g0143 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.936-1317G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408808 | |||||||
chr3:66408913 | A | AGT | 23 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0001c0002t0001g0075 others(20): Show |
23 | HG00609.hp1 HG01192.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.935+1214_935+1215d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | A | AGTGT | 27 | a0001c0002t0001g0062 a0001c0002t0001g0069 a0001c0002t0001g0077 others(24): Show |
27 | HG01123.hp1 HG01123.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.935+1212_935+1215d others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | A | AGTGTGT | 17 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0061 others(14): Show |
17 | HG00099.hp2 HG00738.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.935+1210_935+1215d others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | A | AGTGTGTG others(1): Show |
16 | a0001c0002t0001g0056 a0001c0002t0001g0060 a0001c0002t0001g0070 others(13): Show |
16 | HG00735.hp2 HG01069.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.935+1208_935+1215d others(10): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | A | AGTGTGTG others(3): Show |
14 | a0001c0002t0001g0137 a0001c0002t0001g0198 a0002c0001t0001g0128 others(11): Show |
14 | HG00558.hp1 HG00558.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.935+1206_935+1215d others(12): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | A | AGTGTGTG others(5): Show |
5 | a0002c0001t0001g0090 a0002c0001t0001g0141 a0002c0001t0001g0149 others(2): Show |
5 | HG00673.hp2 HG02451.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.935+1204_935+1215d others(14): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | A | AGTGTGTG others(7): Show |
12 | a0001c0002t0001g0051 a0001c0002t0001g0127 a0002c0001t0001g0110 others(9): Show |
12 | HG02165.hp2 HG02723.hp2 HG03139.hp2 others(9): Show |
intron_variant | MODIFIER | c.935+1202_935+1215d others(16): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | A | AGTGTGTG others(9): Show |
11 | a0001c0002t0001g0189 a0002c0001t0001g0123 a0002c0001t0001g0133 others(8): Show |
11 | HG02040.hp1 HG02056.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.935+1200_935+1215d others(18): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | A | AGTGTGTG others(11): Show |
3 | a0002c0001t0001g0136 a0002c0001t0001g0147 a0002c0001t0001g0170 |
3 | HG00621.hp2 HG00738.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.935+1198_935+1215d others(20): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | A | AGTGTGTG others(13): Show |
4 | a0002c0001t0001g0126 a0002c0001t0001g0140 a0002c0001t0001g0180 others(1): Show |
4 | HG02071.hp1 NA18950.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.935+1196_935+1215d others(22): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | A | AGTGTGTG others(15): Show |
1 | a0002c0018t0001g0175 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.935+1194_935+1215d others(24): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | A | AGTGTGTG others(17): Show |
5 | a0002c0001t0001g0047 a0002c0001t0001g0059 a0002c0001t0001g0101 others(2): Show |
5 | HG00544.hp2 HG03017.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.935+1192_935+1215d others(26): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | A | AGTGTGTG others(19): Show |
3 | a0002c0001t0001g0071 a0002c0001t0001g0134 a0002c0001t0001g0195 |
3 | HG02132.hp2 NA18974.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.935+1190_935+1215d others(28): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | A | AGTGTGTG others(23): Show |
1 | a0002c0001t0001g0048 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.935+1186_935+1215d others(32): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | AGT | A | 23 | a0002c0001t0001g0084 a0002c0001t0001g0086 a0002c0001t0001g0122 others(20): Show |
23 | HG00544.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.935+1214_935+1215d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | AGTGT | A | 42 | a0001c0002t0001g0064 a0001c0002t0001g0117 a0001c0007t0002g0079 others(39): Show |
42 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.935+1212_935+1215d others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | AGTGTGT | A | 17 | a0001c0007t0001g0118 a0001c0007t0002g0099 a0001c0007t0002g0124 others(14): Show |
17 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.935+1210_935+1215d others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | AGTGTGTG others(1): Show |
A | 4 | a0004c0003t0001g0142 a0004c0003t0002g0104 a0004c0003t0002g0193 others(1): Show |
4 | HG02735.hp2 HG03471.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.935+1208_935+1215d others(10): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | AGTGTGTG others(3): Show |
A | 1 | a0004c0003t0002g0088 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.935+1206_935+1215d others(12): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408913 | AGTGTGTG others(5): Show |
A | 2 | a0003c0005t0003g0241 a0009c0013t0004g0214 |
2 | HG01070.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.935+1204_935+1215d others(14): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | |||||||
chr3:66408943 | T | TGTGTGC | 3 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 |
3 | HG02896.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.935+1185_935+1186i others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408943 | |||||||
chr3:66409135 | C | T | 56 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(53): Show |
56 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.935+994G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66409135 | |||||||
chr3:66409188 | A | G | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.935+941T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66409188 | |||||||
chr3:66409353 | C | T | 3 | a0001c0040t0001g0096 a0002c0041t0001g0116 a0013c0043t0022g0009 |
3 | HG00609.hp1 NA18969.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.935+776G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66409353 | |||||||
chr3:66409412 | G | A | 1 | a0009c0037t0002g0017 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.935+717C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66409412 | |||||||
chr3:66409535 | C | G | 4 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(1): Show |
4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.935+594G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66409535 | |||||||
chr3:66409713 | C | T | 4 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.935+416G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66409713 | |||||||
chr3:66409835 | G | C | 4 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.935+294C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66409835 | |||||||
chr3:66409913 | C | A | 56 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(53): Show |
56 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.935+216G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66409913 | |||||||
chr3:66410288 | T | C | 4 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(1): Show |
4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.792-16A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410288 | |||||||
chr3:66410395 | C | A | 5 | a0001c0014t0010g0125 a0001c0014t0010g0186 a0013c0042t0010g0083 others(2): Show |
5 | HG01433.hp1 HG02145.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.792-123G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410395 | |||||||
chr3:66410395 | C | T | 1 | a0004c0003t0002g0144 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.792-123G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410395 | |||||||
chr3:66410434 | T | C | 2 | a0002c0001t0001g0122 a0002c0001t0001g0163 |
2 | HG01074.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.792-162A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410434 | |||||||
chr3:66410508 | C | G | 85 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0001c0014t0011g0058 others(82): Show |
85 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.792-236G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410508 | |||||||
chr3:66410573 | G | A | 1 | a0001c0002t0001g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.792-301C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410573 | |||||||
chr3:66410618 | G | A | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.792-346C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410618 | |||||||
chr3:66410627 | C | T | 3 | a0002c0001t0001g0169 a0008c0008t0001g0013 a0008c0008t0001g0030 |
3 | HG02165.hp2 NA18970.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.792-355G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410627 | |||||||
chr3:66410636 | G | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.792-364C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410636 | |||||||
chr3:66410809 | G | T | 4 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.792-537C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410809 | |||||||
chr3:66410876 | G | A | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.792-604C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410876 | |||||||
chr3:66410944 | C | A | 1 | a0002c0018t0001g0175 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.792-672G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410944 | |||||||
chr3:66410961 | G | A | 1 | a0001c0002t0001g0075 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.792-689C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410961 | |||||||
chr3:66411051 | G | A | 1 | a0004c0003t0001g0142 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.792-779C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411051 | |||||||
chr3:66411203 | C | T | 12 | a0006c0026t0036g0234 a0007c0006t0005g0200 a0007c0006t0005g0215 others(9): Show |
12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.792-931G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411203 | |||||||
chr3:66411365 | A | G | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.792-1093T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411365 | |||||||
chr3:66411538 | G | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.792-1266C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411538 | |||||||
chr3:66411583 | C | T | 12 | a0006c0026t0036g0234 a0007c0006t0005g0200 a0007c0006t0005g0215 others(9): Show |
12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.791+1288G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411583 | |||||||
chr3:66411623 | C | T | 2 | a0003c0012t0014g0233 a0003c0012t0014g0236 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.791+1248G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411623 | |||||||
chr3:66411771 | T | C | 1 | a0002c0001t0032g0199 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.791+1100A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411771 | |||||||
chr3:66411812 | A | G | 51 | a0001c0002t0001g0051 a0002c0001t0001g0047 a0002c0001t0001g0048 others(48): Show |
51 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.791+1059T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411812 | |||||||
chr3:66411855 | T | C | 1 | a0001c0002t0001g0131 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.791+1016A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411855 | |||||||
chr3:66411864 | A | G | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.791+1007T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411864 | |||||||
chr3:66412034 | A | G | 1 | a0006c0009t0004g0224 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.791+837T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412034 | |||||||
chr3:66412083 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.791+788C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412083 | |||||||
chr3:66412104 | A | G | 78 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(75): Show |
79 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.791+767T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412104 | |||||||
chr3:66412170 | C | G | 6 | a0003c0012t0018g0008 a0006c0009t0002g0045 a0011c0016t0013g0204 others(3): Show |
6 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.791+701G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412170 | |||||||
chr3:66412231 | G | A | 4 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.791+640C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412231 | |||||||
chr3:66412259 | C | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.791+612G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412259 | |||||||
chr3:66412345 | G | A | 1 | a0025c0047t0030g0153 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.791+526C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412345 | |||||||
chr3:66412362 | G | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.791+509C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412362 | |||||||
chr3:66412513 | G | T | 1 | a0002c0001t0001g0173 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.791+358C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412513 | |||||||
chr3:66412549 | A | G | 2 | a0002c0001t0001g0121 a0008c0008t0001g0031 |
2 | NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.791+322T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412549 | |||||||
chr3:66412594 | C | T | 1 | a0004c0003t0001g0142 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.791+277G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412594 | |||||||
chr3:66412723 | C | T | 1 | a0019c0038t0003g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.791+148G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412723 | |||||||
chr3:66412808 | C | T | 8 | a0003c0012t0017g0004 a0005c0004t0008g0247 a0005c0004t0008g0248 others(5): Show |
8 | HG01243.hp2 HG01952.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.791+63G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412808 | |||||||
chr3:66412827 | G | A | 232 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.791+44C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412827 | |||||||
chr3:66412830 | C | G | 58 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(55): Show |
58 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.791+41G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412830 | |||||||
chr3:66412862 | C | T | 11 | a0006c0026t0036g0234 a0007c0006t0005g0200 a0007c0006t0005g0215 others(8): Show |
11 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.791+9G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412862 | |||||||
chr3:66413053 | T | C | 1 | a0002c0001t0001g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.648-39A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66413053 | |||||||
chr3:66413212 | C | G | 1 | a0007c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.648-198G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66413212 | |||||||
chr3:66413337 | T | C | 1 | a0001c0002t0001g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.648-323A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66413337 | |||||||
chr3:66413487 | C | A | 3 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 |
3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.648-473G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66413487 | |||||||
chr3:66413628 | T | C | 1 | a0005c0004t0007g0016 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.648-614A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66413628 | |||||||
chr3:66413954 | T | C | 1 | a0001c0007t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.648-940A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66413954 | |||||||
chr3:66413970 | GA | G | 11 | a0002c0001t0001g0110 a0003c0010t0002g0010 a0003c0010t0004g0201 others(8): Show |
11 | HG02647.hp1 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.647+949delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66413970 | |||||||
chr3:66414009 | T | A | 86 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0001c0014t0011g0058 others(83): Show |
86 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.647+911A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414009 | |||||||
chr3:66414119 | C | T | 3 | a0008c0008t0001g0038 a0008c0008t0003g0252 a0008c0008t0003g0256 |
3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.647+801G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414119 | |||||||
chr3:66414135 | T | C | 73 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0001c0014t0011g0058 others(70): Show |
73 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.647+785A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414135 | |||||||
chr3:66414164 | A | G | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.647+756T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414164 | |||||||
chr3:66414313 | T | C | 80 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(77): Show |
81 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.647+607A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414313 | |||||||
chr3:66414325 | G | A | 5 | a0006c0009t0002g0045 a0011c0016t0013g0204 a0011c0016t0013g0205 others(2): Show |
5 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.647+595C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414325 | |||||||
chr3:66414345 | T | C | 1 | a0001c0007t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.647+575A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414345 | |||||||
chr3:66414351 | C | T | 1 | a0001c0007t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.647+569G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414351 | |||||||
chr3:66414352 | A | C | 7 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(4): Show |
7 | HG02055.hp1 HG02572.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.647+568T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414352 | |||||||
chr3:66414352 | A | G | 1 | a0001c0007t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.647+568T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414352 | |||||||
chr3:66414354 | A | G | 2 | a0001c0002t0001g0077 a0001c0007t0001g0118 |
2 | HG00280.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.647+566T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414354 | |||||||
chr3:66414364 | C | T | 2 | a0002c0022t0001g0176 a0002c0022t0001g0179 |
2 | HG01243.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.647+556G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414364 | |||||||
chr3:66414391 | C | G | 8 | a0003c0010t0002g0010 a0003c0010t0004g0201 a0003c0010t0004g0231 others(5): Show |
8 | HG02647.hp1 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.647+529G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414391 | |||||||
chr3:66414392 | G | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.647+528C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414392 | |||||||
chr3:66414403 | T | A | 2 | a0014c0020t0035g0208 a0033c0034t0019g0007 |
2 | HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.647+517A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414403 | |||||||
chr3:66414406 | TAATA | T | 4 | a0005c0004t0007g0016 a0011c0016t0013g0204 a0011c0016t0013g0205 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+510_647+513del others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414406 | |||||||
chr3:66414409 | T | G | 1 | a0001c0002t0001g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.647+511A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414409 | |||||||
chr3:66414418 | AAAT | A | 4 | a0003c0012t0017g0004 a0006c0019t0012g0244 a0006c0019t0012g0245 others(1): Show |
4 | HG01952.hp1 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+499_647+501del others(3): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414418 | |||||||
chr3:66414560 | A | T | 1 | a0002c0001t0016g0003 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.647+360T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414560 | |||||||
chr3:66414584 | A | G | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.647+336T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414584 | |||||||
chr3:66414755 | C | G | 3 | a0009c0015t0002g0032 a0009c0015t0002g0033 a0009c0015t0002g0034 |
3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.647+165G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414755 | |||||||
chr3:66414762 | G | C | 4 | a0003c0012t0017g0004 a0006c0019t0012g0244 a0006c0019t0012g0245 others(1): Show |
4 | HG01952.hp1 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+158C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414762 | |||||||
chr3:66414835 | T | C | 159 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(156): Show |
160 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.647+85A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414835 | |||||||
chr3:66415278 | C | T | 1 | a0006c0019t0012g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.504-215G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415278 | |||||||
chr3:66415412 | C | G | 1 | a0021c0049t0001g0066 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.504-349G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415412 | |||||||
chr3:66415456 | T | C | 3 | a0001c0002t0001g0053 a0001c0002t0001g0060 a0001c0002t0001g0061 |
3 | HG00735.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.504-393A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415456 | |||||||
chr3:66415503 | G | C | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.504-440C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415503 | |||||||
chr3:66415509 | A | G | 1 | a0001c0002t0001g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.504-446T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415509 | |||||||
chr3:66415611 | G | C | 1 | a0002c0001t0001g0173 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.504-548C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415611 | |||||||
chr3:66415693 | G | A | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.504-630C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415693 | |||||||
chr3:66415717 | C | T | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.504-654G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415717 | |||||||
chr3:66415748 | C | T | 1 | a0002c0001t0001g0090 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.504-685G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415748 | |||||||
chr3:66416015 | A | C | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.504-952T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416015 | |||||||
chr3:66416020 | G | A | 60 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(57): Show |
60 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.504-957C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416020 | |||||||
chr3:66416115 | C | G | 60 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(57): Show |
60 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.503+1014G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416115 | |||||||
chr3:66416174 | C | T | 2 | a0003c0005t0003g0216 a0003c0005t0003g0217 |
2 | NA18961.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.503+955G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416174 | |||||||
chr3:66416272 | G | A | 1 | a0003c0012t0017g0004 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.503+857C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416272 | |||||||
chr3:66416383 | G | A | 160 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(157): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.503+746C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416383 | |||||||
chr3:66416685 | A | G | 152 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.503+444T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416685 | |||||||
chr3:66416739 | A | G | 3 | a0002c0001t0001g0170 a0002c0001t0001g0171 a0002c0001t0001g0172 |
3 | HG00738.hp1 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.503+390T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416739 | |||||||
chr3:66416797 | C | T | 4 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.503+332G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416797 | |||||||
chr3:66416813 | A | G | 181 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(178): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.503+316T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416813 | |||||||
chr3:66416941 | G | A | 68 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(65): Show |
68 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.503+188C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416941 | |||||||
chr3:66416954 | G | A | 3 | a0009c0015t0002g0032 a0009c0015t0002g0033 a0009c0015t0002g0034 |
3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.503+175C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416954 | |||||||
chr3:66416977 | G | C | 2 | a0006c0009t0002g0045 a0027c0028t0003g0259 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.503+152C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416977 | |||||||
chr3:66417312 | G | A | 1 | a0005c0004t0007g0016 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.366-46C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417312 | |||||||
chr3:66417330 | T | C | 2 | a0003c0005t0003g0210 a0003c0005t0003g0218 |
2 | HG02040.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.366-64A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417330 | |||||||
chr3:66417539 | T | C | 12 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(9): Show |
12 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.366-273A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417539 | |||||||
chr3:66417665 | A | G | 65 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0001c0014t0011g0058 others(62): Show |
65 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.366-399T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417665 | |||||||
chr3:66417748 | C | G | 3 | a0003c0005t0001g0037 a0003c0005t0001g0039 a0003c0031t0001g0036 |
3 | HG01884.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.366-482G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417748 | |||||||
chr3:66417796 | GA | G | 9 | a0001c0002t0001g0075 a0001c0002t0001g0092 a0006c0009t0002g0045 others(6): Show |
9 | HG00280.hp1 HG01192.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.366-531delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417796 | |||||||
chr3:66417796 | GAA | G | 57 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(54): Show |
57 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.366-532_366-531del others(2): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417796 | |||||||
chr3:66417816 | G | A | 2 | a0008c0008t0003g0237 a0019c0038t0003g0235 |
2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.366-550C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417816 | |||||||
chr3:66417909 | T | C | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-643A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417909 | |||||||
chr3:66417979 | C | T | 1 | a0002c0021t0001g0114 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.366-713G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417979 | |||||||
chr3:66417985 | A | G | 61 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(58): Show |
61 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.366-719T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417985 | |||||||
chr3:66418077 | G | GT | 5 | a0001c0002t0001g0166 a0006c0019t0012g0244 a0006c0019t0012g0245 others(2): Show |
5 | HG01934.hp2 HG01952.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.366-812dupA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418077 | |||||||
chr3:66418083 | T | G | 1 | a0005c0004t0006g0222 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.366-817A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418083 | |||||||
chr3:66418112 | A | T | 2 | a0004c0003t0039g0262 a0023c0052t0038g0263 |
2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.366-846T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418112 | |||||||
chr3:66418115 | C | G | 2 | a0004c0003t0039g0262 a0023c0052t0038g0263 |
2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.366-849G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418115 | |||||||
chr3:66418115 | CAG | C | 44 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(41): Show |
44 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.366-851_366-850del others(2): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418115 | |||||||
chr3:66418117 | G | C | 2 | a0004c0003t0039g0262 a0023c0052t0038g0263 |
2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.366-851C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418117 | |||||||
chr3:66418148 | G | A | 1 | a0003c0012t0017g0004 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.366-882C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418148 | |||||||
chr3:66418172 | A | G | 6 | a0003c0012t0017g0004 a0006c0009t0002g0045 a0006c0019t0012g0244 others(3): Show |
6 | HG01952.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.366-906T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418172 | |||||||
chr3:66418264 | T | A | 4 | a0003c0010t0002g0010 a0004c0003t0002g0105 a0006c0009t0002g0045 others(1): Show |
4 | HG02886.hp1 HG03471.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-998A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418264 | |||||||
chr3:66418340 | G | A | 1 | a0020c0046t0010g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.366-1074C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418340 | |||||||
chr3:66418398 | G | A | 6 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(3): Show |
6 | HG01261.hp1 HG01433.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.366-1132C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418398 | |||||||
chr3:66418698 | C | T | 1 | a0002c0001t0001g0122 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.366-1432G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418698 | |||||||
chr3:66418699 | G | A | 1 | a0015c0051t0002g0054 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.366-1433C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418699 | |||||||
chr3:66418844 | G | C | 7 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(4): Show |
7 | HG01261.hp1 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.366-1578C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418844 | |||||||
chr3:66418859 | A | G | 56 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(53): Show |
56 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.366-1593T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418859 | |||||||
chr3:66418888 | C | T | 59 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(56): Show |
59 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.366-1622G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418888 | |||||||
chr3:66419038 | T | C | 151 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(148): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.366-1772A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419038 | |||||||
chr3:66419039 | G | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-1773C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419039 | |||||||
chr3:66419100 | G | A | 139 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.366-1834C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419100 | |||||||
chr3:66419113 | G | A | 1 | a0001c0002t0001g0150 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.366-1847C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419113 | |||||||
chr3:66419151 | G | A | 1 | a0002c0041t0001g0116 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.366-1885C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419151 | |||||||
chr3:66419157 | G | A | 3 | a0006c0019t0012g0244 a0006c0019t0012g0245 a0017c0025t0012g0253 |
3 | HG01952.hp1 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.366-1891C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419157 | |||||||
chr3:66419287 | T | G | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.366-2021A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419287 | |||||||
chr3:66419295 | G | A | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.366-2029C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419295 | |||||||
chr3:66419409 | T | C | 16 | a0003c0005t0001g0028 a0003c0010t0004g0257 a0007c0006t0005g0200 others(13): Show |
16 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.366-2143A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419409 | |||||||
chr3:66419411 | C | T | 60 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0002c0001t0001g0047 others(57): Show |
60 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.366-2145G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419411 | |||||||
chr3:66419523 | C | T | 1 | a0007c0006t0005g0223 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.366-2257G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419523 | |||||||
chr3:66419605 | T | C | 1 | a0001c0002t0001g0077 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.366-2339A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419605 | |||||||
chr3:66419647 | G | A | 31 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(28): Show |
31 | HG00099.hp1 HG01256.hp1 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.366-2381C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419647 | |||||||
chr3:66419727 | G | T | 11 | a0003c0010t0004g0257 a0007c0006t0005g0200 a0007c0006t0005g0215 others(8): Show |
11 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.366-2461C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419727 | |||||||
chr3:66419788 | C | G | 1 | a0007c0006t0020g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.366-2522G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419788 | |||||||
chr3:66419891 | T | C | 1 | a0002c0001t0001g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.366-2625A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419891 | |||||||
chr3:66419994 | C | T | 134 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.366-2728G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419994 | |||||||
chr3:66420064 | G | A | 1 | a0001c0002t0001g0150 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.366-2798C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420064 | |||||||
chr3:66420073 | C | G | 78 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(75): Show |
79 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.366-2807G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420073 | |||||||
chr3:66420214 | T | C | 10 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(7): Show |
10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.366-2948A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420214 | |||||||
chr3:66420245 | A | C | 1 | a0014c0020t0029g0029 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.366-2979T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420245 | |||||||
chr3:66420261 | C | T | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.366-2995G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420261 | |||||||
chr3:66420356 | C | T | 1 | a0030c0029t0001g0022 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.366-3090G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420356 | |||||||
chr3:66420506 | A | G | 81 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0056 others(78): Show |
82 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.366-3240T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420506 | |||||||
chr3:66420571 | T | C | 1 | a0004c0003t0002g0089 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.366-3305A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420571 | |||||||
chr3:66420614 | A | G | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.366-3348T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420614 | |||||||
chr3:66420624 | C | T | 5 | a0009c0037t0002g0017 a0012c0017t0002g0015 a0012c0017t0002g0019 others(2): Show |
5 | HG00544.hp1 HG00609.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.366-3358G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420624 | |||||||
chr3:66420764 | G | T | 1 | a0007c0006t0005g0215 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.366-3498C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420764 | |||||||
chr3:66420782 | G | A | 1 | a0003c0005t0003g0241 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.366-3516C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420782 | |||||||
chr3:66420800 | G | T | 14 | a0003c0005t0001g0028 a0007c0006t0005g0200 a0007c0006t0005g0215 others(11): Show |
14 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.366-3534C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420800 | |||||||
chr3:66420814 | C | T | 3 | a0004c0003t0002g0080 a0004c0003t0002g0144 a0016c0050t0023g0081 |
3 | HG00099.hp1 HG01256.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.366-3548G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420814 | |||||||
chr3:66420815 | G | A | 41 | a0002c0001t0001g0048 a0002c0001t0001g0059 a0002c0001t0001g0084 others(38): Show |
41 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.366-3549C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420815 | |||||||
chr3:66420835 | T | C | 76 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0056 others(73): Show |
77 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.366-3569A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420835 | |||||||
chr3:66420866 | C | G | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.366-3600G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420866 | |||||||
chr3:66420891 | T | C | 1 | a0001c0007t0002g0161 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.366-3625A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420891 | |||||||
chr3:66420902 | G | T | 3 | a0005c0004t0006g0220 a0005c0004t0006g0221 a0005c0004t0006g0222 |
3 | HG02630.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.366-3636C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420902 | |||||||
chr3:66420952 | G | C | 4 | a0005c0004t0006g0238 a0005c0004t0006g0239 a0005c0004t0006g0240 others(1): Show |
4 | HG01099.hp1 HG01123.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-3686C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420952 | |||||||
chr3:66421099 | C | G | 74 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(71): Show |
75 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.366-3833G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421099 | |||||||
chr3:66421214 | A | T | 10 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(7): Show |
10 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.366-3948T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421214 | |||||||
chr3:66421235 | T | C | 20 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0005c0004t0001g0018 others(17): Show |
20 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.366-3969A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421235 | |||||||
chr3:66421248 | A | G | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.366-3982T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421248 | |||||||
chr3:66421263 | C | G | 130 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(127): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.366-3997G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421263 | |||||||
chr3:66421312 | C | T | 3 | a0009c0015t0002g0032 a0009c0015t0002g0033 a0009c0015t0002g0034 |
3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.366-4046G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421312 | |||||||
chr3:66421321 | T | C | 240 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.366-4055A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421321 | |||||||
chr3:66421322 | G | T | 3 | a0009c0015t0002g0032 a0009c0015t0002g0033 a0009c0015t0002g0034 |
3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.366-4056C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421322 | |||||||
chr3:66421375 | T | C | 72 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0056 others(69): Show |
73 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.366-4109A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421375 | |||||||
chr3:66421462 | G | C | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.366-4196C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421462 | |||||||
chr3:66421470 | A | G | 150 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(147): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.366-4204T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421470 | |||||||
chr3:66421555 | C | G | 8 | a0003c0010t0002g0010 a0003c0010t0004g0201 a0003c0010t0004g0231 others(5): Show |
8 | HG02647.hp1 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.366-4289G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421555 | |||||||
chr3:66421588 | C | T | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.366-4322G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421588 | |||||||
chr3:66421618 | C | T | 50 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.366-4352G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421618 | |||||||
chr3:66421716 | G | A | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-4450C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421716 | |||||||
chr3:66421811 | G | C | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-4545C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421811 | |||||||
chr3:66421866 | T | C | 9 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(6): Show |
9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.366-4600A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421866 | |||||||
chr3:66421981 | T | C | 171 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(168): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.366-4715A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421981 | |||||||
chr3:66421996 | G | A | 1 | a0001c0002t0001g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.366-4730C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421996 | |||||||
chr3:66422015 | T | A | 5 | a0003c0012t0017g0004 a0006c0019t0012g0244 a0006c0019t0012g0245 others(2): Show |
5 | HG01952.hp1 HG02280.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.366-4749A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422015 | |||||||
chr3:66422052 | T | G | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.366-4786A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422052 | |||||||
chr3:66422090 | G | GC | 6 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(3): Show |
6 | HG00735.hp1 HG02970.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.366-4825dupG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422090 | |||||||
chr3:66422132 | G | C | 2 | a0003c0012t0018g0008 a0008c0008t0003g0237 |
2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.366-4866C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422132 | |||||||
chr3:66422217 | T | C | 1 | a0004c0053t0002g0197 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.366-4951A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422217 | |||||||
chr3:66422289 | C | T | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.366-5023G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422289 | |||||||
chr3:66422577 | A | T | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.366-5311T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422577 | |||||||
chr3:66422660 | A | T | 76 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0056 others(73): Show |
77 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.366-5394T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422660 | |||||||
chr3:66422718 | T | G | 27 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(24): Show |
27 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.366-5452A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422718 | |||||||
chr3:66422748 | C | G | 10 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(7): Show |
10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.366-5482G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422748 | |||||||
chr3:66422828 | T | C | 1 | a0001c0007t0002g0157 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.366-5562A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422828 | |||||||
chr3:66422873 | C | T | 166 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(163): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.366-5607G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422873 | |||||||
chr3:66422885 | A | G | 1 | a0004c0003t0002g0102 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.366-5619T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422885 | |||||||
chr3:66423062 | G | A | 71 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0056 others(68): Show |
72 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.366-5796C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423062 | |||||||
chr3:66423088 | A | G | 76 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0056 others(73): Show |
77 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.366-5822T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423088 | |||||||
chr3:66423238 | A | G | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-5972T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423238 | |||||||
chr3:66423240 | G | A | 9 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(6): Show |
9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.366-5974C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423240 | |||||||
chr3:66423249 | T | C | 8 | a0003c0010t0002g0010 a0003c0010t0004g0201 a0003c0010t0004g0231 others(5): Show |
8 | HG02647.hp1 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.366-5983A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423249 | |||||||
chr3:66423308 | C | T | 11 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(8): Show |
11 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.366-6042G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423308 | |||||||
chr3:66423398 | C | A | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.366-6132G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423398 | |||||||
chr3:66423427 | C | T | 2 | a0001c0002t0001g0178 a0003c0005t0003g0241 |
2 | HG01070.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.366-6161G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423427 | |||||||
chr3:66423456 | A | G | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.366-6190T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423456 | |||||||
chr3:66423464 | G | A | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.366-6198C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423464 | |||||||
chr3:66423691 | G | C | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.366-6425C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423691 | |||||||
chr3:66423736 | T | G | 54 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(51): Show |
54 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.366-6470A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423736 | |||||||
chr3:66423749 | T | C | 1 | a0007c0006t0005g0230 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.366-6483A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423749 | |||||||
chr3:66423750 | T | C | 181 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(178): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.366-6484A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423750 | |||||||
chr3:66423865 | G | A | 70 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(67): Show |
71 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.366-6599C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423865 | |||||||
chr3:66424050 | G | T | 2 | a0003c0012t0018g0008 a0008c0008t0003g0237 |
2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.366-6784C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424050 | |||||||
chr3:66424063 | A | G | 53 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(50): Show |
53 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.366-6797T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424063 | |||||||
chr3:66424279 | C | T | 1 | a0002c0001t0001g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.366-7013G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424279 | |||||||
chr3:66424342 | C | G | 7 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(4): Show |
7 | HG01261.hp1 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.366-7076G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424342 | |||||||
chr3:66424403 | G | A | 10 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(7): Show |
10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.366-7137C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424403 | |||||||
chr3:66424445 | C | T | 13 | a0003c0005t0001g0028 a0007c0006t0005g0200 a0007c0006t0005g0215 others(10): Show |
13 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.366-7179G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424445 | |||||||
chr3:66424530 | A | G | 10 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(7): Show |
10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.366-7264T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424530 | |||||||
chr3:66424533 | A | G | 1 | a0002c0018t0001g0175 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.366-7267T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424533 | |||||||
chr3:66424745 | T | C | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-7479A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424745 | |||||||
chr3:66425069 | T | C | 1 | a0004c0003t0002g0152 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.366-7803A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425069 | |||||||
chr3:66425077 | C | T | 9 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(6): Show |
9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.366-7811G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425077 | |||||||
chr3:66425192 | C | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-7926G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425192 | |||||||
chr3:66425213 | C | T | 50 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.366-7947G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425213 | |||||||
chr3:66425214 | T | G | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.366-7948A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425214 | |||||||
chr3:66425309 | T | C | 1 | a0001c0014t0011g0058 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.366-8043A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425309 | |||||||
chr3:66425444 | T | C | 66 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(63): Show |
67 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.366-8178A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425444 | |||||||
chr3:66425550 | AG | A | 66 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(63): Show |
67 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.366-8285delC | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425550 | |||||||
chr3:66425611 | T | C | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.366-8345A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425611 | |||||||
chr3:66425677 | A | G | 12 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(9): Show |
12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.366-8411T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425677 | |||||||
chr3:66425690 | C | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-8424G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425690 | |||||||
chr3:66425696 | TG | T | 3 | a0008c0008t0001g0038 a0008c0008t0003g0252 a0008c0008t0003g0256 |
3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.366-8431delC | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425696 | |||||||
chr3:66425874 | G | T | 1 | a0006c0009t0004g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.366-8608C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425874 | |||||||
chr3:66425976 | T | C | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.366-8710A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425976 | |||||||
chr3:66426284 | A | G | 9 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(6): Show |
9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.366-9018T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66426284 | |||||||
chr3:66426370 | T | C | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-9104A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66426370 | |||||||
chr3:66426707 | G | T | 3 | a0009c0015t0002g0032 a0009c0015t0002g0033 a0009c0015t0002g0034 |
3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.366-9441C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66426707 | |||||||
chr3:66426763 | T | C | 3 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 |
3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.366-9497A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66426763 | |||||||
chr3:66426849 | T | A | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.366-9583A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66426849 | |||||||
chr3:66427094 | C | T | 1 | a0010c0011t0007g0156 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.366-9828G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427094 | |||||||
chr3:66427219 | C | G | 187 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0056 others(184): Show |
188 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(185): Show |
intron_variant | MODIFIER | c.366-9953G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427219 | |||||||
chr3:66427378 | G | A | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.366-10112C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427378 | |||||||
chr3:66427404 | A | G | 9 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(6): Show |
9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.366-10138T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427404 | |||||||
chr3:66427514 | C | T | 238 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.366-10248G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427514 | |||||||
chr3:66427563 | C | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-10297G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427563 | |||||||
chr3:66427894 | C | A | 64 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0001c0014t0011g0058 others(61): Show |
64 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.366-10628G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427894 | |||||||
chr3:66427961 | G | A | 4 | a0001c0002t0001g0051 a0002c0001t0001g0047 a0002c0001t0001g0195 others(1): Show |
4 | HG00544.hp2 HG02132.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-10695C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427961 | |||||||
chr3:66427987 | C | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-10721G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427987 | |||||||
chr3:66427991 | A | G | 5 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.366-10725T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427991 | |||||||
chr3:66427994 | T | C | 4 | a0003c0012t0017g0004 a0006c0019t0012g0244 a0006c0019t0012g0245 others(1): Show |
4 | HG01952.hp1 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-10728A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427994 | |||||||
chr3:66428047 | T | C | 1 | a0008c0008t0025g0043 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.366-10781A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428047 | |||||||
chr3:66428071 | T | C | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.366-10805A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428071 | |||||||
chr3:66428096 | G | A | 1 | a0001c0002t0001g0069 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.366-10830C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428096 | |||||||
chr3:66428218 | C | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-10952G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428218 | |||||||
chr3:66428483 | A | C | 69 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(66): Show |
70 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.366-11217T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428483 | |||||||
chr3:66428486 | A | G | 69 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(66): Show |
70 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.366-11220T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428486 | |||||||
chr3:66428553 | T | A | 65 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0001c0014t0011g0058 others(62): Show |
65 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.366-11287A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428553 | |||||||
chr3:66428581 | C | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-11315G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428581 | |||||||
chr3:66428607 | T | G | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.366-11341A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428607 | |||||||
chr3:66428904 | C | T | 2 | a0002c0001t0001g0121 a0008c0008t0001g0031 |
2 | NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.366-11638G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428904 | |||||||
chr3:66429010 | C | T | 1 | a0004c0003t0002g0152 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.366-11744G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429010 | |||||||
chr3:66429037 | G | C | 4 | a0005c0004t0006g0220 a0005c0004t0006g0221 a0005c0004t0006g0222 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-11771C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429037 | |||||||
chr3:66429063 | G | A | 2 | a0004c0003t0002g0080 a0004c0003t0002g0144 |
2 | HG00099.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.366-11797C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429063 | |||||||
chr3:66429222 | T | C | 3 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 |
3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.366-11956A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429222 | |||||||
chr3:66429480 | C | T | 4 | a0005c0004t0006g0220 a0005c0004t0006g0221 a0005c0004t0006g0222 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-12214G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429480 | |||||||
chr3:66429565 | T | G | 28 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(25): Show |
28 | HG00735.hp1 HG01261.hp1 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.366-12299A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429565 | |||||||
chr3:66429634 | A | AT | 68 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(65): Show |
69 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.366-12369dupA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429634 | |||||||
chr3:66429651 | T | A | 2 | a0002c0001t0001g0123 a0002c0001t0001g0141 |
2 | HG03688.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.366-12385A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429651 | |||||||
chr3:66429787 | G | GGT | 22 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0014t0010g0125 others(19): Show |
22 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.366-12523_366-1252 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429787 | |||||||
chr3:66429787 | G | T | 2 | a0001c0002t0001g0056 a0001c0002t0001g0073 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.366-12521C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429787 | |||||||
chr3:66429787 | GGT | G | 57 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(54): Show |
57 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.366-12523_366-1252 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429787 | |||||||
chr3:66429787 | GGTGT | G | 14 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(11): Show |
14 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.366-12525_366-1252 others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429787 | |||||||
chr3:66429789 | T | G | 1 | a0031c0024t0001g0025 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.366-12523A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429789 | |||||||
chr3:66429833 | G | A | 11 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(8): Show |
11 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.366-12567C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429833 | |||||||
chr3:66429868 | A | ATT | 242 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.366-12604_366-1260 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429868 | |||||||
chr3:66429878 | A | G | 1 | a0004c0003t0026g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.366-12612T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429878 | |||||||
chr3:66429908 | A | AAAAAC | 18 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 others(15): Show |
18 | HG01884.hp2 HG02486.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.366-12647_366-1264 others(9): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429908 | |||||||
chr3:66430078 | T | C | 50 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(47): Show |
50 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.366-12812A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430078 | |||||||
chr3:66430145 | G | A | 1 | a0008c0008t0001g0038 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.366-12879C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430145 | |||||||
chr3:66430175 | C | A | 55 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(52): Show |
55 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.366-12909G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430175 | |||||||
chr3:66430181 | C | T | 3 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 |
3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.366-12915G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430181 | |||||||
chr3:66430182 | A | G | 3 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 |
3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.366-12916T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430182 | |||||||
chr3:66430187 | CAACAAA | C | 64 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0002c0001t0001g0047 others(61): Show |
64 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.366-12927_366-1292 others(10): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430187 | |||||||
chr3:66430190 | CA | C | 56 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(53): Show |
56 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.366-12925delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430190 | |||||||
chr3:66430190 | CAAA | C | 20 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0005c0004t0001g0018 others(17): Show |
20 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.366-12927_366-1292 others(7): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430190 | |||||||
chr3:66430193 | A | C | 80 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(77): Show |
81 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.366-12927T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430193 | |||||||
chr3:66430224 | A | G | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.366-12958T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430224 | |||||||
chr3:66430376 | G | A | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.366-13110C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430376 | |||||||
chr3:66430393 | T | C | 20 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0005c0004t0001g0018 others(17): Show |
20 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.366-13127A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430393 | |||||||
chr3:66430496 | C | T | 1 | a0029c0039t0001g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.366-13230G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430496 | |||||||
chr3:66430533 | G | A | 1 | a0002c0001t0001g0048 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.366-13267C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430533 | |||||||
chr3:66430544 | G | A | 10 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0005c0004t0001g0018 others(7): Show |
10 | HG00544.hp1 HG00609.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.366-13278C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430544 | |||||||
chr3:66430664 | T | C | 9 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(6): Show |
9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.366-13398A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430664 | |||||||
chr3:66430685 | T | C | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-13419A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430685 | |||||||
chr3:66430790 | C | T | 4 | a0005c0004t0006g0220 a0005c0004t0006g0221 a0005c0004t0006g0222 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-13524G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430790 | |||||||
chr3:66430840 | G | A | 1 | a0001c0002t0001g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.366-13574C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430840 | |||||||
chr3:66430870 | C | A | 238 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.366-13604G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430870 | |||||||
chr3:66430967 | C | T | 2 | a0004c0053t0002g0197 a0022c0054t0002g0196 |
2 | HG02300.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.366-13701G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430967 | |||||||
chr3:66430981 | T | C | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-13715A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430981 | |||||||
chr3:66430990 | C | T | 1 | a0004c0003t0002g0100 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.366-13724G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430990 | |||||||
chr3:66431001 | C | T | 1 | a0002c0018t0001g0050 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.366-13735G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431001 | |||||||
chr3:66431029 | C | T | 1 | a0007c0006t0005g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.366-13763G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431029 | |||||||
chr3:66431173 | G | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-13907C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431173 | |||||||
chr3:66431250 | T | G | 14 | a0003c0005t0001g0028 a0007c0006t0005g0200 a0007c0006t0005g0215 others(11): Show |
14 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.366-13984A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431250 | |||||||
chr3:66431345 | T | C | 3 | a0003c0012t0018g0008 a0006c0009t0002g0045 a0008c0008t0003g0237 |
3 | HG02976.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.366-14079A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431345 | |||||||
chr3:66431572 | T | C | 20 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0005c0004t0001g0018 others(17): Show |
20 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.366-14306A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431572 | |||||||
chr3:66431574 | T | C | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.366-14308A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431574 | |||||||
chr3:66431620 | C | T | 8 | a0003c0010t0002g0010 a0003c0010t0004g0201 a0003c0010t0004g0231 others(5): Show |
8 | HG02647.hp1 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.366-14354G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431620 | |||||||
chr3:66431638 | A | G | 10 | a0001c0007t0001g0118 a0001c0007t0002g0124 a0001c0007t0002g0154 others(7): Show |
10 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.366-14372T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431638 | |||||||
chr3:66431646 | T | C | 14 | a0003c0005t0001g0028 a0007c0006t0005g0200 a0007c0006t0005g0215 others(11): Show |
14 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.366-14380A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431646 | |||||||
chr3:66431704 | T | G | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-14438A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431704 | |||||||
chr3:66431890 | A | G | 1 | a0016c0050t0023g0081 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.366-14624T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431890 | |||||||
chr3:66431916 | C | T | 3 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0010c0011t0001g0091 |
3 | NA18943.hp1 NA18970.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.366-14650G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431916 | |||||||
chr3:66431961 | G | A | 1 | a0008c0033t0001g0027 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.366-14695C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431961 | |||||||
chr3:66431982 | C | T | 10 | a0001c0007t0001g0118 a0001c0007t0002g0124 a0001c0007t0002g0154 others(7): Show |
10 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.366-14716G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431982 | |||||||
chr3:66432149 | A | AG | 14 | a0003c0005t0001g0028 a0007c0006t0005g0200 a0007c0006t0005g0215 others(11): Show |
14 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.366-14884_366-1488 others(5): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432149 | |||||||
chr3:66432181 | G | C | 1 | a0001c0002t0001g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.366-14915C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432181 | |||||||
chr3:66432186 | T | C | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.366-14920A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432186 | |||||||
chr3:66432286 | G | A | 1 | a0026c0032t0007g0046 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.366-15020C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432286 | |||||||
chr3:66432489 | C | G | 3 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 |
3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.366-15223G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432489 | |||||||
chr3:66432552 | G | C | 6 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(3): Show |
6 | HG00735.hp1 HG02970.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.366-15286C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432552 | |||||||
chr3:66432557 | G | A | 1 | a0002c0001t0001g0112 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.366-15291C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432557 | |||||||
chr3:66432688 | C | T | 1 | a0021c0049t0001g0066 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.366-15422G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432688 | |||||||
chr3:66432823 | C | A | 1 | a0001c0002t0001g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.366-15557G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432823 | |||||||
chr3:66433031 | T | G | 1 | a0019c0038t0003g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.366-15765A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433031 | |||||||
chr3:66433037 | T | C | 10 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(7): Show |
10 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.366-15771A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433037 | |||||||
chr3:66433097 | T | C | 31 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0007t0002g0079 others(28): Show |
31 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.366-15831A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433097 | |||||||
chr3:66433164 | G | A | 11 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(8): Show |
11 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.366-15898C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433164 | |||||||
chr3:66433277 | G | T | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.366-16011C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433277 | |||||||
chr3:66433476 | G | A | 50 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.366-16210C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433476 | |||||||
chr3:66433543 | T | A | 4 | a0005c0004t0006g0220 a0005c0004t0006g0221 a0005c0004t0006g0222 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-16277A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433543 | |||||||
chr3:66433629 | A | G | 12 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(9): Show |
12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.366-16363T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433629 | |||||||
chr3:66433761 | C | A | 3 | a0009c0015t0002g0032 a0009c0015t0002g0033 a0009c0015t0002g0034 |
3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.366-16495G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433761 | |||||||
chr3:66433868 | A | G | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.366-16602T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433868 | |||||||
chr3:66434082 | A | G | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.366-16816T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434082 | |||||||
chr3:66434271 | A | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-17005T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434271 | |||||||
chr3:66434419 | C | T | 4 | a0005c0004t0006g0220 a0005c0004t0006g0221 a0005c0004t0006g0222 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+17140G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434419 | |||||||
chr3:66434472 | C | T | 11 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0131 others(8): Show |
11 | HG00544.hp1 HG00609.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.365+17087G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434472 | |||||||
chr3:66434532 | A | C | 78 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(75): Show |
79 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.365+17027T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434532 | |||||||
chr3:66434615 | C | T | 1 | a0002c0022t0001g0176 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.365+16944G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434615 | |||||||
chr3:66434616 | G | A | 10 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(7): Show |
10 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+16943C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434616 | |||||||
chr3:66434636 | T | C | 1 | a0006c0009t0004g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.365+16923A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434636 | |||||||
chr3:66434642 | G | A | 22 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(19): Show |
22 | HG00735.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.365+16917C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434642 | |||||||
chr3:66434725 | C | A | 10 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(7): Show |
10 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+16834G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434725 | |||||||
chr3:66434749 | A | G | 3 | a0003c0005t0001g0037 a0003c0005t0001g0039 a0003c0031t0001g0036 |
3 | HG01884.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.365+16810T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434749 | |||||||
chr3:66434755 | T | TA | 44 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0127 others(41): Show |
44 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.365+16803dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434755 | |||||||
chr3:66434755 | TA | T | 33 | a0001c0007t0001g0118 a0001c0007t0002g0079 a0001c0007t0002g0099 others(30): Show |
33 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.365+16803delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434755 | |||||||
chr3:66434766 | A | C | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.365+16793T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434766 | |||||||
chr3:66434775 | C | A | 87 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0131 others(84): Show |
87 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.365+16784G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434775 | |||||||
chr3:66434797 | A | C | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+16762T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434797 | |||||||
chr3:66434873 | G | A | 11 | a0001c0007t0002g0194 a0006c0009t0004g0224 a0006c0009t0004g0225 others(8): Show |
11 | HG00735.hp1 HG01255.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.365+16686C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434873 | |||||||
chr3:66434881 | A | T | 2 | a0007c0006t0009g0011 a0007c0006t0009g0012 |
2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.365+16678T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434881 | |||||||
chr3:66435054 | G | A | 50 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0007t0001g0118 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.365+16505C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435054 | |||||||
chr3:66435071 | A | ATGGC | 63 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(60): Show |
64 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.365+16487_365+1648 others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435071 | |||||||
chr3:66435072 | C | A | 63 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(60): Show |
64 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.365+16487G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435072 | |||||||
chr3:66435072 | C | CGGCA | 15 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(12): Show |
15 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.365+16483_365+1648 others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435072 | |||||||
chr3:66435082 | A | G | 1 | a0008c0008t0003g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.365+16477T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435082 | |||||||
chr3:66435116 | A | G | 1 | a0001c0002t0001g0074 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.365+16443T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435116 | |||||||
chr3:66435161 | C | T | 243 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(240): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.365+16398G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435161 | |||||||
chr3:66435228 | A | T | 12 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(9): Show |
12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.365+16331T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435228 | |||||||
chr3:66435274 | G | C | 1 | a0004c0003t0002g0102 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.365+16285C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435274 | |||||||
chr3:66435285 | A | G | 1 | a0002c0001t0001g0169 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.365+16274T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435285 | |||||||
chr3:66435316 | T | C | 16 | a0001c0002t0001g0053 a0001c0002t0001g0060 a0001c0002t0001g0061 others(13): Show |
17 | HG00673.hp1 HG00735.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.365+16243A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435316 | |||||||
chr3:66435396 | TAAAAACA | T | 31 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0002c0001t0032g0199 others(28): Show |
31 | HG00099.hp1 HG00621.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.365+16156_365+1616 others(11): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435396 | |||||||
chr3:66435406 | A | T | 21 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0131 others(18): Show |
21 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.365+16153T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435406 | |||||||
chr3:66435453 | C | T | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.365+16106G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435453 | |||||||
chr3:66435475 | A | G | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.365+16084T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435475 | |||||||
chr3:66435584 | G | C | 4 | a0005c0004t0006g0220 a0005c0004t0006g0221 a0005c0004t0006g0222 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+15975C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435584 | |||||||
chr3:66435589 | C | T | 10 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(7): Show |
10 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+15970G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435589 | |||||||
chr3:66435651 | C | A | 47 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0002c0001t0001g0047 others(44): Show |
47 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.365+15908G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435651 | |||||||
chr3:66435670 | T | C | 3 | a0001c0002t0001g0062 a0001c0002t0001g0069 a0001c0002t0001g0070 |
3 | HG01167.hp2 HG01515.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.365+15889A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435670 | |||||||
chr3:66435759 | C | T | 1 | a0002c0001t0001g0134 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.365+15800G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435759 | |||||||
chr3:66435781 | CT | C | 31 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(28): Show |
31 | HG00738.hp1 HG01261.hp1 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.365+15777delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435781 | |||||||
chr3:66435781 | CTT | C | 135 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0056 others(132): Show |
136 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.365+15776_365+1577 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435781 | |||||||
chr3:66435784 | T | A | 2 | a0010c0011t0007g0168 a0010c0011t0007g0174 |
2 | HG00280.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.365+15775A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435784 | |||||||
chr3:66435891 | G | C | 21 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0131 others(18): Show |
21 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.365+15668C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435891 | |||||||
chr3:66435918 | C | T | 1 | a0001c0002t0001g0198 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.365+15641G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435918 | |||||||
chr3:66435956 | C | G | 9 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(6): Show |
9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.365+15603G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435956 | |||||||
chr3:66436005 | C | T | 63 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0002c0001t0001g0047 others(60): Show |
63 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.365+15554G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436005 | |||||||
chr3:66436025 | C | T | 2 | a0003c0005t0001g0028 a0011c0030t0027g0021 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.365+15534G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436025 | |||||||
chr3:66436287 | G | A | 4 | a0001c0002t0001g0051 a0002c0001t0001g0047 a0002c0001t0001g0195 others(1): Show |
4 | HG00544.hp2 HG02132.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+15272C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436287 | |||||||
chr3:66436331 | C | T | 1 | a0004c0003t0002g0152 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.365+15228G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436331 | |||||||
chr3:66436335 | C | A | 48 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0007t0001g0118 others(45): Show |
48 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.365+15224G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436335 | |||||||
chr3:66436348 | G | T | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.365+15211C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436348 | |||||||
chr3:66436363 | C | T | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.365+15196G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436363 | |||||||
chr3:66436437 | C | T | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.365+15122G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436437 | |||||||
chr3:66436454 | T | C | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.365+15105A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436454 | |||||||
chr3:66436466 | A | G | 1 | a0003c0005t0001g0026 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.365+15093T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436466 | |||||||
chr3:66436493 | G | A | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.365+15066C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436493 | |||||||
chr3:66436505 | C | T | 1 | a0002c0001t0001g0109 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.365+15054G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436505 | |||||||
chr3:66436528 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.365+15031C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436528 | |||||||
chr3:66436607 | G | A | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.365+14952C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436607 | |||||||
chr3:66436665 | AC | A | 10 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(7): Show |
10 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+14893delG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436665 | |||||||
chr3:66436736 | G | T | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.365+14823C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436736 | |||||||
chr3:66436766 | C | T | 1 | a0002c0001t0001g0165 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.365+14793G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436766 | |||||||
chr3:66436774 | G | A | 1 | a0002c0001t0001g0109 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.365+14785C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436774 | |||||||
chr3:66436815 | C | CA | 14 | a0003c0005t0001g0028 a0007c0006t0005g0200 a0007c0006t0005g0215 others(11): Show |
14 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.365+14743dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436815 | |||||||
chr3:66437028 | C | A | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.365+14531G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437028 | |||||||
chr3:66437077 | C | T | 1 | a0003c0010t0004g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.365+14482G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437077 | |||||||
chr3:66437109 | C | T | 14 | a0003c0005t0001g0028 a0007c0006t0005g0200 a0007c0006t0005g0215 others(11): Show |
14 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.365+14450G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437109 | |||||||
chr3:66437118 | A | G | 49 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0131 others(46): Show |
49 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.365+14441T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437118 | |||||||
chr3:66437189 | G | A | 1 | a0004c0003t0002g0107 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.365+14370C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437189 | |||||||
chr3:66437228 | T | G | 69 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0001c0014t0011g0058 others(66): Show |
69 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.365+14331A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437228 | |||||||
chr3:66437265 | G | T | 1 | a0002c0001t0001g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.365+14294C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437265 | |||||||
chr3:66437282 | G | C | 3 | a0003c0005t0001g0037 a0003c0005t0001g0039 a0003c0031t0001g0036 |
3 | HG01884.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.365+14277C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437282 | |||||||
chr3:66437306 | A | C | 3 | a0009c0015t0002g0032 a0009c0015t0002g0033 a0009c0015t0002g0034 |
3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.365+14253T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437306 | |||||||
chr3:66437314 | G | C | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.365+14245C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437314 | |||||||
chr3:66437337 | A | G | 50 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0131 others(47): Show |
50 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.365+14222T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437337 | |||||||
chr3:66437346 | C | G | 21 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0131 others(18): Show |
21 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.365+14213G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437346 | |||||||
chr3:66437406 | C | A | 73 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0001c0014t0011g0058 others(70): Show |
73 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.365+14153G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437406 | |||||||
chr3:66437549 | T | A | 1 | a0001c0014t0010g0125 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.365+14010A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437549 | |||||||
chr3:66437710 | G | T | 50 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0007t0001g0118 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.365+13849C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437710 | |||||||
chr3:66437722 | G | A | 13 | a0003c0005t0001g0028 a0007c0006t0005g0200 a0007c0006t0005g0215 others(10): Show |
13 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.365+13837C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437722 | |||||||
chr3:66437765 | G | A | 13 | a0003c0005t0001g0028 a0007c0006t0005g0200 a0007c0006t0005g0215 others(10): Show |
13 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.365+13794C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437765 | |||||||
chr3:66438026 | T | C | 1 | a0002c0001t0032g0199 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.365+13533A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438026 | |||||||
chr3:66438030 | T | C | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.365+13529A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438030 | |||||||
chr3:66438103 | G | A | 3 | a0003c0005t0001g0037 a0003c0005t0001g0039 a0003c0031t0001g0036 |
3 | HG01884.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.365+13456C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438103 | |||||||
chr3:66438110 | C | G | 1 | a0007c0006t0005g0223 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.365+13449G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438110 | |||||||
chr3:66438219 | C | T | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+13340G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438219 | |||||||
chr3:66438232 | C | T | 239 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.365+13327G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438232 | |||||||
chr3:66438364 | G | C | 10 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(7): Show |
10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+13195C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438364 | |||||||
chr3:66438388 | C | T | 1 | a0001c0007t0002g0158 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.365+13171G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438388 | |||||||
chr3:66438466 | A | C | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+13093T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438466 | |||||||
chr3:66438611 | T | C | 21 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0005c0004t0001g0018 others(18): Show |
21 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.365+12948A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438611 | |||||||
chr3:66438714 | G | A | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+12845C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438714 | |||||||
chr3:66438948 | C | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.365+12611G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438948 | |||||||
chr3:66438990 | G | T | 60 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(57): Show |
61 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.365+12569C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438990 | |||||||
chr3:66439011 | A | C | 1 | a0015c0051t0002g0054 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.365+12548T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439011 | |||||||
chr3:66439070 | A | G | 1 | a0003c0012t0014g0236 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.365+12489T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439070 | |||||||
chr3:66439187 | G | A | 1 | a0005c0004t0006g0239 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.365+12372C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439187 | |||||||
chr3:66439200 | C | T | 3 | a0009c0013t0001g0041 a0009c0013t0002g0042 a0009c0013t0002g0044 |
3 | NA18991.hp2 NA19000.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.365+12359G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439200 | |||||||
chr3:66439227 | G | A | 2 | a0003c0005t0001g0028 a0011c0030t0027g0021 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.365+12332C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439227 | |||||||
chr3:66439369 | A | G | 1 | a0007c0006t0005g0215 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.365+12190T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439369 | |||||||
chr3:66439419 | A | G | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.365+12140T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439419 | |||||||
chr3:66439561 | CT | C | 6 | a0001c0002t0001g0070 a0001c0002t0001g0078 a0002c0001t0001g0112 others(3): Show |
6 | HG00099.hp2 HG01255.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.365+11997delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439561 | |||||||
chr3:66439575 | T | A | 183 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0056 others(180): Show |
184 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(181): Show |
intron_variant | MODIFIER | c.365+11984A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439575 | |||||||
chr3:66439575 | T | TA | 51 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0106 others(48): Show |
51 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.365+11983dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439575 | |||||||
chr3:66439658 | T | C | 14 | a0003c0005t0001g0028 a0007c0006t0005g0200 a0007c0006t0005g0215 others(11): Show |
14 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.365+11901A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439658 | |||||||
chr3:66439686 | C | G | 1 | a0003c0010t0004g0201 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.365+11873G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439686 | |||||||
chr3:66439701 | C | A | 131 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0056 others(128): Show |
132 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.365+11858G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439701 | |||||||
chr3:66439709 | T | C | 20 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0005c0004t0001g0018 others(17): Show |
20 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.365+11850A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439709 | |||||||
chr3:66439769 | G | A | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+11790C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439769 | |||||||
chr3:66439787 | T | C | 3 | a0008c0008t0001g0038 a0008c0008t0003g0252 a0008c0008t0003g0256 |
3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.365+11772A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439787 | |||||||
chr3:66440019 | A | AG | 39 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0003c0005t0001g0028 others(36): Show |
39 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.365+11539dupC | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440019 | |||||||
chr3:66440019 | A | G | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+11540T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440019 | |||||||
chr3:66440024 | G | GA | 5 | a0001c0002t0001g0094 a0001c0023t0002g0067 a0001c0023t0002g0082 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.365+11534dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440024 | |||||||
chr3:66440160 | C | A | 1 | a0001c0002t0001g0051 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.365+11399G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440160 | |||||||
chr3:66440198 | A | G | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.365+11361T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440198 | |||||||
chr3:66440244 | A | C | 3 | a0003c0005t0001g0037 a0003c0005t0001g0039 a0003c0031t0001g0036 |
3 | HG01884.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.365+11315T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440244 | |||||||
chr3:66440246 | CTCGAGGT others(4): Show |
C | 1 | a0001c0002t0001g0094 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.365+11302_365+1131 others(15): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440246 | |||||||
chr3:66440248 | C | T | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+11311G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440248 | |||||||
chr3:66440275 | C | T | 1 | a0004c0003t0026g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.365+11284G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440275 | |||||||
chr3:66440354 | C | T | 1 | a0004c0003t0002g0132 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.365+11205G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440354 | |||||||
chr3:66440447 | G | A | 237 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.365+11112C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440447 | |||||||
chr3:66440812 | T | C | 1 | a0004c0003t0002g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.365+10747A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440812 | |||||||
chr3:66440853 | G | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.365+10706C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440853 | |||||||
chr3:66441069 | C | T | 4 | a0005c0004t0006g0220 a0005c0004t0006g0221 a0005c0004t0006g0222 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+10490G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66441069 | |||||||
chr3:66441243 | G | A | 48 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0007t0001g0118 others(45): Show |
48 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.365+10316C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66441243 | |||||||
chr3:66441272 | A | G | 3 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 |
3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.365+10287T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66441272 | |||||||
chr3:66441398 | C | G | 144 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0056 others(141): Show |
145 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.365+10161G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66441398 | |||||||
chr3:66441487 | T | C | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.365+10072A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66441487 | |||||||
chr3:66441957 | G | A | 1 | a0001c0002t0001g0117 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.365+9602C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66441957 | |||||||
chr3:66441976 | C | T | 1 | a0002c0001t0001g0141 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.365+9583G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66441976 | |||||||
chr3:66441998 | C | T | 28 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0004c0003t0001g0142 others(25): Show |
28 | HG00099.hp1 HG01256.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.365+9561G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66441998 | |||||||
chr3:66442028 | C | T | 17 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(14): Show |
17 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.365+9531G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442028 | |||||||
chr3:66442091 | T | C | 1 | a0004c0003t0002g0100 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.365+9468A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442091 | |||||||
chr3:66442180 | G | T | 61 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(58): Show |
62 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.365+9379C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442180 | |||||||
chr3:66442214 | T | C | 4 | a0003c0005t0003g0001 a0003c0005t0003g0209 a0003c0005t0003g0211 others(1): Show |
5 | NA18966.hp2 NA18986.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.365+9345A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442214 | |||||||
chr3:66442448 | G | GGGA | 5 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(2): Show |
5 | HG02572.hp1 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+9108_365+9110d others(5): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442448 | |||||||
chr3:66442457 | A | G | 8 | a0001c0002t0001g0065 a0001c0002t0001g0085 a0001c0002t0001g0087 others(5): Show |
8 | HG01261.hp2 HG01433.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.365+9102T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442457 | |||||||
chr3:66442539 | T | C | 1 | a0026c0032t0007g0046 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.365+9020A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442539 | |||||||
chr3:66442553 | A | G | 1 | a0005c0004t0001g0018 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.365+9006T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442553 | |||||||
chr3:66442662 | T | C | 1 | a0009c0037t0002g0017 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.365+8897A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442662 | |||||||
chr3:66442670 | C | A | 3 | a0009c0015t0002g0032 a0009c0015t0002g0033 a0009c0015t0002g0034 |
3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.365+8889G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442670 | |||||||
chr3:66442684 | A | G | 2 | a0002c0001t0001g0188 a0002c0041t0001g0116 |
2 | NA18969.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.365+8875T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442684 | |||||||
chr3:66442784 | C | T | 1 | a0003c0005t0001g0037 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.365+8775G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442784 | |||||||
chr3:66442812 | A | G | 1 | a0001c0002t0001g0065 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.365+8747T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442812 | |||||||
chr3:66442929 | C | CCT | 5 | a0002c0001t0001g0188 a0002c0021t0001g0114 a0002c0021t0001g0115 others(2): Show |
5 | HG00558.hp2 HG02027.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+8628_365+8629d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442929 | |||||||
chr3:66442957 | A | C | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+8602T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442957 | |||||||
chr3:66442957 | A | T | 42 | a0001c0002t0001g0056 a0001c0002t0001g0062 a0001c0002t0001g0064 others(39): Show |
42 | HG00099.hp2 HG00609.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.365+8602T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442957 | |||||||
chr3:66442976 | A | C | 1 | a0001c0002t0001g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.365+8583T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442976 | |||||||
chr3:66443025 | T | C | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+8534A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443025 | |||||||
chr3:66443033 | C | T | 1 | a0010c0011t0007g0156 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.365+8526G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443033 | |||||||
chr3:66443041 | G | A | 73 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0002c0001t0001g0047 others(70): Show |
73 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.365+8518C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443041 | |||||||
chr3:66443162 | G | A | 1 | a0003c0012t0017g0004 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.365+8397C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443162 | |||||||
chr3:66443316 | A | AGGGGATG others(11): Show |
10 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(7): Show |
10 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+8225_365+8242d others(20): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443316 | |||||||
chr3:66443316 | A | AGGGGATG others(30): Show |
9 | a0002c0001t0001g0121 a0002c0001t0001g0126 a0002c0001t0001g0134 others(6): Show |
9 | HG00621.hp2 NA18951.hp1 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.365+8206_365+8242d others(39): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443316 | |||||||
chr3:66443316 | AGGGGATG others(11): Show |
A | 49 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0007t0001g0118 others(46): Show |
49 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.365+8225_365+8242d others(20): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443316 | |||||||
chr3:66443328 | A | AGGGGCGG others(12): Show |
3 | a0006c0019t0012g0244 a0006c0019t0012g0245 a0017c0025t0012g0253 |
3 | HG01952.hp1 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.365+8212_365+8230d others(21): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443328 | |||||||
chr3:66443328 | AGGGGCGG others(12): Show |
A | 10 | a0001c0002t0001g0062 a0001c0002t0001g0064 a0001c0002t0001g0069 others(7): Show |
10 | HG01167.hp2 HG01346.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.365+8212_365+8230d others(21): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443328 | |||||||
chr3:66443466 | C | T | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+8093G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443466 | |||||||
chr3:66443670 | T | C | 1 | a0007c0006t0005g0223 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.365+7889A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443670 | |||||||
chr3:66443779 | A | G | 165 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0056 others(162): Show |
166 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.365+7780T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443779 | |||||||
chr3:66443995 | G | A | 13 | a0001c0002t0001g0077 a0001c0007t0002g0079 a0001c0007t0002g0099 others(10): Show |
13 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.365+7564C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443995 | |||||||
chr3:66444065 | C | T | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.365+7494G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444065 | |||||||
chr3:66444300 | G | T | 1 | a0001c0002t0031g0068 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.365+7259C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444300 | |||||||
chr3:66444326 | A | T | 1 | a0003c0010t0002g0010 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.365+7233T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444326 | |||||||
chr3:66444368 | T | TGC | 25 | a0001c0002t0001g0131 a0005c0004t0001g0018 a0006c0009t0004g0224 others(22): Show |
25 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.365+7189_365+7190d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444368 | |||||||
chr3:66444384 | GC | G | 67 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0002c0001t0001g0047 others(64): Show |
67 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.365+7174delG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444384 | |||||||
chr3:66444489 | G | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.365+7070C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444489 | |||||||
chr3:66444491 | C | CT | 9 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(6): Show |
9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.365+7067dupA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444491 | |||||||
chr3:66444512 | G | A | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+7047C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444512 | |||||||
chr3:66444550 | G | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.365+7009C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444550 | |||||||
chr3:66444565 | C | T | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.365+6994G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444565 | |||||||
chr3:66444869 | TTA | T | 246 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.365+6688_365+6689d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444869 | |||||||
chr3:66444942 | T | C | 67 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(64): Show |
68 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.365+6617A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444942 | |||||||
chr3:66444973 | A | G | 9 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(6): Show |
9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.365+6586T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444973 | |||||||
chr3:66445053 | C | T | 48 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0007t0001g0118 others(45): Show |
48 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.365+6506G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445053 | |||||||
chr3:66445133 | A | G | 5 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.365+6426T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445133 | |||||||
chr3:66445171 | T | A | 1 | a0004c0003t0002g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.365+6388A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445171 | |||||||
chr3:66445274 | G | GT | 12 | a0002c0001t0001g0149 a0007c0006t0005g0200 a0007c0006t0005g0215 others(9): Show |
12 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.365+6284dupA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445274 | |||||||
chr3:66445331 | T | C | 241 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.365+6228A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445331 | |||||||
chr3:66445442 | C | G | 1 | a0002c0001t0001g0133 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.365+6117G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445442 | |||||||
chr3:66445548 | A | G | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.365+6011T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445548 | |||||||
chr3:66445774 | G | A | 1 | a0003c0005t0003g0241 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.365+5785C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445774 | |||||||
chr3:66445803 | A | G | 9 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(6): Show |
9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.365+5756T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445803 | |||||||
chr3:66445961 | A | G | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.365+5598T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445961 | |||||||
chr3:66445988 | T | C | 11 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(8): Show |
11 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.365+5571A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445988 | |||||||
chr3:66446168 | C | T | 94 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(91): Show |
94 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.365+5391G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446168 | |||||||
chr3:66446187 | C | A | 1 | a0001c0002t0001g0127 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.365+5372G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446187 | |||||||
chr3:66446262 | C | T | 1 | a0004c0003t0002g0105 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.365+5297G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446262 | |||||||
chr3:66446299 | G | A | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+5260C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446299 | |||||||
chr3:66446403 | C | CT | 11 | a0001c0002t0001g0162 a0002c0001t0001g0147 a0002c0001t0001g0180 others(8): Show |
11 | HG00621.hp2 HG01928.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.365+5155dupA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446403 | |||||||
chr3:66446403 | CT | C | 14 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0007t0002g0124 others(11): Show |
14 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.365+5155delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446403 | |||||||
chr3:66446469 | G | A | 3 | a0009c0013t0001g0041 a0009c0013t0002g0042 a0009c0013t0002g0044 |
3 | NA18991.hp2 NA19000.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.365+5090C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446469 | |||||||
chr3:66446537 | C | T | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.365+5022G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446537 | |||||||
chr3:66446751 | C | T | 1 | a0001c0002t0001g0076 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.365+4808G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446751 | |||||||
chr3:66446851 | CA | C | 67 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0002c0001t0001g0047 others(64): Show |
67 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.365+4707delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446851 | |||||||
chr3:66446863 | A | T | 1 | a0007c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.365+4696T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446863 | |||||||
chr3:66446945 | G | C | 2 | a0001c0002t0001g0069 a0001c0002t0001g0070 |
2 | HG01167.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.365+4614C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446945 | |||||||
chr3:66447029 | A | T | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+4530T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447029 | |||||||
chr3:66447069 | T | C | 9 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(6): Show |
9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.365+4490A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447069 | |||||||
chr3:66447071 | A | T | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+4488T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447071 | |||||||
chr3:66447139 | A | T | 237 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.365+4420T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447139 | |||||||
chr3:66447177 | T | C | 3 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 |
3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.365+4382A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447177 | |||||||
chr3:66447273 | C | G | 1 | a0007c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.365+4286G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447273 | |||||||
chr3:66447290 | T | C | 66 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(63): Show |
67 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.365+4269A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447290 | |||||||
chr3:66447353 | C | T | 1 | a0003c0010t0004g0201 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.365+4206G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447353 | |||||||
chr3:66447718 | C | T | 12 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(9): Show |
12 | HG00735.hp1 HG01891.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.365+3841G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447718 | |||||||
chr3:66447741 | G | A | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.365+3818C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447741 | |||||||
chr3:66447791 | C | A | 225 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(222): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.365+3768G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447791 | |||||||
chr3:66447859 | G | C | 2 | a0002c0001t0001g0149 a0008c0008t0001g0020 |
2 | NA18975.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.365+3700C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447859 | |||||||
chr3:66448076 | T | G | 9 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(6): Show |
9 | HG01884.hp2 HG02647.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.365+3483A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66448076 | |||||||
chr3:66448087 | C | G | 8 | a0007c0006t0005g0200 a0007c0006t0005g0215 a0007c0006t0005g0219 others(5): Show |
8 | HG01884.hp2 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.365+3472G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66448087 | |||||||
chr3:66448218 | A | C | 253 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(250): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.365+3341T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66448218 | |||||||
chr3:66448223 | A | G | 1 | a0004c0003t0002g0152 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.365+3336T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66448223 | |||||||
chr3:66448382 | T | C | 4 | a0008c0008t0001g0038 a0008c0008t0003g0252 a0008c0008t0003g0256 others(1): Show |
4 | HG02451.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+3177A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66448382 | |||||||
chr3:66448548 | CT | C | 67 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0002c0001t0001g0047 others(64): Show |
67 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.365+3010delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66448548 | |||||||
chr3:66448766 | T | C | 3 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 |
3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.365+2793A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66448766 | |||||||
chr3:66448794 | C | T | 13 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(10): Show |
13 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.365+2765G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66448794 | |||||||
chr3:66449044 | G | A | 4 | a0008c0008t0001g0038 a0008c0008t0003g0252 a0008c0008t0003g0256 others(1): Show |
4 | HG02451.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+2515C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449044 | |||||||
chr3:66449315 | C | T | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+2244G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449315 | |||||||
chr3:66449396 | A | G | 4 | a0008c0008t0001g0038 a0008c0008t0003g0252 a0008c0008t0003g0256 others(1): Show |
4 | HG02451.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+2163T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449396 | |||||||
chr3:66449435 | C | A | 4 | a0008c0008t0001g0038 a0008c0008t0003g0252 a0008c0008t0003g0256 others(1): Show |
4 | HG02451.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+2124G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449435 | |||||||
chr3:66449467 | A | G | 239 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.365+2092T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449467 | |||||||
chr3:66449663 | C | T | 9 | a0002c0001t0001g0170 a0007c0006t0005g0200 a0007c0006t0005g0215 others(6): Show |
9 | HG00738.hp1 HG01884.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.365+1896G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449663 | |||||||
chr3:66449774 | C | T | 239 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.365+1785G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449774 | |||||||
chr3:66449784 | A | G | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.365+1775T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449784 | |||||||
chr3:66449821 | A | G | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.365+1738T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449821 | |||||||
chr3:66449959 | C | T | 2 | a0001c0002t0001g0108 a0002c0001t0001g0180 |
2 | HG02071.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.365+1600G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449959 | |||||||
chr3:66449977 | T | C | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+1582A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449977 | |||||||
chr3:66449996 | C | A | 55 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0131 others(52): Show |
55 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.365+1563G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449996 | |||||||
chr3:66450103 | A | G | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.365+1456T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66450103 | |||||||
chr3:66450140 | G | A | 9 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(6): Show |
9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.365+1419C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66450140 | |||||||
chr3:66450321 | T | C | 9 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(6): Show |
9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.365+1238A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66450321 | |||||||
chr3:66450322 | C | G | 1 | a0010c0011t0024g0063 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.365+1237G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66450322 | |||||||
chr3:66450600 | C | T | 2 | a0001c0002t0001g0070 a0007c0006t0009g0014 |
2 | HG02622.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.365+959G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66450600 | |||||||
chr3:66450671 | G | C | 1 | a0014c0020t0029g0029 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.365+888C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66450671 | |||||||
chr3:66450715 | T | TTA | 2 | a0003c0012t0018g0008 a0008c0008t0003g0237 |
2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.365+842_365+843dup others(2): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66450715 | |||||||
chr3:66450923 | T | C | 12 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(9): Show |
12 | HG00735.hp1 HG01891.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.365+636A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66450923 | |||||||
chr3:66451178 | C | T | 12 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(9): Show |
12 | HG00735.hp1 HG01891.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.365+381G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66451178 | |||||||
chr3:66451213 | T | C | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.365+346A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66451213 | |||||||
chr3:66451298 | C | T | 1 | a0004c0003t0002g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.365+261G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66451298 | |||||||
chr3:66451309 | TA | T | 56 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0093 others(53): Show |
56 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.365+249delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66451309 | |||||||
chr3:66451371 | C | T | 1 | a0009c0013t0002g0024 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.365+188G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66451371 | |||||||
chr3:66451487 | C | A | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+72G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66451487 | |||||||
chr3:66451490 | G | T | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+69C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66451490 | |||||||
chr3:66451670 | T | C | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.291-37A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66451670 | |||||||
chr3:66451810 | A | G | 184 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0056 others(181): Show |
185 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.291-177T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66451810 | |||||||
chr3:66451827 | C | G | 11 | a0001c0002t0001g0198 a0003c0012t0014g0233 a0003c0012t0014g0236 others(8): Show |
11 | HG01099.hp1 HG01123.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.291-194G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66451827 | |||||||
chr3:66451989 | C | G | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.291-356G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66451989 | |||||||
chr3:66452166 | T | TC | 9 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(6): Show |
9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.291-534dupG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452166 | |||||||
chr3:66452322 | T | G | 3 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 |
3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.291-689A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452322 | |||||||
chr3:66452405 | G | T | 4 | a0003c0005t0001g0028 a0005c0004t0006g0220 a0005c0004t0006g0221 others(1): Show |
4 | HG02630.hp2 HG03098.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-772C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452405 | |||||||
chr3:66452507 | C | G | 1 | a0013c0042t0010g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.291-874G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452507 | |||||||
chr3:66452531 | T | G | 12 | a0004c0003t0039g0262 a0007c0006t0005g0200 a0007c0006t0005g0215 others(9): Show |
12 | HG01884.hp2 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.291-898A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452531 | |||||||
chr3:66452551 | G | A | 1 | a0005c0004t0001g0018 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.291-918C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452551 | |||||||
chr3:66452557 | A | C | 69 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(66): Show |
70 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.291-924T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452557 | |||||||
chr3:66452783 | T | C | 21 | a0005c0004t0001g0018 a0006c0009t0004g0224 a0006c0009t0004g0225 others(18): Show |
21 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.291-1150A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452783 | |||||||
chr3:66452872 | T | G | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.291-1239A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452872 | |||||||
chr3:66452942 | C | T | 1 | a0001c0002t0001g0093 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.291-1309G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452942 | |||||||
chr3:66453198 | G | A | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.291-1565C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453198 | |||||||
chr3:66453234 | T | C | 21 | a0005c0004t0001g0018 a0006c0009t0004g0224 a0006c0009t0004g0225 others(18): Show |
21 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.291-1601A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453234 | |||||||
chr3:66453510 | C | G | 1 | a0001c0002t0001g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.291-1877G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453510 | |||||||
chr3:66453584 | A | G | 232 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.291-1951T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453584 | |||||||
chr3:66453625 | G | C | 9 | a0001c0002t0001g0065 a0001c0002t0001g0085 a0001c0002t0001g0087 others(6): Show |
9 | HG01261.hp2 HG01433.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.291-1992C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453625 | |||||||
chr3:66453638 | G | A | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.291-2005C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453638 | |||||||
chr3:66453640 | C | T | 68 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0001c0014t0011g0058 others(65): Show |
68 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.291-2007G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453640 | |||||||
chr3:66453692 | C | G | 14 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(11): Show |
14 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.291-2059G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453692 | |||||||
chr3:66453695 | G | T | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.291-2062C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453695 | |||||||
chr3:66453749 | A | G | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.291-2116T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453749 | |||||||
chr3:66453800 | G | C | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.291-2167C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453800 | |||||||
chr3:66453955 | T | C | 5 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-2322A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453955 | |||||||
chr3:66454068 | C | T | 12 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(9): Show |
12 | HG00735.hp1 HG01891.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.291-2435G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454068 | |||||||
chr3:66454134 | C | T | 1 | a0002c0001t0001g0143 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.291-2501G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454134 | |||||||
chr3:66454458 | T | A | 1 | a0003c0012t0017g0004 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.291-2825A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454458 | |||||||
chr3:66454514 | C | T | 1 | a0001c0014t0010g0186 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.291-2881G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454514 | |||||||
chr3:66454632 | T | C | 1 | a0005c0004t0007g0016 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.291-2999A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454632 | |||||||
chr3:66454740 | C | T | 4 | a0008c0008t0001g0038 a0008c0008t0003g0252 a0008c0008t0003g0256 others(1): Show |
4 | HG02451.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-3107G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454740 | |||||||
chr3:66454745 | C | T | 1 | a0002c0001t0001g0048 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.291-3112G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454745 | |||||||
chr3:66454765 | A | G | 1 | a0005c0004t0021g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.291-3132T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454765 | |||||||
chr3:66454799 | A | G | 1 | a0008c0008t0003g0213 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.291-3166T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454799 | |||||||
chr3:66454965 | G | A | 1 | a0021c0049t0001g0066 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.291-3332C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454965 | |||||||
chr3:66454972 | C | T | 15 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(12): Show |
15 | HG00735.hp1 HG01891.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.291-3339G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454972 | |||||||
chr3:66454980 | G | A | 1 | a0007c0006t0005g0243 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291-3347C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454980 | |||||||
chr3:66455026 | C | T | 1 | a0005c0004t0006g0238 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.291-3393G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66455026 | |||||||
chr3:66455276 | T | C | 12 | a0006c0009t0004g0224 a0006c0009t0004g0225 a0006c0009t0004g0226 others(9): Show |
12 | HG00735.hp1 HG01891.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.291-3643A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66455276 | |||||||
chr3:66455717 | G | C | 1 | a0002c0041t0001g0116 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.291-4084C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66455717 | |||||||
chr3:66455779 | T | C | 1 | a0005c0004t0001g0018 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.291-4146A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66455779 | |||||||
chr3:66455820 | C | T | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.291-4187G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66455820 | |||||||
chr3:66455833 | C | T | 2 | a0001c0002t0001g0198 a0005c0004t0007g0016 |
2 | NA18974.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.291-4200G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66455833 | |||||||
chr3:66455958 | T | C | 134 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.291-4325A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66455958 | |||||||
chr3:66456111 | T | C | 3 | a0006c0009t0004g0246 a0007c0006t0009g0011 a0007c0006t0009g0012 |
3 | HG02559.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.291-4478A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456111 | |||||||
chr3:66456223 | G | C | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.291-4590C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456223 | |||||||
chr3:66456354 | G | A | 1 | a0001c0007t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.291-4721C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456354 | |||||||
chr3:66456450 | G | C | 68 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0002c0001t0001g0047 others(65): Show |
68 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.291-4817C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456450 | |||||||
chr3:66456537 | C | T | 234 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.291-4904G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456537 | |||||||
chr3:66456572 | T | TA | 58 | a0001c0002t0001g0049 a0001c0002t0001g0076 a0001c0002t0001g0094 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.291-4940dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456572 | |||||||
chr3:66456572 | TA | T | 69 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0070 others(66): Show |
69 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.291-4940delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456572 | |||||||
chr3:66456578 | A | AG | 8 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(5): Show |
8 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.291-4946_291-4945i others(3): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456578 | |||||||
chr3:66456729 | T | C | 2 | a0002c0001t0001g0084 a0002c0001t0001g0086 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.291-5096A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456729 | |||||||
chr3:66456745 | T | C | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.291-5112A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456745 | |||||||
chr3:66456859 | T | G | 1 | a0013c0042t0010g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.291-5226A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456859 | |||||||
chr3:66456998 | G | A | 4 | a0003c0005t0001g0028 a0005c0004t0006g0220 a0005c0004t0006g0221 others(1): Show |
4 | HG02630.hp2 HG03098.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-5365C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456998 | |||||||
chr3:66457018 | A | G | 131 | a0001c0002t0001g0049 a0001c0002t0001g0053 a0001c0002t0001g0056 others(128): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.291-5385T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457018 | |||||||
chr3:66457020 | G | A | 63 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(60): Show |
64 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.291-5387C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457020 | |||||||
chr3:66457158 | A | G | 3 | a0009c0015t0002g0032 a0009c0015t0002g0033 a0009c0015t0002g0034 |
3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.290+5280T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457158 | |||||||
chr3:66457167 | T | C | 8 | a0001c0007t0002g0079 a0001c0007t0002g0099 a0001c0014t0010g0125 others(5): Show |
8 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.290+5271A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457167 | |||||||
chr3:66457340 | T | C | 1 | a0002c0001t0001g0146 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.290+5098A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457340 | |||||||
chr3:66457525 | C | A | 4 | a0008c0008t0001g0038 a0008c0008t0003g0252 a0008c0008t0003g0256 others(1): Show |
4 | HG02451.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+4913G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457525 | |||||||
chr3:66457566 | T | C | 22 | a0001c0002t0001g0131 a0005c0004t0001g0018 a0006c0009t0004g0224 others(19): Show |
22 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.290+4872A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457566 | |||||||
chr3:66457580 | G | A | 1 | a0008c0033t0001g0027 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.290+4858C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457580 | |||||||
chr3:66457635 | G | T | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.290+4803C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457635 | |||||||
chr3:66457658 | A | C | 4 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0003c0010t0004g0229 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+4780T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457658 | |||||||
chr3:66457685 | T | C | 4 | a0003c0005t0001g0028 a0005c0004t0006g0220 a0005c0004t0006g0221 others(1): Show |
4 | HG02630.hp2 HG03098.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+4753A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457685 | |||||||
chr3:66457708 | G | A | 62 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(59): Show |
63 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.290+4730C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457708 | |||||||
chr3:66458219 | G | A | 1 | a0020c0046t0010g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.290+4219C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458219 | |||||||
chr3:66458272 | T | C | 1 | a0007c0006t0005g0230 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.290+4166A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458272 | |||||||
chr3:66458339 | C | A | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.290+4099G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458339 | |||||||
chr3:66458381 | AGAAAATG others(17): Show |
A | 4 | a0008c0008t0001g0038 a0008c0008t0003g0252 a0008c0008t0003g0256 others(1): Show |
4 | HG02451.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+4033_290+4056d others(26): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458381 | |||||||
chr3:66458421 | G | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.290+4017C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458421 | |||||||
chr3:66458520 | G | A | 3 | a0001c0014t0011g0058 a0001c0014t0011g0119 a0001c0014t0028g0120 |
3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.290+3918C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458520 | |||||||
chr3:66458632 | G | A | 4 | a0008c0008t0001g0038 a0008c0008t0003g0252 a0008c0008t0003g0256 others(1): Show |
4 | HG02451.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+3806C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458632 | |||||||
chr3:66458729 | A | G | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.290+3709T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458729 | |||||||
chr3:66458833 | A | G | 1 | a0014c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.290+3605T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458833 | |||||||
chr3:66458909 | T | C | 241 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.290+3529A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458909 | |||||||
chr3:66458931 | C | G | 68 | a0001c0002t0001g0051 a0001c0002t0001g0137 a0002c0001t0001g0047 others(65): Show |
68 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.290+3507G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458931 | |||||||
chr3:66458987 | C | A | 1 | a0004c0003t0002g0100 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.290+3451G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458987 | |||||||
chr3:66459014 | C | CA | 151 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0056 others(148): Show |
151 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.290+3423dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66459014 | |||||||
chr3:66459014 | C | CAA | 4 | a0003c0005t0003g0001 a0003c0005t0003g0209 a0003c0005t0003g0211 others(1): Show |
5 | NA18966.hp2 NA18986.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.290+3422_290+3423d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66459014 | |||||||
chr3:66459160 | C | A | 3 | a0009c0013t0001g0041 a0009c0013t0002g0042 a0009c0013t0002g0044 |
3 | NA18991.hp2 NA19000.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.290+3278G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66459160 | |||||||
chr3:66459444 | G | C | 172 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(169): Show |
173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.290+2994C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66459444 | |||||||
chr3:66459628 | T | C | 4 | a0008c0008t0003g0252 a0008c0008t0003g0256 a0011c0030t0027g0021 others(1): Show |
4 | HG02145.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+2810A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66459628 | |||||||
chr3:66459715 | A | G | 6 | a0001c0007t0002g0194 a0002c0001t0001g0059 a0003c0012t0001g0040 others(3): Show |
6 | HG01255.hp1 HG02165.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+2723T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66459715 | |||||||
chr3:66459950 | C | G | 2 | a0011c0030t0027g0021 a0026c0032t0007g0046 |
2 | HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.290+2488G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66459950 | |||||||
chr3:66460071 | T | C | 6 | a0001c0007t0002g0194 a0003c0012t0001g0040 a0008c0008t0025g0043 others(3): Show |
6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+2367A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66460071 | |||||||
chr3:66460074 | C | T | 1 | a0004c0003t0002g0100 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.290+2364G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66460074 | |||||||
chr3:66460075 | G | A | 6 | a0001c0007t0002g0194 a0003c0012t0001g0040 a0008c0008t0025g0043 others(3): Show |
6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+2363C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66460075 | |||||||
chr3:66460205 | T | C | 36 | a0001c0002t0001g0162 a0001c0007t0002g0124 a0001c0007t0002g0154 others(33): Show |
37 | HG01074.hp2 HG01099.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.290+2233A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66460205 | |||||||
chr3:66460421 | C | T | 230 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(227): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.290+2017G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66460421 | |||||||
chr3:66460653 | G | C | 6 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(3): Show |
6 | HG02818.hp1 HG02818.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+1785C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66460653 | |||||||
chr3:66460831 | G | T | 3 | a0003c0012t0018g0008 a0005c0004t0021g0006 a0033c0034t0019g0007 |
3 | HG02886.hp2 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.290+1607C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66460831 | |||||||
chr3:66460868 | G | A | 5 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(2): Show |
5 | HG02818.hp1 HG02818.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+1570C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66460868 | |||||||
chr3:66461261 | C | T | 11 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(8): Show |
11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.290+1177G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66461261 | |||||||
chr3:66461356 | C | T | 10 | a0001c0002t0001g0162 a0001c0007t0002g0124 a0001c0007t0002g0154 others(7): Show |
10 | HG01074.hp2 HG01099.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.290+1082G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66461356 | |||||||
chr3:66461666 | T | G | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.290+772A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66461666 | |||||||
chr3:66461691 | T | C | 3 | a0004c0003t0002g0080 a0016c0050t0023g0081 a0025c0047t0030g0153 |
3 | HG00099.hp1 HG01515.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.290+747A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66461691 | |||||||
chr3:66461725 | T | A | 1 | a0001c0002t0001g0103 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.290+713A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66461725 | |||||||
chr3:66461822 | T | A | 1 | a0001c0002t0001g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.290+616A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66461822 | |||||||
chr3:66461949 | G | C | 254 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.290+489C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66461949 | |||||||
chr3:66462001 | T | C | 1 | a0005c0004t0008g0254 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.290+437A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66462001 | |||||||
chr3:66462015 | C | A | 5 | a0003c0012t0001g0040 a0008c0008t0025g0043 a0009c0013t0001g0041 others(2): Show |
5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.290+423G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66462015 | |||||||
chr3:66462020 | A | C | 173 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.290+418T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66462020 | |||||||
chr3:66462041 | C | T | 5 | a0003c0012t0001g0040 a0008c0008t0025g0043 a0009c0013t0001g0041 others(2): Show |
5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.290+397G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66462041 | |||||||
chr3:66462810 | G | GGTGTCCT others(19): Show |
1 | a0002c0048t0001g0098 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.219-302_219-301ins others(26): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66462810 | |||||||
chr3:66462819 | G | A | 7 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0004c0003t0002g0088 others(4): Show |
7 | HG02280.hp1 HG02486.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-310C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66462819 | |||||||
chr3:66463012 | T | C | 9 | a0001c0002t0001g0178 a0001c0014t0010g0186 a0002c0001t0001g0170 others(6): Show |
9 | HG00738.hp1 HG01433.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-503A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66463012 | |||||||
chr3:66463416 | T | G | 4 | a0003c0012t0018g0008 a0003c0036t0034g0203 a0005c0004t0021g0006 others(1): Show |
4 | HG02572.hp1 HG02886.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-907A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66463416 | |||||||
chr3:66463523 | G | T | 187 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(184): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.219-1014C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66463523 | |||||||
chr3:66463650 | C | T | 4 | a0003c0012t0014g0233 a0003c0012t0014g0236 a0006c0009t0004g0232 others(1): Show |
4 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-1141G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66463650 | |||||||
chr3:66463770 | T | C | 1 | a0002c0001t0001g0109 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.219-1261A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66463770 | |||||||
chr3:66463876 | A | T | 3 | a0005c0004t0006g0238 a0005c0004t0006g0239 a0005c0004t0006g0240 |
3 | HG01099.hp1 HG01358.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.219-1367T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66463876 | |||||||
chr3:66463975 | G | A | 1 | a0003c0005t0001g0039 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.219-1466C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66463975 | |||||||
chr3:66464036 | T | C | 2 | a0008c0033t0001g0027 a0009c0013t0002g0024 |
2 | HG01256.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.219-1527A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464036 | |||||||
chr3:66464043 | G | T | 45 | a0001c0002t0001g0162 a0001c0007t0002g0124 a0001c0007t0002g0154 others(42): Show |
46 | HG01074.hp2 HG01099.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.219-1534C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464043 | |||||||
chr3:66464213 | C | T | 169 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.219-1704G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464213 | |||||||
chr3:66464233 | T | C | 2 | a0001c0002t0001g0113 a0001c0007t0001g0118 |
2 | HG00280.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.219-1724A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464233 | |||||||
chr3:66464505 | T | TA | 217 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(214): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.219-1997dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464505 | |||||||
chr3:66464505 | T | TAA | 15 | a0001c0002t0001g0178 a0001c0007t0002g0194 a0002c0001t0001g0123 others(12): Show |
15 | HG01255.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.219-1998_219-1997d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464505 | |||||||
chr3:66464567 | C | T | 7 | a0001c0023t0002g0067 a0001c0023t0002g0082 a0004c0003t0002g0088 others(4): Show |
7 | HG02280.hp1 HG02486.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-2058G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464567 | |||||||
chr3:66464648 | T | C | 6 | a0001c0007t0002g0194 a0003c0012t0001g0040 a0008c0008t0025g0043 others(3): Show |
6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-2139A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464648 | |||||||
chr3:66464657 | G | C | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-2148C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464657 | |||||||
chr3:66464845 | T | C | 16 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(13): Show |
16 | HG02572.hp1 HG02630.hp2 HG02818.hp1 others(13): Show |
intron_variant | MODIFIER | c.219-2336A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464845 | |||||||
chr3:66465251 | A | G | 2 | a0004c0003t0001g0142 a0004c0003t0002g0057 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.219-2742T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465251 | |||||||
chr3:66465357 | A | AT | 44 | a0001c0002t0001g0162 a0001c0007t0002g0124 a0001c0007t0002g0154 others(41): Show |
45 | HG01074.hp2 HG01099.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-2849dupA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465357 | |||||||
chr3:66465357 | A | ATT | 7 | a0001c0007t0002g0161 a0003c0005t0001g0028 a0003c0005t0001g0039 others(4): Show |
7 | HG01358.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-2850_219-2849d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465357 | |||||||
chr3:66465357 | AT | A | 141 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(138): Show |
141 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.219-2849delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465357 | |||||||
chr3:66465357 | ATT | A | 11 | a0001c0002t0001g0078 a0001c0002t0031g0068 a0001c0007t0001g0118 others(8): Show |
11 | HG00099.hp2 HG00280.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-2850_219-2849d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465357 | |||||||
chr3:66465392 | C | T | 4 | a0003c0012t0014g0233 a0003c0012t0014g0236 a0006c0009t0004g0232 others(1): Show |
4 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-2883G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465392 | |||||||
chr3:66465457 | G | A | 41 | a0001c0002t0001g0162 a0001c0007t0002g0124 a0001c0007t0002g0154 others(38): Show |
42 | HG01074.hp2 HG01099.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.219-2948C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465457 | |||||||
chr3:66465605 | A | T | 9 | a0001c0007t0002g0194 a0003c0012t0001g0040 a0008c0008t0025g0043 others(6): Show |
9 | HG01255.hp1 HG02165.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-3096T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465605 | |||||||
chr3:66465683 | A | C | 40 | a0001c0002t0001g0162 a0001c0007t0002g0124 a0001c0007t0002g0154 others(37): Show |
41 | HG01074.hp2 HG01099.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.219-3174T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465683 | |||||||
chr3:66465790 | C | T | 7 | a0002c0001t0001g0128 a0002c0001t0001g0169 a0002c0001t0015g0002 others(4): Show |
7 | HG01069.hp2 HG02165.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-3281G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465790 | |||||||
chr3:66466021 | T | C | 15 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(12): Show |
15 | HG02572.hp1 HG02630.hp2 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.219-3512A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466021 | |||||||
chr3:66466212 | T | C | 1 | a0004c0053t0002g0197 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.219-3703A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466212 | |||||||
chr3:66466214 | A | G | 1 | a0004c0053t0002g0197 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.219-3705T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466214 | |||||||
chr3:66466215 | G | A | 1 | a0008c0008t0003g0252 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.219-3706C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466215 | |||||||
chr3:66466310 | T | C | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-3801A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466310 | |||||||
chr3:66466380 | T | C | 1 | a0009c0013t0002g0024 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.219-3871A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466380 | |||||||
chr3:66466625 | A | G | 1 | a0009c0013t0002g0024 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.219-4116T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466625 | |||||||
chr3:66466740 | T | C | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.219-4231A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466740 | |||||||
chr3:66466934 | T | C | 2 | a0004c0003t0001g0142 a0004c0003t0002g0057 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.219-4425A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466934 | |||||||
chr3:66467058 | C | G | 13 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0094 others(10): Show |
13 | HG00544.hp1 HG00609.hp2 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.219-4549G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467058 | |||||||
chr3:66467206 | G | A | 1 | a0005c0004t0007g0016 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.219-4697C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467206 | |||||||
chr3:66467246 | C | T | 228 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.219-4737G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467246 | |||||||
chr3:66467357 | A | AT | 19 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0094 others(16): Show |
19 | HG01099.hp1 HG01192.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.219-4849dupA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467357 | |||||||
chr3:66467357 | AT | A | 135 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0056 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.219-4849delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467357 | |||||||
chr3:66467357 | ATT | A | 5 | a0004c0003t0039g0262 a0007c0006t0009g0014 a0008c0033t0001g0027 others(2): Show |
5 | HG01256.hp2 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-4850_219-4849d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467357 | |||||||
chr3:66467430 | G | A | 8 | a0003c0005t0001g0028 a0003c0012t0018g0008 a0003c0036t0034g0203 others(5): Show |
8 | HG01256.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.219-4921C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467430 | |||||||
chr3:66467446 | G | A | 1 | a0003c0005t0001g0037 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.219-4937C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467446 | |||||||
chr3:66467563 | G | A | 1 | a0001c0007t0002g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.219-5054C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467563 | |||||||
chr3:66467572 | A | G | 11 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(8): Show |
11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-5063T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467572 | |||||||
chr3:66467582 | T | C | 11 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(8): Show |
11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-5073A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467582 | |||||||
chr3:66467597 | G | A | 6 | a0001c0007t0002g0194 a0003c0012t0001g0040 a0008c0008t0025g0043 others(3): Show |
6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-5088C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467597 | |||||||
chr3:66467611 | T | G | 1 | a0004c0053t0002g0197 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.219-5102A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467611 | |||||||
chr3:66467615 | C | A | 1 | a0004c0053t0002g0197 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.219-5106G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467615 | |||||||
chr3:66467643 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.219-5134C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467643 | |||||||
chr3:66467652 | C | T | 11 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(8): Show |
11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-5143G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467652 | |||||||
chr3:66467719 | T | C | 230 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(227): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.219-5210A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467719 | |||||||
chr3:66467744 | A | G | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-5235T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467744 | |||||||
chr3:66467896 | A | G | 211 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(208): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.219-5387T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467896 | |||||||
chr3:66467959 | T | C | 6 | a0001c0007t0002g0194 a0003c0012t0001g0040 a0008c0008t0025g0043 others(3): Show |
6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-5450A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467959 | |||||||
chr3:66468014 | T | G | 34 | a0001c0002t0001g0162 a0001c0007t0002g0124 a0001c0007t0002g0154 others(31): Show |
35 | HG01074.hp2 HG01099.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.219-5505A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468014 | |||||||
chr3:66468114 | T | C | 4 | a0003c0012t0018g0008 a0003c0036t0034g0203 a0005c0004t0021g0006 others(1): Show |
4 | HG02572.hp1 HG02886.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-5605A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468114 | |||||||
chr3:66468129 | A | G | 1 | a0001c0002t0001g0076 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.219-5620T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468129 | |||||||
chr3:66468137 | A | T | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-5628T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468137 | |||||||
chr3:66468193 | T | C | 4 | a0006c0009t0004g0225 a0006c0009t0004g0226 a0007c0006t0005g0200 others(1): Show |
4 | HG02970.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-5684A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468193 | |||||||
chr3:66468253 | G | A | 1 | a0007c0006t0009g0035 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.219-5744C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468253 | |||||||
chr3:66468256 | A | G | 1 | a0003c0036t0034g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.219-5747T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468256 | |||||||
chr3:66468294 | T | C | 4 | a0003c0010t0004g0201 a0003c0010t0004g0258 a0003c0010t0004g0260 others(1): Show |
4 | HG02818.hp1 HG02818.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-5785A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468294 | |||||||
chr3:66468348 | G | A | 11 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(8): Show |
11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-5839C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468348 | |||||||
chr3:66468402 | T | C | 17 | a0003c0005t0001g0037 a0003c0010t0002g0010 a0003c0010t0004g0229 others(14): Show |
17 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.219-5893A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468402 | |||||||
chr3:66468416 | G | A | 2 | a0006c0009t0002g0045 a0026c0032t0007g0046 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.219-5907C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468416 | |||||||
chr3:66468483 | A | G | 3 | a0005c0004t0006g0220 a0005c0004t0006g0221 a0005c0004t0006g0222 |
3 | HG02630.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.219-5974T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468483 | |||||||
chr3:66468527 | A | G | 4 | a0006c0009t0004g0225 a0006c0009t0004g0226 a0007c0006t0005g0200 others(1): Show |
4 | HG02970.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-6018T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468527 | |||||||
chr3:66468559 | C | T | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-6050G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468559 | |||||||
chr3:66468993 | G | C | 229 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.219-6484C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468993 | |||||||
chr3:66469385 | G | A | 190 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(187): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.219-6876C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469385 | |||||||
chr3:66469390 | T | C | 15 | a0001c0002t0001g0053 a0001c0002t0001g0056 a0001c0002t0001g0060 others(12): Show |
15 | HG00099.hp2 HG00609.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.219-6881A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469390 | |||||||
chr3:66469440 | T | C | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-6931A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469440 | |||||||
chr3:66469600 | C | A | 11 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(8): Show |
11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-7091G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469600 | |||||||
chr3:66469702 | C | G | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-7193G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469702 | |||||||
chr3:66469824 | C | T | 4 | a0006c0009t0004g0246 a0006c0019t0012g0244 a0006c0019t0012g0245 others(1): Show |
4 | HG01952.hp1 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-7315G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469824 | |||||||
chr3:66469870 | G | C | 6 | a0001c0007t0002g0194 a0003c0012t0001g0040 a0008c0008t0025g0043 others(3): Show |
6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-7361C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469870 | |||||||
chr3:66469901 | C | T | 6 | a0001c0007t0002g0194 a0003c0012t0001g0040 a0008c0008t0025g0043 others(3): Show |
6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-7392G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469901 | |||||||
chr3:66469907 | C | CA | 160 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.219-7399dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469907 | |||||||
chr3:66469907 | C | CAA | 21 | a0001c0002t0001g0070 a0001c0002t0001g0103 a0001c0002t0001g0106 others(18): Show |
21 | HG00735.hp1 HG01891.hp2 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.219-7400_219-7399d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469907 | |||||||
chr3:66469907 | C | CAAA | 40 | a0001c0002t0001g0162 a0001c0007t0002g0124 a0001c0007t0002g0154 others(37): Show |
41 | HG01074.hp2 HG01099.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.219-7401_219-7399d others(5): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469907 | |||||||
chr3:66470126 | G | A | 3 | a0001c0002t0001g0069 a0001c0002t0001g0070 a0013c0042t0010g0083 |
3 | HG01167.hp2 HG03834.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.219-7617C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66470126 | |||||||
chr3:66470382 | A | C | 151 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.219-7873T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66470382 | |||||||
chr3:66470582 | G | T | 1 | a0005c0004t0001g0018 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.219-8073C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66470582 | |||||||
chr3:66470662 | A | G | 10 | a0001c0002t0001g0162 a0001c0007t0002g0124 a0001c0007t0002g0154 others(7): Show |
10 | HG01074.hp2 HG01099.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.219-8153T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66470662 | |||||||
chr3:66470675 | A | C | 1 | a0002c0001t0001g0109 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.219-8166T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66470675 | |||||||
chr3:66470823 | T | C | 1 | a0002c0001t0032g0199 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.219-8314A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66470823 | |||||||
chr3:66470946 | C | A | 1 | a0009c0013t0002g0024 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.219-8437G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66470946 | |||||||
chr3:66470978 | C | A | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-8469G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66470978 | |||||||
chr3:66471001 | T | C | 1 | a0003c0005t0001g0026 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.219-8492A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471001 | |||||||
chr3:66471074 | T | C | 2 | a0008c0033t0001g0027 a0009c0013t0002g0024 |
2 | HG01256.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.219-8565A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471074 | |||||||
chr3:66471190 | C | T | 66 | a0001c0002t0001g0062 a0001c0002t0001g0108 a0001c0002t0001g0117 others(63): Show |
66 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.219-8681G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471190 | |||||||
chr3:66471230 | C | T | 15 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(12): Show |
15 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.219-8721G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471230 | |||||||
chr3:66471324 | T | C | 17 | a0003c0005t0001g0037 a0003c0010t0002g0010 a0003c0010t0004g0229 others(14): Show |
17 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.219-8815A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471324 | |||||||
chr3:66471378 | CT | C | 152 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(149): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.219-8870delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471378 | |||||||
chr3:66471387 | C | T | 1 | a0004c0053t0002g0197 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.219-8878G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471387 | |||||||
chr3:66471447 | G | C | 2 | a0006c0009t0002g0045 a0026c0032t0007g0046 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.219-8938C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471447 | |||||||
chr3:66471995 | G | A | 1 | a0007c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.219-9486C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471995 | |||||||
chr3:66472103 | G | A | 1 | a0002c0001t0001g0164 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.219-9594C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472103 | |||||||
chr3:66472171 | G | C | 2 | a0005c0004t0021g0006 a0033c0034t0019g0007 |
2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.219-9662C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472171 | |||||||
chr3:66472209 | C | T | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-9700G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472209 | |||||||
chr3:66472235 | C | T | 1 | a0002c0001t0001g0149 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.219-9726G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472235 | |||||||
chr3:66472303 | C | CA | 13 | a0001c0007t0002g0124 a0001c0007t0002g0157 a0001c0007t0002g0158 others(10): Show |
14 | HG01074.hp2 HG01123.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-9795dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | |||||||
chr3:66472303 | C | CAA | 8 | a0001c0002t0001g0162 a0001c0007t0002g0154 a0001c0007t0002g0159 others(5): Show |
8 | HG01192.hp2 HG01358.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.219-9796_219-9795d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | |||||||
chr3:66472303 | C | CAAAA | 7 | a0006c0009t0004g0251 a0007c0006t0005g0215 a0007c0006t0005g0219 others(4): Show |
7 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-9798_219-9795d others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | |||||||
chr3:66472303 | CAA | C | 7 | a0003c0005t0001g0028 a0003c0012t0018g0008 a0005c0004t0021g0006 others(4): Show |
7 | HG02886.hp2 HG02970.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-9796_219-9795d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | |||||||
chr3:66472303 | CAAAA | C | 7 | a0001c0002t0001g0178 a0002c0001t0001g0170 a0002c0001t0001g0171 others(4): Show |
7 | HG00738.hp1 HG02055.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-9798_219-9795d others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | |||||||
chr3:66472303 | CAAAAA | C | 32 | a0001c0002t0001g0056 a0001c0002t0001g0073 a0001c0002t0001g0075 others(29): Show |
32 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.219-9799_219-9795d others(7): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | |||||||
chr3:66472303 | CAAAAAA | C | 147 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.219-9800_219-9795d others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | |||||||
chr3:66472303 | CAAAAAAA | C | 9 | a0001c0023t0002g0082 a0002c0001t0001g0188 a0005c0004t0001g0018 others(6): Show |
9 | HG00544.hp1 HG02027.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-9801_219-9795d others(9): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | |||||||
chr3:66472303 | CAAAAAAA others(5): Show |
C | 3 | a0008c0033t0001g0027 a0009c0013t0002g0024 a0014c0020t0035g0208 |
3 | HG01256.hp2 HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-9806_219-9795d others(14): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | |||||||
chr3:66472306 | A | G | 1 | a0033c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.219-9797T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472306 | |||||||
chr3:66472307 | A | G | 1 | a0005c0004t0021g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.219-9798T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472307 | |||||||
chr3:66472332 | A | T | 25 | a0002c0001t0001g0188 a0003c0005t0001g0026 a0003c0005t0001g0039 others(22): Show |
25 | HG00544.hp1 HG00609.hp2 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.219-9823T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472332 | |||||||
chr3:66472333 | A | C | 1 | a0010c0011t0024g0063 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219-9824T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472333 | |||||||
chr3:66472335 | A | C | 1 | a0010c0011t0024g0063 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219-9826T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472335 | |||||||
chr3:66472416 | C | T | 3 | a0001c0002t0001g0103 a0001c0007t0002g0099 a0004c0003t0002g0104 |
3 | HG02735.hp2 HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.219-9907G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472416 | |||||||
chr3:66472439 | C | T | 181 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.219-9930G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472439 | |||||||
chr3:66472676 | C | T | 1 | a0003c0010t0004g0258 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.219-10167G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472676 | |||||||
chr3:66472747 | T | C | 166 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.219-10238A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472747 | |||||||
chr3:66472760 | G | A | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.219-10251C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472760 | |||||||
chr3:66472760 | G | C | 1 | a0001c0002t0001g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.219-10251C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472760 | |||||||
chr3:66472766 | G | A | 195 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(192): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.219-10257C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472766 | |||||||
chr3:66472789 | A | G | 4 | a0006c0009t0004g0246 a0006c0019t0012g0244 a0006c0019t0012g0245 others(1): Show |
4 | HG01952.hp1 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-10280T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472789 | |||||||
chr3:66472880 | C | G | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-10371G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472880 | |||||||
chr3:66473022 | C | T | 1 | a0004c0003t0002g0097 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.219-10513G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473022 | |||||||
chr3:66473039 | T | C | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.219-10530A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473039 | |||||||
chr3:66473269 | A | C | 1 | a0009c0013t0002g0024 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.219-10760T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473269 | |||||||
chr3:66473509 | T | C | 1 | a0003c0012t0001g0040 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.219-11000A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473509 | |||||||
chr3:66473538 | C | T | 1 | a0004c0003t0002g0152 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.219-11029G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473538 | |||||||
chr3:66473657 | T | C | 5 | a0003c0012t0001g0040 a0008c0008t0025g0043 a0009c0013t0001g0041 others(2): Show |
5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-11148A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473657 | |||||||
chr3:66473681 | G | A | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-11172C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473681 | |||||||
chr3:66473720 | T | C | 1 | a0005c0004t0006g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.219-11211A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473720 | |||||||
chr3:66473819 | A | T | 224 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.219-11310T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473819 | |||||||
chr3:66473846 | G | C | 1 | a0004c0003t0002g0152 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.219-11337C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473846 | |||||||
chr3:66473989 | A | G | 16 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0094 others(13): Show |
16 | HG00544.hp1 HG00609.hp2 HG02965.hp2 others(13): Show |
intron_variant | MODIFIER | c.219-11480T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473989 | |||||||
chr3:66474181 | T | C | 1 | a0004c0003t0026g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.219-11672A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474181 | |||||||
chr3:66474293 | C | T | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.219-11784G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474293 | |||||||
chr3:66474347 | CT | C | 14 | a0001c0023t0002g0082 a0003c0005t0001g0039 a0003c0010t0004g0201 others(11): Show |
14 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-11839delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474347 | |||||||
chr3:66474347 | CTT | C | 11 | a0002c0001t0001g0188 a0003c0005t0001g0026 a0005c0004t0001g0018 others(8): Show |
11 | HG00544.hp1 HG00609.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-11840_219-1183 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474347 | |||||||
chr3:66474440 | G | C | 2 | a0001c0002t0001g0074 a0001c0002t0001g0075 |
2 | HG01192.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.219-11931C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474440 | |||||||
chr3:66474545 | C | T | 1 | a0001c0007t0002g0099 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.219-12036G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474545 | |||||||
chr3:66474579 | C | T | 5 | a0003c0012t0001g0040 a0008c0008t0025g0043 a0009c0013t0001g0041 others(2): Show |
5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-12070G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474579 | |||||||
chr3:66474597 | C | T | 3 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0094 |
3 | NA18943.hp1 NA18988.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.219-12088G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474597 | |||||||
chr3:66474598 | G | A | 1 | a0007c0006t0005g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.219-12089C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474598 | |||||||
chr3:66474760 | C | T | 1 | a0003c0036t0034g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.219-12251G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474760 | |||||||
chr3:66474816 | G | C | 1 | a0003c0005t0003g0241 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.219-12307C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474816 | |||||||
chr3:66474874 | T | C | 5 | a0003c0012t0001g0040 a0008c0008t0025g0043 a0009c0013t0001g0041 others(2): Show |
5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-12365A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474874 | |||||||
chr3:66474878 | T | C | 12 | a0001c0002t0001g0053 a0001c0002t0001g0060 a0001c0002t0001g0061 others(9): Show |
12 | HG00099.hp2 HG00609.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.219-12369A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474878 | |||||||
chr3:66474969 | G | A | 196 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(193): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.219-12460C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474969 | |||||||
chr3:66474999 | G | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.219-12490C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474999 | |||||||
chr3:66475001 | G | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.219-12492C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475001 | |||||||
chr3:66475055 | C | T | 1 | a0001c0002t0001g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.219-12546G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475055 | |||||||
chr3:66475099 | T | C | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-12590A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475099 | |||||||
chr3:66475274 | T | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.219-12765A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475274 | |||||||
chr3:66475389 | A | C | 17 | a0001c0002t0001g0049 a0001c0002t0001g0103 a0001c0007t0002g0099 others(14): Show |
17 | HG00544.hp2 HG02071.hp2 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.219-12880T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475389 | |||||||
chr3:66475476 | A | T | 15 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0094 others(12): Show |
15 | HG00544.hp1 HG00609.hp2 HG02965.hp2 others(12): Show |
intron_variant | MODIFIER | c.219-12967T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475476 | |||||||
chr3:66475539 | T | C | 169 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.219-13030A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475539 | |||||||
chr3:66475587 | G | A | 2 | a0003c0012t0018g0008 a0007c0006t0005g0223 |
2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.219-13078C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475587 | |||||||
chr3:66475595 | G | A | 6 | a0001c0007t0002g0194 a0003c0012t0001g0040 a0008c0008t0025g0043 others(3): Show |
6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-13086C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475595 | |||||||
chr3:66475697 | G | A | 222 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.219-13188C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475697 | |||||||
chr3:66475750 | C | G | 2 | a0004c0003t0002g0088 a0004c0003t0002g0089 |
2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.219-13241G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475750 | |||||||
chr3:66475751 | G | C | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.219-13242C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475751 | |||||||
chr3:66475933 | A | G | 6 | a0001c0007t0002g0194 a0003c0012t0001g0040 a0008c0008t0025g0043 others(3): Show |
6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-13424T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475933 | |||||||
chr3:66475993 | G | A | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.219-13484C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475993 | |||||||
chr3:66476013 | T | C | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-13504A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66476013 | |||||||
chr3:66476155 | T | C | 1 | a0001c0002t0001g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.219-13646A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66476155 | |||||||
chr3:66476178 | G | A | 179 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(176): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.219-13669C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66476178 | |||||||
chr3:66476981 | G | C | 11 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(8): Show |
11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-14472C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66476981 | |||||||
chr3:66477234 | GT | G | 209 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(206): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.219-14726delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66477234 | |||||||
chr3:66477396 | TG | T | 15 | a0003c0005t0003g0001 a0003c0005t0003g0209 a0003c0005t0003g0210 others(12): Show |
16 | HG02040.hp2 HG02486.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.219-14888delC | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66477396 | |||||||
chr3:66477856 | A | T | 190 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(187): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.219-15347T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66477856 | |||||||
chr3:66477857 | C | CA | 190 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(187): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.219-15349_219-1534 others(5): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66477857 | |||||||
chr3:66477858 | T | A | 190 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(187): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.219-15349A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66477858 | |||||||
chr3:66477860 | C | T | 190 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(187): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.219-15351G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66477860 | |||||||
chr3:66478032 | G | A | 1 | a0007c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.219-15523C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478032 | |||||||
chr3:66478159 | C | T | 24 | a0003c0005t0001g0028 a0003c0005t0001g0039 a0003c0010t0004g0201 others(21): Show |
24 | HG01256.hp2 HG02165.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.219-15650G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478159 | |||||||
chr3:66478160 | G | A | 1 | a0001c0002t0001g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.219-15651C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478160 | |||||||
chr3:66478279 | A | G | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.219-15770T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478279 | |||||||
chr3:66478320 | T | C | 2 | a0008c0033t0001g0027 a0009c0013t0002g0024 |
2 | HG01256.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.219-15811A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478320 | |||||||
chr3:66478350 | G | A | 1 | a0004c0003t0002g0105 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.219-15841C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478350 | |||||||
chr3:66478378 | G | A | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-15869C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478378 | |||||||
chr3:66478501 | C | A | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.219-15992G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478501 | |||||||
chr3:66478773 | T | C | 3 | a0003c0012t0018g0008 a0005c0004t0021g0006 a0033c0034t0019g0007 |
3 | HG02886.hp2 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.219-16264A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478773 | |||||||
chr3:66479101 | C | T | 2 | a0008c0033t0001g0027 a0009c0013t0002g0024 |
2 | HG01256.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.219-16592G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479101 | |||||||
chr3:66479207 | C | T | 15 | a0003c0005t0003g0001 a0003c0005t0003g0209 a0003c0005t0003g0210 others(12): Show |
16 | HG02040.hp2 HG02486.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.219-16698G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479207 | |||||||
chr3:66479263 | A | G | 4 | a0003c0012t0014g0233 a0003c0012t0014g0236 a0006c0009t0004g0232 others(1): Show |
4 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-16754T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479263 | |||||||
chr3:66479308 | T | C | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-16799A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479308 | |||||||
chr3:66479310 | C | G | 5 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(2): Show |
5 | HG02818.hp1 HG02818.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-16801G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479310 | |||||||
chr3:66479342 | G | C | 1 | a0002c0001t0001g0147 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.219-16833C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479342 | |||||||
chr3:66479716 | G | A | 13 | a0003c0005t0001g0039 a0003c0010t0004g0201 a0003c0010t0004g0257 others(10): Show |
13 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.219-17207C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479716 | |||||||
chr3:66479849 | T | A | 192 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(189): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.219-17340A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479849 | |||||||
chr3:66479859 | G | A | 11 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(8): Show |
11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-17350C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479859 | |||||||
chr3:66479880 | A | G | 153 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.219-17371T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479880 | |||||||
chr3:66480010 | A | G | 20 | a0003c0005t0001g0037 a0003c0010t0002g0010 a0003c0010t0004g0229 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.219-17501T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66480010 | |||||||
chr3:66480040 | C | T | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-17531G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66480040 | |||||||
chr3:66480089 | A | T | 166 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.219-17580T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66480089 | |||||||
chr3:66480447 | T | C | 19 | a0003c0005t0001g0037 a0003c0010t0002g0010 a0003c0010t0004g0229 others(16): Show |
19 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.219-17938A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66480447 | |||||||
chr3:66480577 | C | T | 13 | a0003c0005t0001g0039 a0003c0010t0004g0201 a0003c0010t0004g0257 others(10): Show |
13 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.219-18068G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66480577 | |||||||
chr3:66480672 | C | T | 45 | a0001c0002t0001g0062 a0001c0002t0001g0108 a0001c0002t0001g0131 others(42): Show |
45 | HG00558.hp1 HG00621.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-18163G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66480672 | |||||||
chr3:66480881 | G | A | 2 | a0002c0018t0001g0175 a0002c0022t0001g0176 |
2 | NA18747.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.219-18372C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66480881 | |||||||
chr3:66481155 | T | A | 1 | a0012c0017t0002g0015 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.219-18646A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481155 | |||||||
chr3:66481249 | C | A | 1 | a0001c0007t0002g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.219-18740G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481249 | |||||||
chr3:66481270 | C | A | 1 | a0008c0008t0001g0020 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.219-18761G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481270 | |||||||
chr3:66481364 | G | C | 3 | a0009c0015t0002g0032 a0009c0015t0002g0033 a0009c0015t0002g0034 |
3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.218+18826C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481364 | |||||||
chr3:66481442 | C | T | 158 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.218+18748G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481442 | |||||||
chr3:66481460 | G | C | 4 | a0002c0001t0001g0170 a0002c0001t0001g0171 a0002c0001t0001g0172 others(1): Show |
4 | HG00738.hp1 HG02723.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+18730C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481460 | |||||||
chr3:66481520 | T | TAC | 20 | a0003c0005t0001g0037 a0003c0010t0002g0010 a0003c0010t0004g0229 others(17): Show |
20 | HG00735.hp1 HG01243.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.218+18668_218+1866 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481520 | |||||||
chr3:66481520 | TAC | T | 5 | a0003c0005t0001g0028 a0005c0004t0021g0006 a0008c0033t0001g0027 others(2): Show |
5 | HG01256.hp2 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+18668_218+1866 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481520 | |||||||
chr3:66481520 | TACAC | T | 11 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(8): Show |
11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.218+18666_218+1866 others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481520 | |||||||
chr3:66481691 | C | T | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.218+18499G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481691 | |||||||
chr3:66481835 | C | T | 4 | a0005c0004t0021g0006 a0008c0033t0001g0027 a0009c0013t0002g0024 others(1): Show |
4 | HG01256.hp2 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+18355G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481835 | |||||||
chr3:66482245 | T | C | 6 | a0003c0012t0017g0004 a0005c0004t0021g0006 a0007c0006t0020g0005 others(3): Show |
6 | HG01256.hp2 HG02886.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+17945A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66482245 | |||||||
chr3:66482342 | A | G | 2 | a0002c0048t0001g0098 a0004c0003t0002g0097 |
2 | NA19056.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.218+17848T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66482342 | |||||||
chr3:66482387 | G | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.218+17803C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66482387 | |||||||
chr3:66482720 | T | C | 1 | a0002c0001t0001g0121 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.218+17470A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66482720 | |||||||
chr3:66482754 | T | C | 165 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.218+17436A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66482754 | |||||||
chr3:66482831 | A | G | 4 | a0005c0004t0021g0006 a0008c0033t0001g0027 a0009c0013t0002g0024 others(1): Show |
4 | HG01256.hp2 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+17359T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66482831 | |||||||
chr3:66482841 | T | C | 2 | a0016c0050t0023g0081 a0025c0047t0030g0153 |
2 | HG01515.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.218+17349A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66482841 | |||||||
chr3:66483144 | C | G | 17 | a0003c0005t0001g0039 a0003c0010t0004g0201 a0003c0010t0004g0257 others(14): Show |
17 | HG02451.hp1 HG02630.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.218+17046G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483144 | |||||||
chr3:66483160 | T | C | 17 | a0003c0005t0001g0039 a0003c0010t0004g0201 a0003c0010t0004g0257 others(14): Show |
17 | HG02451.hp1 HG02630.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.218+17030A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483160 | |||||||
chr3:66483264 | C | G | 16 | a0003c0005t0001g0039 a0003c0010t0004g0201 a0003c0010t0004g0257 others(13): Show |
16 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.218+16926G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483264 | |||||||
chr3:66483354 | C | T | 23 | a0001c0007t0002g0194 a0003c0005t0001g0039 a0003c0010t0004g0201 others(20): Show |
23 | HG01255.hp1 HG02165.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.218+16836G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483354 | |||||||
chr3:66483381 | T | C | 6 | a0001c0007t0002g0194 a0003c0012t0001g0040 a0008c0008t0025g0043 others(3): Show |
6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+16809A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483381 | |||||||
chr3:66483610 | G | A | 1 | a0004c0053t0002g0197 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.218+16580C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483610 | |||||||
chr3:66483788 | C | T | 1 | a0001c0002t0001g0127 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.218+16402G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483788 | |||||||
chr3:66483802 | G | A | 1 | a0007c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.218+16388C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483802 | |||||||
chr3:66483814 | G | A | 1 | a0007c0006t0005g0223 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218+16376C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483814 | |||||||
chr3:66483821 | G | GC | 23 | a0001c0007t0002g0194 a0003c0005t0001g0037 a0003c0010t0002g0010 others(20): Show |
23 | HG00735.hp1 HG01255.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.218+16368dupG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483821 | |||||||
chr3:66483839 | C | G | 25 | a0001c0007t0002g0194 a0003c0005t0001g0039 a0003c0010t0004g0201 others(22): Show |
25 | HG01255.hp1 HG02165.hp1 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.218+16351G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483839 | |||||||
chr3:66483915 | G | C | 1 | a0007c0006t0009g0035 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.218+16275C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483915 | |||||||
chr3:66483967 | G | A | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+16223C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483967 | |||||||
chr3:66484024 | G | C | 1 | a0030c0029t0001g0022 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.218+16166C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484024 | |||||||
chr3:66484120 | T | C | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+16070A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484120 | |||||||
chr3:66484130 | T | C | 19 | a0003c0005t0001g0037 a0003c0010t0002g0010 a0003c0010t0004g0229 others(16): Show |
19 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.218+16060A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484130 | |||||||
chr3:66484212 | T | C | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.218+15978A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484212 | |||||||
chr3:66484229 | C | T | 3 | a0011c0016t0013g0204 a0011c0016t0013g0205 a0011c0016t0013g0206 |
3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.218+15961G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484229 | |||||||
chr3:66484231 | C | T | 20 | a0001c0007t0002g0194 a0003c0005t0001g0039 a0003c0010t0004g0201 others(17): Show |
20 | HG01255.hp1 HG02165.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.218+15959G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484231 | |||||||
chr3:66484337 | C | T | 6 | a0001c0007t0002g0194 a0003c0012t0001g0040 a0008c0008t0025g0043 others(3): Show |
6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+15853G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484337 | |||||||
chr3:66484534 | T | G | 6 | a0001c0007t0002g0194 a0003c0012t0001g0040 a0008c0008t0025g0043 others(3): Show |
6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+15656A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484534 | |||||||
chr3:66484715 | T | C | 12 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(9): Show |
12 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+15475A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484715 | |||||||
chr3:66484779 | G | A | 4 | a0005c0004t0001g0018 a0012c0017t0002g0015 a0012c0017t0002g0019 others(1): Show |
4 | HG00544.hp1 NA18950.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+15411C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484779 | |||||||
chr3:66484841 | C | CA | 6 | a0005c0004t0006g0220 a0005c0004t0006g0221 a0005c0004t0006g0222 others(3): Show |
6 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+15348dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484841 | |||||||
chr3:66484936 | T | C | 5 | a0003c0012t0001g0040 a0008c0008t0025g0043 a0009c0013t0001g0041 others(2): Show |
5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+15254A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484936 | |||||||
chr3:66484974 | T | C | 5 | a0003c0012t0001g0040 a0008c0008t0025g0043 a0009c0013t0001g0041 others(2): Show |
5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+15216A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484974 | |||||||
chr3:66485155 | CA | C | 169 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.218+15034delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485155 | |||||||
chr3:66485155 | CAA | C | 5 | a0002c0001t0001g0126 a0004c0003t0002g0097 a0004c0003t0002g0104 others(2): Show |
5 | HG02735.hp2 HG02886.hp2 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+15033_218+1503 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485155 | |||||||
chr3:66485351 | C | T | 5 | a0003c0012t0001g0040 a0008c0008t0025g0043 a0009c0013t0001g0041 others(2): Show |
5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+14839G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485351 | |||||||
chr3:66485415 | C | T | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+14775G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485415 | |||||||
chr3:66485456 | T | C | 19 | a0003c0005t0001g0037 a0003c0010t0002g0010 a0003c0010t0004g0229 others(16): Show |
19 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.218+14734A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485456 | |||||||
chr3:66485572 | G | A | 3 | a0003c0012t0018g0008 a0005c0004t0021g0006 a0033c0034t0019g0007 |
3 | HG02886.hp2 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.218+14618C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485572 | |||||||
chr3:66485649 | A | G | 4 | a0003c0036t0034g0203 a0006c0035t0033g0207 a0008c0008t0003g0237 others(1): Show |
4 | HG02572.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+14541T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485649 | |||||||
chr3:66485692 | C | G | 3 | a0001c0002t0001g0053 a0001c0002t0001g0060 a0001c0002t0001g0061 |
3 | HG00735.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.218+14498G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485692 | |||||||
chr3:66485900 | A | G | 20 | a0003c0005t0001g0037 a0003c0010t0002g0010 a0003c0010t0004g0229 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.218+14290T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485900 | |||||||
chr3:66485974 | T | C | 3 | a0005c0004t0006g0220 a0005c0004t0006g0221 a0005c0004t0006g0222 |
3 | HG02630.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.218+14216A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485974 | |||||||
chr3:66486002 | C | T | 5 | a0003c0012t0001g0040 a0008c0008t0025g0043 a0009c0013t0001g0041 others(2): Show |
5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+14188G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486002 | |||||||
chr3:66486042 | C | T | 5 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(2): Show |
5 | HG02818.hp1 HG02818.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+14148G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486042 | |||||||
chr3:66486071 | T | G | 1 | a0001c0002t0001g0103 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.218+14119A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486071 | |||||||
chr3:66486153 | A | G | 8 | a0005c0004t0008g0255 a0007c0006t0005g0215 a0007c0006t0005g0219 others(5): Show |
8 | HG01256.hp2 HG01884.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+14037T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486153 | |||||||
chr3:66486292 | T | C | 4 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0094 others(1): Show |
4 | NA18943.hp1 NA18981.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+13898A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486292 | |||||||
chr3:66486355 | G | A | 2 | a0004c0003t0002g0080 a0016c0050t0023g0081 |
2 | HG00099.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.218+13835C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486355 | |||||||
chr3:66486358 | C | G | 17 | a0003c0005t0003g0001 a0003c0005t0003g0209 a0003c0005t0003g0210 others(14): Show |
18 | HG02040.hp2 HG02486.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.218+13832G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486358 | |||||||
chr3:66486359 | T | G | 17 | a0003c0005t0003g0001 a0003c0005t0003g0209 a0003c0005t0003g0210 others(14): Show |
18 | HG02040.hp2 HG02486.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.218+13831A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486359 | |||||||
chr3:66486388 | G | A | 13 | a0002c0001t0001g0188 a0003c0005t0001g0026 a0004c0053t0002g0197 others(10): Show |
13 | HG00544.hp1 HG00609.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+13802C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486388 | |||||||
chr3:66486441 | T | G | 1 | a0004c0003t0002g0104 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.218+13749A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486441 | |||||||
chr3:66486466 | A | C | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.218+13724T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486466 | |||||||
chr3:66486736 | C | T | 17 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(14): Show |
17 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(14): Show |
intron_variant | MODIFIER | c.218+13454G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486736 | |||||||
chr3:66487003 | A | G | 1 | a0007c0006t0005g0215 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.218+13187T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66487003 | |||||||
chr3:66487020 | A | G | 2 | a0005c0004t0008g0255 a0008c0008t0003g0256 |
2 | HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.218+13170T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66487020 | |||||||
chr3:66487118 | A | C | 1 | a0003c0010t0004g0260 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.218+13072T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66487118 | |||||||
chr3:66487187 | A | T | 1 | a0001c0014t0010g0125 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.218+13003T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66487187 | |||||||
chr3:66487353 | TA | T | 22 | a0002c0001t0001g0188 a0003c0005t0001g0026 a0003c0005t0001g0028 others(19): Show |
22 | HG00544.hp1 HG00609.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.218+12836delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66487353 | |||||||
chr3:66487474 | T | C | 1 | a0001c0002t0001g0049 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.218+12716A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66487474 | |||||||
chr3:66488030 | A | G | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+12160T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488030 | |||||||
chr3:66488361 | A | T | 1 | a0007c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.218+11829T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488361 | |||||||
chr3:66488420 | A | G | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.218+11770T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488420 | |||||||
chr3:66488464 | T | TA | 6 | a0002c0001t0001g0164 a0003c0005t0001g0026 a0008c0008t0001g0020 others(3): Show |
6 | HG02145.hp2 HG03927.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+11725dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488464 | |||||||
chr3:66488472 | A | AAAC | 14 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0094 others(11): Show |
14 | HG00544.hp1 HG00609.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+11717_218+1171 others(7): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488472 | |||||||
chr3:66488473 | AC | A | 20 | a0001c0002t0001g0053 a0001c0002t0001g0087 a0001c0002t0001g0117 others(17): Show |
20 | HG00280.hp2 HG00558.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.218+11716delG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488473 | |||||||
chr3:66488474 | C | A | 158 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0056 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.218+11716G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488474 | |||||||
chr3:66488477 | A | C | 4 | a0003c0005t0001g0039 a0008c0008t0001g0038 a0008c0033t0001g0027 others(1): Show |
4 | HG01256.hp2 HG02451.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+11713T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488477 | |||||||
chr3:66488538 | G | A | 1 | a0002c0001t0001g0122 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.218+11652C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488538 | |||||||
chr3:66488810 | T | C | 1 | a0013c0042t0010g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.218+11380A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488810 | |||||||
chr3:66488862 | T | G | 3 | a0005c0004t0006g0238 a0005c0004t0006g0239 a0005c0004t0006g0240 |
3 | HG01099.hp1 HG01358.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.218+11328A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488862 | |||||||
chr3:66488867 | C | G | 1 | a0002c0001t0001g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.218+11323G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488867 | |||||||
chr3:66489026 | C | T | 1 | a0001c0007t0002g0124 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.218+11164G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489026 | |||||||
chr3:66489105 | G | A | 1 | a0003c0036t0034g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.218+11085C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489105 | |||||||
chr3:66489204 | T | C | 160 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.218+10986A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489204 | |||||||
chr3:66489278 | C | A | 1 | a0007c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.218+10912G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489278 | |||||||
chr3:66489358 | C | T | 218 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.218+10832G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489358 | |||||||
chr3:66489382 | T | C | 1 | a0001c0002t0001g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.218+10808A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489382 | |||||||
chr3:66489422 | T | G | 22 | a0001c0002t0001g0113 a0001c0002t0001g0117 a0001c0007t0001g0118 others(19): Show |
22 | HG00280.hp2 HG00558.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.218+10768A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489422 | |||||||
chr3:66489432 | G | A | 11 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(8): Show |
11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.218+10758C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489432 | |||||||
chr3:66489465 | T | C | 6 | a0001c0002t0001g0085 a0001c0002t0001g0087 a0001c0002t0001g0166 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+10725A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489465 | |||||||
chr3:66489525 | A | ATG | 14 | a0003c0005t0003g0001 a0003c0005t0003g0209 a0003c0005t0003g0210 others(11): Show |
15 | HG02040.hp2 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.218+10663_218+1066 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489525 | |||||||
chr3:66489525 | A | ATGTG | 4 | a0003c0005t0003g0241 a0011c0016t0013g0204 a0011c0016t0013g0205 others(1): Show |
4 | HG01070.hp2 HG02486.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+10661_218+1066 others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489525 | |||||||
chr3:66489525 | ATG | A | 4 | a0003c0012t0001g0040 a0009c0013t0001g0041 a0009c0013t0002g0042 others(1): Show |
4 | HG02165.hp1 NA18991.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+10663_218+1066 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489525 | |||||||
chr3:66489525 | ATGTG | A | 3 | a0002c0001t0001g0123 a0002c0001t0001g0191 a0003c0005t0001g0028 |
3 | HG03579.hp2 HG03688.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.218+10661_218+1066 others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489525 | |||||||
chr3:66489525 | ATGTGTG | A | 196 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0056 others(193): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.218+10659_218+1066 others(10): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489525 | |||||||
chr3:66489525 | ATGTGTGT others(3): Show |
A | 1 | a0002c0001t0015g0002 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.218+10655_218+1066 others(14): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489525 | |||||||
chr3:66489525 | ATGTGTGT others(5): Show |
A | 12 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(9): Show |
12 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+10653_218+1066 others(16): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489525 | |||||||
chr3:66489565 | C | G | 2 | a0003c0010t0004g0231 a0006c0009t0004g0224 |
2 | HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.218+10625G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489565 | |||||||
chr3:66489567 | G | C | 2 | a0004c0003t0002g0088 a0004c0003t0002g0089 |
2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.218+10623C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489567 | |||||||
chr3:66489583 | T | TTAAG | 12 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(9): Show |
12 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+10603_218+1060 others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489583 | |||||||
chr3:66489679 | A | G | 1 | a0002c0001t0001g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.218+10511T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489679 | |||||||
chr3:66489684 | T | G | 1 | a0007c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.218+10506A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489684 | |||||||
chr3:66489965 | GCAC | G | 5 | a0003c0012t0017g0004 a0003c0012t0018g0008 a0005c0004t0021g0006 others(2): Show |
5 | HG02886.hp2 HG02976.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+10222_218+1022 others(7): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489965 | |||||||
chr3:66490121 | T | C | 1 | a0007c0006t0005g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.218+10069A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490121 | |||||||
chr3:66490132 | T | C | 1 | a0026c0032t0007g0046 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.218+10058A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490132 | |||||||
chr3:66490192 | C | CTCCAAA | 5 | a0003c0012t0017g0004 a0003c0012t0018g0008 a0005c0004t0021g0006 others(2): Show |
5 | HG02886.hp2 HG02976.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+9992_218+9997d others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490192 | |||||||
chr3:66490422 | T | A | 1 | a0007c0006t0005g0223 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218+9768A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490422 | |||||||
chr3:66490612 | T | A | 8 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(5): Show |
8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+9578A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490612 | |||||||
chr3:66490612 | T | C | 158 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.218+9578A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490612 | |||||||
chr3:66490645 | TA | T | 36 | a0002c0001t0001g0110 a0002c0022t0001g0179 a0003c0005t0001g0028 others(33): Show |
37 | HG00280.hp1 HG01099.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.218+9544delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490645 | |||||||
chr3:66490645 | TAA | T | 204 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(201): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.218+9543_218+9544d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490645 | |||||||
chr3:66490669 | G | A | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.218+9521C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490669 | |||||||
chr3:66490738 | T | C | 33 | a0002c0001t0001g0188 a0003c0005t0001g0026 a0003c0005t0001g0037 others(30): Show |
33 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.218+9452A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490738 | |||||||
chr3:66490748 | A | C | 5 | a0003c0012t0017g0004 a0003c0012t0018g0008 a0005c0004t0021g0006 others(2): Show |
5 | HG02886.hp2 HG02976.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+9442T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490748 | |||||||
chr3:66490958 | T | A | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.218+9232A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490958 | |||||||
chr3:66491024 | G | T | 218 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.218+9166C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491024 | |||||||
chr3:66491058 | G | C | 11 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(8): Show |
11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.218+9132C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491058 | |||||||
chr3:66491084 | G | C | 2 | a0002c0001t0001g0090 a0010c0011t0001g0091 |
2 | NA18939.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.218+9106C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491084 | |||||||
chr3:66491102 | CT | C | 4 | a0003c0005t0001g0039 a0008c0008t0001g0038 a0008c0033t0001g0027 others(1): Show |
4 | HG01256.hp2 HG02451.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+9087delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491102 | |||||||
chr3:66491242 | C | T | 3 | a0002c0001t0001g0109 a0002c0001t0001g0110 a0002c0022t0001g0179 |
3 | HG01243.hp1 HG01981.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.218+8948G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491242 | |||||||
chr3:66491389 | G | A | 11 | a0002c0001t0001g0188 a0003c0005t0001g0026 a0005c0004t0001g0018 others(8): Show |
11 | HG00544.hp1 HG00609.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.218+8801C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491389 | |||||||
chr3:66491558 | C | T | 8 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(5): Show |
8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+8632G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491558 | |||||||
chr3:66491678 | T | TA | 9 | a0001c0007t0002g0194 a0003c0012t0001g0040 a0008c0008t0001g0013 others(6): Show |
9 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.218+8511dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491678 | |||||||
chr3:66491836 | C | T | 1 | a0001c0002t0001g0092 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.218+8354G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491836 | |||||||
chr3:66491838 | T | C | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.218+8352A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491838 | |||||||
chr3:66491951 | A | G | 19 | a0003c0005t0001g0037 a0003c0010t0002g0010 a0003c0010t0004g0229 others(16): Show |
19 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.218+8239T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491951 | |||||||
chr3:66491960 | G | C | 1 | a0030c0029t0001g0022 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.218+8230C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491960 | |||||||
chr3:66491980 | T | C | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+8210A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491980 | |||||||
chr3:66492008 | C | G | 3 | a0005c0004t0006g0220 a0005c0004t0006g0221 a0005c0004t0006g0222 |
3 | HG02630.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.218+8182G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492008 | |||||||
chr3:66492250 | G | C | 1 | a0007c0006t0020g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.218+7940C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492250 | |||||||
chr3:66492336 | T | C | 175 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(172): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.218+7854A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492336 | |||||||
chr3:66492339 | G | T | 2 | a0001c0002t0001g0092 a0001c0002t0001g0093 |
2 | NA18943.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.218+7851C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492339 | |||||||
chr3:66492387 | G | A | 1 | a0002c0001t0001g0169 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.218+7803C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492387 | |||||||
chr3:66492439 | A | G | 22 | a0001c0002t0001g0113 a0001c0002t0001g0117 a0001c0007t0001g0118 others(19): Show |
22 | HG00280.hp2 HG00558.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.218+7751T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492439 | |||||||
chr3:66492456 | C | T | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.218+7734G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492456 | |||||||
chr3:66492468 | C | T | 3 | a0005c0004t0006g0220 a0005c0004t0006g0221 a0005c0004t0006g0222 |
3 | HG02630.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.218+7722G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492468 | |||||||
chr3:66492711 | T | C | 4 | a0002c0001t0001g0170 a0002c0001t0001g0171 a0002c0001t0001g0172 others(1): Show |
4 | HG00738.hp1 HG02723.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+7479A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492711 | |||||||
chr3:66492715 | T | TG | 23 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0094 others(20): Show |
23 | HG00544.hp1 HG00609.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.218+7474_218+7475i others(3): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492715 | |||||||
chr3:66492739 | T | G | 8 | a0003c0012t0001g0040 a0008c0008t0001g0013 a0008c0008t0001g0030 others(5): Show |
8 | HG02165.hp1 HG02523.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+7451A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492739 | |||||||
chr3:66492744 | T | C | 1 | a0019c0038t0003g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.218+7446A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492744 | |||||||
chr3:66492777 | G | A | 201 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(198): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.218+7413C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492777 | |||||||
chr3:66492866 | T | C | 4 | a0008c0008t0025g0043 a0009c0013t0001g0041 a0009c0013t0002g0042 others(1): Show |
4 | HG02523.hp1 NA18991.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+7324A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492866 | |||||||
chr3:66493047 | G | A | 1 | a0010c0011t0007g0174 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.218+7143C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493047 | |||||||
chr3:66493072 | GTCCTCCC | G | 12 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(9): Show |
12 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+7111_218+7117d others(9): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493072 | |||||||
chr3:66493114 | G | T | 201 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(198): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.218+7076C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493114 | |||||||
chr3:66493116 | G | A | 1 | a0001c0040t0001g0096 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.218+7074C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493116 | |||||||
chr3:66493160 | C | T | 201 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(198): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.218+7030G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493160 | |||||||
chr3:66493180 | T | C | 1 | a0012c0017t0002g0023 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.218+7010A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493180 | |||||||
chr3:66493212 | T | A | 3 | a0003c0010t0002g0010 a0007c0006t0009g0011 a0007c0006t0009g0012 |
3 | HG02559.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218+6978A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493212 | |||||||
chr3:66493272 | A | G | 201 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(198): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.218+6918T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493272 | |||||||
chr3:66493337 | T | C | 2 | a0002c0018t0001g0175 a0002c0022t0001g0176 |
2 | NA18747.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.218+6853A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493337 | |||||||
chr3:66493839 | G | A | 216 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.218+6351C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493839 | |||||||
chr3:66493843 | G | A | 2 | a0005c0004t0021g0006 a0033c0034t0019g0007 |
2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.218+6347C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493843 | |||||||
chr3:66493912 | A | G | 1 | a0027c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.218+6278T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493912 | |||||||
chr3:66494008 | G | A | 12 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(9): Show |
12 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+6182C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66494008 | |||||||
chr3:66494108 | A | G | 1 | a0008c0008t0037g0261 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.218+6082T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66494108 | |||||||
chr3:66494325 | C | T | 8 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(5): Show |
8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+5865G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66494325 | |||||||
chr3:66494655 | C | T | 4 | a0003c0005t0001g0039 a0008c0008t0001g0038 a0008c0033t0001g0027 others(1): Show |
4 | HG01256.hp2 HG02451.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+5535G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66494655 | |||||||
chr3:66494975 | T | C | 8 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(5): Show |
8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+5215A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66494975 | |||||||
chr3:66495066 | A | G | 1 | a0003c0036t0034g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.218+5124T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66495066 | |||||||
chr3:66495284 | C | T | 2 | a0006c0009t0002g0045 a0026c0032t0007g0046 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.218+4906G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66495284 | |||||||
chr3:66495426 | G | A | 1 | a0001c0002t0001g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.218+4764C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66495426 | |||||||
chr3:66495664 | C | G | 12 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(9): Show |
12 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+4526G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66495664 | |||||||
chr3:66495764 | T | G | 1 | a0007c0006t0005g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.218+4426A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66495764 | |||||||
chr3:66495787 | C | A | 1 | a0008c0033t0001g0027 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.218+4403G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66495787 | |||||||
chr3:66495946 | G | C | 1 | a0004c0003t0002g0105 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.218+4244C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66495946 | |||||||
chr3:66496121 | T | C | 6 | a0003c0005t0001g0028 a0003c0012t0017g0004 a0003c0012t0018g0008 others(3): Show |
6 | HG02886.hp2 HG02976.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+4069A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496121 | |||||||
chr3:66496222 | G | A | 17 | a0001c0002t0001g0049 a0001c0002t0001g0103 a0001c0007t0002g0099 others(14): Show |
17 | HG00544.hp2 HG02071.hp2 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.218+3968C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496222 | |||||||
chr3:66496276 | T | C | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+3914A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496276 | |||||||
chr3:66496366 | A | G | 1 | a0007c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.218+3824T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496366 | |||||||
chr3:66496526 | G | A | 1 | a0001c0002t0001g0106 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.218+3664C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496526 | |||||||
chr3:66496682 | T | A | 2 | a0003c0005t0003g0216 a0003c0005t0003g0217 |
2 | NA18961.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.218+3508A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496682 | |||||||
chr3:66496710 | C | T | 1 | a0004c0003t0002g0057 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.218+3480G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496710 | |||||||
chr3:66496737 | T | TA | 11 | a0003c0005t0001g0028 a0003c0005t0001g0039 a0003c0012t0017g0004 others(8): Show |
11 | HG01256.hp2 HG02451.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.218+3452dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496737 | |||||||
chr3:66496786 | C | G | 12 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(9): Show |
12 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+3404G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496786 | |||||||
chr3:66497004 | A | C | 12 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(9): Show |
12 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+3186T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497004 | |||||||
chr3:66497011 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.218+3179G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497011 | |||||||
chr3:66497104 | T | C | 1 | a0003c0012t0014g0236 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.218+3086A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497104 | |||||||
chr3:66497211 | T | A | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.218+2979A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497211 | |||||||
chr3:66497372 | A | T | 1 | a0001c0002t0001g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.218+2818T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497372 | |||||||
chr3:66497417 | T | TG | 8 | a0003c0012t0001g0040 a0008c0008t0001g0013 a0008c0008t0001g0030 others(5): Show |
8 | HG02165.hp1 HG02523.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+2772dupC | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497417 | |||||||
chr3:66497674 | A | G | 1 | a0002c0001t0001g0055 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.218+2516T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497674 | |||||||
chr3:66497704 | C | CA | 83 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.218+2485dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497704 | |||||||
chr3:66497704 | C | CAA | 88 | a0001c0002t0001g0108 a0001c0002t0001g0113 a0001c0002t0001g0117 others(85): Show |
88 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.218+2484_218+2485d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497704 | |||||||
chr3:66497704 | C | CAAA | 7 | a0001c0007t0002g0194 a0002c0001t0001g0180 a0002c0001t0001g0183 others(4): Show |
7 | HG01243.hp1 HG01255.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+2483_218+2485d others(5): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497704 | |||||||
chr3:66497704 | C | CAAAA | 6 | a0003c0010t0004g0201 a0003c0010t0004g0260 a0005c0004t0006g0202 others(3): Show |
6 | HG02145.hp2 HG02818.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+2482_218+2485d others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497704 | |||||||
chr3:66497704 | C | CCAAA | 3 | a0005c0004t0006g0221 a0005c0004t0006g0222 a0007c0006t0005g0223 |
3 | HG02630.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.218+2485_218+2486i others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497704 | |||||||
chr3:66497744 | C | G | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+2446G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497744 | |||||||
chr3:66497847 | C | A | 164 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.218+2343G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497847 | |||||||
chr3:66497921 | C | G | 9 | a0003c0010t0004g0229 a0003c0010t0004g0231 a0006c0009t0004g0224 others(6): Show |
9 | HG00735.hp1 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.218+2269G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497921 | |||||||
chr3:66497970 | T | C | 1 | a0001c0014t0010g0186 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.218+2220A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497970 | |||||||
chr3:66497996 | C | T | 8 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(5): Show |
8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+2194G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497996 | |||||||
chr3:66498061 | G | T | 5 | a0003c0012t0014g0233 a0003c0012t0014g0236 a0006c0009t0004g0232 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+2129C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498061 | |||||||
chr3:66498232 | A | C | 1 | a0009c0015t0002g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.218+1958T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498232 | |||||||
chr3:66498377 | C | A | 1 | a0002c0001t0001g0187 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.218+1813G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498377 | |||||||
chr3:66498405 | G | C | 2 | a0006c0009t0002g0045 a0026c0032t0007g0046 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.218+1785C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498405 | |||||||
chr3:66498549 | C | T | 5 | a0003c0012t0017g0004 a0003c0012t0018g0008 a0005c0004t0021g0006 others(2): Show |
5 | HG02886.hp2 HG02976.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+1641G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498549 | |||||||
chr3:66498564 | T | TA | 22 | a0001c0002t0001g0189 a0002c0001t0001g0188 a0002c0001t0001g0191 others(19): Show |
22 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.218+1625dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498564 | |||||||
chr3:66498564 | T | TAA | 7 | a0001c0007t0002g0194 a0003c0010t0004g0231 a0003c0012t0001g0040 others(4): Show |
7 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+1624_218+1625d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498564 | |||||||
chr3:66498564 | TA | T | 8 | a0001c0002t0001g0053 a0002c0001t0001g0052 a0003c0012t0017g0004 others(5): Show |
8 | HG01070.hp1 HG01167.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+1625delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498564 | |||||||
chr3:66498564 | TAA | T | 8 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(5): Show |
8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+1624_218+1625d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498564 | |||||||
chr3:66498634 | C | T | 8 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(5): Show |
8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+1556G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498634 | |||||||
chr3:66498671 | CA | C | 8 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(5): Show |
8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+1518delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498671 | |||||||
chr3:66498680 | T | C | 1 | a0004c0003t0002g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.218+1510A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498680 | |||||||
chr3:66498788 | T | A | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+1402A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498788 | |||||||
chr3:66498818 | C | G | 246 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.218+1372G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498818 | |||||||
chr3:66498851 | G | A | 2 | a0003c0005t0001g0039 a0008c0008t0001g0038 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+1339C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498851 | |||||||
chr3:66498909 | G | T | 4 | a0001c0002t0001g0051 a0002c0001t0001g0195 a0002c0001t0032g0199 others(1): Show |
4 | HG00621.hp1 HG00673.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+1281C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498909 | |||||||
chr3:66498933 | T | G | 2 | a0005c0004t0008g0255 a0008c0008t0003g0256 |
2 | HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.218+1257A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498933 | |||||||
chr3:66498979 | T | G | 4 | a0005c0004t0006g0220 a0005c0004t0006g0221 a0005c0004t0006g0222 others(1): Show |
4 | HG02630.hp2 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+1211A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498979 | |||||||
chr3:66499041 | T | C | 2 | a0004c0003t0039g0262 a0023c0052t0038g0263 |
2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.218+1149A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499041 | |||||||
chr3:66499096 | G | A | 6 | a0001c0007t0002g0194 a0003c0012t0001g0040 a0008c0008t0025g0043 others(3): Show |
6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+1094C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499096 | |||||||
chr3:66499152 | T | G | 1 | a0002c0001t0001g0195 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.218+1038A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499152 | |||||||
chr3:66499162 | T | C | 9 | a0003c0010t0004g0229 a0003c0010t0004g0231 a0006c0009t0004g0224 others(6): Show |
9 | HG00735.hp1 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.218+1028A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499162 | |||||||
chr3:66499179 | A | C | 1 | a0001c0002t0001g0049 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.218+1011T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499179 | |||||||
chr3:66499202 | TAC | T | 236 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.218+986_218+987del others(2): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499202 | |||||||
chr3:66499211 | G | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.218+979C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499211 | |||||||
chr3:66499236 | A | G | 3 | a0003c0010t0002g0010 a0007c0006t0009g0011 a0007c0006t0009g0012 |
3 | HG02559.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218+954T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499236 | |||||||
chr3:66499339 | C | A | 2 | a0004c0053t0002g0197 a0022c0054t0002g0196 |
2 | HG02300.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.218+851G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499339 | |||||||
chr3:66499372 | C | T | 5 | a0003c0012t0017g0004 a0003c0012t0018g0008 a0005c0004t0021g0006 others(2): Show |
5 | HG02886.hp2 HG02976.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+818G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499372 | |||||||
chr3:66499534 | A | C | 8 | a0003c0010t0004g0201 a0003c0010t0004g0257 a0003c0010t0004g0258 others(5): Show |
8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+656T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499534 | |||||||
chr3:66499749 | C | T | 1 | a0007c0006t0005g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.218+441G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499749 | |||||||
chr3:66499800 | A | C | 2 | a0002c0001t0001g0047 a0002c0001t0001g0048 |
2 | HG00544.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.218+390T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499800 | |||||||
chr3:66499893 | C | A | 6 | a0003c0010t0004g0257 a0003c0010t0004g0258 a0003c0010t0004g0260 others(3): Show |
6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+297G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499893 | |||||||
chr3:66500145 | G | A | 1 | a0001c0002t0001g0198 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.218+45C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66500145 |