Item | Value |
---|---|
geneid | 161436 |
ensemblid | ENSG00000165521.16 |
hgncid | 18197 |
symbol | EML5 |
name | EMAP like 5 |
refseq_nuc | NM_183387.3 |
refseq_prot | NP_899243.1 |
ensembl_nuc | ENST00000554922.6 |
ensembl_prot | ENSP00000451998.1 |
mane_status | MANE Select |
chr | chr14 |
start | 88612431 |
end | 88792953 |
strand | - |
ver | v1.2 |
region | chr14:88612431-88792953 |
region5000 | chr14:88607431-88797953 |
regionname0 | EML5_chr14_88612431_88792953 |
regionname5000 | EML5_chr14_88607431_88797953 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1977 | 235 | 73 | 43 | 77 | 11 | 29 | 61 | EML5_chr14_88607431_88797953 | EML5 | MAARS others(1972): Show |
chr14 | 88607431 | 88797953 |
a0002 | 0/0 | 1977 | 85 | 8 | 22 | 44 | 4 | 7 | 32 | EML5_chr14_88607431_88797953 | EML5 | MAARS others(1972): Show |
chr14 | 88607431 | 88797953 |
a0003 | 0/0 | 1977 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | MAARS others(1972): Show |
chr14 | 88607431 | 88797953 |
a0004 | 0/0 | 1977 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | MAARS others(1972): Show |
chr14 | 88607431 | 88797953 |
a0005 | 0/0 | 1977 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | MAARS others(1972): Show |
chr14 | 88607431 | 88797953 |
a0006 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | MAARS others(1972): Show |
chr14 | 88607431 | 88797953 |
a0007 | 0/0 | 1977 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | MAARS others(1972): Show |
chr14 | 88607431 | 88797953 |
a0008 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | MAARS others(1972): Show |
chr14 | 88607431 | 88797953 |
a0009 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | MAARS others(1972): Show |
chr14 | 88607431 | 88797953 |
a0010 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | MAARS others(1972): Show |
chr14 | 88607431 | 88797953 |
a0011 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | MAARS others(1972): Show |
chr14 | 88607431 | 88797953 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 5931 | 200 | 53 | 41 | 70 | 11 | 23 | EML5_chr14_88607431_88797953 | EML5 | ATGGC others(5926): Show |
chr14 | 88607431 | 88797953 | ||
a0001c0003 | 0/0 | 5931 | 32 | 19 | 0 | 7 | 0 | 6 | EML5_chr14_88607431_88797953 | EML5 | ATGGC others(5926): Show |
chr14 | 88607431 | 88797953 | ||
a0001c0006 | 0/0 | 5931 | 2 | 0 | 2 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | ATGGC others(5926): Show |
chr14 | 88607431 | 88797953 | ||
a0001c0009 | 0/0 | 5931 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | ATGGC others(5926): Show |
chr14 | 88607431 | 88797953 | ||
a0002c0002 | 0/0 | 5931 | 80 | 8 | 19 | 44 | 3 | 6 | EML5_chr14_88607431_88797953 | EML5 | ATGGC others(5926): Show |
chr14 | 88607431 | 88797953 | ||
a0002c0004 | 0/0 | 5931 | 5 | 0 | 3 | 0 | 1 | 1 | EML5_chr14_88607431_88797953 | EML5 | ATGGC others(5926): Show |
chr14 | 88607431 | 88797953 | ||
a0003c0005 | 0/0 | 5931 | 3 | 3 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | ATGGC others(5926): Show |
chr14 | 88607431 | 88797953 | ||
a0004c0007 | 0/0 | 5931 | 2 | 0 | 0 | 2 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | ATGGC others(5926): Show |
chr14 | 88607431 | 88797953 | ||
a0005c0014 | 0/0 | 5931 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | ATGGC others(5926): Show |
chr14 | 88607431 | 88797953 | ||
a0006c0013 | 0/0 | 5931 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | ATGGC others(5926): Show |
chr14 | 88607431 | 88797953 | ||
a0007c0015 | 0/0 | 5931 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | ATGGC others(5926): Show |
chr14 | 88607431 | 88797953 | ||
a0008c0011 | 0/0 | 5931 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | ATGGC others(5926): Show |
chr14 | 88607431 | 88797953 | ||
a0009c0008 | 0/0 | 5931 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | ATGGC others(5926): Show |
chr14 | 88607431 | 88797953 | ||
a0010c0012 | 0/0 | 5931 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | ATGGC others(5926): Show |
chr14 | 88607431 | 88797953 | ||
a0011c0010 | 0/0 | 5931 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | ATGGC others(5926): Show |
chr14 | 88607431 | 88797953 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 9771 | 7 | 4 | 1 | 0 | 0 | 2 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0002 | 0/0 | 9770 | 68 | 8 | 16 | 35 | 3 | 6 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0003 | 0/0 | 9771 | 35 | 6 | 6 | 11 | 1 | 11 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0005 | 0/0 | 9770 | 17 | 0 | 2 | 14 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0006 | 0/0 | 9770 | 12 | 5 | 4 | 1 | 2 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0007 | 0/0 | 9772 | 10 | 1 | 4 | 0 | 4 | 1 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9767): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0008 | 0/0 | 9770 | 6 | 6 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0009 | 0/0 | 9772 | 5 | 0 | 4 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9767): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0010 | 0/0 | 9770 | 4 | 0 | 0 | 4 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0011 | 0/0 | 9770 | 4 | 4 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0012 | 0/0 | 9780 | 4 | 0 | 0 | 4 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9775): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0014 | 0/0 | 9771 | 3 | 3 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0017 | 0/0 | 9769 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9764): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0018 | 1/0 | 9771 | 1 | 0 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0019 | 0/0 | 9770 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0022 | 0/0 | 9767 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9762): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0023 | 0/0 | 9768 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9763): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0024 | 0/0 | 9767 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9762): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0025 | 0/0 | 9770 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0026 | 0/0 | 9770 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0027 | 0/0 | 9770 | 2 | 1 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0028 | 0/0 | 9771 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0029 | 0/0 | 9770 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0030 | 0/0 | 9770 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0031 | 0/0 | 9772 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9767): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0032 | 0/1 | 9773 | 1 | 0 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9768): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0033 | 0/0 | 9771 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0035 | 0/0 | 9771 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0036 | 0/0 | 9768 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9763): Show |
chr14 | 88607431 | 88797953 |
a0001c0001t0037 | 0/0 | 9767 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9762): Show |
chr14 | 88607431 | 88797953 |
a0001c0003t0002 | 0/0 | 9770 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0001c0003t0004 | 0/0 | 9781 | 24 | 14 | 0 | 5 | 0 | 5 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9776): Show |
chr14 | 88607431 | 88797953 |
a0001c0003t0006 | 0/0 | 9770 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0001c0003t0013 | 0/0 | 9781 | 3 | 3 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9776): Show |
chr14 | 88607431 | 88797953 |
a0001c0003t0018 | 0/0 | 9771 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0001c0003t0020 | 0/0 | 9771 | 2 | 0 | 0 | 2 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0001c0006t0003 | 0/0 | 9771 | 2 | 0 | 2 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0001c0009t0013 | 0/0 | 9781 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9776): Show |
chr14 | 88607431 | 88797953 |
a0002c0002t0001 | 0/0 | 9771 | 57 | 2 | 14 | 36 | 2 | 3 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0002c0002t0003 | 0/0 | 9771 | 16 | 6 | 3 | 5 | 0 | 2 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0002c0002t0006 | 0/0 | 9770 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0002c0002t0007 | 0/0 | 9772 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9767): Show |
chr14 | 88607431 | 88797953 |
a0002c0002t0021 | 0/0 | 9771 | 2 | 0 | 2 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0002c0002t0034 | 0/0 | 9811 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9806): Show |
chr14 | 88607431 | 88797953 |
a0002c0002t0038 | 0/0 | 9771 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0002c0002t0039 | 0/0 | 9771 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0002c0004t0001 | 0/0 | 9771 | 5 | 0 | 3 | 0 | 1 | 1 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0003c0005t0015 | 0/0 | 9770 | 3 | 3 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0004c0007t0016 | 0/0 | 9770 | 2 | 0 | 0 | 2 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0005c0014t0001 | 0/0 | 9771 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0006c0013t0003 | 0/0 | 9771 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0007c0015t0007 | 0/0 | 9772 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9767): Show |
chr14 | 88607431 | 88797953 |
a0008c0011t0008 | 0/0 | 9770 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0009c0008t0025 | 0/0 | 9770 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9765): Show |
chr14 | 88607431 | 88797953 |
a0010c0012t0001 | 0/0 | 9771 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
a0011c0010t0003 | 0/0 | 9771 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | CGGCT others(9766): Show |
chr14 | 88607431 | 88797953 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0006g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0006g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0006g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0006g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0006g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0007g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0007g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0007g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0007g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0007g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0007g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0007g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0008g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0009g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0009g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0009g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0009g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0009g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0010g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0010g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0010g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0010g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0011g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0011g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0011g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0011g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0012g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0012g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0012g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0012g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0014g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0014g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0014g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0017g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0017g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0018g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0019g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0019g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0022g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0022g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0023g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0023g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0024g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0024g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0025g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0026g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0026g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0027g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0027g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0028g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0029g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0030g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0031g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0032g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0033g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0035g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0036g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0001t0037g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0004g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0013g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0013g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0013g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0018g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0020g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0003t0020g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0006t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0006t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0001c0009t0013g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0007g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0021g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0021g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0034g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0038g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0002t0039g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0004t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0004t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0002c0004t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0003c0005t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0003c0005t0015g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0003c0005t0015g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0004c0007t0016g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0004c0007t0016g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0005c0014t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0006c0013t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0007c0015t0007g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0008c0011t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0009c0008t0025g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0010c0012t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
a0011c0010t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0007 | g0066 | EUR | GBR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00099 | hp2 | a0002 | c0004 | t0001 | g0241 | EUR | GBR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0156 | EUR | FIN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0276 | EUR | FIN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00323 | hp1 | a0002 | c0002 | t0039 | g0297 | EUR | FIN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00323 | hp2 | a0001 | c0001 | t0007 | g0085 | EUR | FIN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00408 | hp1 | a0001 | c0003 | t0004 | g0319 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00423 | hp1 | a0001 | c0001 | t0005 | g0173 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00544 | hp1 | a0001 | c0001 | t0010 | g0034 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00609 | hp1 | a0001 | c0001 | t0012 | g0326 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0279 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0275 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00639 | hp2 | a0001 | c0001 | t0007 | g0038 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00642 | hp2 | a0001 | c0001 | t0027 | g0296 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00673 | hp1 | a0001 | c0001 | t0005 | g0180 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00733 | hp1 | a0002 | c0002 | t0021 | g0292 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0064 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00738 | hp1 | a0001 | c0001 | t0009 | g0058 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00738 | hp2 | a0002 | c0002 | t0021 | g0273 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG00741 | hp2 | a0001 | c0001 | t0006 | g0284 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0258 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01071 | hp2 | a0001 | c0001 | t0007 | g0073 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01074 | hp1 | a0001 | c0006 | t0003 | g0162 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0246 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0274 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01109 | hp2 | a0001 | c0001 | t0030 | g0135 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0260 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01167 | hp2 | a0001 | c0001 | t0029 | g0157 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01168 | hp2 | a0002 | c0004 | t0001 | g0228 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01175 | hp2 | a0001 | c0006 | t0003 | g0161 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01243 | hp1 | a0001 | c0001 | t0037 | g0205 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0062 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0209 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01256 | hp1 | a0001 | c0001 | t0007 | g0072 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01256 | hp2 | a0001 | c0001 | t0006 | g0286 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01257 | hp1 | a0001 | c0001 | t0006 | g0287 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0239 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01358 | hp2 | a0001 | c0001 | t0009 | g0076 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01361 | hp1 | a0002 | c0002 | t0003 | g0024 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0255 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0186 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01515 | hp1 | a0005 | c0014 | t0001 | g0272 | EUR | IBS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0003 | EUR | IBS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01516 | hp1 | a0001 | c0001 | t0007 | g0070 | EUR | IBS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0113 | EUR | IBS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0003 | EUR | IBS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0112 | EUR | IBS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01884 | hp1 | a0001 | c0001 | t0017 | g0010 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01884 | hp2 | a0001 | c0001 | t0024 | g0206 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01891 | hp1 | a0002 | c0002 | t0003 | g0018 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01928 | hp2 | a0002 | c0002 | t0003 | g0026 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0238 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01943 | hp2 | a0001 | c0001 | t0009 | g0059 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01952 | hp2 | a0002 | c0002 | t0003 | g0027 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0257 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01975 | hp2 | a0001 | c0001 | t0005 | g0185 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01978 | hp1 | a0002 | c0004 | t0001 | g0240 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01993 | hp1 | a0001 | c0001 | t0009 | g0042 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02004 | hp1 | a0001 | c0001 | t0006 | g0285 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0181 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0271 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02027 | hp1 | a0001 | c0001 | t0010 | g0032 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02040 | hp1 | a0004 | c0007 | t0016 | g0008 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02055 | hp2 | a0001 | c0003 | t0004 | g0302 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02135 | hp2 | a0001 | c0003 | t0004 | g0320 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02145 | hp1 | a0001 | c0001 | t0026 | g0294 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0208 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02165 | hp1 | a0006 | c0013 | t0003 | g0022 | EAS | CDX | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | CDX | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02257 | hp1 | a0001 | c0003 | t0004 | g0307 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0230 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0100 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02280 | hp1 | a0001 | c0001 | t0011 | g0214 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02280 | hp2 | a0001 | c0003 | t0004 | g0312 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02293 | hp1 | a0007 | c0015 | t0007 | g0079 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0245 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02451 | hp1 | a0003 | c0005 | t0015 | g0013 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02523 | hp1 | a0001 | c0001 | t0010 | g0033 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02523 | hp2 | a0002 | c0002 | t0006 | g0237 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02572 | hp1 | a0001 | c0003 | t0006 | g0221 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02602 | hp1 | a0001 | c0001 | t0005 | g0183 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02615 | hp1 | a0002 | c0002 | t0003 | g0029 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02615 | hp2 | a0001 | c0001 | t0011 | g0215 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02622 | hp2 | a0001 | c0003 | t0004 | g0306 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02630 | hp2 | a0001 | c0001 | t0011 | g0216 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02647 | hp2 | a0001 | c0001 | t0033 | g0077 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02683 | hp2 | a0001 | c0003 | t0004 | g0315 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02717 | hp1 | a0001 | c0003 | t0004 | g0314 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02717 | hp2 | a0001 | c0001 | t0014 | g0004 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02723 | hp1 | a0003 | c0005 | t0015 | g0015 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02723 | hp2 | a0001 | c0001 | t0011 | g0213 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02735 | hp2 | a0001 | c0003 | t0018 | g0016 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0036 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02809 | hp1 | a0001 | c0003 | t0004 | g0305 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02809 | hp2 | a0001 | c0003 | t0002 | g0012 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02818 | hp1 | a0002 | c0002 | t0003 | g0092 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02886 | hp1 | a0001 | c0001 | t0036 | g0196 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02886 | hp2 | a0001 | c0003 | t0013 | g0299 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02895 | hp1 | a0001 | c0003 | t0004 | g0303 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02895 | hp2 | a0001 | c0001 | t0008 | g0102 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02897 | hp1 | a0001 | c0003 | t0004 | g0304 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02897 | hp2 | a0001 | c0001 | t0008 | g0103 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02922 | hp1 | a0001 | c0003 | t0004 | g0309 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02922 | hp2 | a0001 | c0001 | t0035 | g0198 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02976 | hp1 | a0001 | c0001 | t0022 | g0203 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03017 | hp1 | a0001 | c0003 | t0004 | g0317 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03041 | hp1 | a0001 | c0001 | t0022 | g0204 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03098 | hp1 | a0001 | c0003 | t0013 | g0300 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03098 | hp2 | a0001 | c0001 | t0017 | g0011 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03130 | hp1 | a0001 | c0003 | t0004 | g0313 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0131 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0104 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03139 | hp2 | a0002 | c0002 | t0003 | g0031 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0084 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0219 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03209 | hp1 | a0001 | c0003 | t0013 | g0298 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03209 | hp2 | a0001 | c0001 | t0019 | g0212 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03225 | hp2 | a0002 | c0002 | t0003 | g0017 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03453 | hp1 | a0001 | c0003 | t0004 | g0311 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03453 | hp2 | a0003 | c0005 | t0015 | g0014 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0099 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0045 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0254 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0244 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0046 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0188 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03516 | hp2 | a0001 | c0001 | t0019 | g0217 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03540 | hp1 | a0001 | c0003 | t0004 | g0329 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03540 | hp2 | a0001 | c0009 | t0013 | g0301 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03579 | hp1 | a0001 | c0001 | t0024 | g0207 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03654 | hp1 | a0001 | c0001 | t0007 | g0134 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03669 | hp1 | a0001 | c0003 | t0004 | g0322 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0055 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03704 | hp1 | a0002 | c0002 | t0003 | g0025 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03710 | hp2 | a0001 | c0001 | t0009 | g0060 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | BEB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03927 | hp1 | a0002 | c0004 | t0001 | g0234 | SAS | BEB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03927 | hp2 | a0001 | c0003 | t0004 | g0321 | SAS | BEB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03942 | hp1 | a0001 | c0001 | t0028 | g0009 | SAS | BEB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0074 | SAS | BEB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | STU | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | STU | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0037 | SAS | BEB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0263 | SAS | BEB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG04204 | hp1 | a0002 | c0002 | t0007 | g0030 | SAS | STU | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG04204 | hp2 | a0001 | c0003 | t0004 | g0323 | SAS | STU | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG04228 | hp1 | a0002 | c0002 | t0003 | g0094 | SAS | STU | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0047 | SAS | STU | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18522 | hp1 | a0001 | c0001 | t0014 | g0006 | AFR | YRI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0220 | AFR | YRI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18612 | hp1 | a0001 | c0001 | t0005 | g0176 | EAS | CHB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | CHB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | CHB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18747 | hp2 | a0001 | c0003 | t0004 | g0328 | EAS | CHB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18906 | hp1 | a0001 | c0003 | t0004 | g0310 | AFR | YRI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18906 | hp2 | a0001 | c0001 | t0027 | g0295 | AFR | YRI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18939 | hp2 | a0001 | c0003 | t0020 | g0172 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18948 | hp1 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18948 | hp2 | a0002 | c0002 | t0003 | g0023 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18951 | hp1 | a0002 | c0002 | t0003 | g0093 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18952 | hp1 | a0001 | c0001 | t0005 | g0184 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18953 | hp1 | a0001 | c0001 | t0012 | g0325 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18956 | hp1 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18959 | hp1 | a0002 | c0002 | t0003 | g0021 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18963 | hp2 | a0001 | c0001 | t0005 | g0189 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18964 | hp2 | a0001 | c0001 | t0012 | g0324 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18971 | hp1 | a0001 | c0001 | t0006 | g0202 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18971 | hp2 | a0001 | c0001 | t0010 | g0035 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18978 | hp1 | a0001 | c0001 | t0012 | g0327 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18980 | hp2 | a0004 | c0007 | t0016 | g0007 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18982 | hp2 | a0002 | c0002 | t0003 | g0020 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18983 | hp2 | a0001 | c0001 | t0005 | g0182 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18986 | hp1 | a0001 | c0003 | t0004 | g0316 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18987 | hp1 | a0002 | c0002 | t0034 | g0170 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18990 | hp1 | a0001 | c0003 | t0020 | g0171 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA18995 | hp2 | a0009 | c0008 | t0025 | g0190 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19002 | hp2 | a0001 | c0001 | t0025 | g0191 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19030 | hp1 | a0001 | c0003 | t0004 | g0308 | AFR | LWK | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19030 | hp2 | a0001 | c0001 | t0023 | g0195 | AFR | LWK | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19043 | hp1 | a0001 | c0001 | t0014 | g0005 | AFR | LWK | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19043 | hp2 | a0002 | c0002 | t0003 | g0028 | AFR | LWK | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19054 | hp2 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19056 | hp1 | a0001 | c0003 | t0004 | g0318 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19058 | hp1 | a0010 | c0012 | t0001 | g0247 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19060 | hp2 | a0001 | c0001 | t0005 | g0192 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19065 | hp1 | a0001 | c0001 | t0005 | g0187 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19081 | hp2 | a0002 | c0002 | t0003 | g0019 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19084 | hp2 | a0001 | c0001 | t0005 | g0174 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19086 | hp1 | a0002 | c0002 | t0038 | g0262 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19090 | hp1 | a0001 | c0001 | t0005 | g0179 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19240 | hp1 | a0011 | c0010 | t0003 | g0080 | AFR | YRI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | YRI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0193 | AFR | ASW | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | ASW | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0054 | EUR | TSI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA20752 | hp2 | a0001 | c0001 | t0007 | g0068 | EUR | TSI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0194 | EUR | TSI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA20805 | hp2 | a0001 | c0001 | t0031 | g0067 | EUR | TSI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01123 | hp1 | a0002 | c0004 | t0001 | g0242 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0218 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG02559 | hp2 | a0001 | c0001 | t0023 | g0197 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG06807 | hp1 | a0008 | c0011 | t0008 | g0101 | AFR | USA | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
HG06807 | hp2 | a0001 | c0001 | t0026 | g0293 | AFR | USA | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | USA | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | USA | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
homoSapiens | chm13v2 | a0001 | c0001 | t0032 | g0078 | REF | REF | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
homoSapiens | grch38p0 | a0001 | c0001 | t0018 | g0063 | REF | REF | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:88612433 | C | T | 1 | a0001 | 1 | NA20805.hp2 | splice_region_variant | LOW | c.*3385G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | chr14 | 88612433 | |||||||
chr14:88620769 | G | T | 1 | a0003 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.5360C>A | p.Ala1787Glu | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/44 | 5810/9771 | 5360/5934 | 1787/1977 | chr14 | 88620769 | |||
chr14:88664517 | T | C | 1 | a0009 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.3385A>G | p.Thr1129Ala | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/44 | 3835/9771 | 3385/5934 | 1129/1977 | chr14 | 88664517 | |||
chr14:88664528 | G | A | 1 | a0010 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.3374C>T | p.Thr1125Ile | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/44 | 3824/9771 | 3374/5934 | 1125/1977 | chr14 | 88664528 | |||
chr14:88665408 | G | A | 1 | a0006 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.3206C>T | p.Ala1069Val | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 22/44 | 3656/9771 | 3206/5934 | 1069/1977 | chr14 | 88665408 | |||
chr14:88695454 | G | A | 1 | a0011 | 1 | NA19240.hp1 | missense_variant&splice_region_variant | MODERATE | c.2345C>T | p.Ala782Val | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/44 | 2795/9771 | 2345/5934 | 782/1977 | chr14 | 88695454 | |||
chr14:88705517 | T | C | 1 | a0004 | 2 | HG02040.hp1 NA18980.hp2 |
missense_variant | MODERATE | c.1897A>G | p.Ile633Val | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 12/44 | 2347/9771 | 1897/5934 | 633/1977 | chr14 | 88705517 | |||
chr14:88712367 | T | C | 1 | a0008 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1561A>G | p.Ile521Val | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/44 | 2011/9771 | 1561/5934 | 521/1977 | chr14 | 88712367 | |||
chr14:88738921 | T | C | 4 | a0002 a0005 a0006 others(1): Show |
88 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
missense_variant | MODERATE | c.805A>G | p.Ile269Val | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/44 | 1255/9771 | 805/5934 | 269/1977 | chr14 | 88738921 | |||
chr14:88740517 | G | A | 1 | a0005 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.581C>T | p.Thr194Met | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 5/44 | 1031/9771 | 581/5934 | 194/1977 | chr14 | 88740517 | |||
chr14:88746208 | T | C | 1 | a0007 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.433A>G | p.Met145Val | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/44 | 883/9771 | 433/5934 | 145/1977 | chr14 | 88746208 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:88626910 | A | G | 1 | a0001c0009 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.4668T>C | p.Leu1556Leu | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/44 | 5118/9771 | 4668/5934 | 1556/1977 | chr14 | 88626910 | |||
chr14:88685048 | C | A | 1 | a0002c0004 | 5 | HG00099.hp2 HG01123.hp1 HG01168.hp2 others(2): Show |
synonymous_variant | LOW | c.2949G>T | p.Val983Val | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/44 | 3399/9771 | 2949/5934 | 983/1977 | chr14 | 88685048 | |||
chr14:88688280 | T | C | 2 | a0001c0003 a0001c0009 |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
synonymous_variant | LOW | c.2733A>G | p.Ala911Ala | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/44 | 3183/9771 | 2733/5934 | 911/1977 | chr14 | 88688280 | |||
chr14:88688310 | C | T | 1 | a0001c0006 | 2 | HG01074.hp1 HG01175.hp2 |
synonymous_variant | LOW | c.2703G>A | p.Ala901Ala | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/44 | 3153/9771 | 2703/5934 | 901/1977 | chr14 | 88688310 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:88612583 | A | G | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(48): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
3_prime_UTR_variant | MODIFIER | c.*3235T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 3235 | chr14 | 88612583 | ||||||
chr14:88612690 | T | C | 2 | a0002c0002t0021 a0002c0002t0039 |
3 | HG00323.hp1 HG00733.hp1 HG00738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3128A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 3128 | chr14 | 88612690 | ||||||
chr14:88612752 | G | T | 1 | a0004c0007t0016 | 2 | HG02040.hp1 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3066C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 3066 | chr14 | 88612752 | ||||||
chr14:88612780 | TAC | T | 3 | a0001c0001t0017 a0001c0001t0023 a0001c0001t0036 |
5 | HG01884.hp1 HG02559.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3036_*3037delGT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 3036 | chr14 | 88612780 | ||||||
chr14:88612832 | A | T | 1 | a0001c0001t0030 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2986T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2986 | chr14 | 88612832 | ||||||
chr14:88612979 | T | TA | 5 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0031 others(2): Show |
18 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2838dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2838 | chr14 | 88612979 | ||||||
chr14:88612979 | TA | T | 23 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(20): Show |
138 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*2838delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2838 | chr14 | 88612979 | ||||||
chr14:88613216 | C | T | 2 | a0001c0001t0008 a0008c0011t0008 |
7 | HG02258.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2602G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2602 | chr14 | 88613216 | ||||||
chr14:88613347 | G | C | 2 | a0001c0001t0025 a0009c0008t0025 |
2 | NA18995.hp2 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2471C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2471 | chr14 | 88613347 | ||||||
chr14:88613405 | ATAGT | A | 3 | a0001c0001t0022 a0001c0001t0024 a0001c0001t0037 |
5 | HG01243.hp1 HG01884.hp2 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2409_*2412delACTA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2409 | chr14 | 88613405 | ||||||
chr14:88613524 | T | G | 1 | a0001c0001t0027 | 2 | HG00642.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2294A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2294 | chr14 | 88613524 | ||||||
chr14:88613550 | T | A | 1 | a0003c0005t0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2268A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2268 | chr14 | 88613550 | ||||||
chr14:88613620 | T | C | 1 | a0001c0001t0037 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2198A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2198 | chr14 | 88613620 | ||||||
chr14:88613623 | C | T | 1 | a0001c0001t0029 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2195G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2195 | chr14 | 88613623 | ||||||
chr14:88613907 | G | A | 1 | a0001c0001t0009 | 5 | HG00738.hp1 HG01358.hp2 HG01943.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1911C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 1911 | chr14 | 88613907 | ||||||
chr14:88613933 | T | C | 1 | a0004c0007t0016 | 2 | HG02040.hp1 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1885A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 1885 | chr14 | 88613933 | ||||||
chr14:88614167 | A | G | 1 | a0001c0001t0011 | 4 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1651T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 1651 | chr14 | 88614167 | ||||||
chr14:88614574 | T | C | 1 | a0001c0001t0023 | 2 | HG02559.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1244A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 1244 | chr14 | 88614574 | ||||||
chr14:88614697 | T | A | 1 | a0001c0001t0033 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1121A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 1121 | chr14 | 88614697 | ||||||
chr14:88614799 | G | A | 1 | a0001c0001t0035 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1019C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 1019 | chr14 | 88614799 | ||||||
chr14:88615073 | T | C | 1 | a0002c0002t0038 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*745A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 745 | chr14 | 88615073 | ||||||
chr14:88615112 | G | A | 1 | a0004c0007t0016 | 2 | HG02040.hp1 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*706C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 706 | chr14 | 88615112 | ||||||
chr14:88615254 | T | C | 1 | a0001c0001t0024 | 2 | HG01884.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*564A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 564 | chr14 | 88615254 | ||||||
chr14:88615379 | C | T | 2 | a0001c0001t0011 a0001c0001t0019 |
6 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*439G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 439 | chr14 | 88615379 | ||||||
chr14:88615385 | T | C | 4 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0025 others(1): Show |
23 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*433A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 433 | chr14 | 88615385 | ||||||
chr14:88615399 | A | G | 1 | a0001c0001t0035 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*419T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 419 | chr14 | 88615399 | ||||||
chr14:88792525 | T | TCCCGCTC others(34): Show |
1 | a0002c0002t0034 | 1 | NA18987.hp1 | 5_prime_UTR_variant | MODIFIER | c.-63_-23dupGGCCGCCG others(33): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/44 | 23 | chr14 | 88792525 | ||||||
chr14:88792533 | G | A | 30 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(27): Show |
164 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-30C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/44 | chr14 | 88792533 | |||||||
chr14:88792533 | G | T | 1 | a0001c0001t0028 | 1 | HG03942.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/44 | 30 | chr14 | 88792533 | ||||||
chr14:88792747 | G | C | 2 | a0001c0001t0026 a0001c0001t0027 |
4 | HG00642.hp2 HG02145.hp1 HG06807.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-244C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/44 | 244 | chr14 | 88792747 | ||||||
chr14:88792880 | G | A | 1 | a0002c0002t0039 | 1 | HG00323.hp1 | 5_prime_UTR_variant | MODIFIER | c.-377C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/44 | 377 | chr14 | 88792880 | ||||||
chr14:88792887 | C | G | 1 | a0004c0007t0016 | 2 | HG02040.hp1 NA18980.hp2 |
5_prime_UTR_variant | MODIFIER | c.-384G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/44 | 384 | chr14 | 88792887 | ||||||
chr14:88792920 | A | C | 1 | a0001c0001t0014 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
5_prime_UTR_variant | MODIFIER | c.-417T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/44 | 417 | chr14 | 88792920 | ||||||
chr14:88792946 | G | GCGAGCCG others(3): Show |
4 | a0001c0001t0012 a0001c0003t0004 a0001c0003t0013 others(1): Show |
32 | HG00408.hp1 HG00609.hp1 HG02055.hp2 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-444_-443insGCTCGG others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/44 | 444 | chr14 | 88792946 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:88615905 | C | A | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.5898-51G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 43/43 | chr14 | 88615905 | |||||||
chr14:88615945 | A | G | 105 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0001 others(102): Show |
107 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.5898-91T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 43/43 | chr14 | 88615945 | |||||||
chr14:88615997 | T | G | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.5898-143A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 43/43 | chr14 | 88615997 | |||||||
chr14:88616052 | A | AT | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.5897+89dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 43/43 | chr14 | 88616052 | |||||||
chr14:88616313 | A | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5797-71T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 42/43 | chr14 | 88616313 | |||||||
chr14:88617091 | T | C | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.5643-212A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617091 | |||||||
chr14:88617150 | C | CT | 7 | a0001c0001t0002g0168 a0001c0003t0002g0012 a0001c0003t0006g0221 others(4): Show |
7 | HG01891.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.5643-272dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617150 | |||||||
chr14:88617188 | C | T | 2 | a0001c0001t0002g0112 a0001c0001t0002g0113 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.5643-309G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617188 | |||||||
chr14:88617296 | C | T | 2 | a0001c0001t0017g0010 a0001c0001t0017g0011 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5643-417G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617296 | |||||||
chr14:88617394 | C | T | 6 | a0002c0002t0001g0255 a0002c0002t0001g0256 a0002c0002t0001g0257 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.5643-515G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617394 | |||||||
chr14:88617399 | G | A | 62 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0280 others(59): Show |
62 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.5643-520C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617399 | |||||||
chr14:88617436 | G | A | 3 | a0002c0002t0001g0224 a0002c0002t0001g0225 a0002c0002t0001g0226 |
3 | NA18968.hp1 NA18994.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.5643-557C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617436 | |||||||
chr14:88617493 | G | C | 3 | a0002c0002t0001g0263 a0002c0002t0003g0094 a0002c0002t0007g0030 |
3 | HG04184.hp2 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.5643-614C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617493 | |||||||
chr14:88617604 | T | C | 6 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0215 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.5642+624A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617604 | |||||||
chr14:88617633 | G | C | 1 | a0002c0002t0001g0277 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.5642+595C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617633 | |||||||
chr14:88617902 | G | A | 1 | a0001c0001t0007g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.5642+326C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617902 | |||||||
chr14:88617903 | A | G | 1 | a0001c0001t0002g0088 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.5642+325T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617903 | |||||||
chr14:88618185 | C | T | 1 | a0001c0001t0002g0142 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.5642+43G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88618185 | |||||||
chr14:88618497 | T | G | 5 | a0001c0001t0003g0043 a0001c0001t0003g0052 a0001c0001t0003g0053 others(2): Show |
5 | NA18951.hp2 NA18954.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.5538+153A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 40/43 | chr14 | 88618497 | |||||||
chr14:88618510 | G | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.5538+140C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 40/43 | chr14 | 88618510 | |||||||
chr14:88618907 | C | T | 6 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0215 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.5376-95G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88618907 | |||||||
chr14:88618922 | C | T | 1 | a0001c0001t0011g0216 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5376-110G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88618922 | |||||||
chr14:88618980 | A | G | 1 | a0001c0001t0002g0108 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.5376-168T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88618980 | |||||||
chr14:88619029 | A | G | 1 | a0001c0001t0003g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.5376-217T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88619029 | |||||||
chr14:88619239 | C | T | 1 | a0001c0001t0002g0130 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.5376-427G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88619239 | |||||||
chr14:88619258 | G | A | 9 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.5376-446C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88619258 | |||||||
chr14:88619376 | A | G | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.5376-564T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88619376 | |||||||
chr14:88619487 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5376-675C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88619487 | |||||||
chr14:88619494 | A | C | 274 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0280 others(271): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.5376-682T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88619494 | |||||||
chr14:88619685 | A | AT | 124 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(121): Show |
126 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.5376-874dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88619685 | |||||||
chr14:88619735 | C | T | 7 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(4): Show |
8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.5376-923G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88619735 | |||||||
chr14:88620076 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.5375+678A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88620076 | |||||||
chr14:88620123 | T | C | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.5375+631A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88620123 | |||||||
chr14:88620427 | A | T | 122 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(119): Show |
124 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.5375+327T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88620427 | |||||||
chr14:88620571 | G | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.5375+183C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88620571 | |||||||
chr14:88620616 | A | T | 1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5375+138T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88620616 | |||||||
chr14:88620934 | T | TA | 168 | a0001c0001t0001g0280 a0001c0001t0001g0290 a0001c0001t0002g0001 others(165): Show |
170 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.5203-9dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 38/43 | chr14 | 88620934 | |||||||
chr14:88620934 | T | TAA | 7 | a0001c0001t0003g0069 a0001c0001t0006g0218 a0001c0001t0006g0219 others(4): Show |
7 | HG01496.hp1 HG02559.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.5203-10_5203-9dupT others(1): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 38/43 | chr14 | 88620934 | |||||||
chr14:88620984 | A | G | 1 | a0002c0002t0001g0230 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5203-58T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 38/43 | chr14 | 88620984 | |||||||
chr14:88621457 | A | G | 60 | a0001c0001t0001g0280 a0001c0001t0001g0290 a0001c0001t0003g0036 others(57): Show |
60 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.5014-156T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88621457 | |||||||
chr14:88621747 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.5014-446G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88621747 | |||||||
chr14:88621833 | C | T | 6 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0215 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.5014-532G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88621833 | |||||||
chr14:88621834 | G | A | 1 | a0001c0001t0003g0047 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5014-533C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88621834 | |||||||
chr14:88621922 | C | T | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.5014-621G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88621922 | |||||||
chr14:88622013 | G | A | 92 | a0001c0001t0002g0120 a0001c0001t0002g0133 a0001c0001t0017g0010 others(89): Show |
92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.5013+591C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88622013 | |||||||
chr14:88622144 | G | A | 3 | a0002c0002t0001g0224 a0002c0002t0001g0225 a0002c0002t0001g0226 |
3 | NA18968.hp1 NA18994.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.5013+460C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88622144 | |||||||
chr14:88622256 | C | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.5013+348G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88622256 | |||||||
chr14:88622379 | T | C | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.5013+225A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88622379 | |||||||
chr14:88622391 | A | G | 1 | a0001c0001t0010g0035 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.5013+213T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88622391 | |||||||
chr14:88622418 | T | C | 4 | a0001c0001t0002g0168 a0001c0001t0006g0218 a0001c0001t0006g0219 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.5013+186A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88622418 | |||||||
chr14:88622582 | A | G | 1 | a0001c0001t0002g0147 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.5013+22T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88622582 | |||||||
chr14:88622745 | G | A | 1 | a0001c0003t0004g0323 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4899-27C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88622745 | |||||||
chr14:88622794 | A | T | 2 | a0001c0003t0004g0302 a0001c0003t0004g0329 |
2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4899-76T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88622794 | |||||||
chr14:88622805 | C | CT | 294 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(291): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.4899-88dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88622805 | |||||||
chr14:88622816 | A | T | 1 | a0003c0005t0015g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4899-98T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88622816 | |||||||
chr14:88622895 | A | G | 62 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0280 others(59): Show |
62 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.4899-177T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88622895 | |||||||
chr14:88623017 | C | CT | 208 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0087 others(205): Show |
210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.4899-300dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623017 | |||||||
chr14:88623017 | C | CTT | 16 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(13): Show |
17 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.4899-301_4899-300d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623017 | |||||||
chr14:88623141 | G | A | 104 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0001 others(101): Show |
106 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4899-423C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623141 | |||||||
chr14:88623222 | G | A | 1 | a0001c0009t0013g0301 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4899-504C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623222 | |||||||
chr14:88623466 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4899-748G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623466 | |||||||
chr14:88623648 | G | A | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.4899-930C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623648 | |||||||
chr14:88623655 | G | A | 1 | a0002c0002t0003g0021 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4899-937C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623655 | |||||||
chr14:88623663 | C | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.4899-945G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623663 | |||||||
chr14:88623717 | C | T | 1 | a0001c0003t0004g0322 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4899-999G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623717 | |||||||
chr14:88623773 | T | C | 1 | a0010c0012t0001g0247 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.4899-1055A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623773 | |||||||
chr14:88623790 | A | G | 4 | a0001c0001t0002g0168 a0001c0001t0006g0218 a0001c0001t0006g0219 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4899-1072T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623790 | |||||||
chr14:88623991 | G | A | 3 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0036g0196 |
3 | HG02559.hp2 HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4898+979C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623991 | |||||||
chr14:88624067 | T | A | 1 | a0001c0001t0002g0091 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4898+903A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624067 | |||||||
chr14:88624075 | T | G | 1 | a0001c0001t0002g0091 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4898+895A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624075 | |||||||
chr14:88624127 | G | A | 1 | a0001c0001t0019g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4898+843C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624127 | |||||||
chr14:88624139 | C | T | 7 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(4): Show |
8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.4898+831G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624139 | |||||||
chr14:88624209 | A | T | 294 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(291): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.4898+761T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624209 | |||||||
chr14:88624312 | C | T | 7 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(4): Show |
7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4898+658G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624312 | |||||||
chr14:88624417 | A | T | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.4898+553T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624417 | |||||||
chr14:88624479 | T | C | 152 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0280 others(149): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.4898+491A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624479 | |||||||
chr14:88624584 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4898+386C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624584 | |||||||
chr14:88624858 | G | GGAA | 105 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0001 others(102): Show |
107 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.4898+109_4898+111d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624858 | |||||||
chr14:88624874 | C | G | 1 | a0001c0001t0002g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4898+96G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624874 | |||||||
chr14:88624877 | T | A | 1 | a0001c0001t0002g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4898+93A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624877 | |||||||
chr14:88625317 | T | C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4741-190A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625317 | |||||||
chr14:88625389 | T | C | 1 | a0001c0003t0004g0328 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.4741-262A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625389 | |||||||
chr14:88625480 | C | T | 11 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 others(8): Show |
11 | HG02738.hp1 HG03490.hp1 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.4741-353G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625480 | |||||||
chr14:88625489 | C | T | 2 | a0001c0001t0002g0114 a0001c0001t0002g0115 |
2 | NA18973.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.4741-362G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625489 | |||||||
chr14:88625558 | C | T | 1 | a0001c0001t0003g0081 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4741-431G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625558 | |||||||
chr14:88625559 | G | A | 1 | a0001c0001t0003g0081 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4741-432C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625559 | |||||||
chr14:88625670 | GGGATTAT others(6): Show |
G | 1 | a0002c0002t0001g0226 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.4741-556_4741-544d others(15): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625670 | |||||||
chr14:88625687 | C | T | 6 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0215 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4741-560G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625687 | |||||||
chr14:88625698 | G | A | 4 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0036g0196 others(1): Show |
4 | HG02559.hp2 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.4741-571C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625698 | |||||||
chr14:88625707 | C | T | 1 | a0005c0014t0001g0272 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4741-580G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625707 | |||||||
chr14:88625807 | G | A | 6 | a0001c0003t0002g0012 a0001c0003t0006g0221 a0001c0003t0013g0298 others(3): Show |
6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.4741-680C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625807 | |||||||
chr14:88625912 | C | T | 1 | a0002c0002t0003g0027 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.4741-785G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625912 | |||||||
chr14:88625956 | C | T | 1 | a0001c0003t0004g0302 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4741-829G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625956 | |||||||
chr14:88626063 | T | C | 104 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0001 others(101): Show |
106 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4740+775A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626063 | |||||||
chr14:88626101 | C | T | 1 | a0002c0002t0001g0230 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4740+737G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626101 | |||||||
chr14:88626354 | G | T | 14 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0250 others(11): Show |
14 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.4740+484C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626354 | |||||||
chr14:88626359 | T | C | 79 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0200 others(76): Show |
79 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.4740+479A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626359 | |||||||
chr14:88626576 | C | T | 2 | a0001c0001t0003g0044 a0001c0001t0003g0047 |
2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.4740+262G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626576 | |||||||
chr14:88626616 | C | CA | 7 | a0001c0001t0001g0283 a0001c0001t0002g0138 a0001c0001t0009g0042 others(4): Show |
7 | HG00609.hp1 HG01993.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.4740+221dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626616 | |||||||
chr14:88626616 | CA | C | 94 | a0001c0001t0002g0116 a0001c0001t0002g0122 a0001c0001t0007g0072 others(91): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.4740+221delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626616 | |||||||
chr14:88626634 | C | A | 3 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0220 |
3 | HG02559.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4740+204G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626634 | |||||||
chr14:88626721 | G | A | 10 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 others(7): Show |
10 | HG02738.hp1 HG03490.hp1 HG03492.hp2 others(7): Show |
intron_variant | MODIFIER | c.4740+117C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626721 | |||||||
chr14:88626723 | A | G | 1 | a0001c0001t0033g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4740+115T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626723 | |||||||
chr14:88627137 | A | G | 1 | a0002c0002t0001g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4532-91T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 34/43 | chr14 | 88627137 | |||||||
chr14:88627287 | G | C | 1 | a0001c0001t0014g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4532-241C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 34/43 | chr14 | 88627287 | |||||||
chr14:88627372 | T | C | 4 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0215 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4531+274A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 34/43 | chr14 | 88627372 | |||||||
chr14:88627899 | G | C | 281 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(278): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.4358-80C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88627899 | |||||||
chr14:88628555 | A | G | 1 | a0002c0002t0007g0030 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4358-736T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88628555 | |||||||
chr14:88628653 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4358-834T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88628653 | |||||||
chr14:88628681 | A | G | 1 | a0001c0001t0003g0163 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.4358-862T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88628681 | |||||||
chr14:88628871 | T | A | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.4358-1052A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88628871 | |||||||
chr14:88628908 | C | T | 281 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(278): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.4358-1089G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88628908 | |||||||
chr14:88629115 | T | C | 2 | a0001c0001t0017g0010 a0001c0001t0017g0011 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4358-1296A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88629115 | |||||||
chr14:88629143 | A | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4358-1324T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88629143 | |||||||
chr14:88629206 | A | G | 1 | a0002c0004t0001g0228 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.4358-1387T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88629206 | |||||||
chr14:88629449 | T | C | 1 | a0001c0001t0003g0069 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4358-1630A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88629449 | |||||||
chr14:88629506 | C | G | 104 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0001 others(101): Show |
106 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4358-1687G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88629506 | |||||||
chr14:88629546 | T | C | 3 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4358-1727A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88629546 | |||||||
chr14:88629872 | A | C | 1 | a0002c0002t0001g0231 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.4358-2053T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88629872 | |||||||
chr14:88630008 | T | C | 104 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0001 others(101): Show |
106 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4358-2189A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630008 | |||||||
chr14:88630023 | A | AT | 10 | a0001c0001t0003g0054 a0001c0001t0014g0004 a0001c0001t0014g0005 others(7): Show |
10 | HG01243.hp1 HG02135.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.4358-2205dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630023 | |||||||
chr14:88630023 | AT | A | 103 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0002g0156 others(100): Show |
103 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.4358-2205delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630023 | |||||||
chr14:88630023 | ATT | A | 90 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(87): Show |
91 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.4358-2206_4358-220 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630023 | |||||||
chr14:88630023 | ATTT | A | 24 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(21): Show |
26 | HG01106.hp1 HG01109.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.4358-2207_4358-220 others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630023 | |||||||
chr14:88630341 | T | G | 281 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(278): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.4358-2522A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630341 | |||||||
chr14:88630395 | T | C | 294 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(291): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.4358-2576A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630395 | |||||||
chr14:88630644 | C | T | 1 | a0002c0002t0038g0262 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.4358-2825G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630644 | |||||||
chr14:88630904 | G | A | 7 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(4): Show |
7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4358-3085C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630904 | |||||||
chr14:88631056 | A | C | 1 | a0001c0001t0006g0284 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4358-3237T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88631056 | |||||||
chr14:88631066 | A | G | 1 | a0001c0001t0011g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4358-3247T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88631066 | |||||||
chr14:88631164 | GAT | G | 13 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(10): Show |
14 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.4357+3303_4357+330 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88631164 | |||||||
chr14:88631290 | C | T | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.4357+3179G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88631290 | |||||||
chr14:88631299 | G | A | 13 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(10): Show |
14 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.4357+3170C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88631299 | |||||||
chr14:88631338 | C | A | 2 | a0001c0001t0017g0010 a0001c0001t0017g0011 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4357+3131G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88631338 | |||||||
chr14:88631694 | C | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.4357+2775G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88631694 | |||||||
chr14:88632060 | C | G | 88 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0200 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.4357+2409G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88632060 | |||||||
chr14:88632277 | T | A | 1 | a0001c0001t0002g0155 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4357+2192A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88632277 | |||||||
chr14:88632287 | T | G | 7 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(4): Show |
7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4357+2182A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88632287 | |||||||
chr14:88632306 | G | A | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.4357+2163C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88632306 | |||||||
chr14:88632389 | C | T | 4 | a0001c0001t0026g0293 a0001c0001t0026g0294 a0001c0001t0027g0295 others(1): Show |
4 | HG00642.hp2 HG02145.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.4357+2080G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88632389 | |||||||
chr14:88632746 | G | A | 1 | a0001c0001t0002g0140 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4357+1723C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88632746 | |||||||
chr14:88632775 | G | A | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4357+1694C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88632775 | |||||||
chr14:88632981 | C | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4357+1488G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88632981 | |||||||
chr14:88633027 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4357+1442T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88633027 | |||||||
chr14:88633030 | T | C | 1 | a0001c0001t0019g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4357+1439A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88633030 | |||||||
chr14:88633207 | T | C | 1 | a0001c0001t0003g0039 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.4357+1262A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88633207 | |||||||
chr14:88633635 | AGAT | A | 62 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0280 others(59): Show |
62 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.4357+831_4357+833d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88633635 | |||||||
chr14:88633674 | C | T | 13 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(10): Show |
14 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.4357+795G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88633674 | |||||||
chr14:88633874 | G | A | 104 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0001 others(101): Show |
106 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4357+595C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88633874 | |||||||
chr14:88633938 | T | C | 7 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(4): Show |
7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4357+531A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88633938 | |||||||
chr14:88634109 | T | C | 150 | a0001c0001t0001g0280 a0001c0001t0001g0290 a0001c0001t0003g0036 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.4357+360A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88634109 | |||||||
chr14:88634174 | C | T | 3 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0220 |
3 | HG02559.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4357+295G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88634174 | |||||||
chr14:88634307 | C | A | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4357+162G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88634307 | |||||||
chr14:88634601 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4337-112G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88634601 | |||||||
chr14:88634632 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.4337-143G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88634632 | |||||||
chr14:88634730 | A | C | 1 | a0001c0001t0003g0043 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.4337-241T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88634730 | |||||||
chr14:88634742 | A | G | 1 | a0001c0001t0003g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4337-253T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88634742 | |||||||
chr14:88634910 | G | A | 11 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0209 others(8): Show |
11 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.4337-421C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88634910 | |||||||
chr14:88635022 | C | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4337-533G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88635022 | |||||||
chr14:88635266 | G | C | 105 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0001 others(102): Show |
107 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.4337-777C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88635266 | |||||||
chr14:88635304 | A | G | 1 | a0001c0003t0006g0221 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4337-815T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88635304 | |||||||
chr14:88635500 | AT | A | 3 | a0002c0002t0001g0232 a0002c0002t0001g0233 a0002c0002t0001g0261 |
3 | NA18947.hp2 NA18962.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.4337-1012delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88635500 | |||||||
chr14:88635522 | C | T | 1 | a0001c0001t0005g0182 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4337-1033G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88635522 | |||||||
chr14:88635623 | A | T | 1 | a0002c0002t0001g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4337-1134T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88635623 | |||||||
chr14:88635826 | C | T | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.4337-1337G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88635826 | |||||||
chr14:88636214 | T | C | 59 | a0001c0001t0001g0280 a0001c0001t0001g0290 a0001c0001t0003g0036 others(56): Show |
59 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.4337-1725A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88636214 | |||||||
chr14:88636340 | T | C | 105 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0001 others(102): Show |
107 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.4337-1851A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88636340 | |||||||
chr14:88636370 | G | A | 7 | a0002c0002t0001g0278 a0002c0002t0003g0019 a0002c0002t0003g0020 others(4): Show |
7 | HG02135.hp1 HG02165.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.4337-1881C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88636370 | |||||||
chr14:88636391 | G | A | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4337-1902C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88636391 | |||||||
chr14:88636703 | G | T | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.4336+2106C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88636703 | |||||||
chr14:88637028 | C | A | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.4336+1781G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637028 | |||||||
chr14:88637079 | G | A | 19 | a0001c0001t0006g0208 a0001c0001t0006g0218 a0001c0001t0006g0219 others(16): Show |
19 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.4336+1730C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637079 | |||||||
chr14:88637119 | A | T | 23 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.4336+1690T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637119 | |||||||
chr14:88637162 | T | C | 1 | a0008c0011t0008g0101 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4336+1647A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637162 | |||||||
chr14:88637670 | T | C | 1 | a0001c0001t0002g0107 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.4336+1139A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637670 | |||||||
chr14:88637786 | G | A | 1 | a0001c0001t0010g0034 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4336+1023C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637786 | |||||||
chr14:88637839 | G | A | 1 | a0001c0001t0033g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4336+970C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637839 | |||||||
chr14:88637883 | T | C | 7 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(4): Show |
7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4336+926A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637883 | |||||||
chr14:88637916 | C | T | 1 | a0002c0002t0001g0249 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4336+893G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637916 | |||||||
chr14:88637985 | G | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4336+824C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637985 | |||||||
chr14:88638287 | A | G | 1 | a0002c0002t0001g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.4336+522T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88638287 | |||||||
chr14:88638391 | CT | C | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4336+417delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88638391 | |||||||
chr14:88638411 | C | T | 300 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(297): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.4336+398G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88638411 | |||||||
chr14:88638617 | C | T | 1 | a0002c0002t0001g0278 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4336+192G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88638617 | |||||||
chr14:88638943 | T | A | 151 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0280 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.4238-36A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88638943 | |||||||
chr14:88639142 | C | A | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4238-235G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639142 | |||||||
chr14:88639192 | A | G | 43 | a0001c0001t0001g0280 a0001c0001t0001g0290 a0001c0001t0003g0036 others(40): Show |
43 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.4238-285T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639192 | |||||||
chr14:88639317 | T | C | 7 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(4): Show |
7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4238-410A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639317 | |||||||
chr14:88639461 | C | T | 281 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(278): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.4238-554G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639461 | |||||||
chr14:88639544 | A | G | 105 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0001 others(102): Show |
107 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.4238-637T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639544 | |||||||
chr14:88639572 | A | G | 1 | a0004c0007t0016g0007 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.4238-665T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639572 | |||||||
chr14:88639870 | C | T | 1 | a0001c0001t0011g0213 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4238-963G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639870 | |||||||
chr14:88639877 | A | G | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4238-970T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639877 | |||||||
chr14:88639961 | G | A | 1 | a0001c0001t0002g0128 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4238-1054C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639961 | |||||||
chr14:88640142 | G | T | 4 | a0001c0001t0002g0168 a0003c0005t0015g0013 a0003c0005t0015g0014 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1235C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640142 | |||||||
chr14:88640145 | A | C | 4 | a0001c0001t0002g0168 a0003c0005t0015g0013 a0003c0005t0015g0014 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1238T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640145 | |||||||
chr14:88640146 | G | T | 4 | a0001c0001t0002g0168 a0003c0005t0015g0013 a0003c0005t0015g0014 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1239C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640146 | |||||||
chr14:88640148 | T | C | 4 | a0001c0001t0002g0168 a0003c0005t0015g0013 a0003c0005t0015g0014 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1241A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640148 | |||||||
chr14:88640150 | A | T | 4 | a0001c0001t0002g0168 a0003c0005t0015g0013 a0003c0005t0015g0014 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1243T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640150 | |||||||
chr14:88640152 | C | G | 4 | a0001c0001t0002g0168 a0003c0005t0015g0013 a0003c0005t0015g0014 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1245G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640152 | |||||||
chr14:88640154 | A | T | 4 | a0001c0001t0002g0168 a0003c0005t0015g0013 a0003c0005t0015g0014 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1247T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640154 | |||||||
chr14:88640156 | G | A | 4 | a0001c0001t0002g0168 a0003c0005t0015g0013 a0003c0005t0015g0014 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1249C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640156 | |||||||
chr14:88640158 | A | C | 4 | a0001c0001t0002g0168 a0003c0005t0015g0013 a0003c0005t0015g0014 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1251T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640158 | |||||||
chr14:88640159 | G | T | 4 | a0001c0001t0002g0168 a0003c0005t0015g0013 a0003c0005t0015g0014 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1252C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640159 | |||||||
chr14:88640162 | A | C | 4 | a0001c0001t0002g0168 a0003c0005t0015g0013 a0003c0005t0015g0014 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1255T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640162 | |||||||
chr14:88640397 | G | T | 314 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(311): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.4238-1490C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640397 | |||||||
chr14:88640398 | C | T | 19 | a0001c0001t0006g0208 a0001c0001t0006g0218 a0001c0001t0006g0219 others(16): Show |
19 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.4238-1491G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640398 | |||||||
chr14:88640513 | G | A | 1 | a0001c0001t0002g0133 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4238-1606C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640513 | |||||||
chr14:88640551 | G | A | 2 | a0001c0001t0006g0003 a0001c0001t0006g0286 |
3 | HG01256.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4238-1644C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640551 | |||||||
chr14:88640613 | A | G | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4238-1706T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640613 | |||||||
chr14:88640939 | C | A | 2 | a0002c0002t0003g0017 a0002c0002t0003g0018 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4237+1954G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640939 | |||||||
chr14:88640988 | A | G | 2 | a0001c0001t0011g0214 a0001c0001t0011g0215 |
2 | HG02280.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.4237+1905T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640988 | |||||||
chr14:88641147 | C | G | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.4237+1746G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88641147 | |||||||
chr14:88641162 | G | A | 4 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.4237+1731C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88641162 | |||||||
chr14:88641226 | T | C | 1 | a0002c0002t0003g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4237+1667A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88641226 | |||||||
chr14:88641501 | T | C | 1 | a0001c0001t0006g0003 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4237+1392A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88641501 | |||||||
chr14:88641808 | C | T | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4237+1085G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88641808 | |||||||
chr14:88641851 | T | G | 1 | a0002c0002t0001g0263 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4237+1042A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88641851 | |||||||
chr14:88642002 | T | C | 4 | a0001c0001t0002g0168 a0001c0001t0006g0218 a0001c0001t0006g0219 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4237+891A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88642002 | |||||||
chr14:88642088 | A | G | 4 | a0001c0001t0002g0168 a0001c0001t0006g0218 a0001c0001t0006g0219 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4237+805T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88642088 | |||||||
chr14:88642290 | T | C | 1 | a0001c0001t0009g0059 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.4237+603A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88642290 | |||||||
chr14:88642374 | A | G | 4 | a0001c0001t0002g0168 a0001c0001t0006g0218 a0001c0001t0006g0219 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4237+519T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88642374 | |||||||
chr14:88642434 | G | A | 107 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0001 others(104): Show |
109 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.4237+459C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88642434 | |||||||
chr14:88642527 | C | T | 4 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 others(1): Show |
4 | NA18953.hp2 NA18960.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4237+366G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88642527 | |||||||
chr14:88642588 | A | G | 1 | a0001c0001t0003g0082 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.4237+305T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88642588 | |||||||
chr14:88643138 | G | C | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.4108-116C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88643138 | |||||||
chr14:88643423 | A | C | 1 | a0001c0001t0014g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4108-401T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88643423 | |||||||
chr14:88643523 | A | G | 88 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0200 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.4108-501T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88643523 | |||||||
chr14:88643836 | G | A | 1 | a0001c0001t0005g0173 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.4107+597C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88643836 | |||||||
chr14:88643872 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4107+561C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88643872 | |||||||
chr14:88643884 | G | A | 6 | a0001c0001t0006g0208 a0001c0001t0022g0203 a0001c0001t0022g0204 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.4107+549C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88643884 | |||||||
chr14:88643951 | A | G | 281 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(278): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.4107+482T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88643951 | |||||||
chr14:88644047 | A | G | 1 | a0001c0001t0007g0062 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4107+386T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88644047 | |||||||
chr14:88644200 | A | G | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.4107+233T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88644200 | |||||||
chr14:88644382 | A | G | 1 | a0001c0003t0006g0221 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4107+51T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88644382 | |||||||
chr14:88644629 | C | A | 1 | a0001c0001t0003g0056 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4029-118G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88644629 | |||||||
chr14:88644750 | G | A | 1 | a0001c0001t0002g0140 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4029-239C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88644750 | |||||||
chr14:88644959 | G | A | 5 | a0001c0001t0007g0038 a0001c0001t0007g0070 a0001c0001t0007g0072 others(2): Show |
5 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.4029-448C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88644959 | |||||||
chr14:88645012 | C | T | 2 | a0001c0003t0004g0318 a0001c0003t0004g0319 |
2 | HG00408.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.4029-501G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645012 | |||||||
chr14:88645027 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4029-516G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645027 | |||||||
chr14:88645033 | T | C | 1 | a0002c0004t0001g0234 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4029-522A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645033 | |||||||
chr14:88645045 | T | A | 6 | a0001c0001t0006g0208 a0001c0001t0022g0203 a0001c0001t0022g0204 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.4029-534A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645045 | |||||||
chr14:88645053 | GTTTCAC | G | 61 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0280 others(58): Show |
61 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.4029-548_4029-543d others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645053 | |||||||
chr14:88645083 | G | A | 2 | a0001c0001t0006g0003 a0001c0001t0006g0286 |
3 | HG01256.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4029-572C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645083 | |||||||
chr14:88645210 | G | A | 1 | a0002c0002t0001g0263 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4029-699C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645210 | |||||||
chr14:88645334 | A | C | 61 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0280 others(58): Show |
61 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.4029-823T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645334 | |||||||
chr14:88645350 | G | A | 4 | a0002c0002t0001g0209 a0002c0002t0001g0245 a0002c0002t0003g0024 others(1): Show |
4 | HG01255.hp1 HG01361.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.4029-839C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645350 | |||||||
chr14:88645351 | T | G | 1 | a0001c0001t0003g0081 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4029-840A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645351 | |||||||
chr14:88645449 | C | T | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.4029-938G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645449 | |||||||
chr14:88645555 | C | T | 1 | a0001c0001t0035g0198 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4029-1044G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645555 | |||||||
chr14:88645666 | G | A | 7 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(4): Show |
7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4029-1155C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645666 | |||||||
chr14:88645848 | T | C | 1 | a0001c0001t0007g0038 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4028+1099A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645848 | |||||||
chr14:88645942 | C | T | 1 | a0001c0003t0004g0306 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4028+1005G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645942 | |||||||
chr14:88645968 | T | A | 1 | a0002c0002t0001g0256 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4028+979A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645968 | |||||||
chr14:88646016 | T | C | 1 | a0001c0001t0003g0043 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.4028+931A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88646016 | |||||||
chr14:88646230 | A | C | 1 | a0002c0002t0001g0245 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.4028+717T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88646230 | |||||||
chr14:88646244 | A | G | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4028+703T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88646244 | |||||||
chr14:88646254 | C | T | 3 | a0002c0002t0001g0224 a0002c0002t0001g0225 a0002c0002t0001g0226 |
3 | NA18968.hp1 NA18994.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.4028+693G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88646254 | |||||||
chr14:88646328 | T | A | 2 | a0001c0001t0002g0089 a0001c0001t0002g0090 |
2 | NA19006.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.4028+619A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88646328 | |||||||
chr14:88646364 | A | G | 59 | a0001c0001t0001g0280 a0001c0001t0001g0290 a0001c0001t0003g0036 others(56): Show |
59 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.4028+583T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88646364 | |||||||
chr14:88646833 | A | C | 7 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(4): Show |
8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.4028+114T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88646833 | |||||||
chr14:88646880 | A | G | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4028+67T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88646880 | |||||||
chr14:88646983 | A | G | 1 | a0001c0001t0011g0213 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4020-28T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88646983 | |||||||
chr14:88647231 | G | T | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.4020-276C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647231 | |||||||
chr14:88647235 | G | A | 1 | a0001c0001t0008g0100 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4020-280C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647235 | |||||||
chr14:88647296 | G | A | 1 | a0001c0001t0019g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4020-341C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647296 | |||||||
chr14:88647322 | T | A | 1 | a0002c0002t0003g0021 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4020-367A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647322 | |||||||
chr14:88647325 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4020-370C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647325 | |||||||
chr14:88647421 | G | A | 19 | a0001c0001t0006g0208 a0001c0001t0006g0218 a0001c0001t0006g0219 others(16): Show |
19 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.4020-466C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647421 | |||||||
chr14:88647687 | C | CA | 83 | a0001c0001t0003g0036 a0001c0001t0003g0041 a0001c0001t0003g0044 others(80): Show |
83 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.4020-733dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | |||||||
chr14:88647687 | C | CAA | 21 | a0001c0001t0002g0141 a0001c0001t0008g0103 a0001c0001t0012g0324 others(18): Show |
21 | HG00438.hp1 HG00639.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4020-734_4020-733d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | |||||||
chr14:88647687 | C | CAAA | 89 | a0001c0001t0001g0211 a0001c0001t0002g0001 a0001c0001t0002g0002 others(86): Show |
91 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.4020-735_4020-733d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | |||||||
chr14:88647687 | C | CAAAA | 15 | a0001c0001t0001g0210 a0001c0001t0002g0090 a0001c0001t0002g0105 others(12): Show |
15 | HG01074.hp2 HG01099.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.4020-736_4020-733d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | |||||||
chr14:88647687 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0014g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4020-747_4020-733d others(17): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | |||||||
chr14:88647687 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0014g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4020-748_4020-733d others(18): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | |||||||
chr14:88647687 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0014g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4020-749_4020-733d others(19): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | |||||||
chr14:88647687 | C | CAAAAAAA others(11): Show |
3 | a0001c0001t0022g0204 a0001c0001t0024g0206 a0001c0001t0037g0205 |
3 | HG01243.hp1 HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4020-750_4020-733d others(20): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | |||||||
chr14:88647687 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0022g0203 a0001c0001t0024g0207 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4020-751_4020-733d others(21): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | |||||||
chr14:88647687 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4020-752_4020-733d others(22): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | |||||||
chr14:88647687 | CA | C | 35 | a0001c0001t0003g0040 a0001c0001t0009g0058 a0001c0001t0035g0198 others(32): Show |
35 | HG00408.hp1 HG00738.hp1 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.4020-733delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | |||||||
chr14:88647687 | CAAA | C | 7 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(4): Show |
7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4020-735_4020-733d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | |||||||
chr14:88647777 | G | A | 5 | a0002c0004t0001g0228 a0002c0004t0001g0234 a0002c0004t0001g0240 others(2): Show |
5 | HG00099.hp2 HG01123.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.4020-822C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647777 | |||||||
chr14:88648094 | T | G | 46 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(43): Show |
47 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(44): Show |
intron_variant | MODIFIER | c.4020-1139A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88648094 | |||||||
chr14:88648293 | C | A | 4 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0215 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4020-1338G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88648293 | |||||||
chr14:88648660 | T | C | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(13): Show |
16 | HG00423.hp1 HG00673.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.4019+1252A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88648660 | |||||||
chr14:88648690 | A | T | 3 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0007g0134 |
3 | HG01516.hp2 HG01517.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.4019+1222T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88648690 | |||||||
chr14:88648816 | T | C | 7 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(4): Show |
7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4019+1096A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88648816 | |||||||
chr14:88648872 | A | AT | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4019+1039dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88648872 | |||||||
chr14:88649139 | C | T | 1 | a0001c0001t0002g0133 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4019+773G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88649139 | |||||||
chr14:88649256 | G | C | 2 | a0001c0001t0002g0109 a0001c0001t0002g0110 |
2 | HG02165.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.4019+656C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88649256 | |||||||
chr14:88649336 | T | C | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.4019+576A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88649336 | |||||||
chr14:88649619 | T | G | 1 | a0001c0001t0003g0055 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4019+293A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88649619 | |||||||
chr14:88649830 | G | GA | 4 | a0001c0001t0012g0324 a0001c0001t0012g0325 a0001c0001t0012g0326 others(1): Show |
4 | HG00609.hp1 NA18953.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.4019+81dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88649830 | |||||||
chr14:88649978 | A | G | 1 | a0002c0002t0003g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4005-52T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88649978 | |||||||
chr14:88650145 | T | C | 1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4005-219A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650145 | |||||||
chr14:88650174 | T | C | 289 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(286): Show |
292 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.4005-248A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650174 | |||||||
chr14:88650190 | T | C | 7 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(4): Show |
7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4005-264A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650190 | |||||||
chr14:88650282 | G | A | 8 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(5): Show |
9 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.4005-356C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650282 | |||||||
chr14:88650381 | G | A | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4005-455C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650381 | |||||||
chr14:88650849 | C | G | 1 | a0001c0001t0006g0218 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4005-923G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650849 | |||||||
chr14:88650870 | A | G | 269 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(266): Show |
272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.4005-944T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650870 | |||||||
chr14:88650915 | T | C | 1 | a0001c0001t0003g0057 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.4005-989A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650915 | |||||||
chr14:88650957 | G | T | 2 | a0001c0001t0011g0214 a0001c0001t0011g0215 |
2 | HG02280.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.4005-1031C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650957 | |||||||
chr14:88651023 | A | T | 1 | a0002c0002t0001g0278 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4005-1097T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651023 | |||||||
chr14:88651131 | G | A | 325 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(322): Show |
328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.4005-1205C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651131 | |||||||
chr14:88651154 | CT | C | 230 | a0001c0001t0001g0283 a0001c0001t0002g0001 a0001c0001t0002g0002 others(227): Show |
232 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.4005-1229delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651154 | |||||||
chr14:88651154 | CTT | C | 40 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0096 others(37): Show |
41 | HG00673.hp2 HG00738.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.4005-1230_4005-122 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651154 | |||||||
chr14:88651160 | T | C | 2 | a0001c0001t0017g0010 a0001c0001t0017g0011 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4005-1234A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651160 | |||||||
chr14:88651163 | T | C | 6 | a0001c0001t0006g0208 a0001c0001t0022g0203 a0001c0001t0022g0204 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.4005-1237A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651163 | |||||||
chr14:88651208 | C | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4005-1282G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651208 | |||||||
chr14:88651246 | T | TGTC | 4 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0035g0198 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.4005-1323_4005-132 others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651246 | |||||||
chr14:88651398 | A | G | 1 | a0001c0001t0002g0114 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.4005-1472T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651398 | |||||||
chr14:88651554 | T | A | 1 | a0001c0003t0018g0016 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4005-1628A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651554 | |||||||
chr14:88651807 | G | A | 5 | a0002c0004t0001g0228 a0002c0004t0001g0234 a0002c0004t0001g0240 others(2): Show |
5 | HG00099.hp2 HG01123.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.4005-1881C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651807 | |||||||
chr14:88652043 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4005-2117A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88652043 | |||||||
chr14:88652347 | C | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.4005-2421G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88652347 | |||||||
chr14:88652433 | C | A | 2 | a0001c0001t0005g0179 a0001c0001t0005g0182 |
2 | NA18983.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.4005-2507G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88652433 | |||||||
chr14:88652535 | T | C | 2 | a0002c0002t0001g0229 a0002c0002t0001g0279 |
2 | HG00609.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.4005-2609A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88652535 | |||||||
chr14:88652720 | T | C | 2 | a0001c0001t0002g0112 a0001c0001t0002g0113 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.4005-2794A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88652720 | |||||||
chr14:88652734 | C | T | 1 | a0001c0001t0008g0100 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4005-2808G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88652734 | |||||||
chr14:88652843 | T | C | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.4005-2917A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88652843 | |||||||
chr14:88652873 | C | T | 2 | a0001c0001t0002g0091 a0001c0001t0002g0155 |
2 | HG01261.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.4005-2947G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88652873 | |||||||
chr14:88653121 | C | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4005-3195G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653121 | |||||||
chr14:88653157 | C | T | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.4005-3231G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653157 | |||||||
chr14:88653340 | A | G | 6 | a0002c0002t0003g0019 a0002c0002t0003g0020 a0002c0002t0003g0021 others(3): Show |
6 | HG02165.hp1 NA18948.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.4005-3414T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653340 | |||||||
chr14:88653408 | T | C | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4005-3482A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653408 | |||||||
chr14:88653472 | C | T | 1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4005-3546G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653472 | |||||||
chr14:88653512 | C | T | 3 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0220 |
3 | HG02559.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4005-3586G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653512 | |||||||
chr14:88653524 | G | A | 1 | a0001c0001t0003g0169 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.4005-3598C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653524 | |||||||
chr14:88653551 | A | G | 1 | a0001c0001t0003g0039 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.4005-3625T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653551 | |||||||
chr14:88653724 | C | T | 10 | a0001c0003t0004g0303 a0001c0003t0004g0304 a0001c0003t0004g0305 others(7): Show |
10 | HG02257.hp1 HG02280.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.4004+3652G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653724 | |||||||
chr14:88653988 | G | C | 6 | a0001c0001t0006g0208 a0001c0001t0022g0203 a0001c0001t0022g0204 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.4004+3388C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653988 | |||||||
chr14:88654097 | A | G | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.4004+3279T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88654097 | |||||||
chr14:88654298 | C | A | 27 | a0001c0003t0004g0302 a0001c0003t0004g0303 a0001c0003t0004g0304 others(24): Show |
27 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.4004+3078G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88654298 | |||||||
chr14:88654528 | C | T | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.4004+2848G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88654528 | |||||||
chr14:88655153 | A | G | 1 | a0002c0002t0003g0019 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.4004+2223T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88655153 | |||||||
chr14:88655279 | T | G | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.4004+2097A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88655279 | |||||||
chr14:88656471 | G | A | 1 | a0001c0001t0017g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4004+905C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88656471 | |||||||
chr14:88656615 | A | AT | 4 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0035g0198 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.4004+760dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88656615 | |||||||
chr14:88656746 | GGACT | G | 175 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(172): Show |
178 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.4004+626_4004+629d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88656746 | |||||||
chr14:88656907 | A | G | 1 | a0010c0012t0001g0247 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.4004+469T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88656907 | |||||||
chr14:88656968 | T | A | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(15): Show |
19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.4004+408A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88656968 | |||||||
chr14:88657019 | G | A | 1 | a0001c0001t0007g0084 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4004+357C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88657019 | |||||||
chr14:88657145 | C | G | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.4004+231G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88657145 | |||||||
chr14:88657286 | T | C | 1 | a0001c0001t0005g0173 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.4004+90A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88657286 | |||||||
chr14:88657337 | A | G | 1 | a0001c0001t0005g0186 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4004+39T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88657337 | |||||||
chr14:88657570 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3878-68T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 26/43 | chr14 | 88657570 | |||||||
chr14:88657647 | C | T | 2 | a0001c0001t0024g0206 a0001c0001t0024g0207 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3878-145G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 26/43 | chr14 | 88657647 | |||||||
chr14:88657830 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3878-328C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 26/43 | chr14 | 88657830 | |||||||
chr14:88657870 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3877+317G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 26/43 | chr14 | 88657870 | |||||||
chr14:88657881 | T | C | 23 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.3877+306A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 26/43 | chr14 | 88657881 | |||||||
chr14:88657937 | A | G | 1 | a0001c0001t0007g0062 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3877+250T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 26/43 | chr14 | 88657937 | |||||||
chr14:88658076 | TACC | T | 175 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(172): Show |
178 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.3877+108_3877+110d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 26/43 | chr14 | 88658076 | |||||||
chr14:88658799 | ATAGT | A | 17 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.3676-415_3676-412d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88658799 | |||||||
chr14:88658918 | G | A | 1 | a0001c0001t0007g0073 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3676-530C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88658918 | |||||||
chr14:88658940 | T | A | 1 | a0001c0001t0017g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3676-552A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88658940 | |||||||
chr14:88658944 | G | A | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3676-556C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88658944 | |||||||
chr14:88659236 | ACT | A | 3 | a0002c0002t0021g0273 a0002c0002t0021g0292 a0002c0002t0039g0297 |
3 | HG00323.hp1 HG00733.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.3676-850_3676-849d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88659236 | |||||||
chr14:88659241 | C | CT | 34 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(31): Show |
36 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.3676-854dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88659241 | |||||||
chr14:88659330 | C | T | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.3676-942G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88659330 | |||||||
chr14:88659540 | G | C | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3676-1152C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88659540 | |||||||
chr14:88659679 | C | T | 2 | a0001c0001t0024g0206 a0001c0001t0024g0207 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3676-1291G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88659679 | |||||||
chr14:88659717 | C | G | 1 | a0001c0001t0002g0091 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3676-1329G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88659717 | |||||||
chr14:88659808 | A | G | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3676-1420T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88659808 | |||||||
chr14:88660011 | C | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3676-1623G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660011 | |||||||
chr14:88660144 | A | G | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3675+1510T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660144 | |||||||
chr14:88660184 | G | A | 51 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(48): Show |
52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.3675+1470C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660184 | |||||||
chr14:88660187 | G | A | 2 | a0001c0001t0003g0044 a0001c0001t0003g0047 |
2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.3675+1467C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660187 | |||||||
chr14:88660202 | G | A | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3675+1452C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660202 | |||||||
chr14:88660282 | T | TA | 57 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(54): Show |
58 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(55): Show |
intron_variant | MODIFIER | c.3675+1371dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660282 | |||||||
chr14:88660282 | TA | T | 7 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0003g0045 others(4): Show |
7 | HG01069.hp2 HG01168.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.3675+1371delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660282 | |||||||
chr14:88660341 | T | A | 1 | a0001c0001t0033g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3675+1313A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660341 | |||||||
chr14:88660517 | C | T | 1 | a0001c0001t0002g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3675+1137G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660517 | |||||||
chr14:88660700 | G | A | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3675+954C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660700 | |||||||
chr14:88660748 | A | AAAAAAAG | 170 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(167): Show |
173 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.3675+899_3675+905d others(9): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660748 | |||||||
chr14:88660806 | T | C | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3675+848A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660806 | |||||||
chr14:88661021 | T | C | 102 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(99): Show |
104 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.3675+633A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88661021 | |||||||
chr14:88661095 | G | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3675+559C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88661095 | |||||||
chr14:88661112 | A | G | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3675+542T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88661112 | |||||||
chr14:88661261 | T | G | 11 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(8): Show |
11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.3675+393A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88661261 | |||||||
chr14:88661449 | T | C | 1 | a0001c0001t0003g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3675+205A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88661449 | |||||||
chr14:88661954 | A | C | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3499-124T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88661954 | |||||||
chr14:88662286 | T | TA | 157 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(154): Show |
160 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.3499-457dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662286 | |||||||
chr14:88662286 | T | TAA | 20 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(17): Show |
20 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.3499-458_3499-457d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662286 | |||||||
chr14:88662339 | G | GT | 148 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(145): Show |
150 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.3499-510dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662339 | |||||||
chr14:88662339 | G | GTT | 69 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0098 others(66): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.3499-511_3499-510d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662339 | |||||||
chr14:88662339 | G | GTTT | 14 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(11): Show |
14 | HG01106.hp2 HG01433.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.3499-512_3499-510d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662339 | |||||||
chr14:88662339 | G | GTTTTTTT others(3): Show |
2 | a0001c0001t0014g0004 a0001c0001t0014g0006 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3499-519_3499-510d others(12): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662339 | |||||||
chr14:88662339 | GTTTTTTT others(11): Show |
G | 4 | a0001c0003t0004g0310 a0001c0003t0004g0311 a0001c0003t0004g0312 others(1): Show |
4 | HG02280.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3499-527_3499-510d others(20): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662339 | |||||||
chr14:88662396 | A | G | 1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3499-566T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662396 | |||||||
chr14:88662407 | C | T | 106 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(103): Show |
108 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.3499-577G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662407 | |||||||
chr14:88662542 | C | CT | 61 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0280 others(58): Show |
61 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.3498+488dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662542 | |||||||
chr14:88662560 | T | A | 24 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(21): Show |
25 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.3498+471A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662560 | |||||||
chr14:88662560 | T | TA | 121 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(118): Show |
123 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.3498+470dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662560 | |||||||
chr14:88662560 | T | TAA | 29 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(26): Show |
29 | HG00408.hp1 HG02055.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.3498+469_3498+470d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662560 | |||||||
chr14:88662628 | C | T | 1 | a0001c0001t0037g0205 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3498+403G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662628 | |||||||
chr14:88662629 | G | A | 1 | a0001c0001t0011g0213 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3498+402C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662629 | |||||||
chr14:88662763 | T | C | 2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | HG01175.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.3498+268A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662763 | |||||||
chr14:88662958 | T | C | 1 | a0002c0002t0001g0209 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3498+73A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662958 | |||||||
chr14:88662960 | G | C | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3498+71C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662960 | |||||||
chr14:88663235 | T | G | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3410-116A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663235 | |||||||
chr14:88663262 | CATTTT | C | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3410-148_3410-144d others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663262 | |||||||
chr14:88663452 | TATATAGT others(8): Show |
T | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(15): Show |
19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3410-348_3410-334d others(17): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663452 | |||||||
chr14:88663467 | A | G | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3410-348T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663467 | |||||||
chr14:88663490 | A | G | 5 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(2): Show |
5 | HG02559.hp1 HG02647.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.3410-371T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663490 | |||||||
chr14:88663731 | C | T | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3410-612G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663731 | |||||||
chr14:88663834 | C | T | 1 | a0001c0001t0014g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3409+659G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663834 | |||||||
chr14:88663908 | C | A | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3409+585G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663908 | |||||||
chr14:88663908 | C | T | 265 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(262): Show |
268 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.3409+585G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663908 | |||||||
chr14:88664044 | A | C | 1 | a0001c0001t0002g0090 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3409+449T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88664044 | |||||||
chr14:88664275 | C | CA | 72 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(69): Show |
73 | HG00408.hp1 HG00642.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.3409+217dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88664275 | |||||||
chr14:88664275 | C | CAAA | 100 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(97): Show |
102 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.3409+215_3409+217d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88664275 | |||||||
chr14:88664275 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0003g0163 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3409+208_3409+217d others(12): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88664275 | |||||||
chr14:88664296 | G | GAAAAAGG others(2): Show |
3 | a0002c0002t0001g0232 a0002c0002t0001g0233 a0002c0002t0001g0261 |
3 | NA18947.hp2 NA18962.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.3409+188_3409+196d others(11): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88664296 | |||||||
chr14:88664881 | T | C | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(15): Show |
19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3278-257A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 22/43 | chr14 | 88664881 | |||||||
chr14:88665089 | A | T | 7 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(4): Show |
8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3277+248T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 22/43 | chr14 | 88665089 | |||||||
chr14:88665103 | G | C | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3277+234C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 22/43 | chr14 | 88665103 | |||||||
chr14:88665644 | T | C | 1 | a0001c0001t0002g0120 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3125-155A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665644 | |||||||
chr14:88665648 | A | G | 9 | a0001c0001t0002g0168 a0001c0001t0023g0195 a0001c0001t0023g0197 others(6): Show |
9 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.3125-159T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665648 | |||||||
chr14:88665739 | A | G | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3125-250T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665739 | |||||||
chr14:88665822 | T | C | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.3125-333A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665822 | |||||||
chr14:88665826 | T | G | 1 | a0001c0001t0003g0165 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3125-337A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665826 | |||||||
chr14:88665836 | A | T | 1 | a0005c0014t0001g0272 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3125-347T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665836 | |||||||
chr14:88665907 | C | CA | 9 | a0001c0001t0002g0124 a0001c0001t0014g0004 a0001c0003t0006g0221 others(6): Show |
9 | HG00544.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3125-419dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665907 | |||||||
chr14:88665907 | CA | C | 6 | a0001c0001t0003g0056 a0002c0002t0001g0268 a0002c0002t0003g0028 others(3): Show |
6 | HG01255.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3125-419delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665907 | |||||||
chr14:88665920 | A | T | 7 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(4): Show |
8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3125-431T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665920 | |||||||
chr14:88666072 | A | G | 2 | a0001c0001t0005g0174 a0001c0001t0005g0175 |
2 | NA18956.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.3125-583T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666072 | |||||||
chr14:88666257 | T | C | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.3125-768A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666257 | |||||||
chr14:88666378 | C | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3125-889G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666378 | |||||||
chr14:88666501 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3125-1012G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666501 | |||||||
chr14:88666511 | C | T | 2 | a0003c0005t0015g0014 a0003c0005t0015g0015 |
2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3125-1022G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666511 | |||||||
chr14:88666588 | G | A | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.3125-1099C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666588 | |||||||
chr14:88666620 | G | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3125-1131C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666620 | |||||||
chr14:88666626 | TTTA | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3125-1140_3125-113 others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666626 | |||||||
chr14:88666629 | A | C | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3125-1140T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666629 | |||||||
chr14:88666948 | T | A | 1 | a0001c0003t0004g0322 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3125-1459A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666948 | |||||||
chr14:88666975 | A | G | 1 | a0001c0001t0002g0141 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3125-1486T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666975 | |||||||
chr14:88667056 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3125-1567C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88667056 | |||||||
chr14:88667096 | T | C | 1 | a0001c0001t0003g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3125-1607A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88667096 | |||||||
chr14:88667104 | A | G | 19 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(16): Show |
20 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3125-1615T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88667104 | |||||||
chr14:88667117 | C | T | 1 | a0001c0001t0027g0295 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3125-1628G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88667117 | |||||||
chr14:88667337 | T | C | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3125-1848A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88667337 | |||||||
chr14:88667597 | G | C | 2 | a0001c0001t0017g0010 a0001c0001t0017g0011 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3125-2108C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88667597 | |||||||
chr14:88667801 | C | T | 1 | a0002c0002t0001g0245 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3125-2312G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88667801 | |||||||
chr14:88668016 | C | T | 269 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(266): Show |
272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.3125-2527G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668016 | |||||||
chr14:88668018 | C | A | 1 | a0002c0002t0003g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3125-2529G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668018 | |||||||
chr14:88668136 | C | T | 88 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0200 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.3125-2647G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668136 | |||||||
chr14:88668270 | C | T | 3 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0220 |
3 | HG02559.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3125-2781G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668270 | |||||||
chr14:88668299 | G | A | 72 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(69): Show |
74 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.3125-2810C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668299 | |||||||
chr14:88668338 | T | G | 2 | a0001c0001t0002g0137 a0001c0001t0002g0138 |
2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3125-2849A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668338 | |||||||
chr14:88668342 | A | G | 176 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(173): Show |
179 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.3125-2853T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668342 | |||||||
chr14:88668371 | A | G | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3125-2882T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668371 | |||||||
chr14:88668434 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0003g0083 |
2 | HG00642.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.3125-2945C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668434 | |||||||
chr14:88668445 | G | C | 1 | a0001c0001t0010g0033 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3125-2956C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668445 | |||||||
chr14:88668937 | C | T | 1 | a0001c0001t0003g0051 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3125-3448G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668937 | |||||||
chr14:88668943 | C | T | 1 | a0002c0002t0003g0025 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3125-3454G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668943 | |||||||
chr14:88668945 | G | A | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3125-3456C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668945 | |||||||
chr14:88669190 | C | T | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.3125-3701G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88669190 | |||||||
chr14:88669391 | T | G | 1 | a0002c0002t0001g0231 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3125-3902A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88669391 | |||||||
chr14:88669528 | G | A | 1 | a0001c0003t0004g0323 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3125-4039C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88669528 | |||||||
chr14:88669790 | T | G | 14 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0250 others(11): Show |
14 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.3125-4301A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88669790 | |||||||
chr14:88669815 | A | G | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3125-4326T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88669815 | |||||||
chr14:88669930 | T | C | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3125-4441A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88669930 | |||||||
chr14:88670012 | T | C | 300 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(297): Show |
303 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.3125-4523A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670012 | |||||||
chr14:88670083 | G | A | 2 | a0001c0001t0002g0124 a0001c0001t0002g0125 |
2 | NA18943.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.3125-4594C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670083 | |||||||
chr14:88670108 | G | A | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.3125-4619C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670108 | |||||||
chr14:88670162 | A | C | 50 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(47): Show |
51 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(48): Show |
intron_variant | MODIFIER | c.3125-4673T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670162 | |||||||
chr14:88670319 | C | CA | 152 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0280 others(149): Show |
155 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.3125-4831dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670319 | |||||||
chr14:88670319 | C | CAA | 30 | a0001c0001t0002g0111 a0001c0001t0002g0149 a0001c0001t0002g0155 others(27): Show |
30 | HG00642.hp2 HG00673.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.3125-4832_3125-483 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670319 | |||||||
chr14:88670347 | G | T | 1 | a0001c0003t0004g0323 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3125-4858C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670347 | |||||||
chr14:88670579 | G | A | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3125-5090C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670579 | |||||||
chr14:88670892 | G | A | 4 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0035g0198 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3125-5403C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670892 | |||||||
chr14:88670980 | G | A | 1 | a0001c0001t0028g0009 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3125-5491C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670980 | |||||||
chr14:88671259 | A | G | 1 | a0001c0001t0005g0182 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3125-5770T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88671259 | |||||||
chr14:88671397 | G | A | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3125-5908C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88671397 | |||||||
chr14:88671479 | C | T | 1 | a0002c0002t0001g0263 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3125-5990G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88671479 | |||||||
chr14:88671516 | G | C | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3125-6027C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88671516 | |||||||
chr14:88671581 | G | T | 1 | a0001c0003t0013g0298 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3125-6092C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88671581 | |||||||
chr14:88671582 | C | T | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3125-6093G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88671582 | |||||||
chr14:88671679 | C | G | 1 | a0001c0001t0003g0064 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3125-6190G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88671679 | |||||||
chr14:88672011 | A | G | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3125-6522T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672011 | |||||||
chr14:88672135 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3125-6646C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672135 | |||||||
chr14:88672286 | C | T | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3125-6797G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672286 | |||||||
chr14:88672287 | C | T | 1 | a0001c0001t0005g0179 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3125-6798G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672287 | |||||||
chr14:88672373 | G | C | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3125-6884C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672373 | |||||||
chr14:88672515 | G | A | 2 | a0001c0001t0024g0206 a0001c0001t0024g0207 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3125-7026C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672515 | |||||||
chr14:88672631 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3125-7142T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672631 | |||||||
chr14:88672636 | A | G | 102 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(99): Show |
104 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.3125-7147T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672636 | |||||||
chr14:88672701 | G | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3125-7212C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672701 | |||||||
chr14:88672778 | G | A | 4 | a0001c0003t0013g0298 a0001c0003t0013g0299 a0001c0003t0013g0300 others(1): Show |
4 | HG02886.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.3125-7289C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672778 | |||||||
chr14:88672829 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3125-7340G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672829 | |||||||
chr14:88672860 | G | A | 1 | a0001c0003t0004g0317 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3125-7371C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672860 | |||||||
chr14:88672865 | A | G | 85 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0200 others(82): Show |
85 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.3125-7376T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672865 | |||||||
chr14:88672888 | G | A | 1 | a0001c0001t0003g0041 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3125-7399C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672888 | |||||||
chr14:88672963 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3125-7474C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672963 | |||||||
chr14:88673344 | C | T | 1 | a0002c0002t0001g0275 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3125-7855G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88673344 | |||||||
chr14:88673611 | T | C | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3125-8122A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88673611 | |||||||
chr14:88673813 | T | C | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.3124+8077A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88673813 | |||||||
chr14:88673848 | C | T | 1 | a0002c0002t0001g0253 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3124+8042G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88673848 | |||||||
chr14:88674272 | AAACAAC | A | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3124+7612_3124+761 others(10): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88674272 | |||||||
chr14:88674412 | C | G | 3 | a0001c0001t0008g0102 a0001c0001t0008g0103 a0001c0001t0008g0104 |
3 | HG02895.hp2 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3124+7478G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88674412 | |||||||
chr14:88674582 | G | A | 1 | a0001c0001t0033g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3124+7308C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88674582 | |||||||
chr14:88674591 | T | C | 2 | a0002c0002t0003g0023 a0002c0002t0034g0170 |
2 | NA18948.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.3124+7299A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88674591 | |||||||
chr14:88674678 | T | C | 1 | a0001c0003t0004g0315 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3124+7212A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88674678 | |||||||
chr14:88674728 | T | C | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.3124+7162A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88674728 | |||||||
chr14:88674821 | TG | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3124+7068delC | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88674821 | |||||||
chr14:88674904 | C | T | 7 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(4): Show |
8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3124+6986G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88674904 | |||||||
chr14:88675052 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3124+6838G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88675052 | |||||||
chr14:88675178 | C | T | 8 | a0001c0001t0002g0095 a0001c0001t0002g0111 a0001c0001t0002g0112 others(5): Show |
8 | HG00438.hp2 HG01099.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.3124+6712G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88675178 | |||||||
chr14:88675298 | G | A | 1 | a0002c0002t0034g0170 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3124+6592C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88675298 | |||||||
chr14:88675506 | G | A | 1 | a0001c0001t0003g0047 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3124+6384C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88675506 | |||||||
chr14:88675518 | G | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3124+6372C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88675518 | |||||||
chr14:88675727 | T | A | 3 | a0002c0002t0021g0273 a0002c0002t0021g0292 a0002c0002t0039g0297 |
3 | HG00323.hp1 HG00733.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.3124+6163A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88675727 | |||||||
chr14:88676077 | A | G | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3124+5813T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88676077 | |||||||
chr14:88676146 | T | C | 1 | a0001c0001t0003g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3124+5744A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88676146 | |||||||
chr14:88676500 | C | T | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3124+5390G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88676500 | |||||||
chr14:88676505 | A | G | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.3124+5385T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88676505 | |||||||
chr14:88676532 | G | A | 1 | a0001c0003t0004g0315 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3124+5358C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88676532 | |||||||
chr14:88676755 | A | G | 1 | a0001c0003t0004g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3124+5135T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88676755 | |||||||
chr14:88676790 | T | C | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3124+5100A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88676790 | |||||||
chr14:88677169 | T | C | 1 | a0001c0001t0011g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3124+4721A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88677169 | |||||||
chr14:88677268 | G | A | 4 | a0001c0003t0004g0310 a0001c0003t0004g0311 a0001c0003t0004g0312 others(1): Show |
4 | HG02280.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3124+4622C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88677268 | |||||||
chr14:88677327 | T | C | 18 | a0001c0001t0002g0168 a0001c0001t0006g0208 a0001c0001t0014g0004 others(15): Show |
18 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.3124+4563A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88677327 | |||||||
chr14:88677390 | C | T | 1 | a0001c0001t0003g0081 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3124+4500G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88677390 | |||||||
chr14:88677415 | G | T | 1 | a0001c0001t0002g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3124+4475C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88677415 | |||||||
chr14:88677473 | G | A | 1 | a0001c0001t0005g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3124+4417C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88677473 | |||||||
chr14:88677507 | G | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3124+4383C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88677507 | |||||||
chr14:88678047 | C | T | 1 | a0001c0001t0002g0107 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3124+3843G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678047 | |||||||
chr14:88678313 | G | C | 1 | a0001c0001t0002g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3124+3577C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678313 | |||||||
chr14:88678534 | T | C | 1 | a0001c0001t0007g0084 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3124+3356A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678534 | |||||||
chr14:88678549 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3124+3341T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678549 | |||||||
chr14:88678645 | T | A | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.3124+3245A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678645 | |||||||
chr14:88678656 | G | T | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(15): Show |
19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3124+3234C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678656 | |||||||
chr14:88678738 | T | C | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(15): Show |
19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3124+3152A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678738 | |||||||
chr14:88678811 | T | C | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(15): Show |
19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3124+3079A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678811 | |||||||
chr14:88678818 | T | C | 1 | a0002c0002t0001g0226 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3124+3072A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678818 | |||||||
chr14:88678946 | T | G | 63 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(60): Show |
65 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.3124+2944A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678946 | |||||||
chr14:88678952 | G | A | 2 | a0002c0002t0001g0243 a0002c0002t0001g0246 |
2 | HG01099.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.3124+2938C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678952 | |||||||
chr14:88679069 | T | C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3124+2821A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88679069 | |||||||
chr14:88679509 | T | C | 1 | a0001c0003t0004g0315 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3124+2381A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88679509 | |||||||
chr14:88679529 | T | C | 1 | a0002c0002t0001g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3124+2361A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88679529 | |||||||
chr14:88679553 | G | A | 3 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0220 |
3 | HG02559.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3124+2337C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88679553 | |||||||
chr14:88679560 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3124+2330G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88679560 | |||||||
chr14:88679561 | G | A | 52 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(49): Show |
53 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(50): Show |
intron_variant | MODIFIER | c.3124+2329C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88679561 | |||||||
chr14:88679566 | C | T | 1 | a0001c0001t0006g0220 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3124+2324G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88679566 | |||||||
chr14:88679624 | G | A | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.3124+2266C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88679624 | |||||||
chr14:88680053 | T | C | 1 | a0002c0002t0003g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3124+1837A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88680053 | |||||||
chr14:88680628 | A | G | 1 | a0001c0001t0002g0118 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3124+1262T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88680628 | |||||||
chr14:88680801 | A | G | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.3124+1089T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88680801 | |||||||
chr14:88680833 | G | C | 1 | a0001c0001t0008g0100 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3124+1057C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88680833 | |||||||
chr14:88680922 | C | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3124+968G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88680922 | |||||||
chr14:88681122 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3124+768A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88681122 | |||||||
chr14:88681365 | C | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3124+525G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88681365 | |||||||
chr14:88681454 | A | G | 2 | a0001c0003t0004g0309 a0001c0003t0004g0313 |
2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3124+436T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88681454 | |||||||
chr14:88681669 | G | A | 10 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(7): Show |
10 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.3124+221C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88681669 | |||||||
chr14:88681742 | A | G | 1 | a0001c0003t0004g0328 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3124+148T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88681742 | |||||||
chr14:88681877 | G | T | 1 | a0001c0001t0003g0169 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3124+13C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88681877 | |||||||
chr14:88682142 | C | T | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.2983-111G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682142 | |||||||
chr14:88682204 | T | C | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2983-173A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682204 | |||||||
chr14:88682208 | T | C | 1 | a0001c0003t0004g0321 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2983-177A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682208 | |||||||
chr14:88682408 | T | TA | 36 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(33): Show |
36 | HG00408.hp1 HG01433.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.2983-378dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682408 | |||||||
chr14:88682408 | TA | T | 20 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0208 others(17): Show |
20 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.2983-378delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682408 | |||||||
chr14:88682622 | C | G | 1 | a0001c0001t0003g0055 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2983-591G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682622 | |||||||
chr14:88682683 | G | A | 1 | a0001c0003t0006g0221 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2983-652C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682683 | |||||||
chr14:88682858 | C | T | 1 | a0001c0003t0013g0299 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2983-827G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682858 | |||||||
chr14:88682866 | G | A | 102 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(99): Show |
104 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.2983-835C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682866 | |||||||
chr14:88682927 | C | T | 1 | a0001c0001t0005g0179 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2983-896G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682927 | |||||||
chr14:88683130 | T | A | 1 | a0002c0002t0001g0282 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2983-1099A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683130 | |||||||
chr14:88683176 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2983-1145C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683176 | |||||||
chr14:88683179 | G | A | 2 | a0001c0001t0005g0179 a0001c0001t0005g0182 |
2 | NA18983.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2983-1148C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683179 | |||||||
chr14:88683231 | G | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2983-1200C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683231 | |||||||
chr14:88683513 | A | G | 7 | a0001c0001t0002g0002 a0001c0001t0002g0086 a0001c0001t0002g0141 others(4): Show |
8 | NA18960.hp2 NA18968.hp2 NA18974.hp2 others(5): Show |
intron_variant | MODIFIER | c.2983-1482T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683513 | |||||||
chr14:88683773 | A | G | 52 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(49): Show |
53 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(50): Show |
intron_variant | MODIFIER | c.2982+1242T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683773 | |||||||
chr14:88683860 | G | C | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2982+1155C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683860 | |||||||
chr14:88683876 | C | T | 1 | a0002c0002t0001g0235 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2982+1139G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683876 | |||||||
chr14:88683938 | T | C | 1 | a0001c0001t0019g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2982+1077A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683938 | |||||||
chr14:88683964 | T | C | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2982+1051A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683964 | |||||||
chr14:88683997 | T | C | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(15): Show |
19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2982+1018A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683997 | |||||||
chr14:88684103 | C | T | 4 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0035g0198 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2982+912G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684103 | |||||||
chr14:88684225 | G | T | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2982+790C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684225 | |||||||
chr14:88684236 | A | ATAAATTT others(2720): Show |
3 | a0001c0001t0003g0043 a0001c0001t0003g0052 a0001c0001t0003g0082 |
3 | NA18954.hp2 NA18995.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2720): Show |
1 | a0001c0001t0003g0053 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2708): Show |
1 | a0001c0001t0033g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2717): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2715): Show |
1 | a0002c0002t0003g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2724): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2717): Show |
1 | a0002c0002t0003g0025 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2726): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2719): Show |
2 | a0001c0001t0003g0039 a0001c0001t0003g0040 |
2 | NA18953.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2728): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2717): Show |
3 | a0002c0004t0001g0234 a0002c0004t0001g0241 a0002c0004t0001g0242 |
3 | HG00099.hp2 HG01123.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2726): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2717): Show |
11 | a0002c0002t0001g0222 a0002c0002t0001g0229 a0002c0002t0001g0254 others(8): Show |
11 | HG00609.hp2 HG01891.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2726): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2717): Show |
52 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0200 others(49): Show |
52 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2726): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2717): Show |
8 | a0002c0002t0001g0231 a0002c0002t0001g0249 a0002c0002t0001g0263 others(5): Show |
8 | HG00438.hp1 HG01978.hp1 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2726): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2711): Show |
1 | a0002c0002t0001g0227 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2720): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2718): Show |
3 | a0002c0002t0001g0232 a0002c0002t0001g0233 a0002c0002t0001g0261 |
3 | NA18947.hp2 NA18962.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2727): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2720): Show |
2 | a0001c0001t0002g0122 a0008c0011t0008g0101 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2718): Show |
1 | a0002c0002t0001g0239 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2727): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2718): Show |
1 | a0002c0002t0001g0288 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2727): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2718): Show |
5 | a0002c0002t0001g0243 a0002c0002t0001g0244 a0002c0002t0001g0246 others(2): Show |
5 | HG01099.hp2 HG01109.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2727): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2719): Show |
4 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0035g0198 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2728): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2719): Show |
2 | a0001c0001t0026g0293 a0001c0001t0026g0294 |
2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2728): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2719): Show |
2 | a0001c0001t0027g0295 a0001c0001t0027g0296 |
2 | HG00642.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2728): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2720): Show |
1 | a0001c0001t0003g0055 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2716): Show |
1 | a0001c0001t0022g0204 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2725): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2720): Show |
1 | a0001c0001t0003g0041 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2720): Show |
4 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(1): Show |
4 | HG00741.hp1 HG01069.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2719): Show |
1 | a0001c0003t0013g0298 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2728): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2720): Show |
28 | a0001c0001t0001g0280 a0001c0001t0001g0290 a0001c0001t0003g0045 others(25): Show |
28 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2721): Show |
1 | a0001c0001t0003g0051 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2719): Show |
3 | a0001c0003t0013g0299 a0001c0003t0013g0300 a0001c0009t0013g0301 |
3 | HG02886.hp2 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2728): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2720): Show |
18 | a0001c0001t0003g0044 a0001c0001t0003g0048 a0001c0001t0003g0049 others(15): Show |
18 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2721): Show |
1 | a0001c0003t0004g0323 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2720): Show |
17 | a0001c0003t0004g0305 a0001c0003t0004g0306 a0001c0003t0004g0307 others(14): Show |
17 | HG02257.hp1 HG02280.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2721): Show |
1 | a0001c0003t0004g0315 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2721): Show |
2 | a0001c0003t0004g0316 a0001c0003t0004g0317 |
2 | HG03017.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2714): Show |
2 | a0001c0003t0004g0318 a0001c0003t0004g0319 |
2 | HG00408.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2723): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2719): Show |
1 | a0001c0001t0017g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2728): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2718): Show |
1 | a0001c0001t0017g0011 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2727): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2721): Show |
1 | a0001c0003t0004g0320 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2721): Show |
1 | a0001c0001t0005g0187 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2721): Show |
6 | a0001c0001t0002g0089 a0001c0001t0008g0102 a0001c0001t0008g0103 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2721): Show |
19 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(16): Show |
19 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2721): Show |
62 | a0001c0001t0002g0001 a0001c0001t0002g0087 a0001c0001t0002g0088 others(59): Show |
63 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2722): Show |
1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2731): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2721): Show |
1 | a0001c0001t0005g0184 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2720): Show |
1 | a0001c0001t0002g0148 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2721): Show |
1 | a0001c0001t0002g0116 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2722): Show |
7 | a0001c0001t0002g0002 a0001c0001t0002g0086 a0001c0001t0002g0098 others(4): Show |
8 | NA18960.hp2 NA18968.hp2 NA18974.hp2 others(5): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2731): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2721): Show |
1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2722): Show |
1 | a0001c0001t0012g0326 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2731): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2716): Show |
7 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(4): Show |
7 | HG01243.hp1 HG02145.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2725): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2720): Show |
1 | a0001c0003t0004g0302 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2717): Show |
1 | a0001c0001t0024g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2726): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2719): Show |
2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2728): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2710): Show |
1 | a0001c0001t0019g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2719): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2721): Show |
2 | a0001c0001t0003g0036 a0001c0001t0003g0037 |
2 | HG02738.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2721): Show |
1 | a0001c0001t0019g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2718): Show |
1 | a0001c0001t0006g0220 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2727): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2721): Show |
3 | a0001c0001t0011g0214 a0001c0001t0011g0215 a0001c0001t0011g0216 |
3 | HG02280.hp1 HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2718): Show |
4 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(1): Show |
4 | HG02559.hp1 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2727): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2715): Show |
1 | a0001c0001t0011g0213 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2724): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2721): Show |
7 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(4): Show |
8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2721): Show |
1 | a0001c0001t0008g0100 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2716): Show |
3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2725): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684236 | A | ATAAATTT others(2717): Show |
1 | a0002c0004t0001g0228 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2726): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | |||||||
chr14:88684272 | G | A | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2982+743C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684272 | |||||||
chr14:88684306 | G | A | 4 | a0001c0001t0002g0158 a0001c0001t0006g0284 a0001c0001t0006g0285 others(1): Show |
4 | HG00741.hp2 HG01257.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2982+709C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684306 | |||||||
chr14:88684317 | C | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2982+698G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684317 | |||||||
chr14:88684349 | C | T | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.2982+666G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684349 | |||||||
chr14:88684359 | A | G | 1 | a0001c0001t0003g0056 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2982+656T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684359 | |||||||
chr14:88684391 | C | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2982+624G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684391 | |||||||
chr14:88684421 | C | G | 51 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(48): Show |
52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.2982+594G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684421 | |||||||
chr14:88684459 | C | T | 4 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(1): Show |
4 | HG02622.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2982+556G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684459 | |||||||
chr14:88684460 | G | A | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2982+555C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684460 | |||||||
chr14:88684529 | A | ACATT | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.2982+482_2982+485d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684529 | |||||||
chr14:88684678 | G | T | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.2982+337C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684678 | |||||||
chr14:88684818 | A | T | 1 | a0001c0001t0002g0148 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2982+197T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684818 | |||||||
chr14:88684852 | G | A | 269 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(266): Show |
272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.2982+163C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684852 | |||||||
chr14:88684879 | AT | A | 102 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(99): Show |
104 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.2982+135delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684879 | |||||||
chr14:88684978 | T | C | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2982+37A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684978 | |||||||
chr14:88684999 | T | C | 51 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(48): Show |
52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.2982+16A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684999 | |||||||
chr14:88685303 | T | G | 1 | a0001c0001t0010g0035 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2855-161A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88685303 | |||||||
chr14:88685409 | A | G | 6 | a0002c0002t0003g0019 a0002c0002t0003g0020 a0002c0002t0003g0021 others(3): Show |
6 | HG02165.hp1 NA18948.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.2855-267T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88685409 | |||||||
chr14:88685453 | T | C | 11 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 others(8): Show |
11 | HG02738.hp1 HG03490.hp1 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.2855-311A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88685453 | |||||||
chr14:88685772 | T | C | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2855-630A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88685772 | |||||||
chr14:88685978 | G | T | 1 | a0002c0002t0038g0262 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2855-836C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88685978 | |||||||
chr14:88686051 | C | T | 4 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0215 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2855-909G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88686051 | |||||||
chr14:88686308 | C | T | 27 | a0001c0003t0004g0302 a0001c0003t0004g0303 a0001c0003t0004g0304 others(24): Show |
27 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.2854+908G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88686308 | |||||||
chr14:88686559 | C | T | 1 | a0001c0001t0008g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2854+657G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88686559 | |||||||
chr14:88686634 | G | A | 5 | a0001c0001t0003g0075 a0001c0001t0003g0163 a0001c0001t0003g0164 others(2): Show |
5 | HG00741.hp1 HG01069.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2854+582C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88686634 | |||||||
chr14:88686683 | C | T | 1 | a0001c0003t0004g0309 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2854+533G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88686683 | |||||||
chr14:88686706 | G | A | 1 | a0001c0001t0003g0054 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2854+510C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88686706 | |||||||
chr14:88686765 | T | C | 2 | a0002c0002t0001g0258 a0002c0002t0001g0259 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2854+451A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88686765 | |||||||
chr14:88687401 | G | T | 2 | a0001c0001t0017g0010 a0001c0001t0017g0011 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2743-74C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/43 | chr14 | 88687401 | |||||||
chr14:88687682 | T | TA | 269 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(266): Show |
272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.2743-356_2743-355i others(3): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/43 | chr14 | 88687682 | |||||||
chr14:88687765 | C | CA | 52 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(49): Show |
53 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(50): Show |
intron_variant | MODIFIER | c.2743-439dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/43 | chr14 | 88687765 | |||||||
chr14:88687803 | C | T | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2742+468G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/43 | chr14 | 88687803 | |||||||
chr14:88687910 | A | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2742+361T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/43 | chr14 | 88687910 | |||||||
chr14:88687948 | G | A | 6 | a0001c0003t0004g0303 a0001c0003t0004g0304 a0001c0003t0004g0305 others(3): Show |
6 | HG02257.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2742+323C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/43 | chr14 | 88687948 | |||||||
chr14:88687996 | A | G | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.2742+275T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/43 | chr14 | 88687996 | |||||||
chr14:88688572 | AG | A | 6 | a0001c0003t0004g0303 a0001c0003t0004g0304 a0001c0003t0004g0305 others(3): Show |
6 | HG02257.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2540-100delC | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88688572 | |||||||
chr14:88688811 | C | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2540-338G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88688811 | |||||||
chr14:88688845 | A | G | 1 | a0001c0001t0005g0173 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2540-372T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88688845 | |||||||
chr14:88688864 | T | C | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2540-391A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88688864 | |||||||
chr14:88688875 | C | T | 1 | a0002c0002t0001g0278 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2540-402G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88688875 | |||||||
chr14:88688897 | T | C | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2540-424A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88688897 | |||||||
chr14:88689068 | T | C | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2540-595A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88689068 | |||||||
chr14:88689138 | T | A | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2540-665A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88689138 | |||||||
chr14:88689237 | T | A | 4 | a0001c0003t0013g0298 a0001c0003t0013g0299 a0001c0003t0013g0300 others(1): Show |
4 | HG02886.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2540-764A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88689237 | |||||||
chr14:88689321 | TTA | T | 77 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(74): Show |
79 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.2540-850_2540-849d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88689321 | |||||||
chr14:88689515 | C | A | 1 | a0001c0001t0005g0178 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2540-1042G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88689515 | |||||||
chr14:88689618 | C | T | 11 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(8): Show |
11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2540-1145G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88689618 | |||||||
chr14:88689756 | A | G | 5 | a0001c0001t0008g0102 a0001c0001t0008g0103 a0001c0001t0008g0104 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2540-1283T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88689756 | |||||||
chr14:88689862 | G | A | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.2540-1389C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88689862 | |||||||
chr14:88690067 | A | T | 6 | a0001c0003t0004g0303 a0001c0003t0004g0304 a0001c0003t0004g0305 others(3): Show |
6 | HG02257.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2540-1594T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88690067 | |||||||
chr14:88690129 | A | G | 14 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(11): Show |
15 | HG01256.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2540-1656T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88690129 | |||||||
chr14:88690360 | G | T | 27 | a0001c0003t0004g0302 a0001c0003t0004g0303 a0001c0003t0004g0304 others(24): Show |
27 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.2540-1887C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88690360 | |||||||
chr14:88690434 | C | T | 1 | a0001c0003t0004g0322 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2540-1961G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88690434 | |||||||
chr14:88690598 | G | C | 1 | a0001c0001t0001g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2540-2125C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88690598 | |||||||
chr14:88690599 | T | C | 3 | a0002c0002t0001g0239 a0002c0002t0001g0243 a0002c0002t0001g0246 |
3 | HG01099.hp2 HG01109.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.2540-2126A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88690599 | |||||||
chr14:88690631 | G | A | 1 | a0001c0001t0002g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2540-2158C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88690631 | |||||||
chr14:88691185 | G | C | 1 | a0001c0001t0037g0205 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2540-2712C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88691185 | |||||||
chr14:88691632 | C | T | 2 | a0001c0001t0002g0129 a0001c0001t0002g0130 |
2 | NA18986.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2539+2675G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88691632 | |||||||
chr14:88691652 | T | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2539+2655A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88691652 | |||||||
chr14:88691674 | T | C | 2 | a0001c0001t0019g0212 a0001c0001t0019g0217 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2539+2633A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88691674 | |||||||
chr14:88691739 | A | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2539+2568T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88691739 | |||||||
chr14:88691823 | T | C | 1 | a0001c0001t0003g0052 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2539+2484A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88691823 | |||||||
chr14:88692015 | C | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2539+2292G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692015 | |||||||
chr14:88692146 | G | A | 1 | a0002c0002t0001g0222 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2539+2161C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692146 | |||||||
chr14:88692245 | C | T | 51 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(48): Show |
52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.2539+2062G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692245 | |||||||
chr14:88692308 | T | C | 269 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(266): Show |
272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.2539+1999A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692308 | |||||||
chr14:88692342 | A | C | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2539+1965T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692342 | |||||||
chr14:88692379 | A | G | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.2539+1928T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692379 | |||||||
chr14:88692668 | A | T | 269 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(266): Show |
272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.2539+1639T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692668 | |||||||
chr14:88692703 | C | T | 106 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(103): Show |
108 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2539+1604G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692703 | |||||||
chr14:88692710 | G | A | 3 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2539+1597C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692710 | |||||||
chr14:88692783 | C | T | 1 | a0002c0002t0007g0030 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2539+1524G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692783 | |||||||
chr14:88692861 | G | C | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2539+1446C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692861 | |||||||
chr14:88693371 | G | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.2539+936C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693371 | |||||||
chr14:88693379 | T | C | 1 | a0001c0001t0010g0033 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2539+928A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693379 | |||||||
chr14:88693432 | G | C | 1 | a0001c0001t0019g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2539+875C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693432 | |||||||
chr14:88693614 | C | A | 1 | a0001c0001t0005g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2539+693G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693614 | |||||||
chr14:88693763 | C | CT | 14 | a0001c0001t0001g0210 a0001c0001t0003g0036 a0001c0001t0003g0051 others(11): Show |
14 | HG00733.hp2 HG01175.hp2 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.2539+543dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693763 | |||||||
chr14:88693763 | CT | C | 202 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0002g0001 others(199): Show |
204 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2539+543delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693763 | |||||||
chr14:88693763 | CTT | C | 14 | a0001c0001t0002g0107 a0001c0001t0002g0125 a0001c0001t0002g0129 others(11): Show |
14 | HG00642.hp2 HG01167.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.2539+542_2539+543d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693763 | |||||||
chr14:88693763 | CTTTT | C | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2539+540_2539+543d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693763 | |||||||
chr14:88693819 | T | G | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2539+488A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693819 | |||||||
chr14:88693848 | G | A | 1 | a0001c0001t0007g0084 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2539+459C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693848 | |||||||
chr14:88693937 | A | AT | 17 | a0001c0001t0002g0151 a0001c0001t0003g0040 a0001c0001t0007g0062 others(14): Show |
17 | HG00642.hp2 HG01109.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.2539+369dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693937 | |||||||
chr14:88694015 | C | G | 3 | a0002c0002t0001g0224 a0002c0002t0001g0225 a0002c0002t0001g0226 |
3 | NA18968.hp1 NA18994.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2539+292G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88694015 | |||||||
chr14:88694074 | A | G | 1 | a0002c0002t0001g0264 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2539+233T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88694074 | |||||||
chr14:88694280 | T | C | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2539+27A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88694280 | |||||||
chr14:88694737 | A | G | 1 | a0001c0001t0005g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2439-330T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/43 | chr14 | 88694737 | |||||||
chr14:88694796 | T | C | 1 | a0002c0002t0001g0279 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2439-389A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/43 | chr14 | 88694796 | |||||||
chr14:88694951 | A | C | 2 | a0001c0001t0022g0203 a0001c0001t0022g0204 |
2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2438+410T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/43 | chr14 | 88694951 | |||||||
chr14:88695063 | C | T | 1 | a0002c0002t0001g0279 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2438+298G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/43 | chr14 | 88695063 | |||||||
chr14:88695171 | C | T | 2 | a0001c0001t0002g0120 a0001c0001t0002g0133 |
2 | NA18962.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.2438+190G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/43 | chr14 | 88695171 | |||||||
chr14:88695175 | G | A | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2438+186C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/43 | chr14 | 88695175 | |||||||
chr14:88695209 | CTATGAT | C | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.2438+146_2438+151d others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/43 | chr14 | 88695209 | |||||||
chr14:88695299 | A | T | 1 | a0001c0003t0004g0323 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2438+62T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/43 | chr14 | 88695299 | |||||||
chr14:88695626 | A | C | 19 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(16): Show |
20 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.2345-172T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88695626 | |||||||
chr14:88695665 | G | A | 2 | a0001c0001t0003g0044 a0001c0001t0003g0047 |
2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2345-211C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88695665 | |||||||
chr14:88695808 | A | G | 1 | a0002c0002t0003g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2345-354T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88695808 | |||||||
chr14:88695844 | T | C | 2 | a0001c0001t0002g0109 a0001c0001t0002g0110 |
2 | HG02165.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.2345-390A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88695844 | |||||||
chr14:88695847 | T | A | 1 | a0001c0001t0009g0076 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2345-393A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88695847 | |||||||
chr14:88695894 | C | T | 2 | a0001c0001t0024g0206 a0001c0001t0024g0207 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2345-440G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88695894 | |||||||
chr14:88696015 | G | A | 4 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2345-561C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696015 | |||||||
chr14:88696164 | A | AAT | 20 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(17): Show |
21 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.2344+681_2344+682d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696164 | |||||||
chr14:88696164 | AAT | A | 204 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(201): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2344+681_2344+682d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696164 | |||||||
chr14:88696199 | T | C | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.2344+648A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696199 | |||||||
chr14:88696238 | A | G | 11 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(8): Show |
11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2344+609T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696238 | |||||||
chr14:88696452 | A | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2344+395T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696452 | |||||||
chr14:88696565 | A | G | 4 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0116 others(1): Show |
4 | HG01168.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.2344+282T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696565 | |||||||
chr14:88696584 | G | A | 52 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(49): Show |
53 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(50): Show |
intron_variant | MODIFIER | c.2344+263C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696584 | |||||||
chr14:88696634 | A | G | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.2344+213T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696634 | |||||||
chr14:88696774 | C | G | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.2344+73G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696774 | |||||||
chr14:88697167 | T | C | 6 | a0001c0003t0002g0012 a0001c0003t0006g0221 a0001c0003t0013g0298 others(3): Show |
6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2239-215A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697167 | |||||||
chr14:88697217 | T | C | 4 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0035g0198 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2239-265A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697217 | |||||||
chr14:88697231 | A | G | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2239-279T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697231 | |||||||
chr14:88697496 | C | T | 4 | a0001c0001t0002g0091 a0001c0001t0002g0155 a0001c0001t0002g0156 others(1): Show |
4 | HG00280.hp1 HG01167.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2239-544G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697496 | |||||||
chr14:88697536 | C | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2239-584G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697536 | |||||||
chr14:88697607 | C | T | 3 | a0002c0002t0001g0200 a0002c0002t0001g0248 a0002c0002t0001g0249 |
3 | HG00438.hp1 HG00673.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2239-655G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697607 | |||||||
chr14:88697693 | TAATA | T | 7 | a0002c0002t0001g0227 a0002c0002t0001g0264 a0002c0002t0001g0265 others(4): Show |
7 | HG02132.hp1 NA18943.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.2239-745_2239-742d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697693 | |||||||
chr14:88697712 | A | G | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.2239-760T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697712 | |||||||
chr14:88697806 | G | C | 1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2239-854C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697806 | |||||||
chr14:88697896 | C | T | 17 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2239-944G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697896 | |||||||
chr14:88697897 | A | G | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.2239-945T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697897 | |||||||
chr14:88697963 | C | G | 5 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(2): Show |
5 | HG01099.hp1 HG01168.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2239-1011G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697963 | |||||||
chr14:88698083 | C | T | 5 | a0001c0001t0008g0102 a0001c0001t0008g0103 a0001c0001t0008g0104 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2239-1131G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698083 | |||||||
chr14:88698172 | A | T | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.2239-1220T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698172 | |||||||
chr14:88698203 | T | C | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(15): Show |
19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2239-1251A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698203 | |||||||
chr14:88698265 | C | CT | 189 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(186): Show |
191 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.2239-1314dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698265 | |||||||
chr14:88698265 | C | CTT | 56 | a0001c0001t0001g0211 a0001c0001t0001g0283 a0001c0001t0006g0003 others(53): Show |
57 | HG00408.hp1 HG00609.hp1 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.2239-1315_2239-131 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698265 | |||||||
chr14:88698265 | C | CTTT | 13 | a0001c0001t0001g0210 a0001c0001t0002g0168 a0001c0001t0006g0208 others(10): Show |
13 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.2239-1316_2239-131 others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698265 | |||||||
chr14:88698307 | C | T | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2239-1355G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698307 | |||||||
chr14:88698391 | C | G | 11 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(8): Show |
11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2239-1439G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698391 | |||||||
chr14:88698813 | T | G | 2 | a0002c0002t0001g0288 a0002c0002t0001g0289 |
2 | HG02040.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.2239-1861A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698813 | |||||||
chr14:88698878 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2239-1926C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698878 | |||||||
chr14:88698895 | C | T | 1 | a0001c0001t0003g0169 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2239-1943G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698895 | |||||||
chr14:88698989 | T | A | 1 | a0002c0002t0003g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2239-2037A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698989 | |||||||
chr14:88699166 | C | G | 1 | a0001c0003t0004g0306 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2239-2214G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88699166 | |||||||
chr14:88699320 | T | G | 1 | a0002c0002t0003g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2239-2368A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88699320 | |||||||
chr14:88699451 | C | T | 1 | a0001c0001t0002g0141 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2239-2499G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88699451 | |||||||
chr14:88699453 | C | A | 1 | a0001c0001t0003g0075 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2239-2501G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88699453 | |||||||
chr14:88699472 | A | G | 2 | a0001c0003t0020g0171 a0001c0003t0020g0172 |
2 | NA18939.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2239-2520T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88699472 | |||||||
chr14:88699579 | G | C | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.2239-2627C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88699579 | |||||||
chr14:88699680 | A | G | 1 | a0001c0001t0002g0148 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2239-2728T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88699680 | |||||||
chr14:88699839 | C | T | 6 | a0001c0001t0006g0208 a0001c0001t0022g0203 a0001c0001t0022g0204 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.2238+2607G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88699839 | |||||||
chr14:88700224 | G | A | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2238+2222C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88700224 | |||||||
chr14:88700308 | A | T | 22 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(19): Show |
23 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2238+2138T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88700308 | |||||||
chr14:88700495 | A | G | 5 | a0001c0003t0004g0318 a0001c0003t0004g0319 a0001c0003t0004g0322 others(2): Show |
5 | HG00408.hp1 HG03669.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.2238+1951T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88700495 | |||||||
chr14:88700614 | C | T | 11 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 others(8): Show |
11 | HG02738.hp1 HG03490.hp1 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.2238+1832G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88700614 | |||||||
chr14:88701075 | G | A | 1 | a0002c0002t0001g0274 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2238+1371C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88701075 | |||||||
chr14:88701083 | T | C | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.2238+1363A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88701083 | |||||||
chr14:88701186 | T | C | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.2238+1260A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88701186 | |||||||
chr14:88701499 | A | G | 1 | a0001c0001t0002g0120 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2238+947T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88701499 | |||||||
chr14:88701603 | G | A | 2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | HG01175.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2238+843C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88701603 | |||||||
chr14:88701771 | A | T | 1 | a0002c0002t0001g0275 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2238+675T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88701771 | |||||||
chr14:88701962 | G | A | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2238+484C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88701962 | |||||||
chr14:88702024 | C | A | 1 | a0001c0001t0003g0047 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2238+422G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88702024 | |||||||
chr14:88702088 | A | T | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2238+358T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88702088 | |||||||
chr14:88702278 | T | C | 1 | a0002c0002t0001g0249 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2238+168A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88702278 | |||||||
chr14:88702752 | T | C | 1 | a0002c0002t0001g0230 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2052-120A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88702752 | |||||||
chr14:88702958 | T | C | 2 | a0001c0001t0017g0010 a0001c0001t0017g0011 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2052-326A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88702958 | |||||||
chr14:88703005 | C | T | 5 | a0001c0001t0002g0097 a0001c0001t0002g0118 a0001c0001t0002g0132 others(2): Show |
5 | HG00408.hp2 NA18954.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.2052-373G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88703005 | |||||||
chr14:88703184 | T | C | 3 | a0001c0001t0002g0089 a0001c0001t0002g0090 a0001c0001t0006g0202 |
3 | NA18971.hp1 NA19006.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2052-552A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88703184 | |||||||
chr14:88703419 | C | T | 10 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(7): Show |
10 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.2052-787G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88703419 | |||||||
chr14:88703721 | T | C | 1 | a0001c0001t0002g0115 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2052-1089A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88703721 | |||||||
chr14:88703957 | T | C | 101 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(98): Show |
103 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.2051+903A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88703957 | |||||||
chr14:88704197 | T | C | 1 | a0001c0001t0002g0142 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2051+663A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88704197 | |||||||
chr14:88704200 | T | G | 1 | a0010c0012t0001g0247 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2051+660A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88704200 | |||||||
chr14:88704253 | T | C | 1 | a0001c0001t0014g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2051+607A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88704253 | |||||||
chr14:88704298 | C | G | 3 | a0001c0001t0009g0042 a0001c0001t0009g0059 a0001c0001t0009g0060 |
3 | HG01943.hp2 HG01993.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2051+562G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88704298 | |||||||
chr14:88704357 | A | C | 4 | a0001c0001t0002g0158 a0001c0001t0006g0284 a0001c0001t0006g0285 others(1): Show |
4 | HG00741.hp2 HG01257.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051+503T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88704357 | |||||||
chr14:88704662 | A | T | 5 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 others(2): Show |
5 | HG02040.hp1 HG02717.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.2051+198T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88704662 | |||||||
chr14:88704993 | A | G | 6 | a0001c0001t0006g0208 a0001c0001t0022g0203 a0001c0001t0022g0204 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1933-15T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 12/43 | chr14 | 88704993 | |||||||
chr14:88705031 | T | G | 1 | a0001c0001t0028g0009 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1933-53A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 12/43 | chr14 | 88705031 | |||||||
chr14:88705182 | C | T | 78 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(75): Show |
80 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1933-204G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 12/43 | chr14 | 88705182 | |||||||
chr14:88705251 | T | C | 1 | a0001c0001t0014g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1932+231A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 12/43 | chr14 | 88705251 | |||||||
chr14:88705367 | C | T | 51 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(48): Show |
52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.1932+115G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 12/43 | chr14 | 88705367 | |||||||
chr14:88705615 | C | T | 1 | a0002c0002t0007g0030 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1826-27G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 11/43 | chr14 | 88705615 | |||||||
chr14:88705645 | G | T | 1 | a0001c0001t0002g0123 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1826-57C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 11/43 | chr14 | 88705645 | |||||||
chr14:88705762 | A | G | 1 | a0001c0001t0002g0117 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1826-174T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 11/43 | chr14 | 88705762 | |||||||
chr14:88705873 | C | T | 1 | a0001c0001t0007g0084 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1826-285G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 11/43 | chr14 | 88705873 | |||||||
chr14:88705948 | A | T | 1 | a0001c0001t0002g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1825+311T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 11/43 | chr14 | 88705948 | |||||||
chr14:88706563 | T | C | 106 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(103): Show |
108 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1658-137A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88706563 | |||||||
chr14:88706573 | G | A | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1658-147C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88706573 | |||||||
chr14:88706796 | G | T | 1 | a0001c0003t0004g0317 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1658-370C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88706796 | |||||||
chr14:88706984 | T | C | 1 | a0001c0003t0004g0310 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1658-558A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88706984 | |||||||
chr14:88707200 | T | C | 7 | a0001c0001t0002g0106 a0001c0001t0002g0123 a0001c0001t0002g0136 others(4): Show |
7 | HG01109.hp2 HG02055.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1658-774A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707200 | |||||||
chr14:88707270 | T | TTTTA | 139 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0280 others(136): Show |
142 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.1658-848_1658-845d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707270 | |||||||
chr14:88707270 | T | TTTTATTT others(1): Show |
31 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0119 others(28): Show |
31 | HG00438.hp2 HG00642.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1658-852_1658-845d others(10): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707270 | |||||||
chr14:88707270 | T | TTTTATTT others(5): Show |
3 | a0001c0001t0005g0187 a0001c0001t0014g0005 a0001c0001t0023g0195 |
3 | NA19030.hp2 NA19043.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1658-856_1658-845d others(14): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707270 | |||||||
chr14:88707270 | TTTTA | T | 3 | a0001c0001t0007g0062 a0001c0001t0017g0010 a0002c0004t0001g0240 |
3 | HG01243.hp2 HG01884.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1658-848_1658-845d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707270 | |||||||
chr14:88707270 | TTTTATTT others(5): Show |
T | 5 | a0002c0002t0001g0200 a0002c0002t0001g0238 a0002c0002t0001g0248 others(2): Show |
5 | HG00438.hp1 HG00673.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.1658-856_1658-845d others(14): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707270 | |||||||
chr14:88707276 | T | G | 1 | a0001c0001t0003g0053 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1658-850A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707276 | |||||||
chr14:88707343 | G | A | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1658-917C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707343 | |||||||
chr14:88707496 | T | C | 1 | a0002c0002t0003g0029 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1658-1070A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707496 | |||||||
chr14:88707549 | C | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1658-1123G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707549 | |||||||
chr14:88707948 | A | G | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(15): Show |
19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1658-1522T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707948 | |||||||
chr14:88707951 | A | G | 1 | a0002c0002t0001g0232 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1658-1525T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707951 | |||||||
chr14:88708242 | A | C | 1 | a0001c0001t0008g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1658-1816T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88708242 | |||||||
chr14:88708323 | T | C | 1 | a0001c0001t0002g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1658-1897A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88708323 | |||||||
chr14:88708616 | C | T | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1658-2190G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88708616 | |||||||
chr14:88708871 | T | C | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1658-2445A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88708871 | |||||||
chr14:88709008 | G | A | 1 | a0002c0002t0003g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1658-2582C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709008 | |||||||
chr14:88709024 | T | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1658-2598A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709024 | |||||||
chr14:88709083 | A | C | 1 | a0001c0001t0003g0052 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1658-2657T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709083 | |||||||
chr14:88709158 | A | AT | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1658-2733_1658-273 others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709158 | |||||||
chr14:88709381 | A | ATATAAAG others(191): Show |
3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1657+2889_1657+289 others(202): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709381 | |||||||
chr14:88709479 | C | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1657+2792G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709479 | |||||||
chr14:88709809 | T | A | 1 | a0002c0002t0001g0253 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1657+2462A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709809 | |||||||
chr14:88709819 | A | G | 1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1657+2452T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709819 | |||||||
chr14:88709911 | T | C | 1 | a0001c0001t0028g0009 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1657+2360A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709911 | |||||||
chr14:88710057 | C | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1657+2214G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710057 | |||||||
chr14:88710159 | C | T | 1 | a0002c0002t0007g0030 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1657+2112G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710159 | |||||||
chr14:88710208 | T | A | 107 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(104): Show |
109 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1657+2063A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710208 | |||||||
chr14:88710216 | G | T | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1657+2055C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710216 | |||||||
chr14:88710268 | G | A | 51 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(48): Show |
52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.1657+2003C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710268 | |||||||
chr14:88710409 | T | C | 1 | a0001c0001t0002g0142 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1657+1862A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710409 | |||||||
chr14:88710739 | C | CA | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1657+1531dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710739 | |||||||
chr14:88710910 | A | C | 5 | a0001c0001t0002g0087 a0001c0001t0002g0088 a0001c0001t0002g0089 others(2): Show |
5 | HG00423.hp2 NA18944.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1657+1361T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710910 | |||||||
chr14:88710974 | A | G | 1 | a0002c0002t0001g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1657+1297T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710974 | |||||||
chr14:88711085 | A | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1657+1186T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711085 | |||||||
chr14:88711090 | A | C | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1657+1181T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711090 | |||||||
chr14:88711251 | G | A | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1657+1020C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711251 | |||||||
chr14:88711328 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1657+943C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711328 | |||||||
chr14:88711354 | T | C | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1657+917A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711354 | |||||||
chr14:88711376 | G | GCAGTTCC others(1381): Show |
1 | a0001c0003t0018g0016 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1390): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1382): Show |
25 | a0001c0003t0004g0303 a0001c0003t0004g0304 a0001c0003t0004g0305 others(22): Show |
25 | HG00408.hp1 HG02135.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1391): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1383): Show |
1 | a0001c0001t0024g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1392): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1383): Show |
1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1392): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1383): Show |
9 | a0001c0001t0002g0127 a0001c0001t0002g0152 a0001c0003t0002g0012 others(6): Show |
9 | HG02055.hp2 HG02572.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1392): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1384): Show |
1 | a0001c0001t0027g0296 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1384): Show |
10 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 others(7): Show |
10 | HG02145.hp1 HG02559.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1384): Show |
5 | a0001c0001t0002g0168 a0001c0001t0022g0203 a0001c0001t0022g0204 others(2): Show |
5 | HG01243.hp1 HG01891.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1384): Show |
2 | a0001c0001t0019g0212 a0001c0001t0019g0217 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1384): Show |
6 | a0001c0001t0002g0158 a0001c0001t0006g0003 a0001c0001t0006g0284 others(3): Show |
7 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1384): Show |
9 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(6): Show |
9 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1384): Show |
1 | a0001c0001t0002g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1384): Show |
1 | a0001c0001t0005g0184 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1384): Show |
1 | a0001c0001t0002g0141 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1383): Show |
1 | a0001c0001t0002g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1392): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1385): Show |
1 | a0001c0001t0005g0177 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1394): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1384): Show |
86 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(83): Show |
88 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1376): Show |
1 | a0001c0001t0002g0126 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1385): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1385): Show |
3 | a0001c0001t0006g0208 a0004c0007t0016g0007 a0004c0007t0016g0008 |
3 | HG02040.hp1 HG02145.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1394): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1385): Show |
1 | a0001c0001t0001g0283 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1394): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1385): Show |
10 | a0001c0001t0002g0091 a0001c0001t0002g0106 a0001c0001t0002g0114 others(7): Show |
10 | HG00423.hp1 HG01261.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1394): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711376 | G | GCAGTTCC others(1386): Show |
1 | a0003c0005t0015g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1395): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | |||||||
chr14:88711488 | A | G | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1657+783T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711488 | |||||||
chr14:88711857 | G | A | 1 | a0001c0001t0033g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1657+414C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711857 | |||||||
chr14:88711942 | C | CA | 26 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(23): Show |
28 | HG00673.hp2 HG01074.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1657+328dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711942 | |||||||
chr14:88711942 | C | T | 4 | a0001c0001t0010g0032 a0001c0001t0010g0033 a0001c0001t0010g0034 others(1): Show |
4 | HG00544.hp1 HG02027.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1657+329G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711942 | |||||||
chr14:88711942 | CA | C | 43 | a0001c0001t0008g0102 a0001c0001t0023g0195 a0001c0001t0023g0197 others(40): Show |
43 | HG00408.hp1 HG00642.hp2 HG02055.hp2 others(40): Show |
intron_variant | MODIFIER | c.1657+328delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711942 | |||||||
chr14:88712001 | G | A | 1 | a0001c0003t0004g0320 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1657+270C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88712001 | |||||||
chr14:88712058 | C | A | 1 | a0001c0001t0002g0146 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1657+213G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88712058 | |||||||
chr14:88712095 | T | C | 1 | a0001c0001t0037g0205 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1657+176A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88712095 | |||||||
chr14:88712120 | C | G | 27 | a0001c0003t0004g0302 a0001c0003t0004g0303 a0001c0003t0004g0304 others(24): Show |
27 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.1657+151G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88712120 | |||||||
chr14:88712574 | T | C | 1 | a0002c0002t0001g0263 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1445-91A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88712574 | |||||||
chr14:88712799 | G | A | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1445-316C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88712799 | |||||||
chr14:88712964 | G | A | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1445-481C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88712964 | |||||||
chr14:88713082 | C | T | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.1445-599G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713082 | |||||||
chr14:88713326 | A | G | 11 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 others(8): Show |
11 | HG02738.hp1 HG03490.hp1 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.1445-843T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713326 | |||||||
chr14:88713329 | C | A | 1 | a0002c0002t0003g0026 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1445-846G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713329 | |||||||
chr14:88713334 | G | C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1445-851C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713334 | |||||||
chr14:88713382 | A | T | 1 | a0002c0002t0003g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1445-899T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713382 | |||||||
chr14:88713391 | CA | C | 265 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(262): Show |
268 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.1445-909delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713391 | |||||||
chr14:88713468 | T | C | 269 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(266): Show |
272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1445-985A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713468 | |||||||
chr14:88713499 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1445-1016G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713499 | |||||||
chr14:88713572 | G | T | 2 | a0001c0003t0020g0171 a0001c0003t0020g0172 |
2 | NA18939.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1445-1089C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713572 | |||||||
chr14:88713619 | A | AT | 9 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0140 others(6): Show |
9 | HG00738.hp1 HG01943.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.1445-1137dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713619 | |||||||
chr14:88713619 | AT | A | 17 | a0001c0001t0001g0283 a0001c0001t0002g0136 a0001c0001t0002g0158 others(14): Show |
18 | HG00741.hp2 HG01109.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.1445-1137delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713619 | |||||||
chr14:88713698 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1445-1215G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713698 | |||||||
chr14:88713785 | A | C | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1444+1154T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713785 | |||||||
chr14:88713840 | G | GT | 23 | a0001c0001t0002g0109 a0001c0001t0002g0111 a0001c0001t0002g0117 others(20): Show |
23 | HG00099.hp2 HG00438.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.1444+1098dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713840 | |||||||
chr14:88713840 | GT | G | 84 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0280 others(81): Show |
85 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1444+1098delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713840 | |||||||
chr14:88713929 | C | T | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1444+1010G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713929 | |||||||
chr14:88713971 | G | A | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1444+968C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713971 | |||||||
chr14:88713996 | C | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1444+943G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713996 | |||||||
chr14:88714096 | C | T | 4 | a0001c0003t0004g0315 a0001c0003t0004g0316 a0001c0003t0004g0317 others(1): Show |
4 | HG02683.hp2 HG03017.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1444+843G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88714096 | |||||||
chr14:88714249 | C | T | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1444+690G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88714249 | |||||||
chr14:88714250 | A | C | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1444+689T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88714250 | |||||||
chr14:88714318 | T | C | 2 | a0001c0001t0017g0010 a0001c0001t0017g0011 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1444+621A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88714318 | |||||||
chr14:88714332 | T | C | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1444+607A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88714332 | |||||||
chr14:88714388 | G | A | 4 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1444+551C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88714388 | |||||||
chr14:88714553 | C | CCA | 3 | a0002c0002t0001g0263 a0002c0002t0003g0094 a0002c0002t0007g0030 |
3 | HG04184.hp2 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1444+384_1444+385d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88714553 | |||||||
chr14:88714575 | A | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1444+364T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88714575 | |||||||
chr14:88715349 | A | G | 1 | a0001c0001t0022g0204 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1188-154T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88715349 | |||||||
chr14:88715464 | A | G | 88 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0200 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1188-269T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88715464 | |||||||
chr14:88716310 | A | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1188-1115T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716310 | |||||||
chr14:88716511 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1188-1316C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716511 | |||||||
chr14:88716732 | A | AAC | 81 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(78): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1188-1539_1188-153 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716732 | |||||||
chr14:88716732 | A | AACAC | 11 | a0001c0001t0003g0048 a0002c0002t0001g0230 a0002c0002t0001g0255 others(8): Show |
11 | HG01433.hp1 HG01978.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.1188-1541_1188-153 others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716732 | |||||||
chr14:88716732 | AAC | A | 163 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0280 others(160): Show |
165 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1188-1539_1188-153 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716732 | |||||||
chr14:88716732 | AACAC | A | 55 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(52): Show |
56 | HG00408.hp1 HG00741.hp2 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.1188-1541_1188-153 others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716732 | |||||||
chr14:88716797 | C | CTGAT | 3 | a0001c0003t0004g0320 a0001c0003t0004g0321 a0001c0003t0004g0328 |
3 | HG02135.hp2 HG03927.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1188-1606_1188-160 others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716797 | |||||||
chr14:88716835 | T | C | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1188-1640A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716835 | |||||||
chr14:88716861 | A | G | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1188-1666T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716861 | |||||||
chr14:88716890 | A | G | 11 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(8): Show |
11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1188-1695T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716890 | |||||||
chr14:88716995 | A | G | 107 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(104): Show |
109 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1188-1800T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716995 | |||||||
chr14:88717056 | G | C | 2 | a0001c0001t0024g0206 a0001c0001t0024g0207 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1188-1861C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717056 | |||||||
chr14:88717083 | C | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1188-1888G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717083 | |||||||
chr14:88717165 | TC | T | 3 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 |
3 | NA18953.hp2 NA18960.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1188-1971delG | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717165 | |||||||
chr14:88717291 | C | A | 7 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(4): Show |
8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1188-2096G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717291 | |||||||
chr14:88717297 | C | T | 6 | a0001c0003t0004g0303 a0001c0003t0004g0304 a0001c0003t0004g0305 others(3): Show |
6 | HG02257.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1188-2102G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717297 | |||||||
chr14:88717326 | C | A | 24 | a0001c0001t0002g0141 a0001c0001t0005g0173 a0001c0001t0005g0174 others(21): Show |
24 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1188-2131G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717326 | |||||||
chr14:88717454 | G | C | 1 | a0001c0001t0005g0187 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1188-2259C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717454 | |||||||
chr14:88717482 | G | T | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.1188-2287C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717482 | |||||||
chr14:88717505 | T | A | 92 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0017g0010 others(89): Show |
92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1188-2310A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717505 | |||||||
chr14:88717679 | C | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1188-2484G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717679 | |||||||
chr14:88717700 | A | C | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1188-2505T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717700 | |||||||
chr14:88717756 | A | AAAC | 76 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0200 others(73): Show |
76 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.1188-2564_1188-256 others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717756 | |||||||
chr14:88717756 | A | AAACAAC | 9 | a0002c0002t0001g0224 a0002c0002t0001g0239 a0002c0002t0001g0250 others(6): Show |
9 | HG00099.hp2 HG01123.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1188-2567_1188-256 others(10): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717756 | |||||||
chr14:88717756 | AAAC | A | 3 | a0002c0002t0001g0248 a0002c0002t0001g0249 a0002c0002t0001g0276 |
3 | HG00280.hp2 HG00438.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1188-2564_1188-256 others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717756 | |||||||
chr14:88717756 | AAACAAC | A | 174 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(171): Show |
177 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.1188-2567_1188-256 others(10): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717756 | |||||||
chr14:88717756 | AAACAACA others(5): Show |
A | 3 | a0001c0001t0006g0208 a0001c0001t0024g0206 a0001c0001t0024g0207 |
3 | HG01884.hp2 HG02145.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1188-2573_1188-256 others(16): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717756 | |||||||
chr14:88717806 | T | C | 88 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0200 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1188-2611A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717806 | |||||||
chr14:88717861 | T | A | 2 | a0001c0001t0002g0158 a0001c0001t0006g0287 |
2 | HG01257.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1188-2666A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717861 | |||||||
chr14:88717931 | G | A | 51 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(48): Show |
52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.1188-2736C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717931 | |||||||
chr14:88718174 | T | G | 1 | a0001c0003t0013g0300 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1188-2979A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88718174 | |||||||
chr14:88718654 | T | C | 1 | a0001c0003t0004g0329 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1188-3459A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88718654 | |||||||
chr14:88718740 | G | C | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(15): Show |
19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1188-3545C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88718740 | |||||||
chr14:88718902 | C | T | 1 | a0001c0001t0033g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1188-3707G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88718902 | |||||||
chr14:88718986 | T | C | 14 | a0001c0001t0002g0141 a0001c0001t0005g0173 a0001c0001t0005g0178 others(11): Show |
14 | HG00423.hp1 HG00673.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.1188-3791A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88718986 | |||||||
chr14:88719121 | C | G | 3 | a0001c0003t0004g0320 a0001c0003t0004g0321 a0001c0003t0004g0328 |
3 | HG02135.hp2 HG03927.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1188-3926G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88719121 | |||||||
chr14:88719182 | T | C | 1 | a0002c0002t0003g0025 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1188-3987A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88719182 | |||||||
chr14:88719214 | A | G | 3 | a0001c0001t0022g0203 a0001c0001t0022g0204 a0001c0001t0037g0205 |
3 | HG01243.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1188-4019T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88719214 | |||||||
chr14:88719318 | C | G | 269 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(266): Show |
272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1188-4123G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88719318 | |||||||
chr14:88719327 | AGTGAGCT | A | 102 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(99): Show |
104 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.1188-4139_1188-413 others(11): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88719327 | |||||||
chr14:88719563 | T | C | 11 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(8): Show |
11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1188-4368A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88719563 | |||||||
chr14:88719673 | C | CT | 13 | a0001c0001t0003g0043 a0001c0001t0003g0052 a0001c0001t0003g0053 others(10): Show |
13 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1188-4479dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88719673 | |||||||
chr14:88719724 | G | A | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1188-4529C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88719724 | |||||||
chr14:88720147 | T | C | 1 | a0002c0002t0001g0254 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1188-4952A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88720147 | |||||||
chr14:88720271 | C | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1188-5076G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88720271 | |||||||
chr14:88720292 | C | T | 1 | a0001c0001t0005g0187 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1188-5097G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88720292 | |||||||
chr14:88720546 | G | A | 1 | a0008c0011t0008g0101 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1188-5351C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88720546 | |||||||
chr14:88720613 | T | C | 79 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(76): Show |
81 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1188-5418A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88720613 | |||||||
chr14:88720673 | T | C | 2 | a0001c0001t0002g0112 a0001c0001t0002g0113 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1188-5478A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88720673 | |||||||
chr14:88720882 | G | A | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1187+5659C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88720882 | |||||||
chr14:88721249 | G | T | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187+5292C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88721249 | |||||||
chr14:88721348 | G | A | 6 | a0001c0003t0002g0012 a0001c0003t0006g0221 a0001c0003t0013g0298 others(3): Show |
6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1187+5193C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88721348 | |||||||
chr14:88721361 | A | G | 5 | a0001c0001t0008g0102 a0001c0001t0008g0103 a0001c0001t0008g0104 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1187+5180T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88721361 | |||||||
chr14:88721538 | T | C | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.1187+5003A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88721538 | |||||||
chr14:88721568 | G | A | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1187+4973C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88721568 | |||||||
chr14:88721724 | G | T | 2 | a0001c0001t0026g0293 a0001c0001t0026g0294 |
2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1187+4817C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88721724 | |||||||
chr14:88721730 | G | A | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1187+4811C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88721730 | |||||||
chr14:88721990 | G | A | 3 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0220 |
3 | HG02559.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1187+4551C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88721990 | |||||||
chr14:88722076 | G | A | 11 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(8): Show |
11 | HG00642.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1187+4465C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722076 | |||||||
chr14:88722329 | G | C | 1 | a0001c0001t0033g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1187+4212C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722329 | |||||||
chr14:88722331 | A | G | 1 | a0011c0010t0003g0080 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1187+4210T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722331 | |||||||
chr14:88722371 | C | G | 2 | a0001c0001t0010g0032 a0001c0001t0010g0033 |
2 | HG02027.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1187+4170G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722371 | |||||||
chr14:88722553 | G | A | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1187+3988C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722553 | |||||||
chr14:88722565 | G | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1187+3976C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722565 | |||||||
chr14:88722688 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1187+3853G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722688 | |||||||
chr14:88722783 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1187+3758T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722783 | |||||||
chr14:88722825 | A | G | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1187+3716T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722825 | |||||||
chr14:88722944 | A | T | 1 | a0001c0001t0003g0051 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1187+3597T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722944 | |||||||
chr14:88723168 | T | C | 51 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(48): Show |
52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.1187+3373A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88723168 | |||||||
chr14:88723242 | G | A | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1187+3299C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88723242 | |||||||
chr14:88723385 | T | C | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1187+3156A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88723385 | |||||||
chr14:88723533 | G | A | 1 | a0001c0001t0002g0129 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1187+3008C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88723533 | |||||||
chr14:88723534 | C | T | 7 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(4): Show |
8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1187+3007G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88723534 | |||||||
chr14:88723992 | C | T | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1187+2549G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88723992 | |||||||
chr14:88724114 | C | CA | 164 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(161): Show |
167 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1187+2426dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724114 | |||||||
chr14:88724114 | C | CAA | 102 | a0001c0001t0002g0120 a0001c0001t0002g0133 a0001c0001t0006g0285 others(99): Show |
102 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1187+2425_1187+242 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724114 | |||||||
chr14:88724157 | C | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1187+2384G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724157 | |||||||
chr14:88724224 | G | A | 4 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0215 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1187+2317C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724224 | |||||||
chr14:88724273 | C | CA | 8 | a0001c0001t0002g0095 a0001c0001t0002g0098 a0001c0001t0002g0106 others(5): Show |
8 | HG01361.hp2 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1187+2267dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724273 | |||||||
chr14:88724273 | CA | C | 71 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(68): Show |
72 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(69): Show |
intron_variant | MODIFIER | c.1187+2267delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724273 | |||||||
chr14:88724338 | A | C | 5 | a0001c0001t0003g0043 a0001c0001t0003g0052 a0001c0001t0003g0053 others(2): Show |
5 | NA18951.hp2 NA18954.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1187+2203T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724338 | |||||||
chr14:88724382 | T | TAAGAAGA others(309): Show |
3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1187+2158_1187+215 others(320): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724382 | |||||||
chr14:88724569 | T | TA | 98 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(95): Show |
100 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1187+1971dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724569 | |||||||
chr14:88724595 | T | C | 284 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(281): Show |
287 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.1187+1946A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724595 | |||||||
chr14:88724659 | A | G | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1187+1882T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724659 | |||||||
chr14:88724740 | A | C | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187+1801T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724740 | |||||||
chr14:88725059 | T | C | 1 | a0002c0002t0001g0270 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1187+1482A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88725059 | |||||||
chr14:88725213 | G | C | 107 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(104): Show |
109 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1187+1328C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88725213 | |||||||
chr14:88725502 | T | C | 2 | a0001c0001t0019g0212 a0001c0001t0019g0217 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1187+1039A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88725502 | |||||||
chr14:88725652 | G | A | 3 | a0002c0002t0003g0017 a0002c0002t0003g0018 a0002c0002t0003g0092 |
3 | HG01891.hp1 HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1187+889C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88725652 | |||||||
chr14:88725799 | C | A | 1 | a0001c0001t0003g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1187+742G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88725799 | |||||||
chr14:88725908 | A | C | 1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1187+633T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88725908 | |||||||
chr14:88725945 | A | C | 2 | a0001c0001t0026g0293 a0001c0001t0026g0294 |
2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1187+596T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88725945 | |||||||
chr14:88725985 | T | C | 1 | a0001c0003t0002g0012 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1187+556A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88725985 | |||||||
chr14:88726038 | T | C | 51 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(48): Show |
52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.1187+503A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88726038 | |||||||
chr14:88726102 | TTACTC | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1187+434_1187+438d others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88726102 | |||||||
chr14:88726228 | T | C | 1 | a0001c0003t0004g0319 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1187+313A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88726228 | |||||||
chr14:88726472 | A | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1187+69T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88726472 | |||||||
chr14:88726735 | A | C | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1050-57T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88726735 | |||||||
chr14:88726876 | G | C | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(15): Show |
19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1050-198C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88726876 | |||||||
chr14:88726888 | C | T | 2 | a0001c0001t0008g0099 a0001c0001t0008g0100 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1050-210G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88726888 | |||||||
chr14:88726903 | C | T | 3 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0220 |
3 | HG02559.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1050-225G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88726903 | |||||||
chr14:88727038 | T | TTTG | 90 | a0001c0001t0005g0174 a0001c0001t0005g0175 a0001c0001t0017g0010 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1050-363_1050-361d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727038 | |||||||
chr14:88727121 | C | A | 87 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0200 others(84): Show |
87 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1050-443G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727121 | |||||||
chr14:88727367 | T | A | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1050-689A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727367 | |||||||
chr14:88727396 | A | G | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1050-718T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727396 | |||||||
chr14:88727401 | A | AT | 24 | a0001c0001t0003g0056 a0001c0001t0023g0195 a0001c0001t0023g0197 others(21): Show |
24 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1050-724dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727401 | |||||||
chr14:88727401 | A | ATT | 156 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0001 others(153): Show |
159 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1050-725_1050-724d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727401 | |||||||
chr14:88727401 | A | ATTT | 10 | a0001c0001t0001g0283 a0001c0001t0002g0106 a0001c0001t0002g0118 others(7): Show |
10 | HG01109.hp2 HG02040.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1050-726_1050-724d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727401 | |||||||
chr14:88727447 | G | A | 1 | a0005c0014t0001g0272 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1050-769C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727447 | |||||||
chr14:88727598 | A | G | 59 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(56): Show |
60 | HG00408.hp1 HG00642.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1050-920T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727598 | |||||||
chr14:88727796 | C | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1050-1118G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727796 | |||||||
chr14:88727849 | A | C | 1 | a0002c0002t0003g0025 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1050-1171T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727849 | |||||||
chr14:88727918 | G | A | 4 | a0001c0003t0004g0315 a0001c0003t0004g0316 a0001c0003t0004g0317 others(1): Show |
4 | HG02683.hp2 HG03017.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1050-1240C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727918 | |||||||
chr14:88727928 | T | TAAGAATT others(358): Show |
1 | a0001c0001t0002g0147 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1050-1251_1050-125 others(369): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727928 | |||||||
chr14:88728093 | A | C | 1 | a0002c0002t0001g0271 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1050-1415T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728093 | |||||||
chr14:88728200 | C | CT | 259 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0001 others(256): Show |
261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.1050-1523dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728200 | |||||||
chr14:88728211 | T | TG | 7 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(4): Show |
8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1050-1534dupC | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728211 | |||||||
chr14:88728289 | A | G | 1 | a0001c0001t0017g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1050-1611T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728289 | |||||||
chr14:88728321 | TGCACCAG others(6): Show |
T | 99 | a0001c0001t0002g0168 a0001c0001t0017g0010 a0001c0001t0017g0011 others(96): Show |
99 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1050-1656_1050-164 others(17): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728321 | |||||||
chr14:88728334 | A | G | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1050-1656T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728334 | |||||||
chr14:88728608 | T | A | 1 | a0002c0002t0003g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1050-1930A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728608 | |||||||
chr14:88728788 | C | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1050-2110G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728788 | |||||||
chr14:88728834 | A | C | 1 | a0001c0001t0007g0062 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1050-2156T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728834 | |||||||
chr14:88729084 | A | G | 5 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(2): Show |
5 | HG02559.hp1 HG02647.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1050-2406T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729084 | |||||||
chr14:88729088 | C | CAT | 91 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0200 others(88): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1050-2412_1050-241 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729088 | |||||||
chr14:88729474 | T | C | 111 | a0001c0001t0002g0168 a0001c0001t0006g0208 a0001c0001t0014g0004 others(108): Show |
111 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1050-2796A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729474 | |||||||
chr14:88729558 | G | GT | 20 | a0001c0003t0004g0302 a0001c0003t0004g0309 a0001c0003t0004g0311 others(17): Show |
20 | HG00280.hp2 HG02055.hp2 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.1050-2881dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729558 | |||||||
chr14:88729561 | TTTTG | T | 6 | a0001c0003t0002g0012 a0001c0003t0006g0221 a0001c0003t0013g0298 others(3): Show |
6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050-2887_1050-288 others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729561 | |||||||
chr14:88729565 | G | T | 282 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(279): Show |
285 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.1050-2887C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729565 | |||||||
chr14:88729568 | T | G | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1050-2890A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729568 | |||||||
chr14:88729569 | T | G | 4 | a0002c0002t0001g0263 a0002c0002t0001g0278 a0002c0002t0003g0094 others(1): Show |
4 | HG02135.hp1 HG04184.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1050-2891A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729569 | |||||||
chr14:88729569 | T | TG | 6 | a0001c0003t0004g0303 a0001c0003t0004g0304 a0001c0003t0004g0305 others(3): Show |
6 | HG02257.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1050-2892_1050-289 others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729569 | |||||||
chr14:88729572 | G | T | 6 | a0001c0003t0002g0012 a0001c0003t0006g0221 a0001c0003t0013g0298 others(3): Show |
6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050-2894C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729572 | |||||||
chr14:88729577 | T | G | 6 | a0001c0003t0002g0012 a0001c0003t0006g0221 a0001c0003t0013g0298 others(3): Show |
6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050-2899A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729577 | |||||||
chr14:88729685 | G | T | 1 | a0001c0001t0022g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1050-3007C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729685 | |||||||
chr14:88729742 | G | A | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.1050-3064C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729742 | |||||||
chr14:88729857 | G | A | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1050-3179C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729857 | |||||||
chr14:88729866 | T | TTTTC | 182 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(179): Show |
184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.1050-3189_1050-318 others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729866 | |||||||
chr14:88729869 | T | TCTTTG | 12 | a0001c0001t0001g0283 a0001c0001t0002g0087 a0001c0001t0002g0143 others(9): Show |
13 | HG00423.hp2 HG00741.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.1050-3192_1050-319 others(9): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729869 | |||||||
chr14:88729870 | G | C | 74 | a0001c0001t0002g0106 a0001c0001t0002g0121 a0001c0001t0002g0122 others(71): Show |
74 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1050-3192C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729870 | |||||||
chr14:88729870 | G | T | 16 | a0001c0001t0001g0283 a0001c0001t0002g0087 a0001c0001t0002g0143 others(13): Show |
17 | HG00423.hp2 HG00741.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.1050-3192C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729870 | |||||||
chr14:88729871 | T | TTTG | 74 | a0001c0001t0002g0106 a0001c0001t0002g0121 a0001c0001t0002g0122 others(71): Show |
74 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1050-3194_1050-319 others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729871 | |||||||
chr14:88729883 | G | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1050-3205C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729883 | |||||||
chr14:88729976 | C | T | 6 | a0001c0001t0002g0095 a0001c0001t0002g0111 a0001c0001t0002g0112 others(3): Show |
6 | HG01099.hp1 HG01168.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050-3298G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729976 | |||||||
chr14:88730022 | A | C | 1 | a0001c0001t0011g0216 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1050-3344T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730022 | |||||||
chr14:88730045 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1050-3367T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730045 | |||||||
chr14:88730112 | A | G | 1 | a0001c0001t0003g0061 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1050-3434T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730112 | |||||||
chr14:88730120 | T | C | 2 | a0002c0002t0001g0248 a0002c0002t0001g0249 |
2 | HG00438.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1050-3442A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730120 | |||||||
chr14:88730178 | T | C | 1 | a0001c0001t0002g0108 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1050-3500A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730178 | |||||||
chr14:88730473 | T | C | 1 | a0001c0001t0006g0003 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1050-3795A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730473 | |||||||
chr14:88730684 | C | G | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1050-4006G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730684 | |||||||
chr14:88730746 | C | A | 1 | a0001c0001t0003g0037 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1050-4068G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730746 | |||||||
chr14:88730875 | G | A | 91 | a0001c0001t0002g0168 a0001c0001t0017g0010 a0001c0001t0017g0011 others(88): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1050-4197C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730875 | |||||||
chr14:88730904 | T | C | 1 | a0002c0002t0003g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1050-4226A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730904 | |||||||
chr14:88730949 | T | A | 4 | a0001c0003t0004g0315 a0001c0003t0004g0316 a0001c0003t0004g0317 others(1): Show |
4 | HG02683.hp2 HG03017.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1050-4271A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730949 | |||||||
chr14:88731146 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1050-4468G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731146 | |||||||
chr14:88731208 | A | G | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1050-4530T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731208 | |||||||
chr14:88731218 | C | G | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1050-4540G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731218 | |||||||
chr14:88731226 | C | T | 1 | a0002c0002t0003g0029 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1050-4548G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731226 | |||||||
chr14:88731269 | T | A | 1 | a0001c0001t0011g0213 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1050-4591A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731269 | |||||||
chr14:88731315 | C | T | 2 | a0001c0003t0013g0300 a0001c0009t0013g0301 |
2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1050-4637G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731315 | |||||||
chr14:88731316 | A | G | 2 | a0001c0003t0013g0300 a0001c0009t0013g0301 |
2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1050-4638T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731316 | |||||||
chr14:88731324 | G | GT | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1050-4647dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731324 | |||||||
chr14:88731755 | A | G | 1 | a0002c0002t0003g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1049+4609T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731755 | |||||||
chr14:88731809 | C | T | 1 | a0001c0001t0014g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1049+4555G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731809 | |||||||
chr14:88732052 | A | G | 1 | a0001c0001t0009g0058 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1049+4312T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732052 | |||||||
chr14:88732087 | A | G | 24 | a0001c0001t0002g0141 a0001c0001t0005g0173 a0001c0001t0005g0174 others(21): Show |
24 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1049+4277T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732087 | |||||||
chr14:88732126 | G | A | 1 | a0004c0007t0016g0007 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1049+4238C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732126 | |||||||
chr14:88732219 | A | C | 1 | a0001c0001t0001g0280 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1049+4145T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732219 | |||||||
chr14:88732325 | C | T | 4 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0215 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1049+4039G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732325 | |||||||
chr14:88732326 | G | A | 14 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0250 others(11): Show |
14 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1049+4038C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732326 | |||||||
chr14:88732380 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1049+3984C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732380 | |||||||
chr14:88732385 | G | A | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1049+3979C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732385 | |||||||
chr14:88732466 | T | C | 2 | a0001c0001t0005g0173 a0001c0001t0005g0181 |
2 | HG00423.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1049+3898A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732466 | |||||||
chr14:88732540 | G | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1049+3824C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732540 | |||||||
chr14:88732593 | T | C | 1 | a0002c0002t0034g0170 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1049+3771A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732593 | |||||||
chr14:88732888 | G | T | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1049+3476C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732888 | |||||||
chr14:88732917 | A | G | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1049+3447T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732917 | |||||||
chr14:88733085 | A | C | 1 | a0001c0001t0003g0075 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1049+3279T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733085 | |||||||
chr14:88733143 | G | C | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1049+3221C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733143 | |||||||
chr14:88733147 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1049+3217G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733147 | |||||||
chr14:88733203 | T | C | 5 | a0001c0003t0004g0318 a0001c0003t0004g0319 a0001c0003t0004g0322 others(2): Show |
5 | HG00408.hp1 HG03669.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.1049+3161A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733203 | |||||||
chr14:88733668 | C | T | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1049+2696G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733668 | |||||||
chr14:88733681 | A | G | 1 | a0001c0003t0013g0300 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1049+2683T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733681 | |||||||
chr14:88733713 | T | A | 7 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(4): Show |
8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1049+2651A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733713 | |||||||
chr14:88733731 | T | C | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1049+2633A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733731 | |||||||
chr14:88733741 | C | G | 4 | a0001c0001t0003g0043 a0001c0001t0003g0052 a0001c0001t0003g0053 others(1): Show |
4 | NA18954.hp2 NA18959.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1049+2623G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733741 | |||||||
chr14:88733922 | T | C | 1 | a0002c0002t0001g0268 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1049+2442A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733922 | |||||||
chr14:88733959 | TAACAAC | T | 17 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1049+2399_1049+240 others(10): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733959 | |||||||
chr14:88734117 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1049+2247T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88734117 | |||||||
chr14:88734160 | A | G | 27 | a0001c0003t0004g0302 a0001c0003t0004g0303 a0001c0003t0004g0304 others(24): Show |
27 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.1049+2204T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88734160 | |||||||
chr14:88734413 | T | C | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1049+1951A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88734413 | |||||||
chr14:88734423 | T | G | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1049+1941A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88734423 | |||||||
chr14:88734910 | A | G | 3 | a0002c0002t0001g0263 a0002c0002t0003g0094 a0002c0002t0007g0030 |
3 | HG04184.hp2 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1049+1454T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88734910 | |||||||
chr14:88735003 | C | T | 2 | a0001c0001t0019g0212 a0001c0001t0019g0217 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1049+1361G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735003 | |||||||
chr14:88735004 | T | C | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(15): Show |
19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1049+1360A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735004 | |||||||
chr14:88735016 | G | T | 1 | a0001c0001t0036g0196 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1049+1348C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735016 | |||||||
chr14:88735158 | C | T | 1 | a0001c0001t0003g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1049+1206G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735158 | |||||||
chr14:88735292 | T | G | 1 | a0001c0001t0003g0075 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1049+1072A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735292 | |||||||
chr14:88735321 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1049+1043T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735321 | |||||||
chr14:88735430 | A | G | 1 | a0001c0001t0009g0042 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1049+934T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735430 | |||||||
chr14:88735510 | C | T | 1 | a0001c0001t0005g0184 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1049+854G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735510 | |||||||
chr14:88735689 | C | T | 1 | a0007c0015t0007g0079 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1049+675G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735689 | |||||||
chr14:88735734 | G | T | 1 | a0002c0002t0006g0237 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1049+630C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735734 | |||||||
chr14:88736003 | CT | C | 246 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(243): Show |
249 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.1049+360delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88736003 | |||||||
chr14:88736028 | G | C | 1 | a0001c0003t0013g0298 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1049+336C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88736028 | |||||||
chr14:88736073 | G | A | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1049+291C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88736073 | |||||||
chr14:88736087 | G | A | 4 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0215 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1049+277C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88736087 | |||||||
chr14:88736187 | G | T | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1049+177C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88736187 | |||||||
chr14:88736225 | C | T | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1049+139G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88736225 | |||||||
chr14:88736282 | A | G | 1 | a0001c0001t0025g0191 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1049+82T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88736282 | |||||||
chr14:88736695 | G | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.848-130C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88736695 | |||||||
chr14:88736798 | A | G | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(15): Show |
19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.848-233T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88736798 | |||||||
chr14:88736921 | C | T | 1 | a0002c0002t0006g0237 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.848-356G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88736921 | |||||||
chr14:88736950 | G | C | 1 | a0001c0001t0025g0191 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.848-385C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88736950 | |||||||
chr14:88736976 | G | A | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.848-411C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88736976 | |||||||
chr14:88737165 | T | G | 2 | a0001c0003t0004g0302 a0001c0003t0004g0329 |
2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.848-600A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88737165 | |||||||
chr14:88737437 | A | G | 284 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(281): Show |
287 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.848-872T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88737437 | |||||||
chr14:88737569 | T | C | 1 | a0001c0001t0003g0057 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.848-1004A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88737569 | |||||||
chr14:88737650 | T | C | 4 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0035g0198 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.848-1085A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88737650 | |||||||
chr14:88737775 | C | T | 1 | a0002c0002t0001g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.847+1104G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88737775 | |||||||
chr14:88737901 | T | A | 1 | a0002c0002t0003g0027 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.847+978A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88737901 | |||||||
chr14:88738010 | C | T | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.847+869G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88738010 | |||||||
chr14:88738397 | A | AT | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.847+481dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88738397 | |||||||
chr14:88738417 | G | GA | 89 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(86): Show |
89 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.847+461dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88738417 | |||||||
chr14:88738417 | GA | G | 9 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0215 others(6): Show |
9 | HG02040.hp1 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.847+461delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88738417 | |||||||
chr14:88738469 | A | T | 20 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(17): Show |
22 | HG01074.hp2 HG01106.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.847+410T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88738469 | |||||||
chr14:88738864 | T | A | 1 | a0001c0001t0002g0090 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.847+15A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88738864 | |||||||
chr14:88738866 | G | A | 1 | a0001c0001t0002g0090 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.847+13C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88738866 | |||||||
chr14:88739328 | T | C | 1 | a0001c0001t0003g0037 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.712-314A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 5/43 | chr14 | 88739328 | |||||||
chr14:88739899 | A | G | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(15): Show |
19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.711+488T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 5/43 | chr14 | 88739899 | |||||||
chr14:88739942 | G | A | 5 | a0001c0003t0004g0318 a0001c0003t0004g0319 a0001c0003t0004g0322 others(2): Show |
5 | HG00408.hp1 HG03669.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.711+445C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 5/43 | chr14 | 88739942 | |||||||
chr14:88740084 | T | C | 1 | a0001c0001t0003g0169 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.711+303A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 5/43 | chr14 | 88740084 | |||||||
chr14:88740196 | T | C | 6 | a0001c0003t0002g0012 a0001c0003t0006g0221 a0001c0003t0013g0298 others(3): Show |
6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.711+191A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 5/43 | chr14 | 88740196 | |||||||
chr14:88740249 | A | G | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.711+138T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 5/43 | chr14 | 88740249 | |||||||
chr14:88740803 | G | T | 5 | a0001c0001t0009g0042 a0001c0001t0009g0058 a0001c0001t0009g0059 others(2): Show |
5 | HG00738.hp1 HG01358.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-231C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88740803 | |||||||
chr14:88740829 | T | C | 2 | a0001c0003t0004g0318 a0001c0003t0004g0319 |
2 | HG00408.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.526-257A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88740829 | |||||||
chr14:88740862 | C | G | 2 | a0001c0001t0024g0206 a0001c0001t0024g0207 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.526-290G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88740862 | |||||||
chr14:88740977 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.526-405T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88740977 | |||||||
chr14:88741122 | C | T | 91 | a0001c0001t0002g0168 a0001c0001t0017g0010 a0001c0001t0017g0011 others(88): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.526-550G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88741122 | |||||||
chr14:88741142 | G | A | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.526-570C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88741142 | |||||||
chr14:88741176 | T | A | 91 | a0001c0001t0002g0168 a0001c0001t0017g0010 a0001c0001t0017g0011 others(88): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.526-604A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88741176 | |||||||
chr14:88741231 | T | C | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-659A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88741231 | |||||||
chr14:88741404 | A | G | 6 | a0001c0001t0006g0208 a0001c0001t0022g0203 a0001c0001t0022g0204 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-832T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88741404 | |||||||
chr14:88741580 | C | T | 17 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.526-1008G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88741580 | |||||||
chr14:88741826 | A | T | 1 | a0001c0001t0002g0116 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.526-1254T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88741826 | |||||||
chr14:88742169 | T | G | 1 | a0002c0002t0001g0236 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.526-1597A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88742169 | |||||||
chr14:88742210 | A | C | 1 | a0001c0001t0003g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.526-1638T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88742210 | |||||||
chr14:88742365 | T | G | 1 | a0001c0003t0004g0319 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.525+1658A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88742365 | |||||||
chr14:88742535 | A | G | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.525+1488T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88742535 | |||||||
chr14:88742563 | G | A | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.525+1460C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88742563 | |||||||
chr14:88742564 | C | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.525+1459G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88742564 | |||||||
chr14:88742623 | A | G | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.525+1400T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88742623 | |||||||
chr14:88743034 | T | C | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.525+989A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88743034 | |||||||
chr14:88743053 | C | T | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.525+970G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88743053 | |||||||
chr14:88743170 | G | A | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.525+853C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88743170 | |||||||
chr14:88743521 | C | T | 1 | a0001c0001t0003g0057 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.525+502G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88743521 | |||||||
chr14:88743613 | G | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.525+410C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88743613 | |||||||
chr14:88744220 | C | G | 1 | a0001c0001t0003g0055 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.457-129G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744220 | |||||||
chr14:88744245 | A | G | 11 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(8): Show |
11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.457-154T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744245 | |||||||
chr14:88744402 | C | T | 1 | a0002c0002t0003g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.457-311G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744402 | |||||||
chr14:88744463 | C | T | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.457-372G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744463 | |||||||
chr14:88744540 | T | A | 51 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(48): Show |
52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.457-449A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744540 | |||||||
chr14:88744679 | C | T | 1 | a0001c0003t0004g0310 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.457-588G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744679 | |||||||
chr14:88744697 | C | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0002c0002t0006g0237 |
3 | HG02451.hp2 HG02523.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.457-606G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744697 | |||||||
chr14:88744951 | T | C | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(15): Show |
19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.457-860A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744951 | |||||||
chr14:88744976 | A | G | 1 | a0002c0002t0001g0274 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.457-885T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744976 | |||||||
chr14:88745045 | C | T | 1 | a0001c0001t0002g0141 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.457-954G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745045 | |||||||
chr14:88745046 | G | A | 1 | a0002c0002t0001g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.457-955C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745046 | |||||||
chr14:88745047 | G | C | 1 | a0001c0001t0022g0204 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457-956C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745047 | |||||||
chr14:88745163 | G | GTGTTTGT others(1): Show |
8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.456+1021_456+1022i others(10): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745163 | |||||||
chr14:88745167 | T | TTG | 66 | a0001c0001t0003g0047 a0001c0001t0003g0166 a0001c0001t0003g0169 others(63): Show |
66 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.456+1016_456+1017d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745167 | T | TTGTG | 9 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0002c0002t0001g0254 others(6): Show |
9 | HG01515.hp1 HG01952.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.456+1014_456+1017d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745167 | T | TTGTGTG | 4 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0003g0017 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.456+1012_456+1017d others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745167 | T | TTGTTTGT others(3): Show |
15 | a0001c0001t0002g0002 a0001c0001t0002g0086 a0001c0001t0002g0096 others(12): Show |
16 | HG00408.hp2 HG02165.hp2 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(12): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745167 | T | TTGTTTGT others(5): Show |
33 | a0001c0001t0002g0087 a0001c0001t0002g0088 a0001c0001t0002g0089 others(30): Show |
33 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(14): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745167 | T | TTGTTTGT others(7): Show |
11 | a0001c0001t0002g0001 a0001c0001t0002g0116 a0001c0001t0002g0139 others(8): Show |
12 | HG01074.hp2 HG01106.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(16): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745167 | T | TTGTTTGT others(9): Show |
2 | a0001c0001t0002g0095 a0001c0001t0002g0147 |
2 | HG01361.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.456+1017_456+1018i others(18): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745167 | T | TTGTTTGT others(18): Show |
1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.456+1017_456+1018i others(27): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745167 | T | TTGTTTGT others(3): Show |
3 | a0001c0001t0008g0099 a0001c0001t0010g0033 a0001c0003t0004g0310 |
3 | HG02523.hp1 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.456+1017_456+1018i others(12): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745167 | T | TTGTTTGT others(5): Show |
40 | a0001c0001t0006g0188 a0001c0001t0008g0102 a0001c0001t0008g0103 others(37): Show |
40 | HG00544.hp1 HG02055.hp2 HG02135.hp2 others(37): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(14): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745167 | T | TTGTTTGT others(7): Show |
29 | a0001c0001t0002g0106 a0001c0001t0002g0121 a0001c0001t0002g0123 others(26): Show |
29 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(16): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745167 | T | TTGTTTGT others(9): Show |
2 | a0001c0001t0002g0122 a0001c0001t0002g0167 |
2 | HG04115.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.456+1017_456+1018i others(18): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745167 | T | TTGTTTGT others(11): Show |
9 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0168 others(6): Show |
10 | HG01515.hp2 HG01517.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(20): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745167 | T | TTGTTTGT others(13): Show |
10 | a0001c0001t0001g0283 a0001c0001t0006g0284 a0001c0001t0006g0285 others(7): Show |
10 | HG00741.hp2 HG02004.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(22): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745167 | T | TTGTTTGT others(15): Show |
4 | a0001c0001t0006g0286 a0001c0001t0011g0214 a0001c0001t0022g0203 others(1): Show |
4 | HG01256.hp2 HG01884.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(24): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745167 | T | TTGTTTGT others(17): Show |
5 | a0001c0001t0002g0158 a0001c0001t0006g0287 a0001c0001t0011g0215 others(2): Show |
5 | HG01243.hp1 HG01257.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(26): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745167 | T | TTGTTTGT others(21): Show |
1 | a0001c0001t0011g0216 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.456+1017_456+1018i others(30): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745167 | TTG | T | 9 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(6): Show |
9 | HG01074.hp1 HG01175.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.456+1016_456+1017d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | |||||||
chr14:88745171 | G | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.456+1014C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745171 | |||||||
chr14:88745201 | T | C | 1 | a0001c0001t0003g0169 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.456+984A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745201 | |||||||
chr14:88745255 | T | C | 1 | a0002c0002t0003g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.456+930A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745255 | |||||||
chr14:88745456 | T | C | 51 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(48): Show |
52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.456+729A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745456 | |||||||
chr14:88745501 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.456+684T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745501 | |||||||
chr14:88745530 | A | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.456+655T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745530 | |||||||
chr14:88745601 | T | C | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.456+584A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745601 | |||||||
chr14:88745611 | G | T | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.456+574C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745611 | |||||||
chr14:88745629 | C | G | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.456+556G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745629 | |||||||
chr14:88745834 | T | C | 2 | a0001c0001t0019g0212 a0001c0001t0019g0217 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.456+351A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745834 | |||||||
chr14:88745890 | A | C | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.456+295T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745890 | |||||||
chr14:88745903 | G | A | 1 | a0001c0001t0007g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.456+282C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745903 | |||||||
chr14:88745931 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.456+254T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745931 | |||||||
chr14:88746933 | T | G | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.358-650A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88746933 | |||||||
chr14:88746980 | G | A | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.358-697C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88746980 | |||||||
chr14:88747057 | G | C | 2 | a0001c0001t0019g0212 a0001c0001t0019g0217 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.358-774C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747057 | |||||||
chr14:88747061 | T | C | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.358-778A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747061 | |||||||
chr14:88747111 | C | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.358-828G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747111 | |||||||
chr14:88747140 | C | T | 3 | a0002c0002t0001g0232 a0002c0002t0001g0233 a0002c0002t0001g0261 |
3 | NA18947.hp2 NA18962.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.358-857G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747140 | |||||||
chr14:88747213 | A | G | 7 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(4): Show |
8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.358-930T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747213 | |||||||
chr14:88747281 | T | C | 2 | a0001c0001t0003g0036 a0001c0001t0003g0037 |
2 | HG02738.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.358-998A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747281 | |||||||
chr14:88747305 | G | A | 1 | a0002c0002t0003g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.358-1022C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747305 | |||||||
chr14:88747366 | C | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.358-1083G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747366 | |||||||
chr14:88747397 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.358-1114C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747397 | |||||||
chr14:88747420 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.358-1137C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747420 | |||||||
chr14:88747558 | A | G | 1 | a0001c0001t0025g0191 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.358-1275T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747558 | |||||||
chr14:88747661 | A | T | 1 | a0001c0001t0010g0034 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.358-1378T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747661 | |||||||
chr14:88747850 | C | A | 7 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(4): Show |
8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.358-1567G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747850 | |||||||
chr14:88747854 | G | A | 2 | a0001c0001t0002g0109 a0001c0001t0002g0110 |
2 | HG02165.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.358-1571C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747854 | |||||||
chr14:88747887 | G | A | 2 | a0001c0001t0003g0052 a0001c0001t0003g0053 |
2 | NA18959.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.358-1604C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747887 | |||||||
chr14:88747974 | G | T | 11 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(8): Show |
11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.358-1691C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747974 | |||||||
chr14:88747976 | G | C | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.358-1693C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747976 | |||||||
chr14:88748024 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.358-1741C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88748024 | |||||||
chr14:88748054 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.358-1771G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88748054 | |||||||
chr14:88748243 | T | G | 1 | a0001c0003t0020g0172 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.358-1960A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88748243 | |||||||
chr14:88748406 | A | G | 2 | a0001c0001t0017g0010 a0001c0001t0017g0011 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.358-2123T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88748406 | |||||||
chr14:88748567 | G | A | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.358-2284C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88748567 | |||||||
chr14:88748978 | GGA | G | 4 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 others(1): Show |
4 | NA18953.hp2 NA18960.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-2697_358-2696d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88748978 | |||||||
chr14:88749075 | G | A | 1 | a0002c0002t0001g0231 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.358-2792C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88749075 | |||||||
chr14:88749412 | A | G | 1 | a0002c0002t0003g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.358-3129T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88749412 | |||||||
chr14:88749666 | T | C | 77 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(74): Show |
79 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.358-3383A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88749666 | |||||||
chr14:88749711 | T | C | 91 | a0001c0001t0002g0168 a0001c0001t0017g0010 a0001c0001t0017g0011 others(88): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.358-3428A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88749711 | |||||||
chr14:88749850 | T | G | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.358-3567A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88749850 | |||||||
chr14:88749868 | A | G | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.358-3585T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88749868 | |||||||
chr14:88750160 | G | T | 1 | a0001c0001t0003g0055 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.358-3877C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88750160 | |||||||
chr14:88750403 | T | C | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.357+4109A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88750403 | |||||||
chr14:88750459 | C | T | 2 | a0001c0001t0008g0099 a0001c0001t0008g0100 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.357+4053G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88750459 | |||||||
chr14:88750511 | G | A | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.357+4001C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88750511 | |||||||
chr14:88750729 | G | T | 1 | a0004c0007t0016g0007 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.357+3783C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88750729 | |||||||
chr14:88750911 | T | C | 4 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(1): Show |
4 | HG02622.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+3601A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88750911 | |||||||
chr14:88750971 | G | C | 1 | a0002c0002t0001g0229 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.357+3541C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88750971 | |||||||
chr14:88751314 | T | C | 1 | a0001c0003t0006g0221 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.357+3198A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88751314 | |||||||
chr14:88751448 | C | T | 63 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(60): Show |
65 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.357+3064G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88751448 | |||||||
chr14:88751507 | G | GT | 7 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(4): Show |
8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.357+3004dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88751507 | |||||||
chr14:88751581 | G | A | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.357+2931C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88751581 | |||||||
chr14:88751614 | AGAGTT | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.357+2893_357+2897d others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88751614 | |||||||
chr14:88751721 | C | T | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.357+2791G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88751721 | |||||||
chr14:88751918 | T | C | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.357+2594A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88751918 | |||||||
chr14:88752194 | C | A | 1 | a0001c0001t0019g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.357+2318G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88752194 | |||||||
chr14:88752194 | C | G | 266 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(263): Show |
269 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.357+2318G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88752194 | |||||||
chr14:88752240 | T | C | 2 | a0001c0001t0017g0010 a0001c0001t0017g0011 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.357+2272A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88752240 | |||||||
chr14:88752298 | T | C | 1 | a0001c0001t0002g0148 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.357+2214A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88752298 | |||||||
chr14:88752471 | T | C | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.357+2041A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88752471 | |||||||
chr14:88752756 | A | G | 9 | a0001c0001t0002g0087 a0001c0001t0002g0088 a0001c0001t0002g0089 others(6): Show |
9 | HG00423.hp2 HG00609.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.357+1756T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88752756 | |||||||
chr14:88752758 | C | A | 1 | a0001c0001t0002g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.357+1754G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88752758 | |||||||
chr14:88753006 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.357+1506G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88753006 | |||||||
chr14:88753229 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.357+1283G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88753229 | |||||||
chr14:88753302 | G | A | 1 | a0001c0001t0003g0041 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.357+1210C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88753302 | |||||||
chr14:88753788 | C | A | 6 | a0002c0002t0001g0255 a0002c0002t0001g0256 a0002c0002t0001g0257 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.357+724G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88753788 | |||||||
chr14:88753996 | G | A | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.357+516C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88753996 | |||||||
chr14:88754005 | T | C | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.357+507A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88754005 | |||||||
chr14:88754044 | G | A | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.357+468C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88754044 | |||||||
chr14:88754047 | A | G | 91 | a0001c0001t0002g0168 a0001c0001t0017g0010 a0001c0001t0017g0011 others(88): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.357+465T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88754047 | |||||||
chr14:88754151 | T | C | 1 | a0001c0001t0003g0051 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.357+361A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88754151 | |||||||
chr14:88754817 | T | C | 91 | a0001c0001t0002g0168 a0001c0001t0017g0010 a0001c0001t0017g0011 others(88): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.198-146A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88754817 | |||||||
chr14:88754828 | G | C | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(15): Show |
19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.198-157C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88754828 | |||||||
chr14:88754963 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.198-292G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88754963 | |||||||
chr14:88755104 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198-433C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755104 | |||||||
chr14:88755147 | C | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.198-476G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755147 | |||||||
chr14:88755289 | T | C | 17 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.198-618A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755289 | |||||||
chr14:88755478 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198-807G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755478 | |||||||
chr14:88755616 | T | G | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.198-945A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755616 | |||||||
chr14:88755719 | G | A | 1 | a0002c0002t0001g0200 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.198-1048C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755719 | |||||||
chr14:88755724 | G | A | 1 | a0001c0001t0028g0009 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.198-1053C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755724 | |||||||
chr14:88755840 | T | A | 6 | a0001c0001t0006g0208 a0001c0001t0022g0203 a0001c0001t0022g0204 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-1169A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755840 | |||||||
chr14:88755984 | C | T | 11 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(8): Show |
11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.198-1313G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755984 | |||||||
chr14:88756090 | C | G | 4 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0002g0109 others(1): Show |
4 | HG02165.hp2 NA18939.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-1419G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756090 | |||||||
chr14:88756217 | A | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.198-1546T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756217 | |||||||
chr14:88756238 | G | T | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.198-1567C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756238 | |||||||
chr14:88756245 | C | A | 1 | a0002c0002t0003g0024 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.198-1574G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756245 | |||||||
chr14:88756312 | T | A | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.198-1641A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756312 | |||||||
chr14:88756372 | T | C | 6 | a0001c0003t0002g0012 a0001c0003t0006g0221 a0001c0003t0013g0298 others(3): Show |
6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-1701A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756372 | |||||||
chr14:88756416 | T | C | 1 | a0001c0001t0012g0327 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.198-1745A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756416 | |||||||
chr14:88756449 | A | G | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-1778T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756449 | |||||||
chr14:88756537 | A | G | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-1866T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756537 | |||||||
chr14:88756693 | C | T | 51 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(48): Show |
52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.198-2022G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756693 | |||||||
chr14:88756752 | A | C | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-2081T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756752 | |||||||
chr14:88756848 | GAC | G | 11 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(8): Show |
11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.198-2179_198-2178d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756848 | |||||||
chr14:88756870 | A | G | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-2199T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756870 | |||||||
chr14:88756908 | T | C | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(15): Show |
19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.198-2237A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756908 | |||||||
chr14:88756987 | C | T | 284 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(281): Show |
287 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.198-2316G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756987 | |||||||
chr14:88757197 | G | T | 1 | a0001c0001t0014g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.198-2526C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88757197 | |||||||
chr14:88757446 | CA | C | 19 | a0001c0001t0002g0106 a0001c0001t0002g0167 a0001c0001t0006g0208 others(16): Show |
19 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.198-2776delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88757446 | |||||||
chr14:88757714 | C | T | 1 | a0001c0001t0002g0133 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.198-3043G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88757714 | |||||||
chr14:88758019 | A | AT | 92 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0054 others(89): Show |
92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.198-3349dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758019 | |||||||
chr14:88758019 | A | ATT | 9 | a0001c0001t0002g0105 a0002c0002t0001g0209 a0002c0002t0001g0229 others(6): Show |
9 | HG01255.hp1 HG01934.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-3350_198-3349d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758019 | |||||||
chr14:88758019 | AT | A | 36 | a0001c0001t0005g0189 a0001c0001t0024g0207 a0001c0001t0037g0205 others(33): Show |
36 | HG00408.hp1 HG01243.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.198-3349delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758019 | |||||||
chr14:88758057 | A | G | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-3386T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758057 | |||||||
chr14:88758093 | G | C | 176 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(173): Show |
179 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.198-3422C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758093 | |||||||
chr14:88758200 | A | T | 2 | a0002c0002t0001g0229 a0002c0002t0001g0279 |
2 | HG00609.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.198-3529T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758200 | |||||||
chr14:88758319 | A | G | 2 | a0001c0001t0010g0032 a0001c0001t0010g0033 |
2 | HG02027.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.198-3648T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758319 | |||||||
chr14:88758487 | G | A | 4 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0215 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-3816C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758487 | |||||||
chr14:88758744 | C | T | 1 | a0001c0001t0022g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.198-4073G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758744 | |||||||
chr14:88758918 | A | G | 2 | a0001c0001t0002g0091 a0001c0001t0002g0155 |
2 | HG01261.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.198-4247T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758918 | |||||||
chr14:88758959 | C | T | 2 | a0001c0003t0020g0171 a0001c0003t0020g0172 |
2 | NA18939.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.198-4288G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758959 | |||||||
chr14:88759026 | G | A | 4 | a0001c0001t0026g0293 a0001c0001t0026g0294 a0001c0001t0027g0295 others(1): Show |
4 | HG00642.hp2 HG02145.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-4355C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759026 | |||||||
chr14:88759032 | G | A | 11 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(8): Show |
11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.198-4361C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759032 | |||||||
chr14:88759117 | T | C | 1 | a0001c0001t0005g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.198-4446A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759117 | |||||||
chr14:88759147 | G | A | 2 | a0001c0001t0006g0003 a0001c0001t0006g0286 |
3 | HG01256.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.198-4476C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759147 | |||||||
chr14:88759175 | GA | G | 51 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(48): Show |
52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.198-4505delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759175 | |||||||
chr14:88759188 | G | T | 1 | a0002c0004t0001g0228 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.198-4517C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759188 | |||||||
chr14:88759313 | C | T | 7 | a0001c0001t0008g0099 a0001c0001t0008g0100 a0001c0001t0008g0102 others(4): Show |
7 | HG02258.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.198-4642G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759313 | |||||||
chr14:88759453 | G | T | 1 | a0002c0002t0003g0024 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.198-4782C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759453 | |||||||
chr14:88759685 | T | TAAAA | 77 | a0001c0001t0002g0168 a0001c0001t0017g0010 a0001c0001t0017g0011 others(74): Show |
77 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.198-5018_198-5015d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | |||||||
chr14:88759685 | T | TAAAAA | 10 | a0002c0002t0001g0223 a0002c0002t0001g0261 a0002c0002t0001g0270 others(7): Show |
10 | HG02165.hp1 NA18948.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.198-5019_198-5015d others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | |||||||
chr14:88759685 | T | TAAAAAAA | 60 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(57): Show |
62 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.198-5021_198-5015d others(9): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | |||||||
chr14:88759685 | T | TAAAAAAA others(1): Show |
37 | a0001c0001t0002g0087 a0001c0001t0002g0088 a0001c0001t0002g0095 others(34): Show |
37 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.198-5022_198-5015d others(10): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | |||||||
chr14:88759685 | T | TAAAAAAA others(7): Show |
1 | a0001c0001t0019g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.198-5028_198-5015d others(16): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | |||||||
chr14:88759685 | T | TAAAAAAA others(8): Show |
6 | a0001c0001t0006g0287 a0001c0001t0019g0217 a0001c0003t0004g0309 others(3): Show |
6 | HG01257.hp1 HG02922.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-5029_198-5015d others(17): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | |||||||
chr14:88759685 | T | TAAAAAAA others(9): Show |
6 | a0001c0003t0004g0302 a0001c0003t0004g0317 a0001c0003t0004g0320 others(3): Show |
6 | HG02055.hp2 HG02135.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-5030_198-5015d others(18): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | |||||||
chr14:88759685 | T | TAAAAAAA others(10): Show |
7 | a0001c0001t0014g0006 a0001c0003t0002g0012 a0001c0003t0004g0310 others(4): Show |
7 | HG02280.hp2 HG02572.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.198-5031_198-5015d others(19): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | |||||||
chr14:88759685 | T | TAAAAAAA others(11): Show |
6 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0024g0207 others(3): Show |
6 | HG02717.hp2 HG03130.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-5032_198-5015d others(20): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | |||||||
chr14:88759685 | T | TAAAAAAA others(12): Show |
9 | a0001c0001t0024g0206 a0001c0003t0004g0303 a0001c0003t0004g0304 others(6): Show |
9 | HG01884.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.198-5033_198-5015d others(21): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | |||||||
chr14:88759685 | T | TAAAAAAA others(13): Show |
3 | a0001c0003t0004g0306 a0001c0003t0004g0307 a0001c0003t0004g0315 |
3 | HG02257.hp1 HG02622.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.198-5015_198-5014i others(22): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | |||||||
chr14:88759685 | T | TAAAAAAA others(14): Show |
1 | a0001c0003t0004g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.198-5015_198-5014i others(23): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | |||||||
chr14:88759698 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0283 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.198-5028_198-5027i others(18): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | |||||||
chr14:88759698 | A | AAAAAAAA others(8): Show |
6 | a0001c0001t0002g0158 a0001c0001t0006g0003 a0001c0001t0006g0284 others(3): Show |
7 | HG00741.hp2 HG01256.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.198-5028_198-5027i others(17): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | |||||||
chr14:88759698 | A | AAAAAAAA others(7): Show |
3 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0215 |
3 | HG02280.hp1 HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.198-5028_198-5027i others(16): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | |||||||
chr14:88759698 | A | AAAAAAAA others(4): Show |
2 | a0003c0005t0015g0014 a0003c0005t0015g0015 |
2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-5028_198-5027i others(13): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | |||||||
chr14:88759698 | A | AAAAAAAA others(3): Show |
1 | a0003c0005t0015g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.198-5028_198-5027i others(12): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | |||||||
chr14:88759698 | A | AAAAACAA others(7): Show |
5 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(2): Show |
5 | HG02559.hp1 HG02647.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.198-5028_198-5027i others(16): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | |||||||
chr14:88759698 | A | AAAACAAA others(6): Show |
3 | a0001c0001t0022g0203 a0001c0001t0022g0204 a0001c0001t0037g0205 |
3 | HG01243.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.198-5028_198-5027i others(15): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | |||||||
chr14:88759698 | A | AAAACAAA others(5): Show |
2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.198-5028_198-5027i others(14): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | |||||||
chr14:88759698 | A | AC | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-5028_198-5027i others(3): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | |||||||
chr14:88759728 | C | T | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.198-5057G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759728 | |||||||
chr14:88759846 | A | C | 1 | a0001c0001t0033g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.198-5175T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759846 | |||||||
chr14:88759870 | C | T | 1 | a0001c0001t0002g0129 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.198-5199G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759870 | |||||||
chr14:88760343 | G | GTTGT | 239 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(236): Show |
242 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.198-5676_198-5673d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88760343 | |||||||
chr14:88760349 | T | TGTTC | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-5679_198-5678i others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88760349 | |||||||
chr14:88760479 | AC | A | 91 | a0001c0001t0002g0168 a0001c0001t0017g0010 a0001c0001t0017g0011 others(88): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.198-5809delG | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88760479 | |||||||
chr14:88760528 | T | C | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.198-5857A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88760528 | |||||||
chr14:88760800 | G | A | 1 | a0002c0002t0001g0270 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.198-6129C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88760800 | |||||||
chr14:88761205 | T | A | 2 | a0001c0001t0002g0124 a0001c0001t0002g0125 |
2 | NA18943.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.198-6534A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88761205 | |||||||
chr14:88761250 | G | A | 176 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(173): Show |
179 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.198-6579C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88761250 | |||||||
chr14:88761813 | A | G | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.198-7142T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88761813 | |||||||
chr14:88761893 | G | A | 1 | a0001c0001t0006g0202 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.198-7222C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88761893 | |||||||
chr14:88762022 | A | G | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.198-7351T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762022 | |||||||
chr14:88762139 | C | T | 27 | a0001c0003t0004g0302 a0001c0003t0004g0303 a0001c0003t0004g0304 others(24): Show |
27 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.198-7468G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762139 | |||||||
chr14:88762141 | CTCTGATG others(16): Show |
C | 1 | a0001c0001t0036g0196 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.198-7493_198-7471d others(25): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762141 | |||||||
chr14:88762167 | T | C | 1 | a0001c0001t0002g0097 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.198-7496A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762167 | |||||||
chr14:88762171 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198-7500G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762171 | |||||||
chr14:88762225 | C | G | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.198-7554G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762225 | |||||||
chr14:88762328 | C | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198-7657G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762328 | |||||||
chr14:88762366 | G | C | 269 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(266): Show |
272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.198-7695C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762366 | |||||||
chr14:88762672 | T | C | 91 | a0001c0001t0002g0168 a0001c0001t0017g0010 a0001c0001t0017g0011 others(88): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.198-8001A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762672 | |||||||
chr14:88762899 | C | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.198-8228G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762899 | |||||||
chr14:88763005 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.198-8334T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763005 | |||||||
chr14:88763018 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198-8347C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763018 | |||||||
chr14:88763247 | T | C | 5 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(2): Show |
5 | HG02559.hp1 HG02647.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.198-8576A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763247 | |||||||
chr14:88763600 | C | T | 1 | a0002c0002t0001g0282 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.198-8929G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763600 | |||||||
chr14:88763622 | T | C | 1 | a0001c0001t0019g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.198-8951A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763622 | |||||||
chr14:88763628 | A | C | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-8957T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763628 | |||||||
chr14:88763662 | C | T | 1 | a0002c0002t0003g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.198-8991G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763662 | |||||||
chr14:88763894 | C | T | 3 | a0002c0002t0001g0224 a0002c0002t0001g0225 a0002c0002t0001g0226 |
3 | NA18968.hp1 NA18994.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.198-9223G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763894 | |||||||
chr14:88763895 | G | T | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-9224C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763895 | |||||||
chr14:88764020 | A | G | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.198-9349T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88764020 | |||||||
chr14:88764277 | T | C | 4 | a0001c0001t0002g0091 a0001c0001t0002g0155 a0001c0001t0002g0156 others(1): Show |
4 | HG00280.hp1 HG01167.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-9606A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88764277 | |||||||
chr14:88764459 | T | C | 91 | a0001c0001t0002g0168 a0001c0001t0017g0010 a0001c0001t0017g0011 others(88): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.198-9788A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88764459 | |||||||
chr14:88764510 | G | C | 2 | a0001c0003t0020g0171 a0001c0003t0020g0172 |
2 | NA18939.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.198-9839C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88764510 | |||||||
chr14:88764907 | G | A | 2 | a0001c0001t0002g0089 a0001c0001t0002g0090 |
2 | NA19006.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.198-10236C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88764907 | |||||||
chr14:88765102 | T | C | 1 | a0002c0002t0003g0018 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.198-10431A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88765102 | |||||||
chr14:88765121 | TCACAAAT others(3): Show |
T | 91 | a0001c0001t0002g0168 a0001c0001t0017g0010 a0001c0001t0017g0011 others(88): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.198-10460_198-1045 others(14): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88765121 | |||||||
chr14:88765141 | A | G | 1 | a0001c0001t0007g0084 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.198-10470T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88765141 | |||||||
chr14:88765145 | C | T | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.198-10474G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88765145 | |||||||
chr14:88765361 | T | C | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-10690A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88765361 | |||||||
chr14:88765473 | T | C | 1 | a0001c0001t0005g0185 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.198-10802A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88765473 | |||||||
chr14:88765501 | T | C | 91 | a0001c0001t0002g0168 a0001c0001t0017g0010 a0001c0001t0017g0011 others(88): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.198-10830A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88765501 | |||||||
chr14:88765940 | G | C | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.198-11269C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88765940 | |||||||
chr14:88766072 | C | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-11401G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766072 | |||||||
chr14:88766185 | A | G | 17 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.198-11514T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766185 | |||||||
chr14:88766199 | C | T | 2 | a0001c0001t0017g0010 a0001c0001t0017g0011 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.198-11528G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766199 | |||||||
chr14:88766201 | G | A | 1 | a0005c0014t0001g0272 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.198-11530C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766201 | |||||||
chr14:88766225 | T | C | 23 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.198-11554A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766225 | |||||||
chr14:88766286 | C | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.198-11615G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766286 | |||||||
chr14:88766337 | C | A | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-11666G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766337 | |||||||
chr14:88766476 | G | A | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.198-11805C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766476 | |||||||
chr14:88766478 | G | A | 2 | a0001c0001t0019g0212 a0001c0001t0019g0217 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.198-11807C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766478 | |||||||
chr14:88766498 | G | A | 104 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(101): Show |
106 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.198-11827C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766498 | |||||||
chr14:88766509 | T | C | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.198-11838A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766509 | |||||||
chr14:88766533 | G | A | 9 | a0001c0001t0012g0326 a0001c0001t0023g0195 a0001c0001t0023g0197 others(6): Show |
9 | HG00609.hp1 HG00642.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.198-11862C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766533 | |||||||
chr14:88766553 | G | T | 269 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(266): Show |
272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.198-11882C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766553 | |||||||
chr14:88766559 | C | T | 1 | a0001c0001t0005g0180 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.198-11888G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766559 | |||||||
chr14:88766560 | T | A | 2 | a0001c0001t0017g0010 a0001c0001t0017g0011 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.198-11889A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766560 | |||||||
chr14:88766758 | G | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.198-12087C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766758 | |||||||
chr14:88766774 | G | A | 4 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-12103C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766774 | |||||||
chr14:88766956 | T | G | 176 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(173): Show |
179 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.198-12285A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766956 | |||||||
chr14:88767149 | C | A | 1 | a0001c0003t0004g0323 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.198-12478G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88767149 | |||||||
chr14:88767631 | T | C | 1 | a0005c0014t0001g0272 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.198-12960A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88767631 | |||||||
chr14:88767822 | C | T | 11 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(8): Show |
11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.198-13151G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88767822 | |||||||
chr14:88767882 | CA | C | 289 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(286): Show |
292 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.198-13212delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88767882 | |||||||
chr14:88767908 | T | C | 1 | a0001c0001t0014g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.198-13237A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88767908 | |||||||
chr14:88768417 | C | CT | 87 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0200 others(84): Show |
87 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.198-13747dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88768417 | |||||||
chr14:88768485 | G | A | 11 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0006g0218 others(8): Show |
11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.198-13814C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88768485 | |||||||
chr14:88768596 | C | G | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.198-13925G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88768596 | |||||||
chr14:88768748 | C | T | 91 | a0001c0001t0002g0168 a0001c0001t0017g0010 a0001c0001t0017g0011 others(88): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.198-14077G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88768748 | |||||||
chr14:88768875 | G | A | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.198-14204C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88768875 | |||||||
chr14:88769290 | G | A | 1 | a0001c0001t0005g0178 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.198-14619C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769290 | |||||||
chr14:88769343 | C | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.198-14672G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769343 | |||||||
chr14:88769357 | T | G | 91 | a0001c0001t0002g0168 a0001c0001t0017g0010 a0001c0001t0017g0011 others(88): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.198-14686A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769357 | |||||||
chr14:88769538 | A | G | 1 | a0001c0001t0010g0033 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.198-14867T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769538 | |||||||
chr14:88769649 | G | C | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-14978C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769649 | |||||||
chr14:88769830 | T | C | 1 | a0001c0001t0019g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.198-15159A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769830 | |||||||
chr14:88769913 | T | C | 1 | a0001c0001t0009g0076 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.198-15242A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769913 | |||||||
chr14:88769966 | G | GT | 97 | a0001c0001t0002g0140 a0001c0001t0002g0168 a0001c0001t0003g0043 others(94): Show |
97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.198-15296dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769966 | |||||||
chr14:88769983 | G | C | 1 | a0001c0001t0005g0186 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.198-15312C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769983 | |||||||
chr14:88770042 | T | C | 1 | a0001c0001t0005g0187 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.198-15371A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770042 | |||||||
chr14:88770314 | A | G | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.198-15643T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770314 | |||||||
chr14:88770464 | A | G | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.198-15793T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770464 | |||||||
chr14:88770477 | G | C | 2 | a0001c0001t0017g0010 a0001c0001t0017g0011 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.198-15806C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770477 | |||||||
chr14:88770570 | T | A | 1 | a0001c0001t0019g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.198-15899A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770570 | |||||||
chr14:88770745 | A | C | 1 | a0001c0001t0019g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.198-16074T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770745 | |||||||
chr14:88770750 | T | C | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-16079A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770750 | |||||||
chr14:88770766 | T | G | 2 | a0001c0001t0024g0206 a0001c0001t0024g0207 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.198-16095A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770766 | |||||||
chr14:88770820 | C | T | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.198-16149G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770820 | |||||||
chr14:88770984 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.198-16313T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770984 | |||||||
chr14:88771066 | T | C | 1 | a0002c0002t0001g0282 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.198-16395A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88771066 | |||||||
chr14:88771352 | C | G | 1 | a0001c0001t0002g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.198-16681G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88771352 | |||||||
chr14:88771398 | C | T | 8 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(5): Show |
9 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.198-16727G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88771398 | |||||||
chr14:88771493 | C | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198-16822G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88771493 | |||||||
chr14:88771635 | C | T | 1 | a0002c0002t0001g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.198-16964G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88771635 | |||||||
chr14:88771729 | T | C | 51 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(48): Show |
52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.198-17058A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88771729 | |||||||
chr14:88771891 | G | A | 1 | a0002c0002t0001g0274 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.198-17220C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88771891 | |||||||
chr14:88771956 | T | G | 1 | a0001c0001t0003g0041 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.198-17285A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88771956 | |||||||
chr14:88772146 | T | A | 1 | a0002c0002t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.198-17475A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772146 | |||||||
chr14:88772147 | C | T | 1 | a0002c0002t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.198-17476G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772147 | |||||||
chr14:88772149 | T | C | 1 | a0002c0002t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.198-17478A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772149 | |||||||
chr14:88772445 | G | A | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-17774C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772445 | |||||||
chr14:88772448 | C | T | 13 | a0001c0003t0004g0303 a0001c0003t0004g0304 a0001c0003t0004g0305 others(10): Show |
13 | HG02257.hp1 HG02280.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.198-17777G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772448 | |||||||
chr14:88772484 | G | A | 1 | a0001c0001t0035g0198 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.198-17813C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772484 | |||||||
chr14:88772614 | G | T | 17 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.198-17943C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772614 | |||||||
chr14:88772686 | G | A | 1 | a0001c0001t0033g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.198-18015C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772686 | |||||||
chr14:88772835 | C | T | 1 | a0001c0001t0028g0009 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.198-18164G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772835 | |||||||
chr14:88772848 | A | G | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.198-18177T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772848 | |||||||
chr14:88772917 | C | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.198-18246G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772917 | |||||||
chr14:88772969 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198-18298G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772969 | |||||||
chr14:88773101 | T | C | 1 | a0002c0002t0001g0275 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.198-18430A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773101 | |||||||
chr14:88773200 | A | C | 1 | a0002c0002t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.198-18529T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773200 | |||||||
chr14:88773206 | C | T | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-18535G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773206 | |||||||
chr14:88773255 | G | A | 23 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.198-18584C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773255 | |||||||
chr14:88773300 | G | C | 2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | HG01175.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.198-18629C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773300 | |||||||
chr14:88773318 | T | C | 1 | a0001c0001t0017g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.198-18647A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773318 | |||||||
chr14:88773379 | A | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-18708T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773379 | |||||||
chr14:88773639 | C | T | 6 | a0002c0002t0003g0019 a0002c0002t0003g0020 a0002c0002t0003g0021 others(3): Show |
6 | HG02165.hp1 NA18948.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.197+18668G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773639 | |||||||
chr14:88773776 | G | C | 1 | a0001c0001t0002g0128 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.197+18531C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773776 | |||||||
chr14:88773819 | TA | T | 268 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(265): Show |
271 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.197+18487delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773819 | |||||||
chr14:88774093 | G | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.197+18214C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774093 | |||||||
chr14:88774128 | A | G | 5 | a0001c0001t0002g0087 a0001c0001t0002g0088 a0001c0001t0002g0089 others(2): Show |
5 | HG00423.hp2 NA18944.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+18179T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774128 | |||||||
chr14:88774135 | G | A | 5 | a0001c0001t0002g0087 a0001c0001t0002g0088 a0001c0001t0002g0089 others(2): Show |
5 | HG00423.hp2 NA18944.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+18172C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774135 | |||||||
chr14:88774187 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+18120A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774187 | |||||||
chr14:88774216 | T | G | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.197+18091A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774216 | |||||||
chr14:88774242 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+18065C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774242 | |||||||
chr14:88774297 | C | T | 1 | a0001c0001t0005g0178 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.197+18010G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774297 | |||||||
chr14:88774305 | G | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(100): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.197+18002C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774305 | |||||||
chr14:88774412 | C | T | 80 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0200 others(77): Show |
80 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.197+17895G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774412 | |||||||
chr14:88774445 | T | A | 1 | a0002c0002t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.197+17862A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774445 | |||||||
chr14:88774807 | A | G | 4 | a0001c0001t0005g0174 a0001c0001t0005g0175 a0001c0001t0005g0176 others(1): Show |
4 | NA18612.hp1 NA18948.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+17500T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774807 | |||||||
chr14:88774991 | C | T | 1 | a0001c0001t0023g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.197+17316G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774991 | |||||||
chr14:88775235 | G | C | 1 | a0002c0002t0001g0276 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.197+17072C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88775235 | |||||||
chr14:88775243 | T | C | 92 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0017g0010 others(89): Show |
92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.197+17064A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88775243 | |||||||
chr14:88775355 | G | C | 8 | a0001c0001t0023g0195 a0001c0001t0023g0197 a0001c0001t0026g0293 others(5): Show |
8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.197+16952C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88775355 | |||||||
chr14:88775610 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+16697C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88775610 | |||||||
chr14:88775679 | G | A | 1 | a0001c0001t0029g0157 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.197+16628C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88775679 | |||||||
chr14:88775905 | A | AAG | 7 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(4): Show |
8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+16400_197+1640 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88775905 | |||||||
chr14:88775905 | AAGAG | A | 17 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(14): Show |
17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.197+16398_197+1640 others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88775905 | |||||||
chr14:88775996 | G | T | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.197+16311C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88775996 | |||||||
chr14:88776244 | C | T | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.197+16063G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88776244 | |||||||
chr14:88776620 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.197+15687G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88776620 | |||||||
chr14:88776691 | C | T | 174 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(171): Show |
177 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.197+15616G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88776691 | |||||||
chr14:88776718 | C | CA | 173 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(170): Show |
176 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.197+15588dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88776718 | |||||||
chr14:88776942 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+15365A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88776942 | |||||||
chr14:88777247 | C | CA | 176 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(173): Show |
179 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.197+15059dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88777247 | |||||||
chr14:88777437 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+14870G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88777437 | |||||||
chr14:88777487 | T | C | 2 | a0001c0001t0024g0206 a0001c0001t0024g0207 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.197+14820A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88777487 | |||||||
chr14:88777699 | G | A | 90 | a0001c0001t0017g0010 a0001c0001t0017g0011 a0002c0002t0001g0193 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.197+14608C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88777699 | |||||||
chr14:88777703 | A | T | 1 | a0001c0001t0005g0173 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.197+14604T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88777703 | |||||||
chr14:88777897 | C | G | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+14410G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88777897 | |||||||
chr14:88778042 | G | A | 3 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0220 |
3 | HG02559.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.197+14265C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88778042 | |||||||
chr14:88778247 | A | G | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.197+14060T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88778247 | |||||||
chr14:88778387 | G | A | 1 | a0001c0001t0002g0130 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.197+13920C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88778387 | |||||||
chr14:88778519 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+13788C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88778519 | |||||||
chr14:88778759 | C | T | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.197+13548G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88778759 | |||||||
chr14:88778778 | A | AAAAAC | 6 | a0001c0001t0006g0208 a0001c0001t0022g0203 a0001c0001t0022g0204 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.197+13524_197+1352 others(9): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88778778 | |||||||
chr14:88778913 | T | G | 1 | a0007c0015t0007g0079 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.197+13394A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88778913 | |||||||
chr14:88779463 | C | T | 5 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0002c0002t0003g0017 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+12844G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88779463 | |||||||
chr14:88779686 | G | A | 1 | a0001c0001t0014g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.197+12621C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88779686 | |||||||
chr14:88780030 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+12277A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780030 | |||||||
chr14:88780043 | C | T | 51 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(48): Show |
52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.197+12264G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780043 | |||||||
chr14:88780254 | G | A | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.197+12053C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780254 | |||||||
chr14:88780381 | TTTG | T | 176 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(173): Show |
179 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.197+11923_197+1192 others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780381 | |||||||
chr14:88780513 | G | A | 2 | a0001c0001t0002g0129 a0001c0001t0002g0130 |
2 | NA18986.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.197+11794C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780513 | |||||||
chr14:88780573 | C | CT | 8 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(5): Show |
9 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.197+11733dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780573 | |||||||
chr14:88780628 | T | C | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.197+11679A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780628 | |||||||
chr14:88780678 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+11629G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780678 | |||||||
chr14:88780968 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+11339C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780968 | |||||||
chr14:88780975 | T | G | 51 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(48): Show |
52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.197+11332A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780975 | |||||||
chr14:88781188 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+11119A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88781188 | |||||||
chr14:88781518 | C | T | 6 | a0001c0001t0006g0208 a0001c0001t0022g0203 a0001c0001t0022g0204 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.197+10789G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88781518 | |||||||
chr14:88781682 | C | T | 50 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0158 others(47): Show |
51 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(48): Show |
intron_variant | MODIFIER | c.197+10625G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88781682 | |||||||
chr14:88781760 | A | G | 1 | a0001c0001t0009g0042 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.197+10547T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88781760 | |||||||
chr14:88781791 | T | C | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.197+10516A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88781791 | |||||||
chr14:88781900 | C | G | 91 | a0001c0001t0002g0098 a0001c0001t0017g0010 a0001c0001t0017g0011 others(88): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.197+10407G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88781900 | |||||||
chr14:88781941 | G | C | 1 | a0011c0010t0003g0080 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.197+10366C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88781941 | |||||||
chr14:88782099 | T | C | 1 | a0001c0001t0003g0081 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.197+10208A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782099 | |||||||
chr14:88782163 | A | G | 102 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(99): Show |
104 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.197+10144T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782163 | |||||||
chr14:88782176 | A | G | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.197+10131T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782176 | |||||||
chr14:88782193 | G | C | 1 | a0001c0003t0004g0314 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.197+10114C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782193 | |||||||
chr14:88782241 | C | T | 4 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 others(1): Show |
4 | NA18953.hp2 NA18960.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+10066G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782241 | |||||||
chr14:88782246 | C | A | 1 | a0001c0001t0003g0082 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.197+10061G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782246 | |||||||
chr14:88782302 | G | C | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.197+10005C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782302 | |||||||
chr14:88782746 | C | G | 1 | a0001c0001t0003g0036 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.197+9561G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782746 | |||||||
chr14:88782794 | C | T | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.197+9513G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782794 | |||||||
chr14:88782807 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.197+9500G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782807 | |||||||
chr14:88782842 | G | A | 1 | a0002c0002t0001g0222 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.197+9465C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782842 | |||||||
chr14:88782855 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.197+9452C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782855 | |||||||
chr14:88782859 | C | A | 2 | a0004c0007t0016g0007 a0004c0007t0016g0008 |
2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.197+9448G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782859 | |||||||
chr14:88782887 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.197+9420G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782887 | |||||||
chr14:88782888 | G | A | 1 | a0001c0001t0012g0327 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.197+9419C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782888 | |||||||
chr14:88783123 | C | T | 17 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0158 others(14): Show |
18 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.197+9184G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783123 | |||||||
chr14:88783129 | C | T | 1 | a0002c0002t0001g0222 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.197+9178G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783129 | |||||||
chr14:88783130 | G | A | 1 | a0001c0001t0014g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.197+9177C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783130 | |||||||
chr14:88783157 | G | A | 1 | a0001c0001t0008g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.197+9150C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783157 | |||||||
chr14:88783168 | G | A | 1 | a0001c0001t0002g0132 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.197+9139C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783168 | |||||||
chr14:88783411 | C | T | 1 | a0001c0001t0002g0096 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.197+8896G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783411 | |||||||
chr14:88783442 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+8865T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783442 | |||||||
chr14:88783813 | C | T | 1 | a0001c0001t0007g0038 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.197+8494G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783813 | |||||||
chr14:88783858 | A | T | 1 | a0001c0001t0001g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.197+8449T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783858 | |||||||
chr14:88783903 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+8404C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783903 | |||||||
chr14:88784021 | G | A | 14 | a0001c0003t0004g0302 a0001c0003t0004g0315 a0001c0003t0004g0316 others(11): Show |
14 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.197+8286C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88784021 | |||||||
chr14:88784099 | C | G | 1 | a0001c0001t0012g0324 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.197+8208G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88784099 | |||||||
chr14:88784198 | G | C | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.197+8109C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88784198 | |||||||
chr14:88784367 | T | A | 19 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0158 others(16): Show |
20 | HG00544.hp2 HG00741.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.197+7940A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88784367 | |||||||
chr14:88784424 | T | C | 1 | a0001c0001t0002g0133 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.197+7883A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88784424 | |||||||
chr14:88784492 | G | A | 1 | a0001c0001t0007g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.197+7815C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88784492 | |||||||
chr14:88784725 | A | T | 2 | a0001c0006t0003g0161 a0001c0006t0003g0162 |
2 | HG01074.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.197+7582T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88784725 | |||||||
chr14:88784887 | C | T | 27 | a0001c0003t0004g0302 a0001c0003t0004g0303 a0001c0003t0004g0304 others(24): Show |
27 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.197+7420G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88784887 | |||||||
chr14:88785131 | A | T | 1 | a0001c0001t0002g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.197+7176T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88785131 | |||||||
chr14:88785157 | T | C | 4 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+7150A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88785157 | |||||||
chr14:88785230 | G | A | 1 | a0001c0001t0007g0084 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.197+7077C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88785230 | |||||||
chr14:88785369 | T | A | 1 | a0002c0002t0001g0278 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.197+6938A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88785369 | |||||||
chr14:88785738 | AC | A | 33 | a0001c0003t0002g0012 a0001c0003t0004g0302 a0001c0003t0004g0303 others(30): Show |
33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.197+6568delG | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88785738 | |||||||
chr14:88785760 | C | A | 1 | a0001c0001t0007g0085 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.197+6547G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88785760 | |||||||
chr14:88785794 | T | C | 6 | a0001c0001t0002g0002 a0001c0001t0002g0086 a0001c0001t0002g0151 others(3): Show |
7 | NA18960.hp2 NA18968.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.197+6513A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88785794 | |||||||
chr14:88785821 | G | C | 177 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(174): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.197+6486C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88785821 | |||||||
chr14:88786077 | C | T | 51 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(48): Show |
52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.197+6230G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88786077 | |||||||
chr14:88786289 | T | C | 1 | a0001c0003t0002g0012 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.197+6018A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88786289 | |||||||
chr14:88786756 | G | A | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.197+5551C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88786756 | |||||||
chr14:88786848 | C | T | 6 | a0001c0003t0004g0303 a0001c0003t0004g0304 a0001c0003t0004g0305 others(3): Show |
6 | HG02257.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.197+5459G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88786848 | |||||||
chr14:88786903 | T | C | 1 | a0001c0001t0017g0011 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.197+5404A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88786903 | |||||||
chr14:88787141 | C | A | 1 | a0002c0002t0001g0279 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.197+5166G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88787141 | |||||||
chr14:88787291 | T | C | 19 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0086 others(16): Show |
21 | HG01074.hp2 HG01106.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.197+5016A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88787291 | |||||||
chr14:88787294 | G | C | 1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.197+5013C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88787294 | |||||||
chr14:88787527 | T | A | 7 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(4): Show |
8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+4780A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88787527 | |||||||
chr14:88787577 | C | T | 267 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(264): Show |
270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.197+4730G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88787577 | |||||||
chr14:88787687 | C | A | 1 | a0001c0001t0014g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.197+4620G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88787687 | |||||||
chr14:88787783 | T | C | 4 | a0001c0001t0002g0091 a0001c0001t0002g0155 a0001c0001t0002g0156 others(1): Show |
4 | HG00280.hp1 HG01167.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+4524A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88787783 | |||||||
chr14:88787821 | T | C | 7 | a0001c0001t0001g0283 a0001c0001t0002g0158 a0001c0001t0006g0003 others(4): Show |
8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+4486A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88787821 | |||||||
chr14:88788183 | C | CA | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.197+4123dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788183 | |||||||
chr14:88788185 | A | C | 2 | a0001c0003t0004g0302 a0001c0003t0004g0329 |
2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.197+4122T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788185 | |||||||
chr14:88788222 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.197+4085G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788222 | |||||||
chr14:88788245 | C | G | 3 | a0003c0005t0015g0013 a0003c0005t0015g0014 a0003c0005t0015g0015 |
3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.197+4062G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788245 | |||||||
chr14:88788245 | C | T | 9 | a0001c0001t0006g0208 a0001c0001t0014g0004 a0001c0001t0014g0005 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.197+4062G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788245 | |||||||
chr14:88788250 | G | A | 2 | a0002c0002t0001g0288 a0002c0002t0001g0289 |
2 | HG02040.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.197+4057C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788250 | |||||||
chr14:88788422 | A | T | 5 | a0001c0001t0002g0087 a0001c0001t0002g0088 a0001c0001t0002g0089 others(2): Show |
5 | HG00423.hp2 NA18944.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+3885T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788422 | |||||||
chr14:88788536 | TA | T | 19 | a0001c0001t0002g0086 a0001c0001t0006g0208 a0001c0001t0014g0004 others(16): Show |
19 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.197+3770delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788536 | |||||||
chr14:88788786 | G | A | 1 | a0001c0001t0005g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.197+3521C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788786 | |||||||
chr14:88788829 | G | A | 2 | a0001c0001t0002g0159 a0001c0001t0002g0160 |
2 | NA18954.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.197+3478C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788829 | |||||||
chr14:88788898 | GA | G | 259 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0283 others(256): Show |
262 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.197+3408delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788898 | |||||||
chr14:88788898 | GAA | G | 9 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.197+3407_197+3408d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788898 | |||||||
chr14:88788980 | C | T | 269 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(266): Show |
272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.197+3327G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788980 | |||||||
chr14:88789070 | A | G | 2 | a0001c0001t0005g0179 a0001c0001t0005g0182 |
2 | NA18983.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.197+3237T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88789070 | |||||||
chr14:88789447 | C | CACTGAGA others(104): Show |
13 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 others(10): Show |
13 | HG00642.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.197+2749_197+2859d others(113): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88789447 | |||||||
chr14:88789447 | C | CACTGAGA others(326): Show |
1 | a0001c0001t0001g0199 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.197+2527_197+2859d others(335): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88789447 | |||||||
chr14:88789447 | CACTGAGA others(104): Show |
C | 101 | a0001c0001t0001g0283 a0001c0001t0001g0290 a0001c0001t0002g0001 others(98): Show |
104 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.197+2749_197+2859d others(2): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88789447 | |||||||
chr14:88789447 | CACTGAGA others(215): Show |
C | 1 | a0001c0001t0002g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.197+2638_197+2859d others(2): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88789447 | |||||||
chr14:88790536 | T | G | 1 | a0001c0003t0004g0329 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.197+1771A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88790536 | |||||||
chr14:88790782 | A | T | 3 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 |
3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.197+1525T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88790782 | |||||||
chr14:88790843 | T | C | 94 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0280 others(91): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.197+1464A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88790843 | |||||||
chr14:88790928 | T | C | 1 | a0002c0002t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.197+1379A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88790928 | |||||||
chr14:88791033 | C | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+1274G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88791033 | |||||||
chr14:88791086 | CTT | C | 28 | a0001c0001t0012g0324 a0001c0001t0012g0325 a0001c0001t0012g0326 others(25): Show |
28 | HG00408.hp1 HG00609.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.197+1219_197+1220d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88791086 | |||||||
chr14:88791249 | G | A | 11 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 others(8): Show |
11 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.197+1058C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88791249 | |||||||
chr14:88791356 | C | T | 11 | a0001c0001t0014g0004 a0001c0001t0014g0005 a0001c0001t0014g0006 others(8): Show |
11 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.197+951G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88791356 | |||||||
chr14:88791917 | G | C | 1 | a0001c0001t0003g0169 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.197+390C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88791917 | |||||||
chr14:88791986 | A | G | 2 | a0002c0002t0001g0193 a0002c0002t0001g0194 |
2 | NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.197+321T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88791986 | |||||||
chr14:88792139 | G | C | 1 | a0002c0002t0021g0292 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.197+168C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88792139 | |||||||
chr14:88792269 | C | T | 54 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(51): Show |
54 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.197+38G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88792269 |