Item | Value |
---|---|
geneid | 284656 |
ensemblid | ENSG00000183317.17 |
hgncid | 19987 |
symbol | EPHA10 |
name | EPH receptor A10 |
refseq_nuc | NM_001099439.2 |
refseq_prot | NP_001092909.1 |
ensembl_nuc | ENST00000373048.9 |
ensembl_prot | ENSP00000362139.4 |
mane_status | MANE Select |
chr | chr1 |
start | 37715976 |
end | 37765120 |
strand | - |
ver | v1.2 |
region | chr1:37715976-37765120 |
region5000 | chr1:37710976-37770120 |
regionname0 | EPHA10_chr1_37715976_37765120 |
regionname5000 | EPHA10_chr1_37710976_37770120 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1008 | 171 | 32 | 39 | 67 | 6 | 26 | 49 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0002 | 0/0 | 1008 | 84 | 17 | 21 | 38 | 3 | 5 | 30 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0003 | 0/0 | 1008 | 41 | 13 | 2 | 24 | 0 | 2 | 13 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0004 | 0/1 | 1008 | 28 | 12 | 6 | 0 | 6 | 3 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0005 | 0/0 | 1008 | 8 | 1 | 4 | 0 | 0 | 3 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0006 | 0/0 | 1008 | 8 | 0 | 0 | 8 | 0 | 0 | 7 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0007 | 0/0 | 1008 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0008 | 0/0 | 1008 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0009 | 0/0 | 1008 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0010 | 0/0 | 1008 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0011 | 0/0 | 1008 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0012 | 0/0 | 1008 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0013 | 0/0 | 1008 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0014 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0015 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0016 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0017 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0018 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0019 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0020 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0021 | 0/0 | 1008 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0022 | 0/0 | 1008 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0023 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0024 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0025 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0026 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0027 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0028 | 0/0 | 1008 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0029 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0030 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0031 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
a0032 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | METCA others(1003): Show |
chr1 | 37710976 | 37770120 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3024 | 135 | 15 | 33 | 57 | 6 | 23 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0001c0005 | 0/0 | 3024 | 17 | 5 | 3 | 9 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0001c0006 | 0/0 | 3024 | 11 | 9 | 2 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0001c0020 | 0/0 | 3024 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0001c0033 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0001c0036 | 0/0 | 3024 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0001c0037 | 0/0 | 3024 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0001c0040 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0001c0042 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0001c0044 | 0/0 | 3024 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0002c0002 | 0/0 | 3024 | 64 | 7 | 19 | 30 | 3 | 5 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0002c0007 | 0/0 | 3024 | 10 | 2 | 0 | 8 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0002c0011 | 0/0 | 3024 | 6 | 6 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0002c0015 | 0/0 | 3024 | 4 | 2 | 2 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0003c0004 | 0/0 | 3024 | 24 | 10 | 0 | 12 | 0 | 2 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0003c0008 | 0/0 | 3024 | 9 | 3 | 2 | 4 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0003c0013 | 0/0 | 3024 | 6 | 0 | 0 | 6 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0003c0024 | 0/0 | 3024 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0003c0025 | 0/0 | 3024 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0004c0003 | 0/1 | 3024 | 27 | 11 | 6 | 0 | 6 | 3 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0004c0038 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0005c0009 | 0/0 | 3024 | 8 | 1 | 4 | 0 | 0 | 3 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0006c0010 | 0/0 | 3024 | 8 | 0 | 0 | 8 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0007c0012 | 0/0 | 3024 | 6 | 0 | 0 | 6 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0008c0014 | 0/0 | 3024 | 5 | 5 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0009c0017 | 0/0 | 3024 | 3 | 0 | 2 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0010c0016 | 0/0 | 3024 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0011c0018 | 0/0 | 3024 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0012c0021 | 0/0 | 3024 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0013c0019 | 0/0 | 3024 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0014c0048 | 0/0 | 3024 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0015c0031 | 0/0 | 3024 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0016c0043 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0017c0023 | 0/0 | 3024 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0018c0029 | 0/0 | 3024 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0019c0032 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0020c0028 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0021c0045 | 0/0 | 3024 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0022c0039 | 0/0 | 3024 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0023c0027 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0024c0049 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0025c0035 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0026c0034 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0027c0026 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0028c0046 | 0/0 | 3024 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0029c0022 | 0/0 | 3024 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0030c0047 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0031c0041 | 0/0 | 3024 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 | ||
a0032c0030 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | ATGGA others(3019): Show |
chr1 | 37710976 | 37770120 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5477 | 79 | 10 | 20 | 32 | 4 | 12 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0001c0001t0002 | 0/0 | 5477 | 50 | 3 | 13 | 24 | 2 | 8 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0001c0001t0004 | 0/0 | 5477 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0001c0001t0009 | 0/0 | 5476 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5471): Show |
chr1 | 37710976 | 37770120 |
a0001c0001t0013 | 0/0 | 5477 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0001c0001t0017 | 0/0 | 5477 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0001c0005t0004 | 0/0 | 5477 | 13 | 1 | 3 | 9 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0001c0005t0011 | 0/0 | 5477 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0001c0005t0015 | 0/0 | 5477 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0001c0006t0002 | 0/0 | 5477 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0001c0006t0007 | 0/0 | 5476 | 8 | 7 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5471): Show |
chr1 | 37710976 | 37770120 |
a0001c0006t0009 | 0/0 | 5476 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5471): Show |
chr1 | 37710976 | 37770120 |
a0001c0020t0002 | 0/0 | 5477 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0001c0033t0002 | 0/0 | 5477 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0001c0036t0001 | 0/0 | 5477 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0001c0037t0004 | 0/0 | 5477 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0001c0040t0011 | 0/0 | 5477 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0001c0042t0001 | 0/0 | 5477 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0001c0044t0001 | 0/0 | 5477 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0002c0002t0001 | 0/0 | 5477 | 41 | 6 | 12 | 17 | 3 | 3 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0002c0002t0002 | 0/0 | 5477 | 22 | 1 | 6 | 13 | 0 | 2 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0002c0002t0018 | 0/0 | 5477 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0002c0007t0004 | 0/0 | 5477 | 8 | 0 | 0 | 8 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0002c0007t0012 | 0/0 | 5477 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0002c0011t0001 | 0/0 | 5477 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0002c0011t0002 | 0/0 | 5477 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0002c0011t0009 | 0/0 | 5476 | 4 | 4 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5471): Show |
chr1 | 37710976 | 37770120 |
a0002c0015t0007 | 0/0 | 5476 | 4 | 2 | 2 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5471): Show |
chr1 | 37710976 | 37770120 |
a0003c0004t0005 | 0/0 | 5477 | 15 | 6 | 0 | 9 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0003c0004t0006 | 0/0 | 5477 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0003c0004t0008 | 0/0 | 5477 | 8 | 4 | 0 | 2 | 0 | 2 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0003c0008t0006 | 0/0 | 5477 | 8 | 3 | 2 | 3 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0003c0008t0021 | 0/0 | 5477 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0003c0013t0006 | 0/0 | 5477 | 6 | 0 | 0 | 6 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0003c0024t0006 | 0/0 | 5477 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0003c0025t0006 | 0/0 | 5477 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0004c0003t0003 | 0/1 | 5476 | 26 | 10 | 6 | 0 | 6 | 3 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5471): Show |
chr1 | 37710976 | 37770120 |
a0004c0003t0016 | 0/0 | 5476 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5471): Show |
chr1 | 37710976 | 37770120 |
a0004c0038t0003 | 0/0 | 5476 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5471): Show |
chr1 | 37710976 | 37770120 |
a0005c0009t0003 | 0/0 | 5476 | 8 | 1 | 4 | 0 | 0 | 3 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5471): Show |
chr1 | 37710976 | 37770120 |
a0006c0010t0002 | 0/0 | 5477 | 8 | 0 | 0 | 8 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0007c0012t0010 | 0/0 | 5476 | 6 | 0 | 0 | 6 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5471): Show |
chr1 | 37710976 | 37770120 |
a0008c0014t0002 | 0/0 | 5477 | 5 | 5 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0009c0017t0003 | 0/0 | 5476 | 3 | 0 | 2 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5471): Show |
chr1 | 37710976 | 37770120 |
a0010c0016t0005 | 0/0 | 5477 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0011c0018t0014 | 0/0 | 5476 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5471): Show |
chr1 | 37710976 | 37770120 |
a0012c0021t0002 | 0/0 | 5477 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0013c0019t0002 | 0/0 | 5477 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0014c0048t0006 | 0/0 | 5477 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0015c0031t0019 | 0/0 | 5476 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5471): Show |
chr1 | 37710976 | 37770120 |
a0016c0043t0003 | 0/0 | 5476 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5471): Show |
chr1 | 37710976 | 37770120 |
a0017c0023t0006 | 0/0 | 5477 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0018c0029t0006 | 0/0 | 5477 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0019c0032t0002 | 0/0 | 5477 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0020c0028t0022 | 0/0 | 5476 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5471): Show |
chr1 | 37710976 | 37770120 |
a0021c0045t0003 | 0/0 | 5476 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5471): Show |
chr1 | 37710976 | 37770120 |
a0022c0039t0001 | 0/0 | 5477 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0023c0027t0005 | 0/0 | 5477 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0024c0049t0020 | 0/0 | 5477 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0025c0035t0001 | 0/0 | 5477 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0026c0034t0001 | 0/0 | 5477 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0027c0026t0005 | 0/0 | 5477 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0028c0046t0001 | 0/0 | 5477 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0029c0022t0001 | 0/0 | 5477 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0030c0047t0001 | 0/0 | 5477 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0031c0041t0002 | 0/0 | 5477 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
a0032c0030t0002 | 0/0 | 5477 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | GCTAG others(5472): Show |
chr1 | 37710976 | 37770120 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0016 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0009g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0009g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0013g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0013g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0001t0017g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0005t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0005t0004g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0005t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0005t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0005t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0005t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0005t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0005t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0005t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0005t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0005t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0005t0011g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0005t0011g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0005t0015g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0005t0015g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0006t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0006t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0006t0007g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0006t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0006t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0006t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0006t0007g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0006t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0006t0007g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0006t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0006t0009g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0020t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0020t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0033t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0036t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0037t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0040t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0042t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0001c0044t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0002t0018g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0007t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0007t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0007t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0007t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0007t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0007t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0007t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0007t0012g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0007t0012g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0011t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0011t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0011t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0011t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0011t0009g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0011t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0015t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0015t0007g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0015t0007g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0002c0015t0007g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0005g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0005g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0005g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0005g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0006g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0008g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0008g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0008g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0008g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0008g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0008g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0008g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0004t0008g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0008t0006g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0008t0006g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0008t0006g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0008t0006g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0008t0006g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0008t0006g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0008t0006g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0008t0006g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0008t0021g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0013t0006g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0013t0006g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0013t0006g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0013t0006g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0024t0006g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0003c0025t0006g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0223 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0003t0016g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0004c0038t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0005c0009t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0005c0009t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0005c0009t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0005c0009t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0005c0009t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0005c0009t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0005c0009t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0005c0009t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0006c0010t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0006c0010t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0006c0010t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0006c0010t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0006c0010t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0006c0010t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0006c0010t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0006c0010t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0007c0012t0010g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0007c0012t0010g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0007c0012t0010g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0008c0014t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0008c0014t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0008c0014t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0008c0014t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0008c0014t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0009c0017t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0009c0017t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0009c0017t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0010c0016t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0010c0016t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0010c0016t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0011c0018t0014g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0012c0021t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0012c0021t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0013c0019t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0013c0019t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0014c0048t0006g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0015c0031t0019g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0016c0043t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0017c0023t0006g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0018c0029t0006g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0019c0032t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0020c0028t0022g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0021c0045t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0022c0039t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0023c0027t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0024c0049t0020g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0025c0035t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0026c0034t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0027c0026t0005g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0028c0046t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0029c0022t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0030c0047t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0031c0041t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
a0032c0030t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00099 | hp2 | a0004 | c0003 | t0003 | g0214 | EUR | GBR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | GBR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0276 | EUR | GBR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | FIN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0251 | EUR | FIN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00323 | hp1 | a0009 | c0017 | t0003 | g0236 | EUR | FIN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0266 | EUR | FIN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00408 | hp1 | a0003 | c0004 | t0005 | g0317 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00544 | hp2 | a0003 | c0008 | t0006 | g0332 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00558 | hp1 | a0002 | c0007 | t0004 | g0014 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00597 | hp2 | a0001 | c0005 | t0004 | g0139 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00609 | hp2 | a0014 | c0048 | t0006 | g0356 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00621 | hp1 | a0015 | c0031 | t0019 | g0267 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00639 | hp2 | a0004 | c0003 | t0003 | g0263 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00642 | hp1 | a0001 | c0006 | t0009 | g0207 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00673 | hp1 | a0003 | c0013 | t0006 | g0006 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00673 | hp2 | a0003 | c0004 | t0005 | g0313 | EAS | CHS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00733 | hp1 | a0004 | c0003 | t0003 | g0196 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00735 | hp1 | a0005 | c0009 | t0003 | g0145 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00735 | hp2 | a0001 | c0005 | t0004 | g0011 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01069 | hp2 | a0002 | c0015 | t0007 | g0043 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01081 | hp1 | a0005 | c0009 | t0003 | g0062 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0245 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01106 | hp1 | a0005 | c0009 | t0003 | g0228 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0239 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01109 | hp1 | a0001 | c0006 | t0007 | g0177 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01167 | hp1 | a0004 | c0003 | t0003 | g0191 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01167 | hp2 | a0009 | c0017 | t0003 | g0237 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01168 | hp1 | a0003 | c0008 | t0006 | g0310 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01169 | hp1 | a0004 | c0003 | t0003 | g0187 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01169 | hp2 | a0003 | c0008 | t0006 | g0309 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01175 | hp1 | a0004 | c0003 | t0003 | g0278 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0230 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01243 | hp2 | a0002 | c0015 | t0007 | g0231 | AMR | PUR | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0015 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0247 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01257 | hp1 | a0009 | c0017 | t0003 | g0224 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01261 | hp1 | a0004 | c0003 | t0003 | g0212 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01346 | hp1 | a0001 | c0044 | t0001 | g0279 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01361 | hp1 | a0002 | c0002 | t0002 | g0254 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0256 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01433 | hp2 | a0001 | c0005 | t0004 | g0011 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0295 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01515 | hp1 | a0004 | c0003 | t0003 | g0013 | EUR | IBS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0248 | EUR | IBS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0243 | EUR | IBS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01517 | hp2 | a0004 | c0003 | t0003 | g0013 | EUR | IBS | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01884 | hp1 | a0003 | c0004 | t0008 | g0325 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0303 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0258 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01975 | hp2 | a0001 | c0005 | t0004 | g0184 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0284 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0282 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02055 | hp1 | a0003 | c0004 | t0008 | g0341 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02055 | hp2 | a0016 | c0043 | t0003 | g0211 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02056 | hp2 | a0003 | c0008 | t0006 | g0334 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02074 | hp1 | a0017 | c0023 | t0006 | g0353 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02074 | hp2 | a0003 | c0008 | t0021 | g0343 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02080 | hp2 | a0003 | c0013 | t0006 | g0328 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02083 | hp1 | a0003 | c0004 | t0006 | g0335 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02129 | hp2 | a0003 | c0013 | t0006 | g0006 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02135 | hp2 | a0001 | c0005 | t0004 | g0298 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02145 | hp1 | a0004 | c0003 | t0003 | g0036 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02148 | hp1 | a0002 | c0002 | t0002 | g0240 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02155 | hp1 | a0003 | c0013 | t0006 | g0346 | EAS | CDX | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0268 | EAS | CDX | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02257 | hp2 | a0002 | c0007 | t0012 | g0028 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02273 | hp2 | a0002 | c0002 | t0002 | g0015 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02280 | hp1 | a0003 | c0004 | t0005 | g0329 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02300 | hp1 | a0002 | c0002 | t0018 | g0255 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02451 | hp1 | a0001 | c0001 | t0009 | g0300 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02451 | hp2 | a0004 | c0003 | t0016 | g0045 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02523 | hp2 | a0018 | c0029 | t0006 | g0308 | EAS | KHV | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02572 | hp1 | a0003 | c0004 | t0005 | g0338 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02602 | hp1 | a0001 | c0001 | t0013 | g0060 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02602 | hp2 | a0004 | c0003 | t0003 | g0204 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02615 | hp1 | a0001 | c0005 | t0011 | g0041 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02615 | hp2 | a0002 | c0011 | t0002 | g0020 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02622 | hp2 | a0011 | c0018 | t0014 | g0007 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02630 | hp1 | a0001 | c0006 | t0007 | g0201 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02630 | hp2 | a0008 | c0014 | t0002 | g0026 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02647 | hp2 | a0001 | c0006 | t0002 | g0047 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02683 | hp2 | a0001 | c0020 | t0002 | g0171 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02698 | hp1 | a0003 | c0004 | t0008 | g0349 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02717 | hp1 | a0019 | c0032 | t0002 | g0033 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02723 | hp1 | a0004 | c0003 | t0003 | g0200 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02723 | hp2 | a0020 | c0028 | t0022 | g0323 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02735 | hp1 | a0021 | c0045 | t0003 | g0123 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02735 | hp2 | a0001 | c0001 | t0017 | g0085 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02738 | hp1 | a0022 | c0039 | t0001 | g0063 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02809 | hp1 | a0004 | c0003 | t0003 | g0197 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02809 | hp2 | a0001 | c0006 | t0007 | g0178 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02818 | hp1 | a0001 | c0001 | t0009 | g0301 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02818 | hp2 | a0002 | c0011 | t0009 | g0035 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02886 | hp1 | a0001 | c0006 | t0007 | g0179 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02895 | hp1 | a0003 | c0008 | t0006 | g0347 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02895 | hp2 | a0002 | c0015 | t0007 | g0232 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02896 | hp1 | a0004 | c0003 | t0003 | g0189 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02896 | hp2 | a0001 | c0005 | t0015 | g0039 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02897 | hp1 | a0003 | c0008 | t0006 | g0348 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02897 | hp2 | a0001 | c0005 | t0015 | g0037 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02922 | hp1 | a0003 | c0004 | t0005 | g0324 | AFR | ESN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02922 | hp2 | a0004 | c0038 | t0003 | g0226 | AFR | ESN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02965 | hp2 | a0003 | c0008 | t0006 | g0339 | AFR | ESN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02970 | hp1 | a0001 | c0005 | t0011 | g0040 | AFR | ESN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02970 | hp2 | a0023 | c0027 | t0005 | g0330 | AFR | ESN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02976 | hp1 | a0002 | c0011 | t0009 | g0023 | AFR | ESN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0302 | AFR | ESN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03098 | hp1 | a0001 | c0006 | t0007 | g0181 | AFR | MSL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03098 | hp2 | a0024 | c0049 | t0020 | g0307 | AFR | MSL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03130 | hp1 | a0003 | c0004 | t0005 | g0337 | AFR | ESN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03130 | hp2 | a0025 | c0035 | t0001 | g0209 | AFR | ESN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03139 | hp1 | a0005 | c0009 | t0003 | g0050 | AFR | ESN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03139 | hp2 | a0026 | c0034 | t0001 | g0051 | AFR | ESN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03195 | hp1 | a0001 | c0006 | t0007 | g0180 | AFR | ESN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03195 | hp2 | a0001 | c0006 | t0002 | g0046 | AFR | ESN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03209 | hp1 | a0008 | c0014 | t0002 | g0027 | AFR | MSL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0305 | AFR | MSL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03225 | hp1 | a0004 | c0003 | t0003 | g0299 | AFR | MSL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03225 | hp2 | a0003 | c0004 | t0005 | g0336 | AFR | MSL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03453 | hp1 | a0001 | c0006 | t0007 | g0182 | AFR | MSL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03453 | hp2 | a0003 | c0004 | t0008 | g0345 | AFR | MSL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03486 | hp1 | a0004 | c0003 | t0003 | g0117 | AFR | MSL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03486 | hp2 | a0027 | c0026 | t0005 | g0340 | AFR | MSL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03490 | hp1 | a0005 | c0009 | t0003 | g0161 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0257 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0246 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03516 | hp1 | a0008 | c0014 | t0002 | g0031 | AFR | ESN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03516 | hp2 | a0004 | c0003 | t0003 | g0222 | AFR | ESN | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03540 | hp1 | a0001 | c0006 | t0007 | g0183 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03540 | hp2 | a0001 | c0040 | t0011 | g0049 | AFR | GWD | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03579 | hp1 | a0002 | c0011 | t0009 | g0022 | AFR | MSL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03669 | hp2 | a0005 | c0009 | t0003 | g0193 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0269 | SAS | STU | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03704 | hp2 | a0003 | c0004 | t0008 | g0322 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03710 | hp1 | a0005 | c0009 | t0003 | g0273 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0252 | SAS | PJL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03831 | hp1 | a0028 | c0046 | t0001 | g0122 | SAS | BEB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | BEB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0217 | SAS | BEB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03834 | hp2 | a0001 | c0001 | t0013 | g0077 | SAS | BEB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG04115 | hp1 | a0004 | c0003 | t0003 | g0080 | SAS | STU | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG04184 | hp1 | a0001 | c0036 | t0001 | g0068 | SAS | BEB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | BEB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | STU | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG04228 | hp2 | a0004 | c0003 | t0003 | g0274 | SAS | STU | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18522 | hp1 | a0011 | c0018 | t0014 | g0007 | AFR | YRI | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18522 | hp2 | a0001 | c0042 | t0001 | g0206 | AFR | YRI | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18612 | hp1 | a0006 | c0010 | t0002 | g0133 | EAS | CHB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CHB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18747 | hp2 | a0003 | c0013 | t0006 | g0006 | EAS | CHB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18906 | hp2 | a0008 | c0014 | t0002 | g0029 | AFR | YRI | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18939 | hp2 | a0002 | c0007 | t0004 | g0292 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18944 | hp1 | a0006 | c0010 | t0002 | g0091 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18944 | hp2 | a0012 | c0021 | t0002 | g0108 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18945 | hp2 | a0003 | c0004 | t0005 | g0318 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0244 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18950 | hp1 | a0013 | c0019 | t0002 | g0289 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18952 | hp2 | a0003 | c0008 | t0006 | g0351 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18954 | hp1 | a0003 | c0025 | t0006 | g0352 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18957 | hp1 | a0002 | c0002 | t0002 | g0286 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18957 | hp2 | a0003 | c0004 | t0008 | g0333 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18962 | hp1 | a0006 | c0010 | t0002 | g0056 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18964 | hp1 | a0029 | c0022 | t0001 | g0124 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18964 | hp2 | a0006 | c0010 | t0002 | g0148 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18966 | hp1 | a0007 | c0012 | t0010 | g0327 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18966 | hp2 | a0001 | c0005 | t0004 | g0102 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18967 | hp1 | a0002 | c0007 | t0004 | g0216 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18967 | hp2 | a0010 | c0016 | t0005 | g0312 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18973 | hp2 | a0002 | c0007 | t0004 | g0241 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18975 | hp1 | a0006 | c0010 | t0002 | g0129 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18980 | hp1 | a0002 | c0007 | t0004 | g0260 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18981 | hp1 | a0003 | c0024 | t0006 | g0354 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18984 | hp1 | a0003 | c0004 | t0005 | g0316 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18986 | hp1 | a0001 | c0005 | t0004 | g0132 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18986 | hp2 | a0006 | c0010 | t0002 | g0111 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18989 | hp1 | a0007 | c0012 | t0010 | g0002 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18992 | hp2 | a0010 | c0016 | t0005 | g0311 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18998 | hp2 | a0001 | c0005 | t0004 | g0058 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18999 | hp2 | a0002 | c0007 | t0004 | g0014 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19001 | hp2 | a0002 | c0007 | t0004 | g0249 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19005 | hp1 | a0003 | c0004 | t0005 | g0314 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19012 | hp1 | a0007 | c0012 | t0010 | g0002 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19012 | hp2 | a0003 | c0004 | t0005 | g0320 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19030 | hp1 | a0002 | c0011 | t0001 | g0034 | AFR | LWK | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19030 | hp2 | a0030 | c0047 | t0001 | g0306 | AFR | LWK | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19056 | hp1 | a0001 | c0037 | t0004 | g0130 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19057 | hp1 | a0002 | c0007 | t0004 | g0235 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19057 | hp2 | a0010 | c0016 | t0005 | g0315 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19058 | hp1 | a0001 | c0005 | t0004 | g0010 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19062 | hp2 | a0006 | c0010 | t0002 | g0147 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19064 | hp1 | a0031 | c0041 | t0002 | g0093 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19064 | hp2 | a0003 | c0004 | t0005 | g0331 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19066 | hp2 | a0007 | c0012 | t0010 | g0002 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19077 | hp1 | a0007 | c0012 | t0010 | g0326 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19077 | hp2 | a0013 | c0019 | t0002 | g0290 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19082 | hp2 | a0003 | c0013 | t0006 | g0342 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19083 | hp1 | a0003 | c0004 | t0008 | g0344 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19083 | hp2 | a0012 | c0021 | t0002 | g0107 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19084 | hp1 | a0003 | c0004 | t0005 | g0319 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19084 | hp2 | a0001 | c0005 | t0004 | g0010 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19085 | hp1 | a0006 | c0010 | t0002 | g0092 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19087 | hp1 | a0001 | c0005 | t0004 | g0110 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19087 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19091 | hp1 | a0003 | c0004 | t0005 | g0321 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA19091 | hp2 | a0001 | c0005 | t0004 | g0136 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA20129 | hp1 | a0008 | c0014 | t0002 | g0030 | AFR | ASW | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA20129 | hp2 | a0004 | c0003 | t0003 | g0208 | AFR | ASW | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA20752 | hp1 | a0004 | c0003 | t0003 | g0073 | EUR | TSI | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA20752 | hp2 | a0004 | c0003 | t0003 | g0215 | EUR | TSI | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA20805 | hp1 | a0004 | c0003 | t0003 | g0192 | EUR | TSI | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0096 | EUR | TSI | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA20905 | hp1 | a0001 | c0020 | t0002 | g0172 | SAS | GIH | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | GIH | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01123 | hp1 | a0005 | c0009 | t0003 | g0100 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0287 | AMR | CLM | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02109 | hp1 | a0002 | c0015 | t0007 | g0025 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02109 | hp2 | a0004 | c0003 | t0003 | g0038 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0019 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02559 | hp1 | a0002 | c0007 | t0012 | g0032 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG02559 | hp2 | a0003 | c0004 | t0005 | g0355 | AFR | ACB | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03471 | hp1 | a0003 | c0004 | t0008 | g0350 | AFR | MSL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | MSL | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | USA | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
HG06807 | hp2 | a0001 | c0033 | t0002 | g0281 | AFR | USA | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18955 | hp1 | a0007 | c0012 | t0010 | g0002 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA20300 | hp1 | a0002 | c0011 | t0009 | g0021 | AFR | USA | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA20300 | hp2 | a0004 | c0003 | t0003 | g0203 | AFR | USA | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA21309 | hp1 | a0001 | c0005 | t0004 | g0225 | AFR | LWK | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
NA21309 | hp2 | a0032 | c0030 | t0002 | g0304 | AFR | LWK | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
homoSapiens | chm13v2 | a0004 | c0003 | t0003 | g0223 | REF | REF | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0016 | REF | REF | EPHA10_chr1_37710976_37770120 | EPHA10 | chr1 | 37710976 | 37770120 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:37718383 | C | T | 3 | a0006 a0010 a0031 |
12 | NA18612.hp1 NA18944.hp1 NA18962.hp1 others(9): Show |
missense_variant | MODERATE | c.3016G>A | p.Val1006Met | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 3070/5477 | 3016/3027 | 1006/1008 | chr1 | 37718383 | |||
chr1:37719444 | G | A | 2 | a0011 a0020 |
3 | HG02622.hp2 HG02723.hp2 NA18522.hp1 |
missense_variant | MODERATE | c.2726C>T | p.Pro909Leu | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 15/17 | 2780/5477 | 2726/3027 | 909/1008 | chr1 | 37719444 | |||
chr1:37720051 | C | T | 3 | a0005 a0007 a0015 |
15 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(12): Show |
missense_variant | MODERATE | c.2420G>A | p.Arg807Gln | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 14/17 | 2474/5477 | 2420/3027 | 807/1008 | chr1 | 37720051 | |||
chr1:37720506 | C | T | 1 | a0022 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.2257G>A | p.Gly753Arg | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 13/17 | 2311/5477 | 2257/3027 | 753/1008 | chr1 | 37720506 | |||
chr1:37720517 | C | T | 4 | a0004 a0009 a0016 others(1): Show |
32 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(29): Show |
missense_variant | MODERATE | c.2246G>A | p.Gly749Glu | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 13/17 | 2300/5477 | 2246/3027 | 749/1008 | chr1 | 37720517 | |||
chr1:37723068 | C | T | 3 | a0005 a0007 a0015 |
15 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(12): Show |
missense_variant | MODERATE | c.1933G>A | p.Val645Ile | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/17 | 1987/5477 | 1933/3027 | 645/1008 | chr1 | 37723068 | |||
chr1:37723076 | G | A | 2 | a0012 a0013 |
4 | NA18944.hp2 NA18950.hp1 NA19077.hp2 others(1): Show |
missense_variant | MODERATE | c.1925C>T | p.Ala642Val | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/17 | 1979/5477 | 1925/3027 | 642/1008 | chr1 | 37723076 | |||
chr1:37723115 | A | G | 3 | a0005 a0007 a0015 |
15 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(12): Show |
missense_variant | MODERATE | c.1886T>C | p.Leu629Pro | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/17 | 1940/5477 | 1886/3027 | 629/1008 | chr1 | 37723115 | |||
chr1:37727153 | G | A | 2 | a0008 a0019 |
6 | HG02630.hp2 HG02717.hp1 HG03209.hp1 others(3): Show |
missense_variant | MODERATE | c.1721C>T | p.Ser574Leu | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/17 | 1775/5477 | 1721/3027 | 574/1008 | chr1 | 37727153 | |||
chr1:37727198 | G | C | 1 | a0018 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1676C>G | p.Ser559Cys | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/17 | 1730/5477 | 1676/3027 | 559/1008 | chr1 | 37727198 | |||
chr1:37731476 | G | T | 1 | a0025 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.1598C>A | p.Ser533Tyr | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/17 | 1652/5477 | 1598/3027 | 533/1008 | chr1 | 37731476 | |||
chr1:37731480 | C | T | 5 | a0008 a0019 a0023 others(2): Show |
9 | HG02630.hp2 HG02717.hp1 HG02970.hp2 others(6): Show |
missense_variant | MODERATE | c.1594G>A | p.Ala532Thr | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/17 | 1648/5477 | 1594/3027 | 532/1008 | chr1 | 37731480 | |||
chr1:37731485 | C | T | 1 | a0026 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.1589G>A | p.Arg530Gln | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/17 | 1643/5477 | 1589/3027 | 530/1008 | chr1 | 37731485 | |||
chr1:37731498 | C | T | 1 | a0017 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.1576G>A | p.Val526Ile | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/17 | 1630/5477 | 1576/3027 | 526/1008 | chr1 | 37731498 | |||
chr1:37731575 | C | T | 1 | a0027 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.1499G>A | p.Ser500Asn | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/17 | 1553/5477 | 1499/3027 | 500/1008 | chr1 | 37731575 | |||
chr1:37753097 | C | A | 1 | a0019 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1136G>T | p.Arg379Leu | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/17 | 1190/5477 | 1136/3027 | 379/1008 | chr1 | 37753097 | |||
chr1:37753098 | G | A | 1 | a0031 | 1 | NA19064.hp1 | missense_variant | MODERATE | c.1135C>T | p.Arg379Cys | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/17 | 1189/5477 | 1135/3027 | 379/1008 | chr1 | 37753098 | |||
chr1:37761414 | A | T | 17 | a0002 a0003 a0007 others(14): Show |
155 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(152): Show |
missense_variant | MODERATE | c.841T>A | p.Phe281Ile | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/17 | 895/5477 | 841/3027 | 281/1008 | chr1 | 37761414 | |||
chr1:37761596 | G | T | 9 | a0003 a0007 a0010 others(6): Show |
56 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(53): Show |
missense_variant | MODERATE | c.659C>A | p.Thr220Lys | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/17 | 713/5477 | 659/3027 | 220/1008 | chr1 | 37761596 | |||
chr1:37761807 | G | T | 1 | a0029 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.448C>A | p.Arg150Ser | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/17 | 502/5477 | 448/3027 | 150/1008 | chr1 | 37761807 | |||
chr1:37762032 | G | C | 1 | a0016 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.223C>G | p.Gln75Glu | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/17 | 277/5477 | 223/3027 | 75/1008 | chr1 | 37762032 | |||
chr1:37762050 | G | A | 2 | a0021 a0028 |
2 | HG02735.hp1 HG03831.hp1 |
missense_variant | MODERATE | c.205C>T | p.Arg69Cys | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/17 | 259/5477 | 205/3027 | 69/1008 | chr1 | 37762050 | |||
chr1:37764973 | T | C | 1 | a0030 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.94A>G | p.Thr32Ala | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/17 | 148/5477 | 94/3027 | 32/1008 | chr1 | 37764973 | |||
chr1:37765006 | G | A | 1 | a0014 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.61C>T | p.Leu21Phe | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/17 | 115/5477 | 61/3027 | 21/1008 | chr1 | 37765006 | |||
chr1:37765027 | G | C | 1 | a0024 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.40C>G | p.Leu14Val | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/17 | 94/5477 | 40/3027 | 14/1008 | chr1 | 37765027 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:37718798 | C | G | 5 | a0004c0003 a0004c0038 a0009c0017 others(2): Show |
32 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(29): Show |
synonymous_variant | LOW | c.2775G>C | p.Ala925Ala | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 16/17 | 2829/5477 | 2775/3027 | 925/1008 | chr1 | 37718798 | |||
chr1:37719497 | G | A | 11 | a0001c0005 a0001c0037 a0001c0040 others(8): Show |
49 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(46): Show |
synonymous_variant | LOW | c.2673C>T | p.Pro891Pro | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 15/17 | 2727/5477 | 2673/3027 | 891/1008 | chr1 | 37719497 | |||
chr1:37719975 | G | A | 5 | a0005c0009 a0007c0012 a0011c0018 others(2): Show |
18 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(15): Show |
synonymous_variant | LOW | c.2496C>T | p.Phe832Phe | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 14/17 | 2550/5477 | 2496/3027 | 832/1008 | chr1 | 37719975 | |||
chr1:37720534 | C | G | 3 | a0005c0009 a0007c0012 a0015c0031 |
15 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(12): Show |
synonymous_variant | LOW | c.2229G>C | p.Val743Val | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 13/17 | 2283/5477 | 2229/3027 | 743/1008 | chr1 | 37720534 | |||
chr1:37721727 | G | A | 1 | a0001c0020 | 2 | HG02683.hp2 NA20905.hp1 |
synonymous_variant | LOW | c.2079C>T | p.Ala693Ala | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/17 | 2133/5477 | 2079/3027 | 693/1008 | chr1 | 37721727 | |||
chr1:37721775 | A | G | 11 | a0001c0006 a0002c0015 a0004c0003 others(8): Show |
64 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(61): Show |
synonymous_variant | LOW | c.2031T>C | p.His677His | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/17 | 2085/5477 | 2031/3027 | 677/1008 | chr1 | 37721775 | |||
chr1:37721781 | G | A | 3 | a0005c0009 a0007c0012 a0015c0031 |
15 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(12): Show |
synonymous_variant | LOW | c.2025C>T | p.Ala675Ala | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/17 | 2079/5477 | 2025/3027 | 675/1008 | chr1 | 37721781 | |||
chr1:37721835 | C | T | 4 | a0001c0037 a0003c0013 a0003c0024 others(1): Show |
9 | HG00609.hp2 HG00673.hp1 HG02080.hp2 others(6): Show |
synonymous_variant | LOW | c.1971G>A | p.Gly657Gly | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/17 | 2025/5477 | 1971/3027 | 657/1008 | chr1 | 37721835 | |||
chr1:37723096 | C | T | 3 | a0005c0009 a0007c0012 a0015c0031 |
15 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(12): Show |
synonymous_variant | LOW | c.1905G>A | p.Leu635Leu | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/17 | 1959/5477 | 1905/3027 | 635/1008 | chr1 | 37723096 | |||
chr1:37727104 | C | T | 1 | a0001c0036 | 1 | HG04184.hp1 | splice_region_variant&synonymous_variant | LOW | c.1770G>A | p.Arg590Arg | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/17 | 1824/5477 | 1770/3027 | 590/1008 | chr1 | 37727104 | |||
chr1:37727152 | C | T | 2 | a0011c0018 a0020c0028 |
3 | HG02622.hp2 HG02723.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.1722G>A | p.Ser574Ser | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/17 | 1776/5477 | 1722/3027 | 574/1008 | chr1 | 37727152 | |||
chr1:37735263 | G | A | 1 | a0001c0040 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.1485C>T | p.Tyr495Tyr | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/17 | 1539/5477 | 1485/3027 | 495/1008 | chr1 | 37735263 | |||
chr1:37752967 | G | T | 5 | a0001c0033 a0003c0024 a0003c0025 others(2): Show |
5 | HG02074.hp1 HG06807.hp2 NA18954.hp1 others(2): Show |
synonymous_variant | LOW | c.1266C>A | p.Thr422Thr | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/17 | 1320/5477 | 1266/3027 | 422/1008 | chr1 | 37752967 | |||
chr1:37754318 | C | A | 1 | a0001c0042 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.903G>T | p.Pro301Pro | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 4/17 | 957/5477 | 903/3027 | 301/1008 | chr1 | 37754318 | |||
chr1:37761757 | C | G | 1 | a0002c0011 | 6 | HG02615.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
synonymous_variant | LOW | c.498G>C | p.Leu166Leu | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/17 | 552/5477 | 498/3027 | 166/1008 | chr1 | 37761757 | |||
chr1:37762036 | C | A | 1 | a0001c0044 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.219G>T | p.Thr73Thr | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/17 | 273/5477 | 219/3027 | 73/1008 | chr1 | 37762036 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:37716047 | T | G | 1 | a0001c0001t0017 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2325A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 2325 | chr1 | 37716047 | ||||||
chr1:37716171 | C | T | 2 | a0001c0006t0007 a0002c0015t0007 |
12 | HG01069.hp2 HG01109.hp1 HG01243.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2201G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 2201 | chr1 | 37716171 | ||||||
chr1:37716266 | G | A | 1 | a0002c0002t0018 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2106C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 2106 | chr1 | 37716266 | ||||||
chr1:37716287 | G | A | 1 | a0004c0003t0016 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2085C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 2085 | chr1 | 37716287 | ||||||
chr1:37716463 | C | T | 20 | a0001c0001t0002 a0001c0001t0017 a0001c0006t0002 others(17): Show |
121 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*1909G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 1909 | chr1 | 37716463 | ||||||
chr1:37716476 | A | G | 17 | a0001c0001t0004 a0001c0005t0004 a0001c0005t0011 others(14): Show |
51 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1896T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 1896 | chr1 | 37716476 | ||||||
chr1:37716492 | T | A | 16 | a0001c0001t0009 a0001c0006t0007 a0001c0006t0009 others(13): Show |
69 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1880A>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 1880 | chr1 | 37716492 | ||||||
chr1:37716561 | TG | T | 16 | a0001c0001t0009 a0001c0006t0007 a0001c0006t0009 others(13): Show |
69 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1810delC | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 1810 | chr1 | 37716561 | ||||||
chr1:37716655 | C | A | 1 | a0002c0007t0012 | 2 | HG02257.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1717G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 1717 | chr1 | 37716655 | ||||||
chr1:37716661 | G | T | 11 | a0004c0003t0003 a0004c0003t0016 a0004c0038t0003 others(8): Show |
50 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1711C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 1711 | chr1 | 37716661 | ||||||
chr1:37716984 | G | C | 14 | a0001c0001t0004 a0001c0005t0004 a0001c0037t0004 others(11): Show |
46 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1388C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 1388 | chr1 | 37716984 | ||||||
chr1:37717075 | G | A | 1 | a0004c0003t0016 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1297C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 1297 | chr1 | 37717075 | ||||||
chr1:37717178 | G | A | 5 | a0001c0001t0009 a0001c0006t0007 a0001c0006t0009 others(2): Show |
19 | HG00642.hp1 HG01069.hp2 HG01109.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1194C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 1194 | chr1 | 37717178 | ||||||
chr1:37717288 | C | T | 11 | a0004c0003t0003 a0004c0003t0016 a0004c0038t0003 others(8): Show |
50 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1084G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 1084 | chr1 | 37717288 | ||||||
chr1:37717466 | C | A | 1 | a0001c0001t0013 | 2 | HG02602.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*906G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 906 | chr1 | 37717466 | ||||||
chr1:37717534 | T | A | 5 | a0001c0001t0009 a0001c0006t0007 a0001c0006t0009 others(2): Show |
19 | HG00642.hp1 HG01069.hp2 HG01109.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*838A>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 838 | chr1 | 37717534 | ||||||
chr1:37717945 | C | T | 1 | a0003c0008t0021 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*427G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 427 | chr1 | 37717945 | ||||||
chr1:37718167 | T | C | 2 | a0007c0012t0010 a0015c0031t0019 |
7 | HG00621.hp1 NA18955.hp1 NA18966.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*205A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 205 | chr1 | 37718167 | ||||||
chr1:37718182 | G | A | 2 | a0011c0018t0014 a0020c0028t0022 |
3 | HG02622.hp2 HG02723.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*190C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 190 | chr1 | 37718182 | ||||||
chr1:37718267 | G | C | 1 | a0001c0005t0015 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*105C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 105 | chr1 | 37718267 | ||||||
chr1:37718293 | C | T | 1 | a0004c0003t0016 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*79G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 79 | chr1 | 37718293 | ||||||
chr1:37718319 | G | A | 1 | a0024c0049t0020 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*53C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 17/17 | 53 | chr1 | 37718319 | ||||||
chr1:37765086 | C | A | 16 | a0003c0004t0005 a0003c0004t0006 a0003c0004t0008 others(13): Show |
56 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(53): Show |
5_prime_UTR_variant | MODIFIER | c.-20G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/17 | 20 | chr1 | 37765086 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:37718511 | G | A | 1 | a0004c0003t0003g0204 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2913-25C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 16/16 | chr1 | 37718511 | |||||||
chr1:37718568 | T | C | 1 | a0004c0003t0016g0045 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2913-82A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 16/16 | chr1 | 37718568 | |||||||
chr1:37718644 | T | C | 45 | a0004c0003t0003g0013 a0004c0003t0003g0036 a0004c0003t0003g0038 others(42): Show |
50 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.2912+17A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 16/16 | chr1 | 37718644 | |||||||
chr1:37718827 | G | A | 2 | a0001c0005t0004g0011 a0001c0005t0004g0184 |
3 | HG00735.hp2 HG01433.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.2757-11C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 15/16 | chr1 | 37718827 | |||||||
chr1:37718836 | T | C | 3 | a0004c0003t0003g0187 a0004c0003t0003g0189 a0004c0003t0003g0191 |
3 | HG01167.hp1 HG01169.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2757-20A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 15/16 | chr1 | 37718836 | |||||||
chr1:37718970 | G | A | 1 | a0001c0033t0002g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2757-154C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 15/16 | chr1 | 37718970 | |||||||
chr1:37719046 | G | A | 2 | a0011c0018t0014g0007 a0020c0028t0022g0323 |
3 | HG02622.hp2 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2757-230C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 15/16 | chr1 | 37719046 | |||||||
chr1:37719073 | G | T | 1 | a0001c0001t0001g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2757-257C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 15/16 | chr1 | 37719073 | |||||||
chr1:37719209 | A | C | 111 | a0001c0001t0001g0280 a0001c0001t0002g0003 a0001c0001t0002g0009 others(108): Show |
120 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.2756+205T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 15/16 | chr1 | 37719209 | |||||||
chr1:37719213 | C | A | 1 | a0001c0020t0002g0172 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2756+201G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 15/16 | chr1 | 37719213 | |||||||
chr1:37719665 | T | C | 34 | a0002c0002t0001g0302 a0002c0002t0001g0303 a0002c0002t0001g0305 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.2563-58A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 14/16 | chr1 | 37719665 | |||||||
chr1:37719685 | CACACAG | C | 2 | a0011c0018t0014g0007 a0020c0028t0022g0323 |
3 | HG02622.hp2 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2563-84_2563-79del others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 14/16 | chr1 | 37719685 | |||||||
chr1:37719724 | A | G | 2 | a0001c0001t0001g0052 a0026c0034t0001g0051 |
2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2563-117T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 14/16 | chr1 | 37719724 | |||||||
chr1:37719737 | C | G | 33 | a0001c0001t0009g0300 a0001c0001t0009g0301 a0001c0006t0007g0177 others(30): Show |
37 | HG00621.hp1 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.2563-130G>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 14/16 | chr1 | 37719737 | |||||||
chr1:37719904 | C | G | 1 | a0001c0001t0002g0162 | 1 | HG02148.hp2 | splice_region_variant&intron_variant | LOW | c.2562+5G>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 14/16 | chr1 | 37719904 | |||||||
chr1:37720142 | G | A | 23 | a0004c0003t0003g0013 a0004c0003t0003g0036 a0004c0003t0003g0038 others(20): Show |
24 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.2413-84C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 13/16 | chr1 | 37720142 | |||||||
chr1:37720143 | C | A | 23 | a0004c0003t0003g0013 a0004c0003t0003g0036 a0004c0003t0003g0038 others(20): Show |
24 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.2413-85G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 13/16 | chr1 | 37720143 | |||||||
chr1:37720588 | C | T | 2 | a0004c0003t0003g0187 a0004c0003t0003g0191 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2209-34G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 12/16 | chr1 | 37720588 | |||||||
chr1:37720622 | C | T | 31 | a0004c0003t0003g0013 a0004c0003t0003g0036 a0004c0003t0003g0038 others(28): Show |
32 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.2209-68G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 12/16 | chr1 | 37720622 | |||||||
chr1:37720638 | G | A | 12 | a0005c0009t0003g0050 a0005c0009t0003g0062 a0005c0009t0003g0100 others(9): Show |
15 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.2209-84C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 12/16 | chr1 | 37720638 | |||||||
chr1:37720760 | T | C | 1 | a0001c0006t0009g0207 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2208+23A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 12/16 | chr1 | 37720760 | |||||||
chr1:37720935 | C | A | 2 | a0004c0003t0003g0117 a0004c0003t0003g0222 |
2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2147-91G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/16 | chr1 | 37720935 | |||||||
chr1:37721019 | G | A | 2 | a0001c0001t0009g0300 a0001c0001t0009g0301 |
2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2147-175C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/16 | chr1 | 37721019 | |||||||
chr1:37721062 | C | T | 1 | a0004c0003t0003g0299 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2147-218G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/16 | chr1 | 37721062 | |||||||
chr1:37721073 | A | C | 1 | a0002c0007t0004g0260 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2147-229T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/16 | chr1 | 37721073 | |||||||
chr1:37721147 | C | T | 1 | a0004c0003t0003g0299 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2147-303G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/16 | chr1 | 37721147 | |||||||
chr1:37721172 | C | G | 13 | a0004c0038t0003g0226 a0005c0009t0003g0050 a0005c0009t0003g0062 others(10): Show |
16 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.2147-328G>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/16 | chr1 | 37721172 | |||||||
chr1:37721255 | T | TA | 7 | a0001c0001t0001g0233 a0002c0007t0004g0260 a0004c0003t0003g0200 others(4): Show |
7 | HG01167.hp2 HG02723.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2146+404dupT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/16 | chr1 | 37721255 | |||||||
chr1:37721255 | T | TAA | 25 | a0004c0003t0003g0013 a0004c0003t0003g0036 a0004c0003t0003g0038 others(22): Show |
26 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.2146+403_2146+404d others(4): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/16 | chr1 | 37721255 | |||||||
chr1:37721271 | C | A | 30 | a0001c0001t0001g0233 a0004c0003t0003g0013 a0004c0003t0003g0036 others(27): Show |
31 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.2146+389G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/16 | chr1 | 37721271 | |||||||
chr1:37721376 | C | A | 1 | a0018c0029t0006g0308 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2146+284G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/16 | chr1 | 37721376 | |||||||
chr1:37721427 | CA | C | 28 | a0001c0005t0015g0039 a0001c0006t0007g0177 a0001c0006t0007g0178 others(25): Show |
32 | HG00621.hp1 HG00642.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.2146+232delT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/16 | chr1 | 37721427 | |||||||
chr1:37721501 | G | A | 12 | a0005c0009t0003g0050 a0005c0009t0003g0062 a0005c0009t0003g0100 others(9): Show |
15 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.2146+159C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/16 | chr1 | 37721501 | |||||||
chr1:37721574 | G | A | 1 | a0002c0002t0001g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2146+86C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/16 | chr1 | 37721574 | |||||||
chr1:37721651 | G | A | 1 | a0001c0006t0009g0207 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2146+9C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 11/16 | chr1 | 37721651 | |||||||
chr1:37721872 | C | T | 1 | a0004c0003t0016g0045 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1961-27G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37721872 | |||||||
chr1:37722130 | CA | C | 24 | a0001c0006t0007g0177 a0001c0006t0007g0178 a0001c0006t0007g0179 others(21): Show |
27 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1961-286delT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37722130 | |||||||
chr1:37722207 | C | T | 12 | a0005c0009t0003g0050 a0005c0009t0003g0062 a0005c0009t0003g0100 others(9): Show |
15 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1961-362G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37722207 | |||||||
chr1:37722216 | T | C | 14 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0001g0059 others(11): Show |
14 | HG00438.hp1 HG00609.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.1961-371A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37722216 | |||||||
chr1:37722317 | T | C | 63 | a0001c0005t0011g0040 a0001c0005t0011g0041 a0001c0005t0015g0037 others(60): Show |
68 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1961-472A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37722317 | |||||||
chr1:37722357 | A | G | 15 | a0002c0002t0001g0302 a0002c0002t0001g0303 a0002c0002t0001g0305 others(12): Show |
18 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1961-512T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37722357 | |||||||
chr1:37722410 | T | A | 1 | a0002c0002t0002g0252 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1961-565A>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37722410 | |||||||
chr1:37722480 | C | T | 1 | a0004c0003t0016g0045 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1960+561G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37722480 | |||||||
chr1:37722487 | G | A | 1 | a0004c0003t0003g0299 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1960+554C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37722487 | |||||||
chr1:37722523 | A | G | 55 | a0001c0006t0002g0046 a0001c0006t0002g0047 a0001c0006t0007g0177 others(52): Show |
59 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1960+518T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37722523 | |||||||
chr1:37722550 | G | A | 37 | a0001c0006t0007g0177 a0001c0006t0007g0178 a0001c0006t0007g0179 others(34): Show |
38 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1960+491C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37722550 | |||||||
chr1:37722581 | T | G | 13 | a0001c0001t0001g0221 a0005c0009t0003g0050 a0005c0009t0003g0062 others(10): Show |
16 | HG00621.hp1 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1960+460A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37722581 | |||||||
chr1:37722614 | T | A | 14 | a0001c0001t0002g0128 a0001c0001t0002g0141 a0001c0001t0002g0205 others(11): Show |
14 | HG01168.hp1 HG01169.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1960+427A>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37722614 | |||||||
chr1:37722725 | C | G | 1 | a0002c0002t0001g0242 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1960+316G>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37722725 | |||||||
chr1:37722902 | G | A | 2 | a0001c0001t0002g0213 a0001c0001t0002g0218 |
2 | HG01074.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1960+139C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37722902 | |||||||
chr1:37722932 | C | T | 12 | a0005c0009t0003g0050 a0005c0009t0003g0062 a0005c0009t0003g0100 others(9): Show |
15 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1960+109G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37722932 | |||||||
chr1:37722984 | C | A | 1 | a0001c0001t0002g0106 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1960+57G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37722984 | |||||||
chr1:37723025 | T | C | 14 | a0005c0009t0003g0050 a0005c0009t0003g0062 a0005c0009t0003g0100 others(11): Show |
18 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1960+16A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 10/16 | chr1 | 37723025 | |||||||
chr1:37723169 | G | A | 43 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0190 others(40): Show |
44 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(41): Show |
splice_region_variant&intron_variant | LOW | c.1835-3C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 9/16 | chr1 | 37723169 | |||||||
chr1:37723208 | C | T | 12 | a0005c0009t0003g0050 a0005c0009t0003g0062 a0005c0009t0003g0100 others(9): Show |
15 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1835-42G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 9/16 | chr1 | 37723208 | |||||||
chr1:37723216 | C | T | 1 | a0008c0014t0002g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1835-50G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 9/16 | chr1 | 37723216 | |||||||
chr1:37723228 | C | A | 6 | a0001c0006t0002g0046 a0001c0006t0002g0047 a0004c0003t0003g0117 others(3): Show |
6 | HG02647.hp2 HG03195.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1835-62G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 9/16 | chr1 | 37723228 | |||||||
chr1:37723236 | G | C | 1 | a0001c0006t0007g0181 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1835-70C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 9/16 | chr1 | 37723236 | |||||||
chr1:37723241 | G | A | 1 | a0004c0003t0016g0045 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1834+70C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 9/16 | chr1 | 37723241 | |||||||
chr1:37723262 | T | C | 12 | a0005c0009t0003g0050 a0005c0009t0003g0062 a0005c0009t0003g0100 others(9): Show |
15 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1834+49A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 9/16 | chr1 | 37723262 | |||||||
chr1:37723279 | C | T | 1 | a0001c0033t0002g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1834+32G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 9/16 | chr1 | 37723279 | |||||||
chr1:37723396 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1773-24G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37723396 | |||||||
chr1:37723409 | C | T | 1 | a0004c0003t0016g0045 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1773-37G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37723409 | |||||||
chr1:37723458 | C | T | 1 | a0004c0038t0003g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1773-86G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37723458 | |||||||
chr1:37723470 | A | C | 47 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0190 others(44): Show |
49 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1773-98T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37723470 | |||||||
chr1:37723535 | C | T | 12 | a0005c0009t0003g0050 a0005c0009t0003g0062 a0005c0009t0003g0100 others(9): Show |
15 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1773-163G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37723535 | |||||||
chr1:37723562 | G | A | 2 | a0004c0003t0016g0045 a0006c0010t0002g0148 |
2 | HG02451.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1773-190C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37723562 | |||||||
chr1:37723594 | C | A | 1 | a0004c0003t0003g0274 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1773-222G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37723594 | |||||||
chr1:37723688 | G | C | 3 | a0004c0003t0016g0045 a0011c0018t0014g0007 a0020c0028t0022g0323 |
4 | HG02451.hp2 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1773-316C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37723688 | |||||||
chr1:37723774 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1773-402T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37723774 | |||||||
chr1:37723873 | G | C | 12 | a0005c0009t0003g0050 a0005c0009t0003g0062 a0005c0009t0003g0100 others(9): Show |
15 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1773-501C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37723873 | |||||||
chr1:37723946 | G | A | 16 | a0004c0003t0003g0117 a0004c0003t0003g0208 a0004c0003t0003g0222 others(13): Show |
19 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1773-574C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37723946 | |||||||
chr1:37724184 | A | G | 1 | a0004c0003t0003g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1773-812T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37724184 | |||||||
chr1:37724226 | G | A | 1 | a0004c0003t0016g0045 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1773-854C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37724226 | |||||||
chr1:37724352 | C | T | 4 | a0004c0003t0003g0117 a0004c0003t0003g0208 a0004c0003t0003g0222 others(1): Show |
4 | HG03225.hp1 HG03486.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1773-980G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37724352 | |||||||
chr1:37724353 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1773-981C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37724353 | |||||||
chr1:37724360 | C | T | 16 | a0004c0003t0003g0117 a0004c0003t0003g0208 a0004c0003t0003g0222 others(13): Show |
19 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1773-988G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37724360 | |||||||
chr1:37724491 | A | G | 3 | a0003c0004t0005g0336 a0003c0004t0005g0337 a0003c0004t0005g0338 |
3 | HG02572.hp1 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1773-1119T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37724491 | |||||||
chr1:37724493 | C | T | 3 | a0023c0027t0005g0330 a0024c0049t0020g0307 a0032c0030t0002g0304 |
3 | HG02970.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1773-1121G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37724493 | |||||||
chr1:37724510 | G | C | 2 | a0001c0020t0002g0171 a0001c0020t0002g0172 |
2 | HG02683.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1773-1138C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37724510 | |||||||
chr1:37724548 | A | C | 1 | a0002c0002t0002g0238 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1773-1176T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37724548 | |||||||
chr1:37724549 | CAGA | C | 16 | a0004c0003t0003g0117 a0004c0003t0003g0208 a0004c0003t0003g0222 others(13): Show |
19 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1773-1180_1773-117 others(7): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37724549 | |||||||
chr1:37724626 | G | T | 4 | a0004c0003t0003g0117 a0004c0003t0003g0208 a0004c0003t0003g0222 others(1): Show |
4 | HG03225.hp1 HG03486.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1773-1254C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37724626 | |||||||
chr1:37724643 | C | T | 1 | a0004c0003t0016g0045 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1773-1271G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37724643 | |||||||
chr1:37724899 | T | C | 2 | a0002c0007t0004g0249 a0002c0007t0004g0260 |
2 | NA18980.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1773-1527A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37724899 | |||||||
chr1:37724953 | T | C | 62 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0190 others(59): Show |
66 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1773-1581A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37724953 | |||||||
chr1:37724963 | T | C | 1 | a0001c0006t0007g0183 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1773-1591A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37724963 | |||||||
chr1:37724992 | G | C | 1 | a0006c0010t0002g0111 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1773-1620C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37724992 | |||||||
chr1:37725003 | T | C | 4 | a0004c0003t0003g0013 a0004c0003t0003g0080 a0004c0003t0003g0192 others(1): Show |
5 | HG00323.hp1 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1773-1631A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725003 | |||||||
chr1:37725020 | C | A | 2 | a0004c0003t0016g0045 a0004c0038t0003g0226 |
2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1773-1648G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725020 | |||||||
chr1:37725054 | G | C | 1 | a0003c0004t0005g0314 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1773-1682C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725054 | |||||||
chr1:37725180 | T | C | 62 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0190 others(59): Show |
66 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1773-1808A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725180 | |||||||
chr1:37725185 | G | T | 9 | a0001c0006t0007g0177 a0001c0006t0007g0178 a0001c0006t0007g0179 others(6): Show |
9 | HG01069.hp2 HG01109.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1773-1813C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725185 | |||||||
chr1:37725377 | G | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0198 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1772+1725C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725377 | |||||||
chr1:37725506 | C | CA | 67 | a0001c0001t0001g0070 a0001c0001t0001g0079 a0001c0001t0001g0098 others(64): Show |
75 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1772+1595dupT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725506 | |||||||
chr1:37725506 | C | CAA | 39 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0190 others(36): Show |
40 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.1772+1594_1772+159 others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725506 | |||||||
chr1:37725506 | C | CAAA | 12 | a0001c0006t0007g0177 a0001c0006t0007g0178 a0001c0006t0007g0179 others(9): Show |
12 | HG01069.hp2 HG01109.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1772+1593_1772+159 others(7): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725506 | |||||||
chr1:37725506 | CA | C | 24 | a0001c0001t0001g0083 a0001c0001t0001g0088 a0001c0001t0001g0164 others(21): Show |
25 | HG00099.hp1 HG01168.hp1 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.1772+1595delT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725506 | |||||||
chr1:37725506 | CAAAAAAA others(2): Show |
C | 11 | a0005c0009t0003g0050 a0005c0009t0003g0062 a0005c0009t0003g0100 others(8): Show |
14 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.1772+1587_1772+159 others(13): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725506 | |||||||
chr1:37725506 | CAAAAAAA others(3): Show |
C | 1 | a0007c0012t0010g0327 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1772+1586_1772+159 others(14): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725506 | |||||||
chr1:37725530 | A | G | 13 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0001g0059 others(10): Show |
13 | HG00438.hp1 HG00609.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1772+1572T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725530 | |||||||
chr1:37725558 | G | A | 2 | a0002c0002t0001g0229 a0002c0002t0001g0230 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1772+1544C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725558 | |||||||
chr1:37725725 | G | C | 62 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0190 others(59): Show |
66 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1772+1377C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725725 | |||||||
chr1:37725726 | G | A | 2 | a0001c0006t0002g0046 a0001c0006t0002g0047 |
2 | HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1772+1376C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725726 | |||||||
chr1:37725809 | G | A | 1 | a0018c0029t0006g0308 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1772+1293C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725809 | |||||||
chr1:37725832 | A | G | 4 | a0004c0003t0003g0117 a0004c0003t0003g0208 a0004c0003t0003g0222 others(1): Show |
4 | HG03225.hp1 HG03486.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1772+1270T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725832 | |||||||
chr1:37725866 | T | C | 20 | a0001c0006t0002g0046 a0001c0006t0002g0047 a0004c0003t0003g0117 others(17): Show |
23 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1772+1236A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725866 | |||||||
chr1:37725875 | G | A | 1 | a0004c0038t0003g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1772+1227C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725875 | |||||||
chr1:37725888 | C | A | 62 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0190 others(59): Show |
66 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1772+1214G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37725888 | |||||||
chr1:37726142 | G | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0075 a0001c0001t0001g0081 |
3 | HG01074.hp2 HG01928.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1772+960C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37726142 | |||||||
chr1:37726397 | C | T | 1 | a0002c0015t0007g0232 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1772+705G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37726397 | |||||||
chr1:37726400 | T | C | 1 | a0004c0038t0003g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1772+702A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37726400 | |||||||
chr1:37726526 | A | G | 125 | a0001c0001t0001g0079 a0001c0001t0001g0098 a0001c0001t0001g0138 others(122): Show |
136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1772+576T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37726526 | |||||||
chr1:37726624 | A | G | 47 | a0001c0001t0001g0087 a0001c0001t0001g0138 a0001c0001t0001g0144 others(44): Show |
48 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1772+478T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37726624 | |||||||
chr1:37726634 | T | C | 1 | a0005c0009t0003g0145 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1772+468A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37726634 | |||||||
chr1:37726665 | A | T | 65 | a0001c0001t0001g0087 a0001c0001t0001g0138 a0001c0001t0001g0144 others(62): Show |
69 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1772+437T>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37726665 | |||||||
chr1:37726754 | G | A | 9 | a0001c0006t0007g0177 a0001c0006t0007g0178 a0001c0006t0007g0179 others(6): Show |
9 | HG01069.hp2 HG01109.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1772+348C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37726754 | |||||||
chr1:37726758 | G | A | 17 | a0001c0001t0004g0149 a0001c0005t0004g0010 a0001c0005t0004g0011 others(14): Show |
19 | HG00544.hp2 HG00597.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1772+344C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37726758 | |||||||
chr1:37726865 | T | C | 12 | a0005c0009t0003g0050 a0005c0009t0003g0062 a0005c0009t0003g0100 others(9): Show |
15 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1772+237A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37726865 | |||||||
chr1:37726932 | G | A | 32 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0190 others(29): Show |
33 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1772+170C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 8/16 | chr1 | 37726932 | |||||||
chr1:37727428 | G | A | 1 | a0002c0002t0001g0247 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1664-218C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37727428 | |||||||
chr1:37727562 | C | T | 1 | a0002c0002t0001g0217 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1664-352G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37727562 | |||||||
chr1:37727855 | C | T | 1 | a0004c0038t0003g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1664-645G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37727855 | |||||||
chr1:37727926 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1664-716T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37727926 | |||||||
chr1:37728177 | C | T | 1 | a0001c0005t0004g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1664-967G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37728177 | |||||||
chr1:37728216 | G | C | 16 | a0001c0001t0001g0188 a0001c0001t0001g0198 a0001c0001t0001g0199 others(13): Show |
16 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1664-1006C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37728216 | |||||||
chr1:37728290 | G | A | 1 | a0005c0009t0003g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1664-1080C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37728290 | |||||||
chr1:37728310 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1664-1100G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37728310 | |||||||
chr1:37728422 | G | C | 44 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0190 others(41): Show |
45 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1664-1212C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37728422 | |||||||
chr1:37728427 | G | A | 1 | a0020c0028t0022g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1664-1217C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37728427 | |||||||
chr1:37728454 | A | G | 3 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG00438.hp1 HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1664-1244T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37728454 | |||||||
chr1:37728484 | G | A | 44 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0190 others(41): Show |
45 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1664-1274C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37728484 | |||||||
chr1:37728517 | C | T | 1 | a0009c0017t0003g0237 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1664-1307G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37728517 | |||||||
chr1:37728519 | C | T | 1 | a0001c0001t0013g0077 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1664-1309G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37728519 | |||||||
chr1:37728558 | T | C | 118 | a0001c0001t0001g0233 a0001c0001t0001g0280 a0001c0001t0002g0003 others(115): Show |
127 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.1664-1348A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37728558 | |||||||
chr1:37729282 | G | A | 1 | a0003c0008t0006g0339 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1664-2072C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37729282 | |||||||
chr1:37729480 | G | A | 3 | a0004c0003t0003g0117 a0004c0003t0003g0208 a0004c0003t0003g0222 |
3 | HG03486.hp1 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1663+1931C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37729480 | |||||||
chr1:37729550 | C | T | 1 | a0010c0016t0005g0311 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1663+1861G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37729550 | |||||||
chr1:37729554 | C | T | 2 | a0004c0003t0016g0045 a0004c0038t0003g0226 |
2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1663+1857G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37729554 | |||||||
chr1:37729602 | G | A | 1 | a0002c0002t0002g0257 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1663+1809C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37729602 | |||||||
chr1:37729647 | G | A | 1 | a0004c0038t0003g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1663+1764C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37729647 | |||||||
chr1:37729661 | C | T | 2 | a0004c0003t0016g0045 a0004c0038t0003g0226 |
2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1663+1750G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37729661 | |||||||
chr1:37729701 | G | A | 11 | a0005c0009t0003g0050 a0005c0009t0003g0100 a0005c0009t0003g0145 others(8): Show |
14 | HG00621.hp1 HG00735.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1663+1710C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37729701 | |||||||
chr1:37729746 | G | A | 16 | a0001c0001t0004g0149 a0001c0005t0004g0010 a0001c0005t0004g0011 others(13): Show |
18 | HG00544.hp2 HG00597.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1663+1665C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37729746 | |||||||
chr1:37729872 | CA | C | 6 | a0001c0001t0001g0104 a0001c0001t0001g0280 a0002c0007t0012g0028 others(3): Show |
6 | HG01168.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663+1538delT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37729872 | |||||||
chr1:37729910 | A | G | 45 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0190 others(42): Show |
46 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1663+1501T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37729910 | |||||||
chr1:37730036 | C | T | 1 | a0001c0001t0001g0008 | 2 | HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1663+1375G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37730036 | |||||||
chr1:37730040 | C | T | 5 | a0001c0001t0002g0067 a0001c0001t0002g0210 a0002c0002t0002g0015 others(2): Show |
6 | HG01255.hp1 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1663+1371G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37730040 | |||||||
chr1:37730052 | C | A | 1 | a0002c0011t0009g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1663+1359G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37730052 | |||||||
chr1:37730119 | A | C | 2 | a0004c0003t0016g0045 a0004c0038t0003g0226 |
2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1663+1292T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37730119 | |||||||
chr1:37730177 | C | T | 1 | a0004c0038t0003g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1663+1234G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37730177 | |||||||
chr1:37730354 | G | A | 31 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0190 others(28): Show |
32 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.1663+1057C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37730354 | |||||||
chr1:37730364 | C | T | 1 | a0005c0009t0003g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1663+1047G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37730364 | |||||||
chr1:37730508 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1663+903C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37730508 | |||||||
chr1:37730981 | C | T | 1 | a0002c0015t0007g0043 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1663+430G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37730981 | |||||||
chr1:37730991 | C | T | 2 | a0004c0003t0016g0045 a0004c0038t0003g0226 |
2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1663+420G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37730991 | |||||||
chr1:37731056 | A | G | 1 | a0004c0003t0016g0045 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1663+355T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37731056 | |||||||
chr1:37731068 | G | A | 1 | a0003c0004t0005g0320 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1663+343C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37731068 | |||||||
chr1:37731169 | T | C | 63 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0190 others(60): Show |
67 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1663+242A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37731169 | |||||||
chr1:37731269 | GTAAT | G | 14 | a0001c0006t0007g0177 a0001c0006t0007g0178 a0001c0006t0007g0179 others(11): Show |
14 | HG01069.hp2 HG01109.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1663+138_1663+141d others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 7/16 | chr1 | 37731269 | |||||||
chr1:37731602 | T | C | 2 | a0002c0002t0001g0248 a0002c0002t0001g0250 |
2 | HG01515.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1492-20A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37731602 | |||||||
chr1:37731729 | T | G | 61 | a0001c0001t0001g0095 a0001c0001t0001g0138 a0001c0001t0001g0144 others(58): Show |
65 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1492-147A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37731729 | |||||||
chr1:37731873 | G | C | 45 | a0001c0001t0001g0098 a0001c0001t0001g0116 a0001c0001t0001g0140 others(42): Show |
49 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1492-291C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37731873 | |||||||
chr1:37731892 | C | T | 35 | a0001c0001t0001g0095 a0001c0001t0001g0138 a0001c0001t0001g0144 others(32): Show |
38 | HG00621.hp1 HG00735.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1492-310G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37731892 | |||||||
chr1:37731957 | A | G | 39 | a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0001g0194 others(36): Show |
40 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.1492-375T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37731957 | |||||||
chr1:37732025 | G | A | 2 | a0002c0007t0012g0028 a0002c0007t0012g0032 |
2 | HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1492-443C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732025 | |||||||
chr1:37732030 | AT | A | 96 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(93): Show |
104 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1492-449delA | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732030 | |||||||
chr1:37732163 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0144 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1492-581G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732163 | |||||||
chr1:37732177 | C | A | 1 | a0003c0008t0006g0339 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1492-595G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732177 | |||||||
chr1:37732192 | A | G | 28 | a0001c0001t0001g0044 a0001c0001t0001g0066 a0001c0001t0001g0072 others(25): Show |
31 | HG00621.hp1 HG01106.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1492-610T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732192 | |||||||
chr1:37732324 | G | A | 1 | a0002c0002t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1492-742C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732324 | |||||||
chr1:37732385 | C | T | 1 | a0001c0033t0002g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1492-803G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732385 | |||||||
chr1:37732433 | T | C | 59 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0174 others(56): Show |
66 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1492-851A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732433 | |||||||
chr1:37732470 | C | A | 1 | a0001c0001t0002g0185 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1492-888G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732470 | |||||||
chr1:37732670 | C | T | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG02056.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1492-1088G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732670 | |||||||
chr1:37732811 | G | C | 2 | a0004c0003t0003g0036 a0004c0003t0003g0038 |
2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1492-1229C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732811 | |||||||
chr1:37732812 | C | G | 2 | a0004c0003t0003g0117 a0004c0003t0003g0222 |
2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1492-1230G>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732812 | |||||||
chr1:37732857 | CTTGTTCT others(12): Show |
C | 4 | a0002c0011t0009g0021 a0002c0011t0009g0022 a0002c0011t0009g0023 others(1): Show |
4 | HG02818.hp2 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1492-1294_1492-127 others(23): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732857 | |||||||
chr1:37732860 | GTTCTTTT others(3): Show |
G | 3 | a0001c0005t0011g0041 a0001c0005t0015g0037 a0001c0005t0015g0039 |
3 | HG02615.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1492-1288_1492-127 others(14): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732860 | |||||||
chr1:37732863 | C | CT | 13 | a0001c0001t0001g0059 a0001c0001t0001g0070 a0001c0001t0001g0084 others(10): Show |
13 | HG00609.hp1 HG01346.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.1492-1282dupA | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | C | CTT | 6 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0076 others(3): Show |
6 | HG00438.hp1 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1492-1283_1492-128 others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | C | CTTT | 9 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0078 others(6): Show |
10 | HG00408.hp1 HG00673.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1492-1284_1492-128 others(7): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | C | CTTTT | 11 | a0001c0001t0001g0066 a0001c0001t0001g0118 a0001c0001t0001g0221 others(8): Show |
11 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(8): Show |
intron_variant | MODIFIER | c.1492-1285_1492-128 others(8): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | C | CTTTTTTT others(4): Show |
2 | a0001c0006t0002g0046 a0001c0006t0002g0047 |
2 | HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1492-1292_1492-128 others(15): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CT | C | 41 | a0001c0001t0001g0055 a0001c0001t0001g0083 a0001c0001t0001g0095 others(38): Show |
44 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1492-1282delA | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTT | C | 36 | a0001c0001t0001g0052 a0001c0001t0001g0140 a0001c0001t0001g0142 others(33): Show |
36 | HG00609.hp2 HG01081.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.1492-1283_1492-128 others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTT | C | 13 | a0001c0001t0001g0190 a0001c0001t0001g0194 a0001c0033t0002g0281 others(10): Show |
13 | HG00099.hp2 HG01261.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.1492-1284_1492-128 others(7): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTT | C | 12 | a0001c0001t0001g0195 a0001c0001t0002g0205 a0001c0001t0002g0213 others(9): Show |
13 | HG00733.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1492-1285_1492-128 others(8): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTT | C | 7 | a0001c0006t0009g0207 a0002c0002t0001g0287 a0002c0002t0002g0001 others(4): Show |
7 | HG00642.hp1 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1492-1286_1492-128 others(9): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTT | C | 15 | a0002c0002t0001g0017 a0002c0002t0001g0227 a0002c0002t0001g0234 others(12): Show |
16 | HG01069.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1492-1287_1492-128 others(10): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTTT | C | 29 | a0001c0001t0001g0054 a0001c0001t0001g0064 a0002c0002t0001g0004 others(26): Show |
29 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.1492-1288_1492-128 others(11): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTTT others(1): Show |
C | 14 | a0001c0001t0001g0071 a0001c0005t0004g0298 a0002c0002t0001g0004 others(11): Show |
18 | HG00323.hp1 HG00597.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1492-1289_1492-128 others(12): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0079 |
2 | HG00280.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1492-1291_1492-128 others(14): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0044 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1492-1293_1492-128 others(16): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0219 a0001c0001t0002g0153 a0001c0001t0002g0154 |
3 | HG03942.hp1 NA18950.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1492-1294_1492-128 others(17): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTTT others(7): Show |
C | 20 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0116 others(17): Show |
20 | HG00621.hp2 HG00735.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1492-1295_1492-128 others(18): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTTT others(8): Show |
C | 68 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0103 others(65): Show |
74 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.1492-1296_1492-128 others(19): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0002g0157 a0005c0009t0003g0161 |
2 | HG03490.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1492-1297_1492-128 others(20): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTTT others(10): Show |
C | 1 | a0011c0018t0014g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1492-1298_1492-128 others(21): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0001g0233 a0001c0044t0001g0279 |
2 | HG01346.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1492-1299_1492-128 others(22): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTTT others(13): Show |
C | 5 | a0002c0002t0001g0024 a0002c0002t0001g0302 a0002c0002t0001g0303 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1492-1301_1492-128 others(24): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTTT others(14): Show |
C | 3 | a0001c0001t0001g0082 a0001c0040t0011g0049 a0003c0004t0005g0314 |
3 | HG02698.hp2 HG03540.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1492-1302_1492-128 others(25): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTTT others(16): Show |
C | 2 | a0001c0001t0001g0220 a0004c0003t0003g0080 |
2 | HG02965.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1492-1304_1492-128 others(27): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTTT others(17): Show |
C | 2 | a0010c0016t0005g0312 a0011c0018t0014g0007 |
2 | NA18522.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1492-1305_1492-128 others(28): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTTT others(18): Show |
C | 2 | a0002c0011t0001g0034 a0002c0011t0002g0020 |
2 | HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1492-1306_1492-128 others(29): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTTT others(19): Show |
C | 1 | a0008c0014t0002g0031 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1492-1307_1492-128 others(30): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732863 | CTTTTTTT others(20): Show |
C | 1 | a0004c0003t0003g0263 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1492-1308_1492-128 others(31): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732863 | |||||||
chr1:37732879 | T | C | 5 | a0001c0001t0001g0044 a0002c0011t0009g0021 a0002c0011t0009g0022 others(2): Show |
5 | HG02145.hp2 HG02818.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1492-1297A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37732879 | |||||||
chr1:37733005 | G | A | 4 | a0002c0011t0009g0021 a0002c0011t0009g0022 a0002c0011t0009g0023 others(1): Show |
4 | HG02818.hp2 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1492-1423C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37733005 | |||||||
chr1:37733072 | T | C | 142 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(139): Show |
149 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(146): Show |
intron_variant | MODIFIER | c.1492-1490A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37733072 | |||||||
chr1:37733113 | G | A | 7 | a0001c0001t0001g0188 a0001c0001t0001g0198 a0001c0001t0001g0199 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1492-1531C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37733113 | |||||||
chr1:37733146 | G | A | 33 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0059 others(30): Show |
33 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1492-1564C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37733146 | |||||||
chr1:37733173 | G | A | 4 | a0002c0002t0001g0024 a0002c0002t0001g0302 a0002c0002t0001g0303 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1492-1591C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37733173 | |||||||
chr1:37733210 | T | C | 1 | a0002c0007t0004g0260 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1492-1628A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37733210 | |||||||
chr1:37733220 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1492-1638C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37733220 | |||||||
chr1:37733314 | C | T | 118 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0103 others(115): Show |
125 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.1492-1732G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37733314 | |||||||
chr1:37733315 | G | A | 1 | a0001c0033t0002g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1492-1733C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37733315 | |||||||
chr1:37733336 | T | A | 2 | a0002c0011t0001g0034 a0002c0011t0002g0020 |
2 | HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1492-1754A>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37733336 | |||||||
chr1:37733466 | G | A | 1 | a0002c0015t0007g0231 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1491+1791C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37733466 | |||||||
chr1:37733870 | T | C | 58 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0057 others(55): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1491+1387A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37733870 | |||||||
chr1:37734011 | C | T | 1 | a0002c0011t0002g0020 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1491+1246G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37734011 | |||||||
chr1:37734023 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1491+1234A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37734023 | |||||||
chr1:37734044 | C | T | 116 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0103 others(113): Show |
123 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.1491+1213G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37734044 | |||||||
chr1:37734242 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1491+1015T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37734242 | |||||||
chr1:37734325 | G | C | 54 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0057 others(51): Show |
55 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1491+932C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37734325 | |||||||
chr1:37734332 | T | C | 9 | a0001c0006t0007g0177 a0001c0006t0007g0178 a0001c0006t0007g0179 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1491+925A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37734332 | |||||||
chr1:37734363 | G | A | 5 | a0001c0033t0002g0281 a0003c0024t0006g0354 a0003c0025t0006g0352 others(2): Show |
5 | HG02074.hp1 HG06807.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1491+894C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37734363 | |||||||
chr1:37734392 | T | G | 196 | a0001c0001t0001g0008 a0001c0001t0001g0053 a0001c0001t0001g0055 others(193): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1491+865A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37734392 | |||||||
chr1:37734535 | A | AAAAT | 6 | a0001c0001t0001g0233 a0002c0002t0001g0024 a0002c0002t0001g0302 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1491+718_1491+721d others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37734535 | |||||||
chr1:37734954 | G | C | 6 | a0001c0001t0001g0233 a0002c0002t0001g0024 a0002c0002t0001g0302 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1491+303C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37734954 | |||||||
chr1:37735098 | G | A | 13 | a0001c0001t0001g0052 a0001c0006t0007g0177 a0001c0006t0007g0178 others(10): Show |
13 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1491+159C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37735098 | |||||||
chr1:37735219 | C | T | 1 | a0018c0029t0006g0308 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1491+38G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 6/16 | chr1 | 37735219 | |||||||
chr1:37735466 | G | A | 3 | a0002c0002t0002g0019 a0008c0014t0002g0026 a0011c0018t0014g0007 |
4 | HG02486.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1358-76C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37735466 | |||||||
chr1:37735636 | G | A | 6 | a0001c0005t0011g0040 a0001c0005t0011g0041 a0001c0005t0015g0037 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-246C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37735636 | |||||||
chr1:37735674 | A | T | 121 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0103 others(118): Show |
128 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.1358-284T>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37735674 | |||||||
chr1:37735681 | A | G | 125 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0103 others(122): Show |
132 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.1358-291T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37735681 | |||||||
chr1:37735699 | C | T | 198 | a0001c0001t0001g0008 a0001c0001t0001g0053 a0001c0001t0001g0055 others(195): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1358-309G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37735699 | |||||||
chr1:37735708 | T | C | 2 | a0004c0003t0003g0117 a0004c0003t0003g0222 |
2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1358-318A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37735708 | |||||||
chr1:37736076 | A | T | 5 | a0001c0033t0002g0281 a0003c0024t0006g0354 a0003c0025t0006g0352 others(2): Show |
5 | HG02074.hp1 HG06807.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358-686T>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736076 | |||||||
chr1:37736235 | G | A | 6 | a0001c0001t0001g0233 a0002c0002t0001g0024 a0002c0002t0001g0302 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1358-845C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736235 | |||||||
chr1:37736253 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1358-863C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736253 | |||||||
chr1:37736311 | G | A | 56 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0057 others(53): Show |
57 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1358-921C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736311 | |||||||
chr1:37736312 | C | A | 56 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0057 others(53): Show |
57 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1358-922G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736312 | |||||||
chr1:37736428 | G | A | 276 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(273): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1358-1038C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736428 | |||||||
chr1:37736476 | C | CA | 55 | a0001c0001t0001g0220 a0001c0001t0001g0233 a0001c0001t0002g0128 others(52): Show |
58 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.1358-1087dupT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736476 | |||||||
chr1:37736476 | C | CAA | 13 | a0001c0001t0001g0195 a0001c0001t0002g0143 a0001c0005t0004g0184 others(10): Show |
13 | HG01168.hp1 HG01975.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1358-1088_1358-108 others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736476 | |||||||
chr1:37736476 | C | CAAA | 99 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0104 others(96): Show |
106 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1358-1089_1358-108 others(7): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736476 | |||||||
chr1:37736476 | C | CAAAA | 13 | a0001c0001t0001g0103 a0001c0001t0001g0109 a0001c0001t0001g0115 others(10): Show |
13 | HG00738.hp2 HG02080.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1358-1090_1358-108 others(8): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736476 | |||||||
chr1:37736476 | CA | C | 6 | a0001c0001t0001g0262 a0001c0006t0007g0178 a0002c0002t0001g0248 others(3): Show |
6 | HG01257.hp2 HG01515.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1358-1087delT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736476 | |||||||
chr1:37736476 | CAAAAAAA | C | 53 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0057 others(50): Show |
54 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1358-1093_1358-108 others(11): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736476 | |||||||
chr1:37736498 | A | G | 1 | a0024c0049t0020g0307 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1358-1108T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736498 | |||||||
chr1:37736534 | C | T | 75 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0054 others(72): Show |
85 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1358-1144G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736534 | |||||||
chr1:37736580 | C | T | 3 | a0002c0015t0007g0043 a0004c0003t0003g0117 a0004c0003t0003g0222 |
3 | HG01069.hp2 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1358-1190G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736580 | |||||||
chr1:37736581 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1358-1191C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736581 | |||||||
chr1:37736601 | G | A | 1 | a0003c0008t0006g0332 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1358-1211C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736601 | |||||||
chr1:37736747 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0221 |
3 | HG00741.hp2 HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1358-1357G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736747 | |||||||
chr1:37736771 | C | T | 1 | a0002c0002t0001g0269 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1358-1381G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736771 | |||||||
chr1:37736856 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1358-1466G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37736856 | |||||||
chr1:37737003 | C | T | 121 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0103 others(118): Show |
128 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.1358-1613G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737003 | |||||||
chr1:37737048 | C | T | 116 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0103 others(113): Show |
123 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.1358-1658G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737048 | |||||||
chr1:37737275 | T | G | 5 | a0001c0033t0002g0281 a0003c0024t0006g0354 a0003c0025t0006g0352 others(2): Show |
5 | HG02074.hp1 HG06807.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358-1885A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737275 | |||||||
chr1:37737343 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1358-1953C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737343 | |||||||
chr1:37737595 | T | G | 116 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0103 others(113): Show |
123 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.1358-2205A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737595 | |||||||
chr1:37737687 | G | C | 116 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0103 others(113): Show |
123 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.1358-2297C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737687 | |||||||
chr1:37737791 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1358-2401C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737791 | |||||||
chr1:37737907 | A | G | 6 | a0001c0001t0001g0233 a0002c0002t0001g0024 a0002c0002t0001g0302 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1358-2517T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737907 | |||||||
chr1:37737932 | C | CT | 49 | a0001c0001t0001g0059 a0001c0001t0001g0069 a0001c0001t0001g0082 others(46): Show |
49 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.1358-2543dupA | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737932 | |||||||
chr1:37737932 | C | CTT | 45 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0055 others(42): Show |
47 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.1358-2544_1358-254 others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737932 | |||||||
chr1:37737932 | C | CTTT | 60 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0057 others(57): Show |
72 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.1358-2545_1358-254 others(7): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737932 | |||||||
chr1:37737932 | C | CTTTT | 26 | a0001c0001t0001g0233 a0001c0005t0011g0040 a0001c0005t0011g0041 others(23): Show |
26 | HG00544.hp1 HG01109.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.1358-2546_1358-254 others(8): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737932 | |||||||
chr1:37737932 | CTT | C | 14 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0190 others(11): Show |
15 | HG00735.hp2 HG01074.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.1358-2544_1358-254 others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737932 | |||||||
chr1:37737932 | CTTT | C | 95 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0103 others(92): Show |
101 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1358-2545_1358-254 others(7): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737932 | |||||||
chr1:37737932 | CTTTT | C | 11 | a0001c0001t0001g0142 a0001c0001t0001g0166 a0001c0001t0001g0167 others(8): Show |
11 | HG00639.hp1 HG02074.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1358-2546_1358-254 others(8): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737932 | |||||||
chr1:37737932 | CTTTTTTT others(3): Show |
C | 4 | a0001c0005t0004g0225 a0002c0002t0002g0019 a0008c0014t0002g0026 others(1): Show |
5 | HG02486.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1358-2552_1358-254 others(14): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737932 | |||||||
chr1:37737932 | CTTTTTTT others(4): Show |
C | 1 | a0001c0037t0004g0130 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1358-2553_1358-254 others(15): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737932 | |||||||
chr1:37737932 | CTTTTTTT others(5): Show |
C | 2 | a0001c0040t0011g0049 a0004c0038t0003g0226 |
2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1358-2554_1358-254 others(16): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737932 | |||||||
chr1:37737932 | CTTTTTTT others(6): Show |
C | 5 | a0002c0011t0001g0034 a0002c0011t0002g0020 a0002c0011t0009g0021 others(2): Show |
5 | HG02615.hp2 HG02818.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358-2555_1358-254 others(17): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737932 | |||||||
chr1:37737932 | CTTTTTTT others(7): Show |
C | 1 | a0002c0011t0009g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1358-2556_1358-254 others(18): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737932 | |||||||
chr1:37737961 | C | T | 6 | a0001c0001t0001g0233 a0002c0002t0001g0024 a0002c0002t0001g0302 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1358-2571G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737961 | |||||||
chr1:37737989 | T | TG | 276 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(273): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1358-2600dupC | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737989 | |||||||
chr1:37737993 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1358-2603G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37737993 | |||||||
chr1:37738091 | A | G | 276 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(273): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1358-2701T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37738091 | |||||||
chr1:37738093 | C | T | 7 | a0002c0007t0004g0014 a0002c0007t0004g0216 a0002c0007t0004g0235 others(4): Show |
8 | HG00544.hp2 HG00558.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358-2703G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37738093 | |||||||
chr1:37738099 | G | A | 1 | a0002c0002t0002g0258 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1358-2709C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37738099 | |||||||
chr1:37738106 | G | A | 6 | a0002c0011t0001g0034 a0002c0011t0002g0020 a0002c0011t0009g0021 others(3): Show |
6 | HG02615.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-2716C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37738106 | |||||||
chr1:37738212 | C | T | 5 | a0001c0033t0002g0281 a0003c0024t0006g0354 a0003c0025t0006g0352 others(2): Show |
5 | HG02074.hp1 HG06807.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358-2822G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37738212 | |||||||
chr1:37738340 | G | C | 198 | a0001c0001t0001g0008 a0001c0001t0001g0053 a0001c0001t0001g0055 others(195): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1358-2950C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37738340 | |||||||
chr1:37738451 | A | T | 1 | a0003c0004t0005g0331 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1358-3061T>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37738451 | |||||||
chr1:37738566 | T | C | 1 | a0001c0001t0002g0151 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1358-3176A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37738566 | |||||||
chr1:37738627 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1358-3237A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37738627 | |||||||
chr1:37738680 | G | A | 6 | a0001c0005t0011g0040 a0001c0005t0011g0041 a0001c0005t0015g0037 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-3290C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37738680 | |||||||
chr1:37738712 | T | C | 5 | a0001c0033t0002g0281 a0003c0024t0006g0354 a0003c0025t0006g0352 others(2): Show |
5 | HG02074.hp1 HG06807.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358-3322A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37738712 | |||||||
chr1:37738821 | TA | T | 130 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0103 others(127): Show |
137 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1358-3432delT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37738821 | |||||||
chr1:37738841 | G | A | 5 | a0001c0033t0002g0281 a0003c0024t0006g0354 a0003c0025t0006g0352 others(2): Show |
5 | HG02074.hp1 HG06807.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358-3451C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37738841 | |||||||
chr1:37738882 | T | TA | 124 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0103 others(121): Show |
131 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.1358-3493dupT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37738882 | |||||||
chr1:37738902 | C | A | 1 | a0001c0001t0002g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1358-3512G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37738902 | |||||||
chr1:37738935 | G | A | 2 | a0004c0003t0003g0117 a0004c0003t0003g0222 |
2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1358-3545C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37738935 | |||||||
chr1:37738990 | G | A | 6 | a0002c0011t0001g0034 a0002c0011t0002g0020 a0002c0011t0009g0021 others(3): Show |
6 | HG02615.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-3600C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37738990 | |||||||
chr1:37739003 | G | A | 3 | a0008c0014t0002g0029 a0008c0014t0002g0030 a0019c0032t0002g0033 |
3 | HG02717.hp1 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1358-3613C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37739003 | |||||||
chr1:37739073 | C | T | 1 | a0002c0002t0001g0024 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1358-3683G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37739073 | |||||||
chr1:37739075 | A | C | 1 | a0001c0001t0002g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1358-3685T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37739075 | |||||||
chr1:37739116 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1358-3726C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37739116 | |||||||
chr1:37739153 | TAAAAA | T | 6 | a0002c0011t0001g0034 a0002c0011t0002g0020 a0002c0011t0009g0021 others(3): Show |
6 | HG02615.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-3768_1358-376 others(9): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37739153 | |||||||
chr1:37739265 | C | A | 116 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0103 others(113): Show |
123 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.1358-3875G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37739265 | |||||||
chr1:37739448 | G | A | 16 | a0002c0002t0001g0004 a0002c0002t0001g0125 a0002c0002t0001g0242 others(13): Show |
22 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.1358-4058C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37739448 | |||||||
chr1:37739535 | A | C | 4 | a0001c0005t0004g0225 a0002c0002t0002g0019 a0008c0014t0002g0026 others(1): Show |
5 | HG02486.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1358-4145T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37739535 | |||||||
chr1:37739616 | G | A | 1 | a0025c0035t0001g0209 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1358-4226C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37739616 | |||||||
chr1:37739688 | C | CA | 9 | a0001c0001t0001g0280 a0002c0002t0001g0024 a0002c0002t0001g0302 others(6): Show |
9 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1358-4299dupT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37739688 | |||||||
chr1:37739688 | CA | C | 190 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0098 others(187): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1358-4299delT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37739688 | |||||||
chr1:37739688 | CAA | C | 6 | a0001c0001t0001g0188 a0001c0001t0002g0157 a0001c0001t0002g0158 others(3): Show |
6 | HG01069.hp1 HG01256.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-4300_1358-429 others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37739688 | |||||||
chr1:37739688 | CAAAAAA | C | 54 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0057 others(51): Show |
55 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1358-4304_1358-429 others(10): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37739688 | |||||||
chr1:37739688 | CAAAAAAA others(3): Show |
C | 1 | a0003c0004t0005g0313 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1358-4308_1358-429 others(14): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37739688 | |||||||
chr1:37739713 | G | C | 1 | a0002c0002t0001g0305 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1358-4323C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37739713 | |||||||
chr1:37739918 | A | T | 1 | a0001c0001t0002g0163 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1358-4528T>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37739918 | |||||||
chr1:37739930 | C | CA | 75 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0005t0004g0298 others(72): Show |
85 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1358-4541dupT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37739930 | |||||||
chr1:37740006 | C | A | 276 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(273): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1358-4616G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740006 | |||||||
chr1:37740074 | T | C | 1 | a0001c0001t0002g0157 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1358-4684A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740074 | |||||||
chr1:37740075 | C | T | 1 | a0001c0001t0002g0157 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1358-4685G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740075 | |||||||
chr1:37740076 | A | C | 1 | a0001c0001t0002g0157 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1358-4686T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740076 | |||||||
chr1:37740298 | T | C | 85 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0103 others(82): Show |
91 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1358-4908A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740298 | |||||||
chr1:37740355 | G | C | 61 | a0001c0005t0004g0298 a0001c0005t0011g0040 a0001c0005t0011g0041 others(58): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1358-4965C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740355 | |||||||
chr1:37740430 | C | T | 1 | a0004c0003t0003g0073 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1358-5040G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740430 | |||||||
chr1:37740455 | G | A | 8 | a0001c0001t0002g0126 a0001c0001t0002g0143 a0001c0001t0002g0153 others(5): Show |
8 | HG00621.hp2 HG02523.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.1358-5065C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740455 | |||||||
chr1:37740466 | C | T | 47 | a0001c0001t0001g0140 a0001c0001t0001g0142 a0001c0001t0001g0166 others(44): Show |
48 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.1358-5076G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740466 | |||||||
chr1:37740467 | A | G | 136 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(133): Show |
143 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.1358-5077T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740467 | |||||||
chr1:37740495 | C | T | 18 | a0001c0001t0001g0220 a0001c0001t0002g0128 a0002c0007t0012g0028 others(15): Show |
18 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1358-5105G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740495 | |||||||
chr1:37740691 | C | T | 9 | a0001c0006t0007g0177 a0001c0006t0007g0178 a0001c0006t0007g0179 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1358-5301G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740691 | |||||||
chr1:37740698 | C | CACACACA others(1): Show |
6 | a0002c0011t0001g0034 a0002c0011t0002g0020 a0002c0011t0009g0021 others(3): Show |
6 | HG02615.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-5316_1358-530 others(12): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740698 | |||||||
chr1:37740731 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | NA18969.hp1 NA19000.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1358-5341C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740731 | |||||||
chr1:37740770 | A | C | 2 | a0001c0001t0002g0065 a0005c0009t0003g0062 |
2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1358-5380T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740770 | |||||||
chr1:37740804 | G | A | 1 | a0001c0005t0004g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1358-5414C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740804 | |||||||
chr1:37740853 | T | C | 4 | a0001c0005t0004g0225 a0002c0002t0002g0019 a0008c0014t0002g0026 others(1): Show |
5 | HG02486.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1358-5463A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740853 | |||||||
chr1:37740966 | A | C | 1 | a0001c0001t0001g0044 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1358-5576T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37740966 | |||||||
chr1:37741125 | A | G | 266 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(263): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1358-5735T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741125 | |||||||
chr1:37741163 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0088 |
2 | NA18981.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1358-5773A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741163 | |||||||
chr1:37741210 | C | T | 3 | a0004c0003t0003g0197 a0004c0003t0003g0203 a0025c0035t0001g0209 |
3 | HG02809.hp1 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1358-5820G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741210 | |||||||
chr1:37741226 | C | T | 1 | a0010c0016t0005g0312 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1358-5836G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741226 | |||||||
chr1:37741341 | G | A | 1 | a0024c0049t0020g0307 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1358-5951C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741341 | |||||||
chr1:37741370 | G | A | 55 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0055 others(52): Show |
56 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1358-5980C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741370 | |||||||
chr1:37741424 | G | C | 1 | a0001c0033t0002g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1358-6034C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741424 | |||||||
chr1:37741439 | G | T | 3 | a0001c0001t0009g0300 a0001c0001t0009g0301 a0004c0003t0003g0299 |
3 | HG02451.hp1 HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1358-6049C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741439 | |||||||
chr1:37741557 | C | T | 6 | a0001c0005t0011g0040 a0001c0005t0011g0041 a0001c0005t0015g0037 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-6167G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741557 | |||||||
chr1:37741582 | A | T | 1 | a0002c0002t0001g0245 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1358-6192T>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741582 | |||||||
chr1:37741595 | A | G | 1 | a0002c0002t0001g0024 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1358-6205T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741595 | |||||||
chr1:37741608 | A | G | 20 | a0002c0002t0001g0005 a0002c0002t0001g0017 a0002c0002t0001g0227 others(17): Show |
24 | HG01123.hp2 HG01496.hp1 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.1358-6218T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741608 | |||||||
chr1:37741643 | A | C | 130 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(127): Show |
137 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1358-6253T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741643 | |||||||
chr1:37741664 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1358-6274G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741664 | |||||||
chr1:37741728 | C | T | 9 | a0001c0006t0007g0177 a0001c0006t0007g0178 a0001c0006t0007g0179 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1358-6338G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741728 | |||||||
chr1:37741758 | T | TA | 134 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(131): Show |
141 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1358-6369dupT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741758 | |||||||
chr1:37741758 | TA | T | 28 | a0002c0007t0004g0014 a0002c0007t0004g0216 a0002c0007t0004g0235 others(25): Show |
31 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1358-6369delT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741758 | |||||||
chr1:37741791 | G | A | 1 | a0003c0013t0006g0342 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1358-6401C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741791 | |||||||
chr1:37741850 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1358-6460A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741850 | |||||||
chr1:37741891 | C | T | 130 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(127): Show |
137 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1358-6501G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741891 | |||||||
chr1:37741925 | G | A | 56 | a0001c0001t0001g0220 a0001c0001t0002g0128 a0002c0007t0004g0014 others(53): Show |
59 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.1358-6535C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37741925 | |||||||
chr1:37742153 | G | T | 130 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(127): Show |
137 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1358-6763C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37742153 | |||||||
chr1:37742328 | C | T | 130 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(127): Show |
137 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1358-6938G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37742328 | |||||||
chr1:37742502 | T | C | 130 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(127): Show |
137 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1358-7112A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37742502 | |||||||
chr1:37742573 | TGAGAATG others(156): Show |
T | 130 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(127): Show |
137 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1358-7346_1358-718 others(4): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37742573 | |||||||
chr1:37742796 | G | A | 7 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0001g0090 others(4): Show |
7 | HG00438.hp1 HG00609.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.1358-7406C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37742796 | |||||||
chr1:37742901 | G | A | 53 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0055 others(50): Show |
54 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1358-7511C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37742901 | |||||||
chr1:37742924 | A | G | 130 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(127): Show |
137 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1358-7534T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37742924 | |||||||
chr1:37742982 | T | C | 5 | a0001c0033t0002g0281 a0003c0024t0006g0354 a0003c0025t0006g0352 others(2): Show |
5 | HG02074.hp1 HG06807.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358-7592A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37742982 | |||||||
chr1:37743065 | T | A | 1 | a0002c0002t0001g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1358-7675A>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37743065 | |||||||
chr1:37743172 | A | C | 2 | a0001c0001t0001g0220 a0023c0027t0005g0330 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1358-7782T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37743172 | |||||||
chr1:37743221 | T | C | 134 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(131): Show |
141 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1358-7831A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37743221 | |||||||
chr1:37743285 | G | A | 1 | a0032c0030t0002g0304 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1358-7895C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37743285 | |||||||
chr1:37743330 | T | G | 2 | a0001c0040t0011g0049 a0004c0038t0003g0226 |
2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1358-7940A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37743330 | |||||||
chr1:37743431 | G | C | 5 | a0002c0002t0001g0024 a0002c0002t0001g0302 a0002c0002t0001g0303 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1358-8041C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37743431 | |||||||
chr1:37743443 | T | C | 6 | a0002c0011t0001g0034 a0002c0011t0002g0020 a0002c0011t0009g0021 others(3): Show |
6 | HG02615.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-8053A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37743443 | |||||||
chr1:37743561 | C | T | 134 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(131): Show |
141 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1358-8171G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37743561 | |||||||
chr1:37743562 | A | G | 134 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(131): Show |
141 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1358-8172T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37743562 | |||||||
chr1:37743673 | T | TGA | 276 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(273): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1358-8285_1358-828 others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37743673 | |||||||
chr1:37743706 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1358-8316C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37743706 | |||||||
chr1:37743714 | C | T | 134 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(131): Show |
141 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1358-8324G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37743714 | |||||||
chr1:37743887 | TATATAGA others(3): Show |
T | 6 | a0001c0005t0011g0040 a0001c0005t0011g0041 a0001c0005t0015g0037 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-8507_1358-849 others(14): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37743887 | |||||||
chr1:37743902 | A | AGAT | 134 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(131): Show |
141 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1358-8515_1358-851 others(7): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37743902 | |||||||
chr1:37744170 | A | G | 2 | a0001c0040t0011g0049 a0004c0038t0003g0226 |
2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1357+8706T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37744170 | |||||||
chr1:37744249 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1357+8627G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37744249 | |||||||
chr1:37744260 | T | A | 134 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(131): Show |
141 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1357+8616A>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37744260 | |||||||
chr1:37744355 | C | CA | 8 | a0001c0006t0007g0181 a0001c0006t0007g0182 a0001c0006t0007g0183 others(5): Show |
8 | HG00738.hp1 HG01496.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1357+8520dupT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37744355 | |||||||
chr1:37744412 | C | T | 1 | a0003c0004t0005g0329 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1357+8464G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37744412 | |||||||
chr1:37744436 | T | C | 134 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(131): Show |
141 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1357+8440A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37744436 | |||||||
chr1:37744627 | G | T | 134 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(131): Show |
141 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1357+8249C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37744627 | |||||||
chr1:37744640 | A | C | 3 | a0001c0001t0001g0064 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG03942.hp2 NA18999.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1357+8236T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37744640 | |||||||
chr1:37744663 | G | GA | 133 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(130): Show |
140 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.1357+8212dupT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37744663 | |||||||
chr1:37744764 | TCTGA | T | 123 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0103 others(120): Show |
130 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.1357+8108_1357+811 others(8): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37744764 | |||||||
chr1:37744892 | T | G | 134 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(131): Show |
141 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1357+7984A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37744892 | |||||||
chr1:37744941 | G | A | 133 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(130): Show |
140 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.1357+7935C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37744941 | |||||||
chr1:37745017 | C | A | 4 | a0002c0002t0001g0288 a0002c0002t0001g0291 a0013c0019t0002g0289 others(1): Show |
4 | NA18950.hp1 NA18961.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.1357+7859G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37745017 | |||||||
chr1:37745018 | G | A | 3 | a0001c0001t0009g0300 a0001c0001t0009g0301 a0004c0003t0003g0299 |
3 | HG02451.hp1 HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1357+7858C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37745018 | |||||||
chr1:37745101 | G | A | 6 | a0002c0011t0001g0034 a0002c0011t0002g0020 a0002c0011t0009g0021 others(3): Show |
6 | HG02615.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1357+7775C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37745101 | |||||||
chr1:37745139 | A | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0142 a0001c0001t0001g0166 others(2): Show |
5 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1357+7737T>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37745139 | |||||||
chr1:37745469 | G | A | 134 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(131): Show |
141 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1357+7407C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37745469 | |||||||
chr1:37745528 | A | C | 134 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(131): Show |
141 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1357+7348T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37745528 | |||||||
chr1:37745533 | A | G | 134 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(131): Show |
141 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1357+7343T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37745533 | |||||||
chr1:37745584 | C | G | 1 | a0003c0013t0006g0328 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1357+7292G>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37745584 | |||||||
chr1:37745654 | A | C | 1 | a0001c0001t0001g0098 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1357+7222T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37745654 | |||||||
chr1:37745710 | C | T | 1 | a0001c0006t0009g0207 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1357+7166G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37745710 | |||||||
chr1:37745720 | C | T | 133 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(130): Show |
140 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.1357+7156G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37745720 | |||||||
chr1:37745731 | T | C | 5 | a0002c0002t0001g0024 a0002c0002t0001g0302 a0002c0002t0001g0303 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1357+7145A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37745731 | |||||||
chr1:37745787 | T | C | 2 | a0004c0003t0003g0117 a0004c0003t0003g0222 |
2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1357+7089A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37745787 | |||||||
chr1:37745983 | G | C | 1 | a0001c0001t0001g0156 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1357+6893C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37745983 | |||||||
chr1:37746087 | T | A | 134 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(131): Show |
141 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1357+6789A>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37746087 | |||||||
chr1:37746101 | C | CT | 28 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0164 others(25): Show |
28 | HG01069.hp1 HG01884.hp2 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1357+6774dupA | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37746101 | |||||||
chr1:37746101 | C | CTT | 116 | a0001c0001t0001g0098 a0001c0001t0001g0103 a0001c0001t0001g0104 others(113): Show |
123 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.1357+6773_1357+677 others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37746101 | |||||||
chr1:37746120 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1357+6756C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37746120 | |||||||
chr1:37746153 | C | T | 133 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(130): Show |
140 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.1357+6723G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37746153 | |||||||
chr1:37746259 | C | T | 2 | a0001c0001t0001g0059 a0022c0039t0001g0063 |
2 | HG02738.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1357+6617G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37746259 | |||||||
chr1:37746453 | A | G | 128 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0098 others(125): Show |
135 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.1357+6423T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37746453 | |||||||
chr1:37746689 | T | C | 2 | a0001c0001t0001g0280 a0005c0009t0003g0273 |
2 | HG02683.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1357+6187A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37746689 | |||||||
chr1:37746793 | A | G | 55 | a0001c0005t0004g0298 a0002c0002t0001g0004 a0002c0002t0001g0005 others(52): Show |
65 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1357+6083T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37746793 | |||||||
chr1:37746806 | T | C | 1 | a0002c0002t0001g0242 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1357+6070A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37746806 | |||||||
chr1:37747390 | A | G | 5 | a0001c0033t0002g0281 a0003c0024t0006g0354 a0003c0025t0006g0352 others(2): Show |
5 | HG02074.hp1 HG06807.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1357+5486T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37747390 | |||||||
chr1:37747393 | A | C | 1 | a0001c0001t0001g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1357+5483T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37747393 | |||||||
chr1:37747466 | G | A | 1 | a0002c0007t0004g0260 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1357+5410C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37747466 | |||||||
chr1:37747552 | C | CA | 57 | a0001c0001t0001g0070 a0001c0001t0001g0095 a0001c0001t0001g0220 others(54): Show |
60 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.1357+5323dupT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37747552 | |||||||
chr1:37747552 | C | CAA | 54 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0055 others(51): Show |
55 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1357+5322_1357+532 others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37747552 | |||||||
chr1:37747552 | CA | C | 143 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(140): Show |
150 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1357+5323delT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37747552 | |||||||
chr1:37747564 | A | C | 2 | a0004c0003t0003g0036 a0004c0003t0003g0038 |
2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1357+5312T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37747564 | |||||||
chr1:37747625 | G | A | 1 | a0002c0007t0012g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1357+5251C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37747625 | |||||||
chr1:37747638 | T | C | 55 | a0001c0005t0004g0298 a0002c0002t0001g0004 a0002c0002t0001g0005 others(52): Show |
65 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1357+5238A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37747638 | |||||||
chr1:37747725 | G | A | 10 | a0001c0001t0001g0233 a0001c0001t0009g0300 a0001c0001t0009g0301 others(7): Show |
10 | HG02451.hp1 HG02615.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1357+5151C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37747725 | |||||||
chr1:37747805 | G | A | 1 | a0004c0003t0003g0274 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1357+5071C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37747805 | |||||||
chr1:37747835 | C | T | 2 | a0004c0003t0003g0196 a0021c0045t0003g0123 |
2 | HG00733.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1357+5041G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37747835 | |||||||
chr1:37747888 | T | G | 1 | a0001c0001t0001g0275 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1357+4988A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37747888 | |||||||
chr1:37747930 | G | C | 1 | a0005c0009t0003g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1357+4946C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37747930 | |||||||
chr1:37747943 | T | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0221 |
3 | HG00741.hp2 HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1357+4933A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37747943 | |||||||
chr1:37748015 | T | G | 130 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(127): Show |
137 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1357+4861A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37748015 | |||||||
chr1:37748049 | G | A | 3 | a0001c0001t0009g0300 a0001c0001t0009g0301 a0004c0003t0003g0299 |
3 | HG02451.hp1 HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1357+4827C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37748049 | |||||||
chr1:37748214 | C | T | 3 | a0001c0006t0002g0046 a0001c0006t0002g0047 a0004c0003t0016g0045 |
3 | HG02451.hp2 HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1357+4662G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37748214 | |||||||
chr1:37748219 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1357+4657G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37748219 | |||||||
chr1:37748428 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1357+4448C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37748428 | |||||||
chr1:37748662 | G | C | 5 | a0002c0002t0001g0024 a0002c0002t0001g0302 a0002c0002t0001g0303 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1357+4214C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37748662 | |||||||
chr1:37748791 | C | T | 72 | a0001c0005t0004g0298 a0001c0005t0011g0040 a0001c0005t0011g0041 others(69): Show |
82 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1357+4085G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37748791 | |||||||
chr1:37748847 | G | A | 7 | a0001c0001t0001g0052 a0001c0006t0009g0207 a0004c0003t0003g0187 others(4): Show |
7 | HG00642.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1357+4029C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37748847 | |||||||
chr1:37748918 | C | CTT | 105 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0104 others(102): Show |
112 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.1357+3956_1357+395 others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37748918 | |||||||
chr1:37748918 | C | CTTT | 18 | a0001c0001t0001g0098 a0001c0001t0001g0103 a0001c0001t0001g0113 others(15): Show |
18 | HG00597.hp2 HG00621.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1357+3955_1357+395 others(7): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37748918 | |||||||
chr1:37748918 | CT | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0057 others(62): Show |
66 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.1357+3957delA | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37748918 | |||||||
chr1:37748918 | CTT | C | 20 | a0001c0005t0011g0040 a0001c0005t0011g0041 a0001c0005t0015g0037 others(17): Show |
20 | HG01109.hp1 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1357+3956_1357+395 others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37748918 | |||||||
chr1:37748918 | CTTT | C | 54 | a0001c0005t0004g0298 a0002c0002t0001g0004 a0002c0002t0001g0005 others(51): Show |
64 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1357+3955_1357+395 others(7): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37748918 | |||||||
chr1:37749025 | A | T | 1 | a0001c0001t0002g0042 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1357+3851T>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37749025 | |||||||
chr1:37749161 | G | A | 3 | a0001c0006t0002g0046 a0001c0006t0002g0047 a0004c0003t0016g0045 |
3 | HG02451.hp2 HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1357+3715C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37749161 | |||||||
chr1:37749225 | G | A | 131 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(128): Show |
138 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.1357+3651C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37749225 | |||||||
chr1:37749251 | A | C | 1 | a0004c0003t0003g0036 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1357+3625T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37749251 | |||||||
chr1:37749282 | G | A | 1 | a0002c0011t0002g0020 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1357+3594C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37749282 | |||||||
chr1:37749288 | T | C | 6 | a0001c0005t0011g0040 a0001c0005t0011g0041 a0001c0005t0015g0037 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1357+3588A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37749288 | |||||||
chr1:37749307 | T | C | 131 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(128): Show |
138 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.1357+3569A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37749307 | |||||||
chr1:37749351 | A | G | 1 | a0024c0049t0020g0307 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1357+3525T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37749351 | |||||||
chr1:37749395 | G | A | 2 | a0004c0003t0003g0117 a0004c0003t0003g0222 |
2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1357+3481C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37749395 | |||||||
chr1:37749532 | T | A | 189 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(186): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1357+3344A>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37749532 | |||||||
chr1:37749581 | G | A | 3 | a0002c0002t0002g0268 a0007c0012t0010g0326 a0015c0031t0019g0267 |
3 | HG00621.hp1 HG02155.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1357+3295C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37749581 | |||||||
chr1:37749605 | G | A | 131 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(128): Show |
138 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.1357+3271C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37749605 | |||||||
chr1:37749721 | A | G | 1 | a0004c0003t0003g0215 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1357+3155T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37749721 | |||||||
chr1:37749775 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1357+3101C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37749775 | |||||||
chr1:37749781 | A | G | 1 | a0005c0009t0003g0062 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1357+3095T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37749781 | |||||||
chr1:37749998 | G | A | 2 | a0001c0040t0011g0049 a0004c0038t0003g0226 |
2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1357+2878C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37749998 | |||||||
chr1:37750120 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1357+2756A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37750120 | |||||||
chr1:37750165 | G | GT | 131 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(128): Show |
138 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.1357+2710dupA | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37750165 | |||||||
chr1:37750245 | C | T | 51 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0055 others(48): Show |
52 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1357+2631G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37750245 | |||||||
chr1:37750246 | G | A | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG02056.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1357+2630C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37750246 | |||||||
chr1:37750398 | A | G | 1 | a0007c0012t0010g0327 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1357+2478T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37750398 | |||||||
chr1:37750401 | C | T | 1 | a0002c0015t0007g0043 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1357+2475G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37750401 | |||||||
chr1:37750464 | G | GGAAGT | 276 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(273): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1357+2407_1357+241 others(9): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37750464 | |||||||
chr1:37750563 | G | A | 1 | a0003c0004t0005g0355 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1357+2313C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37750563 | |||||||
chr1:37750580 | C | CT | 6 | a0001c0001t0002g0097 a0001c0033t0002g0281 a0002c0015t0007g0025 others(3): Show |
6 | HG02074.hp1 HG02109.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1357+2295dupA | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37750580 | |||||||
chr1:37750580 | CT | C | 7 | a0001c0001t0001g0164 a0001c0005t0011g0041 a0001c0005t0015g0037 others(4): Show |
7 | HG01168.hp1 HG02615.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.1357+2295delA | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37750580 | |||||||
chr1:37750661 | C | G | 72 | a0001c0005t0004g0298 a0001c0005t0011g0040 a0001c0005t0011g0041 others(69): Show |
82 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1357+2215G>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37750661 | |||||||
chr1:37750741 | G | A | 9 | a0001c0001t0009g0300 a0001c0001t0009g0301 a0002c0011t0001g0034 others(6): Show |
9 | HG02451.hp1 HG02615.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1357+2135C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37750741 | |||||||
chr1:37750827 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1357+2049A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37750827 | |||||||
chr1:37750866 | A | G | 2 | a0001c0040t0011g0049 a0004c0038t0003g0226 |
2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1357+2010T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37750866 | |||||||
chr1:37751121 | C | T | 1 | a0002c0011t0009g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1357+1755G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751121 | |||||||
chr1:37751122 | G | A | 1 | a0003c0004t0008g0349 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1357+1754C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751122 | |||||||
chr1:37751135 | G | A | 1 | a0001c0001t0002g0128 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1357+1741C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751135 | |||||||
chr1:37751159 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1357+1717G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751159 | |||||||
chr1:37751201 | C | CA | 10 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0005t0011g0040 others(7): Show |
10 | HG00323.hp2 HG01175.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1357+1674dupT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751201 | |||||||
chr1:37751201 | C | CAA | 7 | a0001c0001t0001g0044 a0001c0001t0001g0137 a0001c0001t0001g0188 others(4): Show |
7 | HG01069.hp1 HG01975.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1357+1673_1357+167 others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751201 | |||||||
chr1:37751201 | C | CAAA | 97 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0098 others(94): Show |
103 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1357+1672_1357+167 others(7): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751201 | |||||||
chr1:37751201 | C | CAAAA | 21 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0116 others(18): Show |
22 | HG00621.hp2 HG01106.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1357+1671_1357+167 others(8): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751201 | |||||||
chr1:37751201 | CA | C | 17 | a0001c0001t0001g0061 a0001c0001t0001g0262 a0001c0033t0002g0281 others(14): Show |
17 | HG01243.hp2 HG01257.hp2 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.1357+1674delT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751201 | |||||||
chr1:37751214 | A | G | 6 | a0002c0002t0001g0024 a0002c0002t0001g0302 a0002c0002t0001g0303 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1357+1662T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751214 | |||||||
chr1:37751217 | AGAAAG | A | 3 | a0001c0001t0001g0135 a0001c0006t0009g0207 a0004c0003t0003g0208 |
3 | HG00642.hp1 HG00738.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1357+1654_1357+165 others(9): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751217 | |||||||
chr1:37751218 | G | A | 126 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(123): Show |
133 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.1357+1658C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751218 | |||||||
chr1:37751222 | G | A | 121 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0098 others(118): Show |
128 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.1357+1654C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751222 | |||||||
chr1:37751230 | GAA | G | 3 | a0001c0001t0001g0233 a0004c0003t0003g0117 a0004c0003t0003g0222 |
3 | HG03486.hp1 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1357+1644_1357+164 others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751230 | |||||||
chr1:37751242 | G | GA | 196 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(193): Show |
213 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1357+1633dupT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751242 | |||||||
chr1:37751391 | A | C | 131 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(128): Show |
138 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.1357+1485T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751391 | |||||||
chr1:37751462 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1357+1414C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751462 | |||||||
chr1:37751550 | C | T | 1 | a0004c0003t0003g0192 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1357+1326G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751550 | |||||||
chr1:37751567 | CA | C | 223 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(220): Show |
240 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.1357+1308delT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751567 | |||||||
chr1:37751567 | CAA | C | 53 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0055 others(50): Show |
54 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1357+1307_1357+130 others(6): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751567 | |||||||
chr1:37751599 | C | T | 4 | a0001c0033t0002g0281 a0003c0024t0006g0354 a0017c0023t0006g0353 others(1): Show |
4 | HG02074.hp1 HG06807.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1357+1277G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751599 | |||||||
chr1:37751827 | C | T | 2 | a0001c0040t0011g0049 a0004c0038t0003g0226 |
2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1357+1049G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751827 | |||||||
chr1:37751871 | C | CA | 54 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0055 others(51): Show |
55 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1357+1004dupT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751871 | |||||||
chr1:37751902 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1357+974C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37751902 | |||||||
chr1:37752035 | C | T | 131 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(128): Show |
138 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.1357+841G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37752035 | |||||||
chr1:37752176 | C | T | 3 | a0004c0003t0003g0187 a0004c0003t0003g0189 a0004c0003t0003g0191 |
3 | HG01167.hp1 HG01169.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1357+700G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37752176 | |||||||
chr1:37752269 | G | T | 5 | a0002c0002t0001g0024 a0002c0002t0001g0302 a0002c0002t0001g0303 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1357+607C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37752269 | |||||||
chr1:37752309 | G | A | 2 | a0001c0040t0011g0049 a0004c0038t0003g0226 |
2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1357+567C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37752309 | |||||||
chr1:37752416 | C | T | 1 | a0002c0002t0001g0242 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1357+460G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37752416 | |||||||
chr1:37752474 | T | G | 130 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(127): Show |
137 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1357+402A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37752474 | |||||||
chr1:37752582 | A | G | 131 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(128): Show |
138 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.1357+294T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37752582 | |||||||
chr1:37752767 | T | A | 1 | a0001c0001t0001g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1357+109A>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37752767 | |||||||
chr1:37752793 | C | T | 4 | a0001c0001t0001g0044 a0001c0006t0002g0046 a0001c0006t0002g0047 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1357+83G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37752793 | |||||||
chr1:37752865 | G | A | 1 | a0002c0015t0007g0043 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1357+11C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 5/16 | chr1 | 37752865 | |||||||
chr1:37753248 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1007-22C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 4/16 | chr1 | 37753248 | |||||||
chr1:37753273 | C | T | 2 | a0001c0040t0011g0049 a0004c0038t0003g0226 |
2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1007-47G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 4/16 | chr1 | 37753273 | |||||||
chr1:37753387 | A | G | 1 | a0024c0049t0020g0307 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1007-161T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 4/16 | chr1 | 37753387 | |||||||
chr1:37753552 | G | C | 1 | a0024c0049t0020g0307 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1007-326C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 4/16 | chr1 | 37753552 | |||||||
chr1:37753647 | CGGGAGCA others(25): Show |
C | 218 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(215): Show |
234 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.1007-453_1007-422d others(34): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 4/16 | chr1 | 37753647 | |||||||
chr1:37753663 | CGGGAGCA others(41): Show |
C | 52 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0055 others(49): Show |
53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.1007-485_1007-438d others(50): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 4/16 | chr1 | 37753663 | |||||||
chr1:37753689 | G | T | 1 | a0002c0015t0007g0043 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1007-463C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 4/16 | chr1 | 37753689 | |||||||
chr1:37753700 | GCAGGGGT others(24): Show |
G | 1 | a0004c0003t0003g0013 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1006+484_1007-475d others(33): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 4/16 | chr1 | 37753700 | |||||||
chr1:37753707 | T | C | 1 | a0001c0040t0011g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1007-481A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 4/16 | chr1 | 37753707 | |||||||
chr1:37753727 | C | T | 1 | a0004c0038t0003g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1006+488G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 4/16 | chr1 | 37753727 | |||||||
chr1:37753728 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1006+487C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 4/16 | chr1 | 37753728 | |||||||
chr1:37753855 | C | G | 182 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(179): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1006+360G>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 4/16 | chr1 | 37753855 | |||||||
chr1:37753867 | C | A | 1 | a0001c0001t0002g0173 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1006+348G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 4/16 | chr1 | 37753867 | |||||||
chr1:37754089 | C | T | 131 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(128): Show |
138 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.1006+126G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 4/16 | chr1 | 37754089 | |||||||
chr1:37754104 | A | C | 51 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0055 others(48): Show |
52 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1006+111T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 4/16 | chr1 | 37754104 | |||||||
chr1:37754169 | C | T | 1 | a0001c0001t0002g0096 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1006+46G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 4/16 | chr1 | 37754169 | |||||||
chr1:37754383 | G | A | 2 | a0004c0003t0003g0263 a0004c0003t0003g0278 |
2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.851-13C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37754383 | |||||||
chr1:37754437 | G | T | 55 | a0001c0005t0004g0298 a0002c0002t0001g0004 a0002c0002t0001g0005 others(52): Show |
65 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.851-67C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37754437 | |||||||
chr1:37754486 | G | A | 1 | a0002c0002t0001g0125 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.851-116C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37754486 | |||||||
chr1:37754602 | C | T | 5 | a0002c0002t0001g0024 a0002c0002t0001g0302 a0002c0002t0001g0303 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-232G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37754602 | |||||||
chr1:37754651 | A | AG | 345 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(342): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.851-282dupC | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37754651 | |||||||
chr1:37754705 | G | A | 1 | a0002c0002t0001g0261 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.851-335C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37754705 | |||||||
chr1:37754799 | T | C | 4 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
5 | HG00735.hp2 HG01433.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.851-429A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37754799 | |||||||
chr1:37754802 | A | C | 10 | a0001c0001t0002g0134 a0001c0005t0004g0132 a0001c0033t0002g0281 others(7): Show |
10 | HG00423.hp2 HG02074.hp1 HG06807.hp2 others(7): Show |
intron_variant | MODIFIER | c.851-432T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37754802 | |||||||
chr1:37754821 | C | T | 1 | a0001c0005t0004g0132 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.851-451G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37754821 | |||||||
chr1:37754893 | G | A | 51 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0055 others(48): Show |
52 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.851-523C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37754893 | |||||||
chr1:37754900 | C | T | 4 | a0002c0002t0001g0302 a0002c0002t0001g0303 a0002c0002t0001g0305 others(1): Show |
4 | HG01884.hp2 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-530G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37754900 | |||||||
chr1:37755148 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.851-778C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755148 | |||||||
chr1:37755231 | G | A | 1 | a0004c0003t0003g0215 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.851-861C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755231 | |||||||
chr1:37755284 | G | C | 51 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0055 others(48): Show |
52 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.851-914C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755284 | |||||||
chr1:37755301 | C | T | 136 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(133): Show |
143 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.851-931G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755301 | |||||||
chr1:37755328 | G | GCA | 75 | a0001c0001t0009g0300 a0001c0001t0009g0301 a0001c0005t0004g0298 others(72): Show |
85 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.851-960_851-959dup others(2): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755328 | |||||||
chr1:37755328 | G | GCACA | 5 | a0001c0033t0002g0281 a0003c0024t0006g0354 a0003c0025t0006g0352 others(2): Show |
5 | HG02074.hp1 HG06807.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.851-962_851-959dup others(4): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755328 | |||||||
chr1:37755334 | A | G | 51 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0055 others(48): Show |
52 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.851-964T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755334 | |||||||
chr1:37755349 | CCCA | C | 131 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(128): Show |
138 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.851-982_851-980del others(3): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755349 | |||||||
chr1:37755359 | CCAT | C | 6 | a0002c0011t0001g0034 a0002c0011t0002g0020 a0002c0011t0009g0021 others(3): Show |
6 | HG02615.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.851-992_851-990del others(3): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755359 | |||||||
chr1:37755372 | G | A | 1 | a0001c0006t0002g0046 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.851-1002C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755372 | |||||||
chr1:37755436 | A | G | 351 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(348): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.851-1066T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755436 | |||||||
chr1:37755537 | G | C | 1 | a0002c0015t0007g0043 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.851-1167C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755537 | |||||||
chr1:37755548 | T | C | 1 | a0003c0008t0006g0351 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.851-1178A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755548 | |||||||
chr1:37755708 | C | A | 51 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0055 others(48): Show |
52 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.851-1338G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755708 | |||||||
chr1:37755772 | C | T | 125 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0098 others(122): Show |
132 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.851-1402G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755772 | |||||||
chr1:37755817 | T | G | 276 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(273): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.851-1447A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755817 | |||||||
chr1:37755916 | G | A | 2 | a0001c0006t0009g0207 a0004c0003t0003g0208 |
2 | HG00642.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.851-1546C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755916 | |||||||
chr1:37755936 | C | T | 1 | a0003c0004t0008g0325 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.851-1566G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755936 | |||||||
chr1:37755948 | CA | C | 5 | a0001c0033t0002g0281 a0003c0024t0006g0354 a0003c0025t0006g0352 others(2): Show |
5 | HG02074.hp1 HG06807.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.851-1579delT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37755948 | |||||||
chr1:37756032 | C | T | 2 | a0003c0004t0005g0324 a0020c0028t0022g0323 |
2 | HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.851-1662G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37756032 | |||||||
chr1:37756375 | C | G | 1 | a0002c0002t0002g0240 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.851-2005G>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37756375 | |||||||
chr1:37756418 | C | T | 4 | a0001c0001t0001g0044 a0001c0006t0002g0046 a0001c0006t0002g0047 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-2048G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37756418 | |||||||
chr1:37756449 | A | G | 189 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(186): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.851-2079T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37756449 | |||||||
chr1:37756482 | G | GGATTC | 51 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0055 others(48): Show |
52 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.851-2113_851-2112i others(7): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37756482 | |||||||
chr1:37756485 | C | G | 51 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0055 others(48): Show |
52 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.851-2115G>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37756485 | |||||||
chr1:37756486 | A | ATTCAG | 51 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0055 others(48): Show |
52 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.851-2117_851-2116i others(7): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37756486 | |||||||
chr1:37756520 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.851-2150G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37756520 | |||||||
chr1:37756521 | T | C | 138 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(135): Show |
145 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.851-2151A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37756521 | |||||||
chr1:37756527 | A | G | 51 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0055 others(48): Show |
52 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.851-2157T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37756527 | |||||||
chr1:37756621 | T | G | 6 | a0002c0011t0001g0034 a0002c0011t0002g0020 a0002c0011t0009g0021 others(3): Show |
6 | HG02615.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.851-2251A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37756621 | |||||||
chr1:37756818 | G | A | 133 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(130): Show |
140 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.851-2448C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37756818 | |||||||
chr1:37756876 | A | G | 1 | a0001c0037t0004g0130 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.851-2506T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37756876 | |||||||
chr1:37756890 | A | G | 1 | a0006c0010t0002g0129 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.851-2520T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37756890 | |||||||
chr1:37756987 | G | T | 5 | a0002c0002t0001g0024 a0002c0002t0001g0302 a0002c0002t0001g0303 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-2617C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37756987 | |||||||
chr1:37756988 | C | T | 5 | a0002c0002t0001g0024 a0002c0002t0001g0302 a0002c0002t0001g0303 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-2618G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37756988 | |||||||
chr1:37757078 | T | C | 134 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0098 others(131): Show |
141 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.851-2708A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37757078 | |||||||
chr1:37757104 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.851-2734C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37757104 | |||||||
chr1:37757133 | G | T | 133 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0053 others(130): Show |
140 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.851-2763C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37757133 | |||||||
chr1:37757167 | T | C | 9 | a0001c0001t0009g0300 a0001c0001t0009g0301 a0002c0011t0001g0034 others(6): Show |
9 | HG02451.hp1 HG02615.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.851-2797A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37757167 | |||||||
chr1:37757278 | G | A | 6 | a0001c0001t0001g0044 a0001c0001t0001g0233 a0001c0033t0002g0281 others(3): Show |
6 | HG02074.hp1 HG02145.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.851-2908C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37757278 | |||||||
chr1:37757422 | G | A | 267 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0001g0053 others(264): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.851-3052C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37757422 | |||||||
chr1:37757431 | A | C | 280 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(277): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.851-3061T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37757431 | |||||||
chr1:37757434 | A | G | 9 | a0001c0001t0009g0300 a0001c0001t0009g0301 a0002c0011t0001g0034 others(6): Show |
9 | HG02451.hp1 HG02615.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.851-3064T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37757434 | |||||||
chr1:37757494 | T | C | 210 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0098 others(207): Show |
228 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.851-3124A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37757494 | |||||||
chr1:37757511 | T | G | 1 | a0025c0035t0001g0209 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.851-3141A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37757511 | |||||||
chr1:37757558 | G | T | 1 | a0002c0002t0001g0229 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.851-3188C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37757558 | |||||||
chr1:37757618 | A | G | 259 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(256): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.851-3248T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37757618 | |||||||
chr1:37757645 | T | C | 3 | a0001c0006t0002g0046 a0001c0006t0002g0047 a0004c0003t0016g0045 |
3 | HG02451.hp2 HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.851-3275A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37757645 | |||||||
chr1:37757690 | T | A | 140 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0098 others(137): Show |
147 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.851-3320A>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37757690 | |||||||
chr1:37757751 | G | A | 8 | a0001c0001t0001g0044 a0001c0006t0002g0046 a0001c0006t0002g0047 others(5): Show |
8 | HG01884.hp2 HG02145.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.851-3381C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37757751 | |||||||
chr1:37757817 | A | G | 11 | a0003c0004t0005g0313 a0003c0004t0005g0314 a0003c0004t0005g0316 others(8): Show |
11 | HG00408.hp1 HG00673.hp2 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.851-3447T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37757817 | |||||||
chr1:37757841 | A | G | 2 | a0001c0040t0011g0049 a0004c0038t0003g0226 |
2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.851-3471T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37757841 | |||||||
chr1:37758169 | C | CT | 5 | a0001c0001t0001g0044 a0001c0006t0002g0046 a0001c0006t0002g0047 others(2): Show |
5 | HG01069.hp2 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+3235dupA | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37758169 | |||||||
chr1:37758189 | A | G | 1 | a0001c0001t0002g0128 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+3216T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37758189 | |||||||
chr1:37758285 | T | C | 2 | a0002c0015t0007g0231 a0002c0015t0007g0232 |
2 | HG01243.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.850+3120A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37758285 | |||||||
chr1:37758677 | T | G | 4 | a0002c0011t0009g0021 a0002c0011t0009g0022 a0002c0011t0009g0023 others(1): Show |
4 | HG02818.hp2 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+2728A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37758677 | |||||||
chr1:37758744 | G | A | 58 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0017 others(55): Show |
69 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.850+2661C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37758744 | |||||||
chr1:37758963 | T | G | 177 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0131 others(174): Show |
193 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.850+2442A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37758963 | |||||||
chr1:37759044 | C | T | 64 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0017 others(61): Show |
75 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.850+2361G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37759044 | |||||||
chr1:37759079 | C | T | 1 | a0001c0001t0002g0127 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.850+2326G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37759079 | |||||||
chr1:37759170 | C | A | 64 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0017 others(61): Show |
75 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.850+2235G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37759170 | |||||||
chr1:37759190 | G | A | 6 | a0001c0005t0011g0040 a0001c0005t0011g0041 a0001c0005t0015g0037 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.850+2215C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37759190 | |||||||
chr1:37759415 | T | C | 70 | a0001c0005t0011g0040 a0001c0005t0011g0041 a0001c0005t0015g0037 others(67): Show |
81 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.850+1990A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37759415 | |||||||
chr1:37759419 | A | G | 263 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(260): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.850+1986T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37759419 | |||||||
chr1:37759462 | T | C | 64 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0017 others(61): Show |
75 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.850+1943A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37759462 | |||||||
chr1:37759706 | C | G | 2 | a0003c0008t0006g0309 a0003c0008t0006g0310 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.850+1699G>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37759706 | |||||||
chr1:37759795 | T | TA | 185 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(182): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.850+1609dupT | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37759795 | |||||||
chr1:37760231 | T | C | 1 | a0001c0006t0002g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.850+1174A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37760231 | |||||||
chr1:37760329 | C | A | 2 | a0004c0003t0003g0117 a0004c0003t0003g0222 |
2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.850+1076G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37760329 | |||||||
chr1:37760329 | C | T | 1 | a0001c0044t0001g0279 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.850+1076G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37760329 | |||||||
chr1:37760407 | C | G | 51 | a0003c0004t0005g0313 a0003c0004t0005g0314 a0003c0004t0005g0316 others(48): Show |
56 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.850+998G>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37760407 | |||||||
chr1:37760533 | C | A | 4 | a0002c0002t0001g0229 a0002c0002t0001g0230 a0002c0015t0007g0231 others(1): Show |
4 | HG01243.hp1 HG01243.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+872G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37760533 | |||||||
chr1:37760685 | G | A | 4 | a0001c0001t0002g0012 a0001c0001t0002g0185 a0001c0001t0002g0186 others(1): Show |
5 | HG00741.hp1 HG01261.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+720C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37760685 | |||||||
chr1:37760778 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00408.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.850+627A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37760778 | |||||||
chr1:37760812 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.850+593C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37760812 | |||||||
chr1:37760821 | C | T | 1 | a0004c0038t0003g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.850+584G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37760821 | |||||||
chr1:37760822 | G | T | 4 | a0002c0002t0001g0302 a0002c0002t0001g0303 a0002c0002t0001g0305 others(1): Show |
4 | HG01884.hp2 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+583C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37760822 | |||||||
chr1:37760852 | G | A | 3 | a0001c0001t0009g0300 a0001c0001t0009g0301 a0004c0003t0003g0299 |
3 | HG02451.hp1 HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.850+553C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37760852 | |||||||
chr1:37760913 | G | A | 2 | a0004c0003t0003g0263 a0004c0003t0003g0278 |
2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.850+492C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37760913 | |||||||
chr1:37761036 | A | T | 1 | a0002c0002t0001g0284 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.850+369T>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37761036 | |||||||
chr1:37761085 | AT | A | 146 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0059 others(143): Show |
155 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.850+319delA | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37761085 | |||||||
chr1:37761088 | T | TA | 9 | a0002c0002t0001g0229 a0002c0002t0001g0230 a0002c0002t0002g0238 others(6): Show |
9 | HG00099.hp2 HG00323.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.850+316_850+317ins others(1): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37761088 | |||||||
chr1:37761088 | T | TAA | 59 | a0001c0001t0009g0300 a0001c0001t0009g0301 a0002c0002t0001g0004 others(56): Show |
70 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.850+316_850+317ins others(2): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37761088 | |||||||
chr1:37761088 | TTA | T | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
6 | HG01069.hp2 HG01074.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+315_850+316del others(2): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37761088 | |||||||
chr1:37761089 | T | A | 187 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0121 others(184): Show |
203 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.850+316A>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37761089 | |||||||
chr1:37761105 | C | A | 84 | a0001c0001t0001g0008 a0001c0001t0001g0053 a0001c0001t0001g0054 others(81): Show |
87 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.850+300G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37761105 | |||||||
chr1:37761110 | A | G | 70 | a0002c0002t0001g0024 a0002c0002t0002g0019 a0002c0007t0012g0028 others(67): Show |
76 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.850+295T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37761110 | |||||||
chr1:37761213 | G | A | 1 | a0004c0038t0003g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.850+192C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37761213 | |||||||
chr1:37761292 | C | T | 69 | a0001c0001t0001g0131 a0001c0001t0001g0135 a0001c0001t0001g0137 others(66): Show |
73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.850+113G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37761292 | |||||||
chr1:37761304 | C | T | 70 | a0002c0002t0001g0024 a0002c0002t0002g0019 a0002c0007t0012g0028 others(67): Show |
76 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.850+101G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 3/16 | chr1 | 37761304 | |||||||
chr1:37762108 | GC | G | 6 | a0001c0005t0011g0040 a0001c0005t0011g0041 a0001c0005t0015g0037 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-26delG | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762108 | |||||||
chr1:37762344 | T | C | 332 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(329): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.172-261A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762344 | |||||||
chr1:37762349 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.172-266C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762349 | |||||||
chr1:37762359 | C | T | 1 | a0002c0002t0001g0234 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.172-276G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762359 | |||||||
chr1:37762452 | T | G | 4 | a0001c0001t0002g0213 a0004c0003t0003g0212 a0004c0003t0003g0214 others(1): Show |
4 | HG00099.hp2 HG01261.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+333A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762452 | |||||||
chr1:37762544 | A | G | 332 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(329): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.171+241T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762544 | |||||||
chr1:37762585 | C | CT | 166 | a0001c0001t0001g0131 a0001c0001t0001g0135 a0001c0001t0001g0137 others(163): Show |
177 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.171+199dupA | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762585 | |||||||
chr1:37762585 | C | CTT | 87 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(84): Show |
90 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.171+198_171+199dup others(2): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762585 | |||||||
chr1:37762585 | CT | C | 25 | a0002c0002t0001g0005 a0002c0002t0001g0017 a0002c0002t0001g0227 others(22): Show |
29 | HG01123.hp2 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.171+199delA | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762585 | |||||||
chr1:37762585 | CTT | C | 7 | a0001c0005t0011g0040 a0001c0005t0011g0041 a0001c0005t0015g0037 others(4): Show |
7 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+198_171+199del others(2): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762585 | |||||||
chr1:37762602 | G | T | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+183C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762602 | |||||||
chr1:37762603 | A | G | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+182T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762603 | |||||||
chr1:37762604 | C | A | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+181G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762604 | |||||||
chr1:37762607 | T | G | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+178A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762607 | |||||||
chr1:37762608 | C | T | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+177G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762608 | |||||||
chr1:37762610 | A | G | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+175T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762610 | |||||||
chr1:37762611 | A | T | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+174T>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762611 | |||||||
chr1:37762613 | T | C | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+172A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762613 | |||||||
chr1:37762614 | G | C | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+171C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762614 | |||||||
chr1:37762615 | G | T | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+170C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762615 | |||||||
chr1:37762618 | G | T | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+167C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762618 | |||||||
chr1:37762620 | A | G | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+165T>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762620 | |||||||
chr1:37762621 | G | T | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+164C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762621 | |||||||
chr1:37762623 | C | A | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+162G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762623 | |||||||
chr1:37762630 | T | A | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+155A>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762630 | |||||||
chr1:37762632 | T | A | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+153A>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762632 | |||||||
chr1:37762633 | T | G | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+152A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762633 | |||||||
chr1:37762634 | C | T | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+151G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762634 | |||||||
chr1:37762638 | C | G | 1 | a0005c0009t0003g0161 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.171+147G>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762638 | |||||||
chr1:37762643 | C | A | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+142G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762643 | |||||||
chr1:37762644 | A | T | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+141T>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762644 | |||||||
chr1:37762647 | C | T | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+138G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762647 | |||||||
chr1:37762649 | G | A | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+136C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762649 | |||||||
chr1:37762650 | G | T | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+135C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762650 | |||||||
chr1:37762654 | G | T | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+131C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762654 | |||||||
chr1:37762663 | G | A | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+122C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762663 | |||||||
chr1:37762664 | C | T | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+121G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762664 | |||||||
chr1:37762666 | G | C | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+119C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762666 | |||||||
chr1:37762669 | G | A | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+116C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762669 | |||||||
chr1:37762691 | C | A | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+94G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762691 | |||||||
chr1:37762694 | T | A | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+91A>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762694 | |||||||
chr1:37762701 | T | A | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+84A>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762701 | |||||||
chr1:37762702 | G | C | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+83C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762702 | |||||||
chr1:37762703 | A | T | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+82T>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762703 | |||||||
chr1:37762705 | G | C | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+80C>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762705 | |||||||
chr1:37762706 | T | A | 1 | a0002c0011t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+79A>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 2/16 | chr1 | 37762706 | |||||||
chr1:37762881 | A | T | 1 | a0001c0001t0001g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.107-32T>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37762881 | |||||||
chr1:37763125 | A | T | 266 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(263): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.107-276T>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37763125 | |||||||
chr1:37763266 | C | T | 1 | a0002c0015t0007g0043 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.107-417G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37763266 | |||||||
chr1:37763345 | G | T | 4 | a0001c0001t0001g0044 a0001c0006t0002g0046 a0001c0006t0002g0047 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-496C>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37763345 | |||||||
chr1:37763383 | T | C | 292 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(289): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.107-534A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37763383 | |||||||
chr1:37763431 | C | T | 346 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(343): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.107-582G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37763431 | |||||||
chr1:37763521 | A | C | 74 | a0002c0002t0001g0024 a0002c0002t0001g0229 a0002c0002t0001g0230 others(71): Show |
80 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.107-672T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37763521 | |||||||
chr1:37763621 | C | T | 1 | a0002c0002t0002g0019 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.107-772G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37763621 | |||||||
chr1:37763628 | T | C | 1 | a0005c0009t0003g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.107-779A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37763628 | |||||||
chr1:37763658 | C | T | 4 | a0002c0002t0001g0229 a0002c0002t0001g0230 a0002c0015t0007g0231 others(1): Show |
4 | HG01243.hp1 HG01243.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-809G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37763658 | |||||||
chr1:37763662 | TAG | T | 197 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0052 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.107-815_107-814del others(2): Show |
EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37763662 | |||||||
chr1:37763841 | A | C | 1 | a0001c0001t0002g0042 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.107-992T>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37763841 | |||||||
chr1:37763958 | C | T | 6 | a0001c0005t0011g0040 a0001c0005t0011g0041 a0001c0005t0015g0037 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+1003G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37763958 | |||||||
chr1:37764193 | G | A | 1 | a0001c0033t0002g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.106+768C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37764193 | |||||||
chr1:37764489 | G | A | 18 | a0002c0002t0001g0005 a0002c0002t0001g0017 a0002c0002t0001g0282 others(15): Show |
22 | HG01123.hp2 HG01496.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+472C>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37764489 | |||||||
chr1:37764538 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.106+423A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37764538 | |||||||
chr1:37764554 | C | A | 1 | a0001c0005t0004g0298 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.106+407G>T | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37764554 | |||||||
chr1:37764718 | C | T | 69 | a0002c0002t0001g0024 a0002c0002t0002g0019 a0002c0007t0012g0028 others(66): Show |
75 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.106+243G>A | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37764718 | |||||||
chr1:37764837 | T | G | 7 | a0001c0001t0009g0300 a0001c0001t0009g0301 a0002c0002t0001g0302 others(4): Show |
7 | HG01884.hp2 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.106+124A>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37764837 | |||||||
chr1:37764873 | C | G | 51 | a0003c0004t0005g0313 a0003c0004t0005g0314 a0003c0004t0005g0316 others(48): Show |
56 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.106+88G>C | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37764873 | |||||||
chr1:37764901 | T | C | 1 | a0024c0049t0020g0307 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.106+60A>G | EPHA10 | ENSG00000183317.17 | transcript | ENST00000373048.9 | protein_coding | 1/16 | chr1 | 37764901 |